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All over body with itching

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prurigo nodularis multiple papules nodules all over body itching

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papular urticaria scabies nodular lesions arms itching differential diagnosis

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prurigo nodularis papules arms itching

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Clinical Assessment

Most likely diagnosis: Prurigo Nodularis (PN)
The images show multiple discrete, dome-shaped papules and nodules distributed over the extensor surface of the arms, several with white/crusted tops consistent with excoriation — a classic presentation.

Morphology from the Images

FeatureObservation
Lesion typeDome-shaped firm papules/nodules
SurfaceSome with white/hyperkeratotic tops (excoriated/crusted)
DistributionExtensor arms, spreading proximally and distally
Background skinPost-inflammatory hyperpigmentation
SymptomIntense generalized pruritus

Diagnosis: Prurigo Nodularis

Prurigo nodularis is a chronic inflammatory skin disease driven by an itch-scratch cycle. Repeated scratching induces nerve proliferation and chronic skin changes, perpetuating the itch.
Pathophysiology: Intense pruritus → scratching → trauma → epidermal hyperplasia, dermal fibrosis, nerve proliferation → more itch (self-perpetuating cycle).
Key clinical features:
  • Multiple firm, dome-shaped nodules (5–20 mm) on extensor surfaces
  • Severe, intractable pruritus
  • Post-inflammatory hyperpigmentation common in darker skin types
  • Sparing of the mid-back ("butterfly sign") is characteristic but not always present

Reference Image (Prurigo Nodularis)

Prurigo Nodularis – extensor arm involvement

Differential Diagnoses to Consider

ConditionDistinguishing Features
Nodular scabiesBurrows in web spaces/genitalia; household contacts affected; responds to scabicides
Papular urticariaUrticarial base, insect bite history, transient lesions
Lichen planusViolaceous flat-topped papules, Wickham striae, oral lesions
Hypertrophic lichen planusThick plaques on shins, overlapping features with PN
Pemphigoid nodularisRare; blister formation; IgG/C3 on IF
Important: In any new or severe case of PN, screen for underlying systemic triggers (see below), especially given the widespread distribution.

Workup — Screen for Underlying Causes

CategoryTests
RenalBUN, creatinine (CKD is a major cause)
HepaticLFTs, HBsAg, anti-HCV (cholestatic itch)
HaematologicCBC, peripheral smear (polycythemia vera, lymphoma)
EndocrineTFTs (thyroid disease), FBS (diabetes)
InfectiousHIV serology (PN is a well-known HIV-associated dermatosis — Harrison's, p. 5916)
AtopicIgE, eosinophil count (atopic diathesis)
Iron storesSerum ferritin, iron studies

Management

Step 1 — General Measures
  • Emollients (thick moisturizers) liberally and frequently
  • Trim fingernails short; cotton gloves at night
  • Avoid hot water baths
Step 2 — Topical Therapy
  • High-potency topical corticosteroids (clobetasol propionate 0.05%) under occlusion to individual nodules
  • Topical calcineurin inhibitors (tacrolimus 0.1%) for maintenance
  • Topical capsaicin (0.025–0.075%) — desensitizes C-fibers; burning sensation initially
Step 3 — Intralesional Therapy
  • Intralesional triamcinolone acetonide (10–40 mg/mL) for individual thick nodules — highly effective
Step 4 — Systemic Therapy (for widespread/refractory cases)
DrugDoseNotes
AntihistaminesCetirizine/hydroxyzineAdjunct for itch relief
Gabapentin/pregabalin300–1800 mg/dayFor neuropathic itch component
Naltrexone (low-dose)4.5 mg/nightOpioid antagonist for refractory pruritus
Dupilumab300 mg SC every 2 weeksIL-4/IL-13 blockade; FDA-approved for PN (2022)
Thalidomide/lenalidomideSpecialist useFor severe refractory PN
Narrowband UVB phototherapy2–3×/weekEffective for widespread disease
Step 5 — Address Underlying Cause Treating the trigger (e.g., correcting iron deficiency, managing CKD, treating HIV) can lead to significant improvement.

Summary

This presentation is highly consistent with Prurigo Nodularis. The priority is:
  1. Rule out nodular scabies (treat empirically with permethrin if clinical suspicion)
  2. Screen for HIV, CKD, hepatic disease, and haematologic malignancy
  3. Start topical high-potency steroids ± intralesional triamcinolone for thickest lesions
  4. Add gabapentin or dupilumab for widespread/refractory disease
(Harrison's Principles of Internal Medicine, 21st Ed., p. 5916)
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