I now have authoritative textbook content for every major pediatric triad. Here is the complete, exam-question-formatted reference:
Pediatric "Triad" Diagnosis Patterns - Exam Q&A Master List
Each entry is formatted the way examiners write vignettes: trigger phrase → triad → diagnosis → key next step.
HOW TO USE THIS
Examiners almost never give you all three components of a triad - that would be too easy. The trick is: 2 out of 3 components in a child = you name the diagnosis and supply the third. Practice these bidirectionally.
TIER 1 - Highest Frequency (Appear in Almost Every Exam)
1. Kawasaki Disease
(Tintinalli's Emergency Medicine; Bradley & Daroff's Neurology)
Vignette trigger: Child <5 years, fever >5 days, irritable, won't bear weight
Classic (Complete) Criteria - Fever ≥5 days PLUS 4 of 5:
| # | Feature | Exam Buzzword |
|---|
| 1 | Bilateral nonexudative conjunctivitis | "red eyes, no discharge" |
| 2 | Mucous membrane changes | "strawberry tongue, cracked/red lips" |
| 3 | Extremity changes | "swollen hands/feet → later peeling fingertips" |
| 4 | Polymorphous rash | "non-vesicular, perineal predilection" |
| 5 | Cervical lymphadenopathy | ">1.5 cm, usually unilateral" (least common) |
Incomplete/Atypical Kawasaki = Fever ≥5 days + only 2-3 criteria → still diagnose if CRP ≥3 mg/L + ESR ≥40 mm/h + 3 of: albumin <3 g/dL, anemia for age, elevated ALT, platelets >450,000 after day 7, WBC >12,000, sterile pyuria.
The feared complication: Coronary artery aneurysm - "leading cause of acquired heart disease in children."
Treatment: IVIG + aspirin (one of the FEW indications for aspirin in children).
Q trap: A child gets aspirin for Kawasaki. Is Reye syndrome a risk? Answer: No - aspirin here is given for its anti-inflammatory/antiplatelet effect at therapeutic doses under specialist guidance, not for a viral illness.
2. Intussusception
(Rosen's Emergency Medicine)
Classic Triad:
- Colicky, intermittent abdominal pain (episodes 10-15 min, intervals 15-30 min)
- Palpable sausage-shaped mass (RUQ/right abdomen)
- "Currant jelly" stool (blood + mucus - ischemic mucosa) - late and infrequent
Exam trap: "All three features are present in a minority of patients." The question will likely give you 1 or 2 features. Pain + vomiting in a 6-18 month old = think intussusception first.
Age peak: 6 months - 2 years. Most common cause = idiopathic (lead point in older children - lymphoma, Meckel's).
Imaging pearl: Ultrasound = investigation of choice. Classic sign = "target sign" / "bull's eye" / "doughnut sign" on transverse view; "pseudo-kidney sign" on longitudinal view.
Treatment: Air/contrast enema (diagnostic + therapeutic). If failed or perforation suspected → surgery.
3. Hemolytic Uremic Syndrome (HUS)
(Henry's Lab Methods; Sleisenger & Fordtran's GI)
Classic Triad:
- Microangiopathic hemolytic anemia (schistocytes on blood film)
- Thrombocytopenia
- Acute kidney injury (oliguria, hematuria, rising creatinine)
Trigger: Bloody diarrhea 5-10 days prior → E. coli O157:H7 (Shiga toxin-producing STEC)
Exam rule: Child + bloody diarrhea → AKI 1 week later = HUS until proven otherwise.
Q trap: Should you give antibiotics for the STEC diarrhea? Answer: No - antibiotics increase Shiga toxin release and worsen HUS risk. Treatment is supportive.
Alternate triggers (atypical HUS): Streptococcus pneumoniae, complement dysregulation, drugs.
4. Henoch-Schönlein Purpura (HSP / IgA Vasculitis)
(Tintinalli's; Sleisenger & Fordtran's)
Classic Triad:
- Palpable purpura (below the waist - buttocks, lower limbs; non-thrombocytopenic)
- Arthritis (knees and ankles)
- Colicky abdominal pain ± GI bleeding
Plus: Renal involvement (IgA nephropathy pattern) - hematuria/proteinuria
GI involvement: Up to 90% of patients. Subepithelial edema → ischemia → bleeding.
Exam tip: Purpura below the waist in a child after a URI = HSP. The purpura is NOT from thrombocytopenia (platelet count is normal - this distinguishes it from ITP and meningococcemia).
5. Pyloric Stenosis
(Robbins Pathology; Tintinalli's; Quick Compendium)
Classic Triad:
- Projectile, nonbilious vomiting after every feeding (1-6 weeks of age)
- Palpable "olive" mass - firm, ovoid, 1-2 cm in epigastrium
- Hypochloremic, hypokalemic metabolic alkalosis (from losing HCl in vomit)
Age: 2-8 weeks. Male > Female (4:1). First-born males.
Abnormal peristaltic waves visible across upper abdomen before vomiting (exam-specific detail).
Diagnosis: Ultrasound (pyloric muscle thickness >3-4 mm, channel length >17 mm).
Treatment: Surgical pyloromyotomy (after correcting electrolytes first).
Q trap: Vomiting is NONBILIOUS (obstruction is above ampulla of Vater). Bilious vomiting in a newborn = surgical emergency until proven otherwise (think malrotation/volvulus).
TIER 2 - Frequently Tested
6. Epiglottitis
Triad (the "4 Ds"):
- Drooling
- Dysphagia
- Dyspnea (stridor, respiratory distress)
- (+ Distress / high fever - often quoted as the actual 4th D)
Buzzword on X-ray: "Thumbprint sign" (swollen epiglottis on lateral neck X-ray)
Rule: Do NOT examine the throat. Do NOT lie the child flat. Secure the airway in OR with anesthesia standing by.
Cause: H. influenzae type B (now rare due to Hib vaccine) → increasingly S. aureus, S. pyogenes.
7. Croup (Laryngotracheobronchitis)
Triad:
- Barky/seal-like cough
- Inspiratory stridor
- Hoarseness
X-ray: "Steeple sign" (subglottic narrowing on AP neck X-ray)
Cause: Parainfluenza virus. Age 6 months - 3 years. Worse at night.
Treatment: Single dose dexamethasone (oral/IM) + racemic epinephrine nebulization for moderate-severe.
8. Meningococcemia
Triad:
- Fever
- Petechial/purpuric rash (non-blanching, trunk → spreading)
- Meningismus (neck stiffness, photophobia)
Rule: Non-blanching purpuric rash in a child = treat immediately with IV ceftriaxone. Do not wait for LP results.
9. Shaken Baby Syndrome / Abusive Head Trauma
(Grainger & Allison's Diagnostic Radiology)
Classic Triad:
- Subdural hematoma (SDH)
- Retinal hemorrhages
- Encephalopathy (altered consciousness, seizures)
Note: Biomechanical studies show shaking alone may not generate the full triad - impact is also involved ("shaken-impact syndrome"). Current preferred term: non-accidental head injury (NAHI).
Exam trap: No external signs of trauma does NOT exclude abusive head trauma.
10. Meckel Diverticulum
Classic Triad ("Rule of 2s"):
- Occurs in 2% of the population
- Within 2 feet of ileocecal valve
- Usually presents within first 2 years of life
- (2 types of ectopic mucosa: gastric and pancreatic)
- (2:1 male predominance)
Presentation triad:
- Painless rectal bleeding (hematochezia)
- Iron-deficiency anemia
- Age <5 years
Diagnosis: Meckel scan (Tc-99m pertechnetate - detects ectopic gastric mucosa).
11. Tetralogy of Fallot
Anatomical tetrad (4 defects in 1):
- VSD (ventricular septal defect)
- Overriding aorta
- Pulmonary stenosis (RVOT obstruction)
- Right ventricular hypertrophy
Clinical triad in an exam vignette:
- Cyanotic infant
- Harsh systolic murmur (LLSB)
- "Tet spells" (paroxysmal cyanosis during crying/feeding → child squats to relieve)
CXR: "Boot-shaped heart" (coeur en sabot)
Immediate treatment for a Tet spell: Knee-chest position, IV propranolol, IV phenylephrine (raises SVR → reduces right-to-left shunt).
TIER 3 - Rarer but Classically Tested
12. Hand-Schüller-Christian Disease (Langerhans Cell Histiocytosis)
(Cummings Otolaryngology)
Classic Triad (present in ~25% of cases):
- Lytic skull lesions
- Exophthalmos (orbital bone involvement)
- Diabetes insipidus (pituitary/hypothalamus involvement)
13. Prune Belly Syndrome (Eagle-Barrett / "Triad Syndrome")
Triad:
- Absent/deficient abdominal wall muscles
- Bilateral cryptorchidism
- Urinary tract abnormalities (dilated ureters, bladder, renal dysplasia)
QUICK EXAM DRILL TABLE
| Vignette Gives You | Diagnosis | Completing Feature |
|---|
| Fever >5d + strawberry tongue + peeling fingertips | Kawasaki | Coronary aneurysm risk → IVIG + aspirin |
| 9-month-old + colicky pain + sausage mass | Intussusception | Currant jelly stool → air enema |
| Bloody diarrhea → AKI + hemolytic anemia | HUS | Thrombocytopenia → no antibiotics |
| Purpura below waist + arthralgia + abdo pain | HSP | Normal platelets + renal involvement |
| 4-week-old + projectile nonbilious vomiting | Pyloric stenosis | Olive mass + hypochloremic alkalosis |
| Drooling + dysphagia + thumbprint sign | Epiglottitis | Secure airway - do NOT examine throat |
| Barky cough + stridor + steeple sign | Croup | Dexamethasone ± epinephrine |
| Non-blanching purpura + fever | Meningococcemia | IV ceftriaxone IMMEDIATELY |
| Cyanotic infant + tet spells + squatting | Tetralogy of Fallot | Boot-shaped heart on CXR |
| Painless PR bleed + anemia in toddler | Meckel diverticulum | Tc-99m pertechnetate scan |
| Lytic skull + exophthalmos + DI | LCH (Hand-Schüller-Christian) | Histiocyte infiltration |
| SDH + retinal hemorrhage + no external trauma | Shaken baby (NAHI) | Encephalopathy; mandatory reporting |
Study tip: For each row above, practice reading it in reverse - given the diagnosis, name all 3 components AND the single most important next step. That is exactly what MCQ vignettes test.