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  • Presentation

Unusual Infectious and Autoimmune Dermatopathology Cases: Cryptococcosis, Leptospirosis, and Mpox-Associated Pemphigus Vulgaris

Description

This presentation highlighted three unusual dermatopathology cases linking infection and autoimmune disease. The first case was primary cutaneous cryptococcosis in an older woman with a worsening violaceous ulcer on the chest after applying a powder later identified as lycopodium powder, a flammable industrial material marketed as “dragon’s breath”; biopsy showed granulomatous inflammation with encapsulated yeast highlighted by fungal stains, and the diagnosis was made after excluding disseminated disease. The second case involved a man returning from travel and freshwater exposure in Jamaica who developed jaundice, purpura, and severe bullous lesions with multiorgan failure; biopsy showed vasculopathic changes and hemorrhage, and the illness was ultimately leptospirosis, emphasizing the importance of recognizing exposure history, pre-tibial petechiae/purpura, and conjunctival suffusion because early treatment is critical. The final case described a woman who initially had mpox confirmed by PCR, then developed widespread mucosal and cutaneous erosive bullae with biopsy and DIF consistent with pemphigus vulgaris; after IVIG, prednisone, and rituximab she improved significantly, raising the question of whether mpox could act as a trigger for new-onset pemphigus vulgaris.

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Conclusions

  • The presentation argues that unusual skin eruptions can reveal rare systemic or opportunistic infections, so dermatopathology remains crucial for diagnosis.
  • Primary cutaneous cryptococcosis can present as a localized ulcerative lesion in an apparently immunocompetent patient and may require treatment as disseminated disease because of the risk of severe outcomes.
  • Environmental exposure histories matter, because the cryptococcosis case suggests a contaminated or unsafe topical product, even if the exact source could not be proven.
  • Leptospirosis should be strongly considered after freshwater or flood exposure, especially when patients develop fever, jaundice, renal failure, purpura, or conjunctival suffusion.
  • Because leptospirosis is often underrecognized outside endemic regions, clinicians need a high index of suspicion and early treatment to reduce mortality.
  • Mpox may be temporally associated with new-onset pemphigus vulgaris in rare cases, but the presentation emphasizes that causation cannot be established from a single case.
  • Severe blistering disease after mpox can worsen rapidly and may require escalation to systemic immunosuppression and burn-center-level supportive care.
  • Overall, the cases highlight that careful history taking, biopsy, special stains, and targeted infectious workup are essential for identifying unexpected causes of complex skin disease.
  • Nishiyama-Fujita Y, Kondapi DS, Parkerson GR, Xu Y. Primary Cutaneous Cryptococcosis of Nose With Extensive Tissue Destruction: A Rare Case Report. Ear, Nose & Throat Journal. 2025;104(7):NP460-NP462.#10.1177/01455613221126324
  • Rijnink EC, Chandie Shaw PK. Subconjunctival Hemorrhage in Leptospirosis. N Engl J Med. 2022 Dec 29;387(26):e71.#10.1056/nejmicm2202675