Atypical cutaneous lymphoproliferative disorder in patients with HIV infection

Int J Dermatol. 1999 Feb;38(2):111-8. doi: 10.1046/j.1365-4362.1999.00417.x.

Abstract

Background: An inflammatory pruritic eruption which is characterized histologically by CD8+, atypical lymphocytes has been described in human immunodeficiency virus (HIV)-infected patients. This disorder has been described as "pseudo-Sezary" or a "cutaneous T cell lymphoma (CTCL)-simulant", however, as these patients do not resemble CTCL clinically, and the relationship between this entity and CTCL is unclear, a more descriptive term is "atypical cutaneous lymphoproliferative disorder" (ACLD). The purpose of this study is to categorize the clinical, histologic, and immunophenotypic features of 16 HIV-infected patients with this skin disorder seen at the New York Department of Veterans Affairs Medical Center.

Methods: A retrospective chart review was conducted on 16 HIV-infected patients with a histologic diagnosis of an atypical cutaneous lymphoproliferative infiltrate on skin biopsy. Skin biopsies were reviewed, and histologic features noted. Immunophenotyping was performed on 14 out of 16 samples; electron microscopy was performed on samples from five patients. Clinical manifestations, disease course, medication history, and response to treatment were noted.

Results: The patients presented with a pruritic, persistent, generalized, papular eruption. Pigment changes, including hyperpigmentation and hypopigmentation were common. Histologically, lesional biopsies were characterized by a superficial and deep polymorphous infiltrate with atypical lymphocytes which were CD8+ predominant, Ki-1 negative, and occasionally CD7 antigen depleted. Sezary-like cells were present in the infiltrate in four out of five patients by electron microscopy. None of the patients has systemic manifestations of lymphoma; however, one of the 16 patients eventually developed frank CTCL.

Conclusions: HIV-infected patients can present with a pruritic, widespread disorder, often with pigment changes characterized by an atypical cutaneous lymphocytic infiltrate. This clinicopathologic disorder is a rare, reactive inflammatory condition which generally occurs in late stage HIV infection and rarely progresses to frank lymphoma.

Publication types

  • Review

MeSH terms

  • Acquired Immunodeficiency Syndrome / complications
  • Acquired Immunodeficiency Syndrome / virology
  • Adult
  • Aged
  • Antigens, CD / analysis
  • Diagnosis, Differential
  • Follow-Up Studies
  • HIV Infections / complications*
  • Humans
  • Immunohistochemistry
  • Lymphoproliferative Disorders / complications
  • Lymphoproliferative Disorders / metabolism
  • Lymphoproliferative Disorders / pathology*
  • Male
  • Microscopy, Electron
  • Middle Aged
  • Skin / chemistry
  • Skin / pathology
  • Skin / ultrastructure
  • Skin Diseases / complications
  • Skin Diseases / metabolism
  • Skin Diseases / pathology*
  • T-Lymphocytes / chemistry
  • T-Lymphocytes / pathology
  • T-Lymphocytes / ultrastructure

Substances

  • Antigens, CD