Literature DB >> 11907856

Pseudoporphyria: an atypical variant resembling toxic epidermal necrolysis.

A J Papadopoulos1, R A Schwartz, Z Fekete, G Kihiczak, J A Samady, S H Atkin, W C Lambert.   

Abstract

BACKGROUND: Pseudoporphyria has been attributed to both medication usage and chronic hemodialysis. Histologically, it is identical to porphyria cutanea tarda. It is most commonly seen as localized bullae on sun-exposed skin, often on the dorsum of the hands and fingers.
OBJECTIVES: We describe a 31-year-old man with rapidly evolving bullae which became denuded, clinically suggestive of toxic epidermal necrolysis. Pseudoporphyria was proven histologically. However, our patient's eruption was not localized as small bullae but was widespread, with large bullae evolving into large, cutaneous, denuded erosions.
CONCLUSIONS: We describe a previously unreported, generalized variant of pseudoporphyria that resembles toxic epidermal necrolysis. We provide a review of pseudoporphyria and compare our variant to toxic epidermal necrolysis and mimicking disorders.

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Year:  2001        PMID: 11907856     DOI: 10.1007/s10227-001-0013-1

Source DB:  PubMed          Journal:  J Cutan Med Surg        ISSN: 1203-4754            Impact factor:   2.092


  1 in total

1.  A case of toxic epidermal necrosis-like cutaneous eruption as the first manifestation and clue to the diagnosis of systemic lupus erythematosus: A case report.

Authors:  Hanieh Zargham; Stephanie Ghazal; Kevin Watters; Khue Huu Nguyen
Journal:  SAGE Open Med Case Rep       Date:  2020-07-15
  1 in total

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