Answer the following questions as per bds 3rd year oriented for university exam pattern of general surgery: Question for gs Long questions 1. Fistula in ano – etiology, classification, management 2. Hypovolemic shock (most asked) 3. Fluid therapy in burns (Parkland formula) 4. Mandibular fractures: classification + management * Principles of fracture healing 5. Oral cancer: etiology, clinical features, staging, management 6. Precancerous lesions (leukoplakia, OSMF) 7. Approach to a swelling (inspection, palpation) 8. Classification of tumors 9. Goiter classification + management 10. Lymphadenopathy approach 11. Types of head injury * Extradural vs subdural hematoma 12. Carcinoma larynx 13. Hyperthyroidism Short questions: * Stages of shock * Cross matching * Massive transfusion * Le Fort fractures * Complications of fractures * Immobilization methods * TNM staging * Biopsy in oral cancer * Benign vs malignant tumor * Signs of malignancy * Cyst vs tumor * Lymph node examination * Sialolithiasis * Parotid swelling causes * Facial nerve in parotid surgery * Thyroid swelling examination * Complications of thyroidectomy * Tubercular lymphadenitis * Hodgkin vs Non-Hodgkin * Glasgow coma scale * Concussion * Tonsillitis * Indications of tonsillectomy * Dehydration * IV fluids * Electrolyte imbalance * Acidosis vs alkalosis * ABG basics * TB * HIV basics * Ulnar nerve injury * Wrist drop * Common surgical specimens * Sutures & Needles Types,Absorbable vs non-absorbable * Local anesthesia basics,Complications * Types of biopsy ,Indications

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I have the library available. Given the very large scope of this request (30+ topics), I'll deliver this as a comprehensive, well-structured exam guide from my medical knowledge, supplemented by the textbooks available. Let me now produce the full answer.

BDS 3rd Year - General Surgery: Complete Exam Guide


LONG QUESTIONS


1. Fistula in Ano

Etiology

A fistula-in-ano is an abnormal communication between the anal canal/rectum and the perianal skin. It is almost always the result of a previous anorectal abscess that drained spontaneously or was surgically drained but did not heal completely.
Causes:
  • Cryptoglandular (most common ~90%): Infection of the anal glands (located at the dentate line) spreads through the intersphincteric plane
  • Specific infections: Tuberculosis, Crohn's disease, actinomycosis
  • Trauma: Foreign bodies, injury
  • Malignancy: Carcinoma of rectum/anal canal
  • Radiation: Post-radiotherapy fistulas
  • Obstetric injury

Classification (Parks Classification - Most Important)

Based on the relationship of the fistula tract to the sphincter complex:
TypeDescriptionFrequency
IntersphinctericPasses through internal sphincter only, tracks downward between sphincters~70% (most common)
TranssphinctericCrosses both internal and external sphincters~25%
SuprasphinctericGoes above puborectalis, loops over it~5%
ExtrasphinctericCompletely outside sphincter mechanism~1% (rarest)
Goodsall's Rule: Helps predict internal opening - fistulas with external opening anterior to transverse anal line open directly into the anal canal; those posterior to the line have a curved tract opening at the posterior midline of the anal canal.

Management

Principles - Must NOT damage sphincters (risk of incontinence)
Surgical options:
  1. Fistulotomy (Lay-open): Opening the entire fistula tract - for low, simple intersphincteric fistulas; most common procedure
  2. Fistulectomy: Complete excision of the tract (higher risk of incontinence if high fistula)
  3. Seton placement:
    • Cutting seton: Gradually tightens, cuts through sphincter slowly (fibrous reaction forms around it)
    • Draining seton: Controls sepsis while awaiting definitive surgery
  4. Advancement flap: Mucosal or anodermal flap to cover internal opening - for high complex fistulas
  5. LIFT procedure (Ligation of Intersphincteric Fistula Tract): Sphincter-preserving; ligates and divides the tract at the intersphincteric plane
  6. Fibrin glue/collagen plug: Minimally invasive; lower success rates
Key point for BDS exam: Low fistulas (intersphincteric) - fistulotomy is standard. High fistulas (supra/extrasphincteric) - seton or advancement flap to preserve continence.

2. Hypovolemic Shock (Most Asked)

Definition

Hypovolemic shock is circulatory failure due to inadequate circulating blood volume, leading to tissue hypoperfusion and cellular hypoxia.

Etiology

  • Hemorrhagic: Trauma, GI bleed, ruptured aortic aneurysm, ectopic pregnancy
  • Non-hemorrhagic: Burns (plasma loss), severe diarrhea/vomiting, diabetic ketoacidosis (dehydration), peritonitis (third-spacing)

Pathophysiology

Volume loss → decreased venous return (preload) → decreased cardiac output → decreased tissue perfusion → compensatory mechanisms activate:
  • Sympathetic activation: tachycardia, vasoconstriction
  • RAAS activation: sodium and water retention
  • ADH release: water retention
  • If not corrected: cellular ischemia → SIRS → MODS → death

Classification/Stages of Shock (ATLS - 4 Classes)

ParameterClass IClass IIClass IIIClass IV
Blood loss (mL)Up to 750750-15001500-2000>2000
Blood loss (%)Up to 15%15-30%30-40%>40%
HR<100100-120120-140>140
BPNormalNormalDecreasedVery low
Pulse pressureNormal/↑DecreasedDecreasedDecreased
RR14-2020-3030-40>35
Urine output (mL/hr)>3020-305-15Negligible
CNS/Mental statusSlightly anxiousMildly anxiousConfusedLethargic/unconscious
Fluid replacementCrystalloidCrystalloidCrystalloid + bloodBlood + crystalloid
Exam tip: Class I and II - BP maintained (compensated shock). Class III onward - BP falls (decompensated).

Management

Immediate (ABCDE approach):
  1. Airway + Oxygen
  2. Two large-bore IV lines (14-16G in antecubital fossae)
  3. IV fluid resuscitation: 2 liters Ringer's Lactate bolus (or Normal Saline)
  4. Blood transfusion if inadequate response (for hemorrhagic shock)
  5. Identify and control source of hemorrhage (pressure, tourniquet, surgical control)
  6. Monitor: HR, BP, urine output (target >0.5 mL/kg/hr), CVP
  7. Vasopressors (dopamine, norepinephrine) only if volume is adequate but BP remains low
Monitoring response: "3-for-1 rule" - give 3 mL crystalloid for every 1 mL estimated blood loss.
Types of Responders:
  • Rapid responder: Responds to initial bolus and stays stable - blood loss <20%
  • Transient responder: Responds initially but deteriorates - ongoing bleeding
  • Non-responder: No response - massive ongoing hemorrhage, needs emergency surgery

3. Fluid Therapy in Burns (Parkland Formula)

Initial Assessment

Rule of Nines (Wallace) for estimating TBSA (Total Body Surface Area) burned:
AreaAdultsChildren (9's modified)
Head + Neck9%18% (0-1yr)
Each arm9%9%
Trunk (ant)18%18%
Trunk (post)18%18%
Each leg18%14%
Perineum1%1%
Lund and Browder chart - more accurate for children (accounts for age-related head/leg variation)

Parkland Formula (Most Important)

Formula: 4 mL × Body Weight (kg) × % TBSA burned (2nd + 3rd degree only)
  • Fluid used: Ringer's Lactate (Hartmann's solution)
  • First 8 hours: Give HALF of total calculated volume (time calculated from time of burn, NOT time of arrival)
  • Next 16 hours: Give remaining HALF
Example: 70 kg patient with 30% TBSA burns
  • Total = 4 × 70 × 30 = 8,400 mL in first 24 hours
  • First 8 hours: 4,200 mL
  • Next 16 hours: 4,200 mL
Day 2 onwards: Colloids (albumin, FFP) and 5% dextrose in water are added. No standard formula - guided by clinical response.

Modified Brooke Formula

2 mL × Weight × % TBSA = total RL in 24 hrs (less fluid)

Monitoring Adequacy

  • Urine output: 0.5-1 mL/kg/hr in adults (best indicator); 1 mL/kg/hr in children
  • Inhalation injury: Add 30-50% to calculated volume
  • Electrical burns: Target urine output 1-1.5 mL/kg/hr (myoglobinuria risk)

Important Points

  • Burns <15% TBSA (adult) or <10% (child) - may manage with oral fluids
  • Don't count 1st degree (superficial/epidermal) burns
  • Fluid overload risk: Abdominal compartment syndrome, pulmonary edema

4. Mandibular Fractures: Classification + Management

Classification

By Location:
  1. Symphysis/Parasymphysis - midline and 1 cm lateral
  2. Body - between canine and angle
  3. Angle - at the gonial angle (third molar region) - most common
  4. Ramus - vertical part
  5. Condyle - most common in children; subcondylar most frequent
  6. Coronoid process - rare
  7. Alveolar process
By Fracture Pattern:
  • Simple (closed), Compound (open into oral cavity), Comminuted, Pathological, Greenstick (children)
By Favorability (Kazanjian classification):
  • Favorable: Muscle pull tends to reduce/maintain the fracture
  • Unfavorable: Muscle pull tends to displace the fracture

Clinical Features

  • Pain, swelling, trismus
  • Malocclusion (most reliable sign)
  • Step deformity at fracture site
  • Anesthesia/paresthesia of lower lip (inferior alveolar nerve injury)
  • Intraoral laceration, hematoma in floor of mouth
  • Abnormal mobility of fragments

Management

Principles of Fracture Management (4 R's):
  1. Resuscitation - airway, hemorrhage control
  2. Reduction - restore normal anatomy
  3. Retention (fixation) - maintain reduction
  4. Rehabilitation
Methods:
1. Closed Reduction + Intermaxillary Fixation (IMF/MMF):
  • Arch bars + wiring (Erich arch bar system)
  • Used for: Simple, minimally displaced fractures, condylar fractures (especially in children)
  • Duration: 4-6 weeks
  • Disadvantage: Patient cannot eat normally; airway concerns
2. Open Reduction Internal Fixation (ORIF):
  • Plates and screws (miniplates - Champy's technique)
  • Indications: Displaced fractures, comminuted, failed closed reduction, bilateral fractures, edentulous patients, condylar fractures with significant displacement
  • Approach: Intraoral or extraoral (submandibular incision for angle/body)
  • Champy's lines of osteosynthesis: Single miniplate along the oblique line for angle fractures; two miniplates at symphysis
3. External Fixation:
  • Rarely used; for highly comminuted or infected fractures
Condylar Fractures: Mostly managed conservatively with IMF + early mobilization. Surgery for displacement into middle cranial fossa, open joint injury, or gross displacement in adults.

Principles of Fracture Healing

Primary (Direct) Healing

  • Requires rigid fixation with compression plates
  • Direct bone formation without callus
  • Cutting cones (osteoclasts) traverse the fracture line, followed by osteoblasts

Secondary (Indirect) Healing - More common

Stages:
  1. Hematoma formation (0-48 hrs): Bleeding fills fracture gap; fibrin clot forms; inflammatory mediators released
  2. Inflammatory phase (days 1-5): Granulation tissue replaces clot; macrophages, neutrophils; vasodilation
  3. Soft callus stage (weeks 1-3): Fibroblasts and chondroblasts produce fibrocartilaginous callus; bridging between fragments
  4. Hard callus stage (weeks 3-12): Cartilage calcifies and ossifies; woven bone replaces fibrocartilage
  5. Remodeling (months to years): Woven bone replaced by lamellar bone; medullary canal restored; follows Wolff's law

Factors Affecting Healing

Local: Severity of injury, blood supply, infection, soft tissue interposition, movement at fracture site, bone loss Systemic: Age (children heal faster), nutritional status (Vit C, D, Ca, protein), steroids, diabetes, osteoporosis, malignancy

5. Oral Cancer: Etiology, Clinical Features, Staging, Management

Etiology

  • Tobacco (smoking + smokeless/chewing) - most important
  • Alcohol (synergistic with tobacco - 15x risk)
  • Betel nut (areca nut) chewing - particularly relevant in India/South Asia
  • HPV 16 and 18 (oropharyngeal cancers, especially tonsillar/base of tongue)
  • Chronic irritation: Ill-fitting dentures, jagged teeth
  • Poor oral hygiene
  • Sunlight (lip cancer)
  • Nutritional deficiency: Iron deficiency (Plummer-Vinson syndrome predisposes), Vitamins A/C/E
  • Pre-existing precancerous lesions (leukoplakia, erythroplakia, OSMF)
  • Immune suppression

Histology

  • Squamous cell carcinoma (SCC) - 95% of oral cancers
  • Other: Adenocarcinoma (salivary glands), mucoepidermoid carcinoma, verrucous carcinoma

Clinical Features

Early:
  • Non-healing ulcer (>2 weeks) - most important warning sign
  • White or red patch that cannot be scraped off
  • Painless initially; pain is a late feature
Late:
  • Irregular, indurated (hard) ulcer with everted/raised edges
  • Restricted mouth opening (trismus) - involvement of masticatory muscles
  • Referred otalgia (ear pain via auriculotemporal nerve)
  • Cervical lymphadenopathy (hard, fixed nodes)
  • Loose teeth, altered speech, dysphagia
  • Bleeding from lesion

Staging (TNM + AJCC)

T Stage (Primary Tumor):
StageDescription
T1≤2 cm
T22-4 cm
T3>4 cm
T4aModerately advanced local disease (invades adjacent structures like cortical bone, floor of mouth, skin)
T4bVery advanced (masticator space, pterygoid plates, skull base, carotid)
N Stage (Nodes):
StageDescription
N0No nodes
N1Single ipsilateral node ≤3 cm
N2aSingle ipsilateral node 3-6 cm
N2bMultiple ipsilateral nodes, none >6 cm
N2cBilateral or contralateral nodes, none >6 cm
N3Node >6 cm
M Stage: M0 = no distant mets; M1 = distant mets present
Overall Stage:
  • Stage I: T1N0M0
  • Stage II: T2N0M0
  • Stage III: T3N0 or T1-3N1
  • Stage IV: T4 or N2-3 or M1

Management

Biopsy first - incisional biopsy (not excisional for large lesions)
Treatment by stage:
StageTreatment
Early (I, II)Surgery OR radiotherapy alone
Advanced (III, IVA)Surgery + adjuvant radiotherapy (± chemotherapy)
Stage IVB/IVCChemoradiation or palliative
Surgery:
  • Wide local excision with 1-1.5 cm margins
  • Neck dissection: Radical, modified radical, or selective (for N+ or N0 with >20% occult node risk)
  • Reconstruction: Primary closure, local flaps, regional flaps (pectoralis major), free flaps (radial forearm, fibula for jaw)
Radiotherapy: External beam RT; brachytherapy for tongue cancers
Chemotherapy (adjuvant): Cisplatin-based for high-risk features (positive margins, extracapsular spread, perineural/vascular invasion)

6. Precancerous Lesions

Leukoplakia

Definition: "A white patch on the mucous membrane which cannot be scraped off and cannot be attributed to any other disease." (WHO) - Diagnosis of exclusion.
Etiology: Tobacco (most common), alcohol, chronic irritation, Candida infection, syphilis (syphilitic leukoplakia has high malignant potential), HPV
Clinical Types:
  • Homogeneous: Uniform white, flat, well-defined - lowest malignant potential (~5%)
  • Non-homogeneous:
    • Nodular (speckled): Mixed white and red patches
    • Verrucous: Thick, warty surface
    • Erythroleukoplakia: Red and white mixed - highest malignant potential (~40%)
Histology (Grading):
  • Hyperkeratosis without dysplasia
  • Mild, moderate, severe dysplasia (carcinoma in situ)
  • SCC
Malignant transformation rate: ~5-6% overall; erythroplakia much higher (~40%)
Management:
  • Remove causative agent (stop tobacco/alcohol)
  • Biopsy mandatory
  • Small lesions: Surgical excision
  • Larger: Laser ablation (CO2 laser), cryotherapy
  • Vitamin A analogues (retinoids) - medical management
  • Regular follow-up

Oral Submucous Fibrosis (OSMF)

Definition: Chronic, insidious disease affecting the oral mucosa (and sometimes pharynx and esophagus), characterized by juxta-epithelial inflammatory reaction and progressive fibrosis of the submucosal tissues.
Etiology:
  • Areca nut (betel nut) chewing - primary cause
  • Arecoline (alkaloid in areca nut) stimulates fibroblasts, increases collagen production, inhibits collagenase
  • Genetic predisposition (HLA associations)
  • Nutritional deficiency (iron, B vitamins)
  • Autoimmune component (antinuclear antibodies)
Clinical Features:
  • Burning sensation in mouth (early) - especially with spicy food
  • Blanching and stiffness of oral mucosa
  • Trismus (restricted mouth opening) - hallmark symptom; fibrotic bands palpable in buccal mucosa
  • Palpable fibrous bands
  • Depapillation of tongue
  • Uvula may become small and pale
Grading (Khanna & Andrade):
GradeFeatures
IBurning, hypersalivation, early blanching
IIBlanching, fibrous bands, mouth opening 26-35 mm
IIIStiff mucosa, mouth opening 15-25 mm, early dysplasia
IVAMouth opening <15 mm, moderate dysplasia
IVBSevere dysplasia or carcinoma in situ
Malignant Transformation: ~7-13% lifetime risk (considered an obligate precancerous condition)
Management:
  • Cessation of areca nut/betel quid chewing - essential
  • Medical:
    • Corticosteroid injections (intralesional triamcinolone) - reduces inflammation
    • Hyaluronidase injections
    • Lycopene, beta-carotene (antioxidants)
    • Vitamins A, C, E, B complex
    • Iron supplements
    • Pentoxifylline (vasodilator, reduces fibrosis)
  • Surgical (for severe trismus):
    • Release of fibrous bands + split-thickness skin graft
    • Buccal fat pad grafting
    • Nasolabial flap
  • Physiotherapy (mouth exercises after surgery)

7. Approach to a Swelling (Clinical Examination)

Inspection

S - Site: Exact anatomical location S - Size: Approximate dimensions S - Shape: Regular, irregular, lobulated S - Surface: Smooth, nodular, bosselated S - Skin over swelling: Normal, tethered, stretched, ulcerated, erythematous, puckered ("peau d'orange" in breast cancer), dilated veins S - Swelling: Confirm it is indeed a swelling S - Spontaneous pulsations: Expansile pulsations suggest vascular lesion S - Scars: Previous surgery/trauma

Palpation

  1. Temperature: Warm (inflammatory/vascular), cold (ischemia)
  2. Tenderness: Presence, degree, site
  3. Size: More precise measurement
  4. Surface: Smooth or irregular; lobulated
  5. Edge/Border: Well-defined (cyst, lipoma) vs. ill-defined (infiltrating carcinoma)
  6. Consistency:
    • Soft (lipoma, abscess)
    • Firm (fibroma, lymph node)
    • Hard (bone, calcified)
    • Fluctuant (fluid-filled - cyst, abscess)
    • Rubbery (lymphoma)
    • Stony hard (malignancy, calcified)
  7. Reducibility: Can the swelling be reduced (hernia, varicocele)?
  8. Compressibility: Blood/lymph can be compressed temporarily (hemangioma, lymphangioma)
  9. Pulsatility:
    • Transmitted pulsations (overlying an artery)
    • Expansile pulsations (aneurysm - pushes fingers apart in two planes)
  10. Transillumination: Fluid-filled, thin-walled cysts transilluminate (e.g., hydrocele, lymphangioma)
  11. Plane of swelling: Skin, subcutaneous, deep fascia, muscle, bone
  12. Mobility/Fixity: Free, tethered to skin, fixed to underlying structures
  13. Regional lymph nodes: Always examine
  14. Relation to underlying/overlying structures
  15. Special tests: Fluctuation test, fluid thrill, slip sign (lipoma), etc.

8. Classification of Tumors

By Behavior

TypeBenignMalignant
CapsuleWell-encapsulatedPoorly defined/none
GrowthSlow, expansileRapid, infiltrative
MarginsWell-definedIll-defined
DifferentiationWell-differentiatedPoorly differentiated
MitosisRare, normalFrequent, atypical
MetastasisNonePresent
RecurrenceRare after excisionCommon
Effect on hostUsually noneCachexia, death
NucleiNormal N:C ratioHigh N:C ratio, pleomorphism
NecrosisAbsentOften present

By Tissue of Origin (Histogenesis)

TissueBenignMalignant
Squamous epitheliumPapillomaSquamous cell carcinoma
Glandular epitheliumAdenomaAdenocarcinoma
Fibrous tissueFibromaFibrosarcoma
FatLipomaLiposarcoma
Muscle (smooth)LeiomyomaLeiomyosarcoma
Muscle (striated)RhabdomyomaRhabdomyosarcoma
BoneOsteomaOsteosarcoma
CartilageChondromaChondrosarcoma
Blood vesselsHemangiomaAngiosarcoma
Lymphoid-Lymphoma
Nerve sheathNeurofibroma/SchwannomaNeurofibrosarcoma
MelanocytesNevusMelanoma
Hematopoietic-Leukemia

Special Types

  • Teratoma: From all 3 germ layers (totipotent cells)
  • Hamartoma: Disorganized but normal tissue elements for that site
  • Choristoma: Normal tissue in abnormal location
  • Carcinoid: Neuroendocrine tumor (low-grade malignant)

9. Goiter: Classification + Management

Definition

Goiter = any enlargement of the thyroid gland, regardless of cause.

Classification

Etiological:
  1. Physiological: Puberty, pregnancy
  2. Simple/Colloid (Non-toxic):
    • Endemic goiter (iodine deficiency - most common cause worldwide)
    • Sporadic
  3. Toxic Goiter:
    • Diffuse toxic (Graves' disease)
    • Toxic multinodular goiter
    • Toxic adenoma (Plummer's disease)
  4. Autoimmune:
    • Hashimoto's thyroiditis (hypothyroid)
    • Graves' disease (hyperthyroid)
  5. Inflammatory: De Quervain's (subacute), Riedel's (fibrous)
  6. Neoplastic:
    • Benign: Follicular adenoma
    • Malignant: Papillary, Follicular, Medullary, Anaplastic carcinoma
By size:
  • Grade 0: Not visible or palpable
  • Grade 1: Palpable but not visible
  • Grade 2: Visible and palpable
By morphology:
  • Diffuse (uniform enlargement)
  • Nodular (single/multinodular)

Thyroid Swelling Examination (Salient Points)

  • Moves with swallowing - key feature (attached to pretracheal fascia)
  • Pemberton's sign: Facial congestion on raising arms above head - SVC obstruction by goiter
  • Berry's sign: Absence of carotid pulsation behind goiter
  • Kocher's test: Trachea compression test

Management

Simple Non-toxic Goiter:
  • Small: Reassure; levothyroxine to suppress TSH
  • Iodine supplementation (endemic)
  • Surgery: For pressure symptoms, cosmesis, large goiter, suspected malignancy
Toxic Goiter (Hyperthyroidism):
  1. Antithyroid drugs (Carbimazole/Propylthiouracil):
    • First-line in Graves' disease; block thyroid peroxidase
    • Propranolol (beta-blocker) for symptom control
  2. Radioactive Iodine (RAI - I-131):
    • Preferred definitive treatment in adults
    • Destroys thyroid tissue
    • Contraindicated in pregnancy/children
  3. Surgery (Total/Near-total thyroidectomy):
    • Indications: Large goiter with pressure symptoms, failed medical therapy, pregnancy, young patients, suspected malignancy, cosmesis
Thyroid Cancer:
  • Papillary (most common, best prognosis): Total thyroidectomy + RAI ablation
  • Follicular: Total thyroidectomy + RAI
  • Medullary: Total thyroidectomy + neck dissection (no RAI useful)
  • Anaplastic (worst prognosis): Palliative; chemotherapy/radiotherapy

10. Lymphadenopathy - Approach

Causes (mnemonic MINT-CRAP)

M - Malignancy (lymphoma, leukemia, metastases) I - Infection (TB, EBV, HIV, bacterial) N - Normal variant (reactive nodes) T - Trauma C - Connective tissue diseases (SLE, RA) R - Reaction (drug reaction - phenytoin) A - Autoimmune P - Parasites

Clinical Approach

History:
  • Duration, associated fever, weight loss, night sweats (B symptoms of lymphoma)
  • Sore throat, dental problems, scalp lesions
  • Risk factors: TB contact, HIV risk, travel history
  • Medications
Examination of Lymph Node:
FeatureSuggests
Tender, softReactive/Inflammatory
Hard, fixedMalignant (metastatic)
Rubbery, non-tenderLymphoma
Matted, collar-studTB
FluctuantAbscess/TB (cold abscess)
Lymph Node Groups (Head and Neck): Submental, submandibular, parotid, pre-auricular, post-auricular, occipital, anterior cervical (along IJV), posterior cervical, supraclavicular (Virchow's node - GI/pelvic malignancy), deep cervical, axillary, inguinal

Investigations

  • CBC, ESR, CRP
  • Mantoux test, chest X-ray (TB)
  • HIV testing
  • FNAC - first investigation for single enlarged node
  • Excisional biopsy - if FNAC inconclusive
  • CT neck/chest/abdomen
  • PET scan (lymphoma staging)
  • Bone marrow biopsy (hematological malignancy)

11. Head Injury

Classification

By severity (GCS):
  • Mild: GCS 13-15
  • Moderate: GCS 9-12
  • Severe: GCS ≤8
By pathology:
  1. Primary injury: Direct result of impact
    • Concussion, contusion, laceration, diffuse axonal injury (DAI)
  2. Secondary injury: Develops after primary impact
    • Intracranial hematoma (EDH, SDH, ICH)
    • Brain edema, herniation, ischemia, infection
Extradural Hematoma (EDH) vs Subdural Hematoma (SDH):
FeatureEDHSDH
Source of bleedingMiddle meningeal artery (arterial)Bridging veins (venous)
LocationBetween skull and duraBetween dura and arachnoid
Shape on CTBiconvex (lenticular) - does not cross suturesCrescent-shaped - crosses sutures
Lucid intervalClassic (loss → recovery → deterioration)Less common
Associated fractureTemporal bone fracture (80%)Not necessarily
PrognosisBetter if treated earlyWorse (brain damage often underlying)
Age groupYoung adultsElderly (acute), all ages (chronic)
OnsetRapid (hours)Acute (<3 days), Subacute (3-21 days), Chronic (>21 days)
CT appearance:
  • EDH: Biconvex hyperdense (white) collection, does not cross suture lines
  • Acute SDH: Crescent hyperdense collection; chronic SDH = hypodense (black)
Management:
  • Mild TBI: Observation, neurological monitoring
  • EDH >30 mL, thickness >15 mm, midline shift >5 mm: Urgent surgical evacuation (burr hole/craniotomy)
  • Acute SDH with midline shift/deterioration: Urgent craniotomy
  • ICP monitoring for severe TBI
  • Mannitol (osmotic agent) for raised ICP
  • Hyperventilation (temporary ICP reduction)

12. Carcinoma Larynx

Etiology

  • Cigarette smoking (most important)
  • Alcohol
  • Asbestos exposure
  • HPV
  • Radiation

Anatomy (relevant)

Three sites with different prognosis:
  1. Glottis (vocal cord) - 60%; most common; BEST prognosis (poor lymphatic supply)
  2. Supraglottis (above vocal cord) - 30%; worse prognosis (rich lymphatics, late presentation)
  3. Subglottis (below vocal cord) - 10%; rarest; worst prognosis

Clinical Features

  • Hoarseness (earliest symptom in glottic SCC) - hallmark; any hoarseness >3 weeks needs laryngoscopy
  • Dysphagia (supraglottic)
  • Dyspnea, stridor (advanced disease)
  • Sore throat, referred otalgia
  • Neck mass (lymph node metastasis)
  • Hemoptysis
  • Weight loss

Investigations

  • Indirect laryngoscopy, fiber-optic laryngoscopy
  • CT neck and chest
  • Biopsy (definitive diagnosis)
  • MRI (soft tissue involvement)

Staging (T staging)

  • T1: Tumor limited to one subsite, normal cord mobility
  • T2: Extended to other subsite or impaired mobility
  • T3: Cord fixation or invasion of pre-epiglottic space
  • T4: Invasion beyond larynx (thyroid cartilage, trachea, soft tissue of neck)

Management

StageManagement
Early (T1, T2)Radiotherapy OR conservation surgery (partial laryngectomy)
Advanced (T3, T4)Total laryngectomy + neck dissection + adjuvant RT
UnresectableConcurrent chemoradiotherapy (larynx preservation)
Total laryngectomy = permanent tracheostoma; voice rehabilitation via tracheoesophageal puncture (TEP) with voice prosthesis.

13. Hyperthyroidism

Definition

Excess circulating thyroid hormones (T3 and T4) leading to hypermetabolic state.

Etiology

  • Graves' disease (diffuse toxic goiter) - most common (80%); autoimmune - TSH receptor antibodies (TRAb)
  • Toxic multinodular goiter
  • Toxic adenoma (Plummer's disease)
  • Thyroiditis (De Quervain's) - transient
  • Excess iodine (Jod-Basedow)
  • Thyroid cancer (rare)
  • TSH-secreting pituitary adenoma (rare)

Clinical Features

Metabolic: Weight loss despite increased appetite, heat intolerance, sweating CVS: Palpitations, tachycardia, atrial fibrillation, high cardiac output failure CNS: Anxiety, irritability, tremor, insomnia GIT: Diarrhea, increased bowel frequency Skin: Warm, moist, pretibial myxedema (Graves') Eyes (Graves'): Exophthalmos, lid lag, lid retraction, ophthalmoplegia (thyroid eye disease) Musculoskeletal: Proximal myopathy, bone loss Reproductive: Oligomenorrhea, gynecomastia

Investigations

  • TSH low (most sensitive; suppressed in primary hyperthyroidism)
  • T3, T4 elevated
  • TRAb (positive in Graves')
  • Radioactive iodine uptake scan: Diffuse uptake (Graves'), hot nodule (toxic adenoma)
  • ECG: Sinus tachycardia, AF

Management

  1. Antithyroid drugs:
    • Carbimazole (first-line in UK) or Methimazole - blocks peroxidase; inhibits T3/T4 synthesis
    • Propylthiouracil (PTU) - also blocks peripheral T4 → T3 conversion; preferred in pregnancy (first trimester) and thyroid storm
    • Duration: 12-18 months; 50% remission rate in Graves'
    • Side effects: Agranulocytosis (stop drug, urgent blood count), rash, hepatotoxicity (PTU)
  2. Beta-blockers (Propranolol/Atenolol): Symptomatic control of tachycardia, tremor; does not affect thyroid hormone production
  3. Radioactive Iodine (I-131):
    • Definitive treatment for Graves' and toxic MNG
    • Leads to hypothyroidism (requires lifelong levothyroxine)
    • Contraindicated: Pregnancy, breastfeeding, severe Graves' ophthalmopathy
  4. Surgery (Total/Near-total thyroidectomy):
    • For large goiter, failed medical therapy, young patients, malignancy suspicion
    • Preoperative preparation: Antithyroid drugs for 6-8 weeks + Lugol's iodine 10 days pre-op (reduces vascularity)
Thyroid Storm (Crisis): Life-threatening exacerbation
  • Treat with: PTU high dose, iodine (Lugol's), hydrocortisone, propranolol, cooling, supportive care


SHORT QUESTIONS


Stages of Shock

See Class I-IV table under Hypovolemic Shock (Q2 above) Also: Warm shock (early/compensated) vs Cold shock (decompensated).

Cross-Matching

The process of testing compatibility between donor blood and recipient before transfusion.
Types:
  1. Major cross-match (most important): Recipient's serum + donor's RBCs - tests for antibodies in recipient against donor cells
  2. Minor cross-match: Donor's serum + recipient's RBCs - tests for antibodies in donor against recipient
  3. In-silico (electronic cross-match): Computer-based using blood bank records
Steps:
  1. ABO + Rh typing (forward and reverse)
  2. Antibody screening (indirect Coombs test)
  3. Cross-match (major)
Type and Screen: ABO/Rh typing + antibody screen only (no actual cross-match; used for low-risk procedures where blood likely not needed)

Massive Transfusion

Definition: Transfusion of ≥10 units of pRBCs within 24 hours (or entire blood volume within 24 hours; or >4 units in 1 hour).
Complications (DILUTIONAL + METABOLIC):
  • Dilutional coagulopathy (loss of clotting factors)
  • Dilutional thrombocytopenia
  • Hypothermia (use blood warmers)
  • Hypocalcemia (citrate in stored blood chelates calcium - give IV calcium)
  • Hyperkalemia (RBC breakdown releases K+)
  • Metabolic acidosis
  • TRALI (Transfusion-Related Acute Lung Injury)
  • TACO (Transfusion-Associated Circulatory Overload)
  • ABO/Rh incompatibility reactions
  • Citrate toxicity (in liver failure - can't metabolize citrate)
Massive Transfusion Protocol (MTP): Target ratio pRBC:FFP:Platelets = 1:1:1 (damage control resuscitation)
  • Cryoprecipitate for fibrinogen (<1.5 g/L)
  • Tranexamic acid (antifibrinolytic) early in trauma (within 3 hours)

Le Fort Fractures

Classification of mid-face fractures (described by René Le Fort):
LevelLine of fractureSeparated part
Le Fort I (Horizontal)Horizontal line above tooth apices, through piriform aperture and pterygoid platesHard palate + upper teeth (floating palate)
Le Fort II (Pyramidal)Through nasal bones, lacrimal bones, orbital floor, zygomaticomaxillary suture, pterygoid platesNose + maxilla (floating middle face)
Le Fort III (Craniofacial disjunction)Through nasofrontal junction, orbital walls, zygomaticofrontal suture, zygomatic archEntire midface separates from skull base
Clinical features common to all:
  • Dish-face deformity
  • CSF rhinorrhea (Le Fort II, III - dural tear)
  • Bilateral periorbital ecchymosis ("Panda eyes/Raccoon eyes")
  • Malocclusion
Management: ORIF with miniplates via coronal/facial approach.

Complications of Fractures

Early:
  • Hemorrhage, shock
  • Nerve injury
  • Vascular injury (ischemia)
  • Wound/open fracture infection
  • Fat embolism (48-72 hrs after long bone fracture: confusion, hypoxia, petechiae)
  • Compartment syndrome (5 P's: Pain, Pallor, Pulselessness, Paraesthesia, Paralysis - treat with FASCIOTOMY)
Late:
  • Malunion (healed in wrong position)
  • Non-union (failure to heal >4-6 months; types: hypertrophic, atrophic, infected)
  • Delayed union
  • Avascular necrosis (head of femur, scaphoid, talus - watershed areas)
  • Contractures (Volkmann's ischemic contracture - forearm after compartment syndrome)
  • Post-traumatic arthritis
  • Myositis ossificans (heterotopic ossification)
  • Osteomyelitis (open fractures)

Immobilization Methods

  1. Plaster of Paris (POP): Calcium sulfate hemihydrate; exothermic setting; used for casting
  2. Fiberglass cast: Lighter, water-resistant alternative
  3. Splint: Partial cast; allows swelling
  4. External fixation: Pins through bone connected by external frame; open/infected fractures
  5. Traction:
    • Skin traction (sticky traction) - limited force
    • Skeletal traction (pin through bone - Steinmann pin, Kirschner wire)
    • Types: Fixed traction (Thomas splint), Balanced traction
  6. Internal fixation:
    • Plates and screws (ORIF)
    • Intramedullary nails (IMN) - femur, tibia fractures
    • Kirschner wires (K-wires)
    • Dynamic Hip Screw (DHS) - femoral neck fractures
  7. Functional bracing: Allows joint movement while fracture heals (tibial shaft)

TNM Staging

See Oral Cancer section above for full T/N/M description
General principles:
  • T: Primary tumor size/extent (T0 to T4)
  • N: Regional lymph node involvement (N0 to N3)
  • M: Distant metastasis (M0 = absent, M1 = present)
  • p prefix = pathological staging (after surgery)
  • c prefix = clinical staging
  • Stage grouping: I to IV based on T, N, M combinations

Biopsy in Oral Cancer

Types:
  1. Incisional biopsy: Remove a representative piece from the lesion - preferred for large lesions
  2. Excisional biopsy: Remove entire lesion - for small lesions (<1 cm)
  3. Punch biopsy: For flat lesions
  4. Brush biopsy / cytology: Screening tool, not definitive
Rules for biopsy in oral cancer:
  • Include representative tissue with some normal margin
  • Include area of most abnormal appearance (erythroplakia component, indurated area)
  • Avoid necrotic center (non-diagnostic)
  • Must include subepithelial connective tissue (depth)
  • No prior cauterization/electrosurgery
  • Avoid crushing with forceps
  • Use Toluidine blue as vital stain to guide biopsy site (stains dysplastic/malignant tissue blue)

Benign vs Malignant Tumor

FeatureBenignMalignant
CapsulePresentAbsent
MarginsWell-definedIll-defined
Growth rateSlowRapid
MetastasisNonePresent
DifferentiationHighLow (anaplastic)
NecrosisAbsentCommon
MitosisRare, normalFrequent, atypical
N:C ratioNormalIncreased
RecurrenceRareCommon
Effect on hostLocal pressureSystemic (cachexia)

Signs of Malignancy (in a swelling/ulcer)

Signs of malignancy in an ulcer:
  • Raised, everted, rolled edges (SCC)
  • Indurated base and edges
  • Sloughing/necrotic floor
  • Fixed to underlying structures
  • Regional lymphadenopathy (hard, fixed)
  • Satellite nodules
  • Bleeding on touch
Systemic signs:
  • Unexplained weight loss, anorexia
  • Cachexia (malignant cachexia - cytokine-driven)
  • Anemia of chronic disease
  • Paraneoplastic syndromes

Cyst vs Tumor

FeatureCystTumor
DefinitionPathological cavity lined by epithelium, containing fluid/semi-solid materialAbnormal mass of tissue (neoplasm)
FluctuationPositive (tense may be negative)Negative (unless necrotic center)
TransilluminationPositive (thin-walled)Negative
ConsistencySoft to tenseFirm to hard
GrowthSlowVariable
Malignant potentialSome (e.g., dermoid, jaw cysts)Depends on type
ContentsFluid/keratin/debrisCells, stroma

Lymph Node Examination

  1. Inspect for visible swelling
  2. Palpate systematically (all groups bilateral):
    • Submental, submandibular, parotid
    • Pre and post auricular, occipital
    • Anterior cervical (along SCM, IJV)
    • Posterior cervical (behind SCM)
    • Supraclavicular (Virchow's node on left)
    • Axillary, inguinal
  3. Note: Size, number, consistency (soft/firm/hard/rubbery), tenderness, mobility/fixity, matting, skin changes over it, surface character

Sialolithiasis

Definition: Formation of calculi (stones) in the salivary glands or ducts.
Most common: Submandibular gland (80-90%) - because:
  • Wharton's duct is long (5 cm), runs upward against gravity
  • Saliva is more alkaline and mucous-rich (higher calcium content)
  • Orifice is at floor of mouth (wider, more contaminated)
  • Duct bends over mylohyoid muscle
Clinical features:
  • Painful swelling of the gland at meal times (postprandial pain and swelling)
  • Obstruction symptoms: swelling subsides between meals
  • Pus from duct orifice (secondary infection)
  • Stone palpable bimanually in floor of mouth
Investigations:
  • Plain X-ray (80% of submandibular stones are radio-opaque)
  • Ultrasonography
  • CT scan (best)
  • Sialography (shows filling defect - now less used)
Management:
  • Small stones near orifice: Milking/massage + warm fluids + sialogogues
  • Duct stones: Sialolithotomy (intraoral incision and extraction)
  • Gland stones / recurrent disease: Submandibular gland excision
  • Parotid: Stenson's duct accessible intraorally; parotidectomy if intraglandular

Parotid Swelling - Causes

Inflammatory:
  • Acute bacterial parotitis (Staphylococcus aureus - dehydrated elderly)
  • Viral: Mumps (bilateral, tender, child)
  • Chronic recurrent parotitis
  • Sarcoidosis (Heerfordt syndrome)
  • Sjogren's syndrome
Obstruction:
  • Parotid duct stone (rare, <20% of sialoliths)
Neoplastic:
  • Benign: Pleomorphic adenoma (most common parotid tumor, 70%)
  • Benign: Warthin's tumor (adenolymphoma - bilateral, smokers, males)
  • Malignant: Mucoepidermoid carcinoma (most common parotid malignancy), Acinic cell, Adenoid cystic carcinoma
  • Lymphoma, metastatic deposits
Cysts:
  • Branchial cyst (within parotid)
  • HIV-associated cysts

Facial Nerve in Parotid Surgery

The facial nerve (CN VII) runs through the parotid gland, dividing it into superficial and deep lobes.
Surgical anatomy:
  • Nerve exits the stylomastoid foramen
  • Divides into upper (temporofacial) and lower (cervicofacial) divisions in the parotid
  • Further divides into 5 branches: Temporal, Zygomatic, Buccal, Marginal Mandibular, Cervical (mnemonic: Ten Zebras Bought My Car)
Identification landmarks:
  • Tragal pointer (cartilage of tragus points to main trunk ~1 cm medially and inferiorly) - most reliable
  • Posterior belly of digastric (nerve lies just above it)
  • Tympanomastoid suture (nerve 6-8 mm deep)
  • Mastoid process and styloid process
Complications of parotid surgery:
  • Facial nerve palsy (temporary ~10%, permanent ~1%) - most feared complication
  • Frey's syndrome (auriculotemporal nerve syndrome): Sweating and flushing over cheek during eating (gustatory sweating) - due to aberrant regeneration of parasympathetic fibers to sweat glands
  • Salivary fistula
  • Hematoma, infection
  • Great auricular nerve damage (numbness of earlobe)

Thyroid Swelling Examination

  1. Inspection: Neck midline swelling; moves with swallowing and protrusion of tongue (distinguishes thyroid from non-thyroid)
  2. Palpation (from behind patient):
    • Size, shape, surface, consistency
    • Single nodule vs multinodular
    • Tenderness
    • Mobility - moves with swallowing
    • Tracheal position (deviation)
  3. Percussion: Over sternum for retrosternal extension
  4. Auscultation: Bruit over thyroid (Graves' disease - hypervascular)
  5. Pemberton's sign: Raise arms above head → facial congestion, cyanosis = SVC obstruction by retrosternal goiter
  6. Kocher's test: Lateral pressure on each side of thyroid → stridor if tracheal narrowing
  7. Berry's sign: Loss of carotid pulsation behind enlarged thyroid lobe
  8. Cervical lymph nodes: For malignancy
  9. Check for thyroid status: Pulse rate, tremor, eye signs (exophthalmos, lid lag), reflexes, temperature

Complications of Thyroidectomy

Immediate:
  • Primary hemorrhage (within 24 hrs) - may cause airway compromise by hematoma compressing trachea (EMERGENCY - remove clips/sutures at bedside)
  • Airway obstruction (hematoma, tracheomalacia)
  • Thyroid storm (in uncontrolled hyperthyroidism)
Early (within days):
  • Hypocalcemia (most common complication): Due to inadvertent parathyroid gland removal or devascularization → tetany, positive Chvostek's sign (facial nerve tapping), Trousseau's sign (carpal spasm with BP cuff). Treat with IV calcium gluconate, then oral calcium + Vitamin D
  • Recurrent laryngeal nerve (RLN) injury: Unilateral RLN injury → hoarseness; Bilateral → aphonia + respiratory distress (tracheostomy needed)
  • External laryngeal nerve injury: Loss of high-pitched voice (singer's nerve - Semon's law)
  • Wound infection
Late:
  • Hypothyroidism: Post total thyroidectomy; requires lifelong levothyroxine
  • Hypoparathyroidism (permanent)
  • Keloid scar
  • Recurrence (of toxic goiter/malignancy)

Tubercular Lymphadenitis

Most common form of extrapulmonary TB in India
Pathology:
  • Mycobacterium tuberculosis
  • Starts as reactive lymphadenopathy → caseation necrosis → collar-stud abscess (pus tracks through deep fascia, creating abscess with narrow neck between deep and superficial compartments)
  • Cold abscess: No overlying signs of acute inflammation (cold, painless)
Clinical features:
  • Cervical nodes most commonly affected (posterior triangle)
  • Multiple, matted nodes
  • Painless initially → cold abscess → collar-stud abscess → discharging sinus
Investigations:
  • FNAC (shows caseating granulomas, Langerhans giant cells)
  • AFB stain and culture (gold standard)
  • Mantoux test (often positive)
  • PCR (rapid, sensitive)
  • Chest X-ray (rule out pulmonary TB)
  • Excisional biopsy (if FNAC inconclusive)
Management:
  • Anti-TB therapy: HRZE for 2 months (Intensive phase), then HR for 4-7 months (Continuation phase)
  • H = Isoniazid, R = Rifampicin, Z = Pyrazinamide, E = Ethambutol
  • Surgical: Excision for large nodes, cold abscess drainage, discharging sinus excision

Hodgkin vs Non-Hodgkin Lymphoma

FeatureHodgkin's Lymphoma (HL)Non-Hodgkin's Lymphoma (NHL)
AgeBimodal (15-35 yrs, >55 yrs)>50 yrs (mostly)
Cell of originReed-Sternberg cells (B-cell origin)B cells (85%), T cells
Pathognomonic cellReed-Sternberg cell ("Owl-eye" appearance)None specific
SpreadContiguous (orderly, node by node)Non-contiguous (skips)
DistributionCervical > mediastinal > para-aorticMore widespread, extranodal common
B symptomsFever, night sweats, weight loss (30%)Less common initially
Extranodal involvementRareCommon
PrognosisGenerally betterVariable (indolent to aggressive)
Cure rate~80%Variable
Reed-Sternberg cell: Large binucleate cell with prominent eosinophilic "owl-eye" nucleoli - pathognomonic of Hodgkin's lymphoma.
Staging (Ann Arbor):
  • Stage I: Single lymph node region
  • Stage II: 2+ regions, same side of diaphragm
  • Stage III: Both sides of diaphragm
  • Stage IV: Disseminated extranodal involvement
Treatment:
  • HL: ABVD chemotherapy (Adriamycin, Bleomycin, Vinblastine, Dacarbazine) ± radiotherapy
  • NHL: CHOP regimen ± rituximab (R-CHOP for CD20+ B-cell)

Glasgow Coma Scale (GCS)

ComponentResponseScore
Eye Opening (E)Spontaneous4
To voice3
To pain2
None1
Verbal (V)Oriented5
Confused4
Inappropriate words3
Incomprehensible sounds2
None1
Motor (M)Obeys commands6
Localizes pain5
Withdraws from pain4
Flexion (decorticate)3
Extension (decerebrate)2
None1
Total = E + V + M (Range: 3 to 15)
  • 3-8 = Severe TBI (Intubate! GCS ≤8, intubate)
  • 9-12 = Moderate
  • 13-15 = Mild

Concussion

Definition: A transient, self-limited alteration in brain function resulting from biomechanical forces - no structural injury (no abnormality on CT/MRI).
Features:
  • Brief loss of consciousness (<30 min) or no LOC
  • Post-traumatic amnesia (<24 hours)
  • Confusion, disorientation, headache, dizziness
  • No focal neurological deficit
  • CT/MRI: Normal (structural imaging is normal by definition)
Post-concussion syndrome: Headache, dizziness, cognitive difficulties, mood changes persisting weeks-months after concussion.
Management:
  • Physical and cognitive rest
  • Avoid returning to sport/activity too soon (risk of second impact syndrome)
  • Gradual return-to-play protocol (stepwise)
  • No specific pharmacological treatment
Differentiation: Concussion (no structural damage) vs Contusion (bruising of brain parenchyma - visible on CT as hemorrhagic areas).

Tonsillitis

Acute tonsillitis:
  • Commonest organisms: Streptococcus pyogenes (Group A beta-haemolytic) - most important; also Adenovirus, EBV
  • Features: Sore throat, fever, dysphagia, odynophagia, tonsillar enlargement, exudate on tonsils, cervical lymphadenopathy
  • Complications: Peritonsillar abscess (quinsy), rheumatic fever, post-streptococcal glomerulonephritis, retropharyngeal abscess
  • Treatment: Penicillin V / Amoxicillin; Azithromycin if allergic; avoid Ampicillin (can cause rash in EBV)
Chronic tonsillitis:
  • Recurrent acute episodes, persistent sore throat, halitosis, hypertrophied tonsils with crypts

Indications of Tonsillectomy

Absolute indications:
  • Obstructive sleep apnea (OSA) from tonsillar hypertrophy
  • Peritonsillar abscess (quinsy) - after 6 weeks
  • Suspicion of malignancy (unilateral enlargement)
  • Diphtheria carrier not responding to antibiotics
Relative (Paradise criteria - most commonly used):
  • ≥7 episodes of tonsillitis in 1 year
  • ≥5 episodes/year for 2 consecutive years
  • ≥3 episodes/year for 3 consecutive years

Dehydration

Classification by severity:
Severity% Body weight lossFeatures
Mild<5% (infants <5%, adults <3%)Thirst, slightly dry mouth
Moderate5-10%Dry mucous membranes, decreased skin turgor, sunken eyes, reduced urine output
Severe>10%Above + hypotension, tachycardia, poor capillary refill, altered consciousness
Types by tonicity:
  • Isotonic (most common): Equal loss of water and sodium (diarrhea, vomiting)
  • Hypertonic: Water loss > sodium loss (diabetes insipidus, inadequate oral intake)
  • Hypotonic: Sodium loss > water loss (excess sweating replaced with plain water)
Management:
  • Mild/moderate: Oral rehydration therapy (ORS)
  • Severe: IV fluids (Normal saline 0.9% or Ringer's Lactate)
  • Reassess and adjust

IV Fluids

Crystalloids:
FluidNa (mEq/L)Uses
Normal Saline (0.9% NaCl)154Hypovolemia, hyponatremia (initial resuscitation)
Ringer's Lactate (Hartmann's)130Burns, trauma resuscitation - closest to plasma
5% Dextrose0Maintenance, hypoglycemia, hypernatremia treatment
0.45% NaCl (Half-normal)77Maintenance fluids
Hypertonic saline (3%)513Severe hyponatremia, raised ICP
Colloids:
  • Human albumin (4.5%, 20%)
  • Hydroxyethyl starch (Voluven)
  • Gelatin solutions (Gelofusine, Haemaccel)
  • Dextran
  • FFP, blood products
Maintenance fluid requirement (Holliday-Segar formula):
  • 100 mL/kg for first 10 kg + 50 mL/kg for next 10 kg + 20 mL/kg for each kg >20 kg

Electrolyte Imbalance

Hyponatremia (<135 mEq/L): Symptoms: confusion, seizures, headache. Causes: SIADH, heart failure, cirrhosis, hypothyroidism. Treatment: fluid restriction, hypertonic saline for severe symptomatic.
Hypernatremia (>145 mEq/L): Causes: diabetes insipidus, inadequate fluid intake. Treatment: free water replacement.
Hypokalemia (<3.5 mEq/L): Weakness, arrhythmias (U waves on ECG), paralytic ileus. Causes: diuretics, vomiting, diarrhea, hyperaldosteronism. Treatment: IV/oral KCl.
Hyperkalemia (>5.5 mEq/L): Peaked T waves → wide QRS → sine wave → VF. Causes: renal failure, ACE inhibitors, acidosis, hemolysis. Treatment: IV calcium gluconate (stabilizes membrane), insulin+dextrose, salbutamol, kayexalate, dialysis.
Hypocalcemia: Tetany, Chvostek's, Trousseau's signs. Causes: hypoparathyroidism, vitamin D deficiency, pancreatitis, massive transfusion. Treatment: IV calcium gluconate, then oral calcium + Vit D.

Acidosis vs Alkalosis / ABG Basics

Normal ABG values:
  • pH: 7.35-7.45
  • PaCO2: 35-45 mmHg
  • HCO3-: 22-26 mEq/L
  • PaO2: 80-100 mmHg
  • SaO2: 95-100%
  • BE: -2 to +2
Approach:
  1. Look at pH: <7.35 = acidosis; >7.45 = alkalosis
  2. Look at PaCO2: Elevated = respiratory acidosis; Low = respiratory alkalosis
  3. Look at HCO3: Low = metabolic acidosis; High = metabolic alkalosis
  4. Check for compensation
DisorderpHPaCO2HCO3
Respiratory acidosisCompensatory ↑
Respiratory alkalosisCompensatory ↓
Metabolic acidosisCompensatory ↓
Metabolic alkalosisCompensatory ↑
Anion Gap = Na - (Cl + HCO3) → Normal 8-12 mEq/L
  • High anion gap metabolic acidosis (MUDPILES): Methanol, Uremia, DKA, Propylene glycol, Isoniazid, Lactic acidosis, Ethylene glycol, Salicylates

Tuberculosis (TB)

Organism: Mycobacterium tuberculosis (acid-fast, obligate aerobe)
Transmission: Droplet inhalation
Primary TB: Ghon focus (lower zone) + hilar lymph nodes = Ghon complex/primary complex
Post-primary (Secondary) TB: Reactivation, apical lung involvement
Pulmonary TB features: Chronic cough >2 weeks, hemoptysis, weight loss, night sweats, fever, anorexia
Investigations:
  • Sputum AFB smear (3 samples), culture (gold standard - Lowenstein-Jensen medium)
  • GeneXpert MTB/RIF (rapid PCR, detects rifampicin resistance)
  • Chest X-ray: Upper lobe infiltrates, cavitation
  • Mantoux (TST), IGRA (QuantiFERON)
Treatment (RNTCP/DOTS):
  • Intensive phase: HRZE × 2 months
  • Continuation phase: HR × 4 months
  • Drug-resistant TB: Longer regimens with second-line drugs
BCG vaccine: Neonatal vaccination - protects against severe pediatric TB (miliary, meningeal)

HIV Basics

Virus: HIV-1 (predominantly), HIV-2; Retrovirus, infects CD4+ T lymphocytes (also macrophages, dendritic cells)
Transmission: Sexual (most common), blood (transfusion, needle sharing), mother to child (vertical)
Stages:
  1. Acute HIV infection (seroconversion illness) - fever, rash, lymphadenopathy, 2-6 weeks after exposure
  2. Chronic asymptomatic infection (clinical latency) - CD4 decline over years
  3. AIDS: CD4 <200 cells/mm³ OR AIDS-defining illness
AIDS-defining illnesses: PCP pneumonia, CMV retinitis, Cryptococcal meningitis, Toxoplasmosis, MAC, Kaposi's sarcoma, Cerebral lymphoma, Esophageal candidiasis, Cryptosporidiosis
Investigations: HIV ELISA (screening), Western blot (confirmatory), CD4 count, HIV viral load
Treatment (ART): Start in all HIV+ patients regardless of CD4 count; Preferred first-line: Tenofovir + Lamivudine + Dolutegravir (TLD)
Surgical considerations:
  • Universal precautions, double gloving
  • Post-exposure prophylaxis (PEP) within 72 hours of needlestick
  • Avoid unnecessary procedures; higher infection/wound healing risk

Ulnar Nerve Injury

Ulnar nerve: C8, T1; medial cord of brachial plexus
Sites of injury:
  1. Medial epicondyle (cubital tunnel) - most common
  2. Wrist (canal of Guyon) - e.g., cyclist's palsy
Deformity: "Claw hand" (especially with low lesions) - hyperextension of MCPJs + flexion of IPJs of ring and little finger
Motor loss:
  • Hypothenar muscles (ADM, ODM, FDM)
  • All palmar and dorsal interossei
  • 3rd and 4th lumbricals (ring and little)
  • Adductor pollicis (Froment's sign: can't pinch paper without flexing thumb IP joint)
Sensory loss: Little finger, medial half of ring finger, ulnar palm
High vs Low lesion:
  • Low (at wrist): Claw hand more pronounced (clawing of ring and little fingers - "ulnar paradox")
  • High (at elbow): Flexor digitorum profundus to ring/little also lost → less clawing paradoxically

Wrist Drop

Radial nerve injury (posterior cord, C5-C8)
Common causes:
  • Humeral shaft fracture (most common)
  • "Saturday night palsy" / "Park bench palsy" - compression in axilla (crutch) or upper arm (falling asleep on arm)
  • Penetrating injuries
Deformity: Wrist drop (inability to extend wrist and fingers)
Motor loss:
  • Wrist extensors (ECRL, ECRB, ECU)
  • Finger extensors (EDC, EI, EDM)
  • Thumb extensors and abductor (ECRB, APL, EPL, EPB)
  • Brachioradialis (elbow flexion in mid-prone position)
Sensory loss: Dorsal webspace between thumb and index finger (first dorsal webspace - radial nerve autonomous zone)
Test: "Prayer position" - can't extend wrists to flat

Common Surgical Specimens

  1. Appendix - appendectomy (most common surgical specimen)
  2. Gallbladder - cholecystectomy
  3. Colorectal resections - right hemicolectomy, sigmoid colectomy
  4. Mastectomy specimens (breast)
  5. Thyroid (thyroidectomy specimens)
  6. Lymph node - biopsy specimens
  7. Hernia sac - open/laparoscopic hernia repair
  8. Tonsils (tonsillectomy)
  9. Skin biopsies - melanoma, SCC
  10. Prostate - TURP chips, prostatectomy

Sutures and Needles

Types of Sutures

Absorbable:
SutureMaterialAbsorption timeUses
Plain catgutCollagen (sheep/cow intestine)10-14 daysSubcutaneous (rarely used now)
Chromic catgutChromium-treated collagen21-28 daysGynecological, oral surgery
Polyglycolic acid (Dexon)Synthetic60-90 daysDeep tissues
Polyglactin 910 (Vicryl)Synthetic56-70 daysMost widely used absorbable; deep tissues, subcuticular
Poliglecaprone (Monocryl)Synthetic monofilament90-120 daysSubcuticular skin closure
Polydioxanone (PDS)Synthetic monofilament180-210 daysFascial closure (prolonged strength)
Non-absorbable:
SutureMaterialUses
SilkNatural protein (multifilament)Ligation, oral/mucosa (knot handling excellent)
Nylon (Ethilon)Synthetic monofilamentSkin closure
Prolene (Polypropylene)Synthetic monofilamentVascular surgery, skin, permanent sutures
Steel wireStainless steelSternal closure, tendons
Properties:
  • Monofilament: Less infection risk, harder to tie, cuts through tissue
  • Multifilament (braided): Easier to tie, better knot security, more infection risk (harbors bacteria)

Types of Needles

TypeDescriptionUses
Cutting (triangular cross-section, cutting on outer edge)Sharp, passes through tough tissueSkin
Reverse cutting (cutting on outer edge)Less tissue tearingSkin (preferred over cutting)
Round body/taperNo cutting edge; displaces tissueBowel, fascia, blood vessels
BluntNo sharp pointLiver, very friable tissue
Needle parts: Swaged (needle-suture junction), body (curved/straight), tip

Local Anesthesia

Mechanism: Blocks voltage-gated sodium channels → prevents depolarization → nerve conduction blocked. Smaller unmyelinated fibers blocked first (pain > temperature > touch > pressure > motor).
Types:
AgentOnsetDurationMax DoseSpecial features
Lignocaine (Lidocaine)Fast (5 min)1-2 hrs4 mg/kg plain; 7 mg/kg with adrenalineMost widely used in dentistry
BupivacaineSlow (15-20 min)4-8 hrs2 mg/kgLong-acting; postoperative pain
ArticaineFast1-2 hrs7 mg/kg with epiHigh bone penetration; popular in dentistry
PrilocaineModerate1.5-2 hrs6 mg/kgMethemoglobinemia with high doses
RopivacaineModerate4-8 hrs3 mg/kgLess cardiotoxic than bupivacaine
Vasoconstrictors (Adrenaline/Epinephrine):
  • 1:80,000 or 1:100,000 concentration
  • Prolongs duration, reduces systemic absorption, reduces bleeding
  • Contraindicated: Uncontrolled thyrotoxicosis, severe cardiac disease, pheochromocytoma, end-arteries (fingers, toes, nose, penis, ears)

Complications of Local Anesthesia

Local:
  • Hematoma (intravascular injection)
  • Nerve damage (direct trauma, intraneural injection)
  • Infection
  • Broken needle (rare, with sudden movement)
  • Trismus (inferior alveolar nerve block)
Systemic:
  • Intravascular injection (most dangerous):
    • CNS: Perioral tingling, tinnitus → confusion → seizures → CNS depression → coma
    • CVS: Bradycardia, hypotension, cardiac arrest (bupivacaine particularly cardiotoxic)
  • Allergic reaction: True allergy rare (more to preservatives - paraben); anaphylaxis
  • Methaemoglobinaemia (prilocaine overdose)
  • Syncope (vasovagal - most common "reaction" in dental practice)
Management of LA toxicity: Stop injection, oxygen, IV benzodiazepine for seizures, cardiovascular support, Intralipid 20% (lipid emulsion for bupivacaine toxicity)

Types of Biopsy + Indications

TypeDescriptionIndication
Incisional biopsyRemoval of part of lesionLarge lesions, when excision not feasible, suspected malignancy
Excisional biopsyComplete removal of lesionSmall lesions (<1-1.5 cm), benign presumed lesion
Punch biopsyCircular punch removes cylinder of tissueSkin lesions, flat mucosal lesions
Core needle biopsy (Tru-cut)Core of tissue via hollow needleBreast, liver, prostate, kidney
Fine Needle Aspiration Cytology (FNAC)22-25G needle aspirates cellsThyroid nodule, lymph nodes, salivary glands, breast lumps; NOT for bone tumors
Shave biopsyTangential shavingSuperficial skin lesions
Sentinel lymph node biopsyFirst draining node identified by dye/isotopeBreast cancer, melanoma - avoid full node dissection if negative
Bone marrow biopsy (trephine)Core of bone marrowHematological malignancies, unexplained anemia
Brush cytologyCells brushed from mucosal surfaceScreening (lung bronchoscopy, cervical Pap smear)
Liquid biopsyCirculating tumor DNA in bloodNovel technique; monitoring cancer treatment

This guide covers all the topics listed for BDS 3rd Year General Surgery university examinations. For each long question, present an introduction, relevant classification/etiology, clinical features, and management. For short questions, keep answers concise (half to one page) and include a key table or mnemonic where possible. Always mention the most important single fact first - examiners look for that.
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