Lepromatous leprosy masquerading as acute sarcoidosis: a case report and literature review.

Mrinal M. Patnaik, Dale Hammerschmidt, Jo Anne H. van Burik, Jose Jessurun, Peter Smyth

Research output: Contribution to journalReview article

1 Scopus citations

Abstract

Leprosy is uncommon in North America. Because it has a prolonged incubation period and can masquerade with a variety of manifestations, many patients with leprosy experience a significant delay in diagnosis and treatment. Lepra reactions are of 2 types: reversal (type 1) and erythema nodosum leprosum (ENL) (type 2). Type 1 or reversal reactions represent an increase in cell-mediated immunity, whereas type 2 or ENL is caused by antigen-antibody complex formation and deposition after antigen release from dying lepra bacilli. This article describes the diagnostic challenges presented by a Minnesota patient eventually found to have lepromatous leprosy. That challenge was compounded by the fact that the clinical scenario closely mimicked connective tissue/immune complex disease and by the fact that the patient presented in a location where the incidence and prevalence of leprosy is extremely low.

Original languageEnglish (US)
Pages (from-to)30-33
Number of pages4
JournalMinnesota medicine
Volume91
Issue number11
StatePublished - Nov 2008

ASJC Scopus subject areas

  • Medicine(all)

Fingerprint Dive into the research topics of 'Lepromatous leprosy masquerading as acute sarcoidosis: a case report and literature review.'. Together they form a unique fingerprint.

  • Cite this

    Patnaik, M. M., Hammerschmidt, D., van Burik, J. A. H., Jessurun, J., & Smyth, P. (2008). Lepromatous leprosy masquerading as acute sarcoidosis: a case report and literature review. Minnesota medicine, 91(11), 30-33.