# An Atypical Pediatric Dermatologic Presentation Unmasking an Unexpected Systemic Diagnosis: A Diagnostic Challenge

**Authors:** Brooke Heyer, Leonardo Bonifanti, David R Jetha, Cristina Figallo

PMC · DOI: 10.7759/cureus.103019 · Cureus · 2026-02-05

## TL;DR

A 13-year-old boy with unusual skin and joint symptoms was found to have HIV and rare IgA vasculitis, highlighting the need for broad differential diagnosis in complex pediatric cases.

## Contribution

This case report highlights the diagnostic challenge of atypical pediatric presentations leading to an unexpected HIV diagnosis.

## Key findings

- A 13-year-old male presented with persistent bilateral pedal edema and bullous lesions resistant to antibiotics.
- HIV-1 was diagnosed via serologic testing, with non-perinatal transmission confirmed.
- Atypical IgA vasculitis was concurrently diagnosed, emphasizing the need for broad differential diagnosis in complex pediatric cases.

## Abstract

Dermatologic and musculoskeletal presentations in pediatric patients can pose significant diagnostic challenges, particularly when findings are atypical, persistent, and resistant to therapy. We present a diagnostically complex case of a 13-year-old male with a history of multiple psychiatric comorbidities who developed progressive bilateral pedal edema, bullous lower extremity lesions with excoriations, and severe pain, all symptoms seemingly refractory to antibiotics. Despite initial concern for skin and soft-tissue infection, symptoms persisted, prompting inpatient evaluation and an expanded serologic workup. Screening for immunologic and infectious causes, including human immunodeficiency virus (HIV) and sexually transmitted infections, revealed a new diagnosis of HIV-1 acquired through non-perinatal transmission. The patient was concurrently diagnosed with atypical IgA vasculitis, raising consideration of infectious versus drug-related triggers based on his medication regimen. Although vasculitis is uncommon in HIV-positive patients, and IgA vasculitis is even rarer, this case emphasizes the importance of a broad differential diagnosis in pediatric patients with multisystem involvement. Ultimately, close attention to atypical presentations can ensure timely diagnoses and better care for patients facing similarly complex conditions.

## Linked entities

- **Diseases:** IgA vasculitis (MONDO:0019167)

## Full-text entities

- **Genes:** HLA-B (major histocompatibility complex, class I, B) [NCBI Gene 3106] {aka AS, B-4901, HLAB}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, CD79A (CD79a molecule) [NCBI Gene 973] {aka IGA, IGAlpha, MB-1, MB1}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}
- **Diseases:** linear IgA dermatosis (MESH:D062027), bronchospasm (MESH:D001986), acute disease (MESH:D000208), fever (MESH:D005334), Kaposi sarcoma (MESH:D012514), HIV-associated vasculitis (MESH:D016263), Yersinia enterocolitica (MESH:D015009), polyarteritis nodosa (MESH:D010488), emesis (MESH:D014839), Henoch-Schonlein purpura (MESH:D011695), lymphadenopathy (MESH:D008206), erythematous maculopapular rashes (MESH:D005076), pruritic (MESH:C535817), AIDS (MESH:D000163), hypersensitivity vasculitis (MESH:D018366), lesions (MESH:D009059), autoimmune (MESH:D001327), mononucleosis (MESH:D007244), ankle-localized edema (MESH:D016512), fatigue (MESH:D005221), multisystem dysfunction (MESH:D019578), diarrhea (MESH:D003967), desquamation of the palms (MESH:D017490), neoplastic lesions (MESH:D009062), small-vessel vasculitis (MESH:C565222), STI (MESH:D012749), psychiatric (MESH:D001523), erythema multiforme (MESH:D004892), malignancy (MESH:D009369), opportunistic infections (MESH:D009894), medium-vessel disease (MESH:C536223), ODD (MESH:D019958), bullous pemphigoid (MESH:D010391), hepatitis B and C (MESH:D006509), edema (MESH:D004487), anxiety (MESH:D001007), vasculitides (MESH:D014657), inflammatory (MESH:D007249), gastrointestinal symptoms (MESH:D012817), PJP (MESH:D011020), foot pain (MESH:D010146), Reiter's syndrome (MESH:D016918), skin (MESH:D012871), immune dysregulation (OMIM:614878), HIV (MESH:D015658), fungal infections (MESH:D009181), erythema (MESH:D004890), necrosis (MESH:D009336), maculopapular lesions (MESH:D010267), infectious disease (MESH:D003141), Dermatologic and musculoskeletal (MESH:D009140), petechiae (MESH:D011693), dryness of the skin (MESH:D014987), bacterial and (MESH:D001424), bipolar disorder (MESH:D001714), peripheral neuropathy (MESH:D010523), myalgias (MESH:D063806), Systemic vasculitides (MESH:D056647), hypersensitivity (MESH:D004342), infection (MESH:D007239)
- **Chemicals:** acyclovir (MESH:D000212), pentamidine (MESH:D010419), clindamycin (MESH:D002981), famotidine (MESH:D015738), levofloxacin (MESH:D064704), mupirocin (MESH:D016712), bictegravir-emtricitabine-tenofovir alafenamide (MESH:C000654125), acetaminophen (MESH:D000082), Bactrim (MESH:D015662), ceftriaxone (MESH:D002443), aminopenicillins (-), cephalexin (MESH:D002506)
- **Species:** Human immunodeficiency virus 1 (no rank) [taxon 11676], Yersinia enterocolitica (species) [taxon 630], Homo sapiens (human, species) [taxon 9606], Human immunodeficiency virus (species) [taxon 12721]

## Full text

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## References

11 references — full list in the complete paper: https://tomesphere.com/paper/PMC12967028/full.md

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Source: https://tomesphere.com/paper/PMC12967028