Literature DB >> 7802169

Woringer-Kolopp disease. A lymphomatoid hypersensitivity reaction.

A N Crowson1, C M Magro.   

Abstract

We report two cases of unilesional pagetoid reticulosis (Woringer-Kolopp disease). Histopathological, immunohistological, ultrastructural, and genotypic studies showed both lesions to be lymphomatoid hypersensitivity reactions, as characterized by polyclonal proliferations of T-lymphocytes; CD8+ T cytotoxic-suppressor (Tc/s) lymphocytes were predominant in one case, whereas CD4+ T helper (Th) lymphocytes were predominant in the other. The nosology of Woringer-Kolopp disease is discussed.

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Year:  1994        PMID: 7802169     DOI: 10.1097/00000372-199410000-00017

Source DB:  PubMed          Journal:  Am J Dermatopathol        ISSN: 0193-1091            Impact factor:   1.533


  3 in total

1.  CD8+ Pagetoid Reticulosis Presenting as a Solitary Foot Plaque in a Young Woman.

Authors:  Stephanie J Martin; Philip R Cohen; Jeong Hee Cho-Vega; Jaime A Tschen
Journal:  J Clin Aesthet Dermatol       Date:  2010-10

2.  Pagetoid reticulosis in a 5-year-old boy.

Authors:  John D Miedler; Arni K Kristjansson; Jennifer Gould; Joan Tamburro; Anita C Gilliam
Journal:  J Am Acad Dermatol       Date:  2008-04       Impact factor: 11.527

3.  A Case of Ketron-Goodman Disease.

Authors:  M Carlesimo; A Tammaro; C Cox; E Mari; L Fidanza; A Narcisi; C Cacchi; G Camplone
Journal:  Case Rep Dermatol       Date:  2009-09-12
  3 in total

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