Lymphocytic vasculitis involving the central nervous system occurs in patients with X-linked lymphoproliferative disease in the absence of Epstein-Barr virus infection

Pediatr Blood Cancer. 2009 Dec;53(6):1120-3. doi: 10.1002/pbc.22185.

Abstract

X-linked lymphoproliferative disease (XLP) is an immunodeficiency caused by defects in the adaptor molecule SAP. The manifestations of XLP generally occur following Epstein-Barr virus (EBV) infection and include fulminant mononucleosis, hypogammaglobulinemia and lymphoma. In this report, we describe two unrelated patients with fatal T-cell-mediated central nervous system vasculitis for whom repeated serologic and molecular testing for EBV was negative. In both patients, clonal T-cell populations were observed, but neither demonstrated evidence of lymphoma. Thus, loss of SAP function can lead to dysregulated immune responses characterized by the uncontrolled expansion and activation of T cells independent of EBV infection.

Publication types

  • Case Reports
  • Research Support, N.I.H., Extramural

MeSH terms

  • Adolescent
  • Adult
  • Central Nervous System / immunology*
  • Epstein-Barr Virus Infections
  • Fatal Outcome
  • Genetic Diseases, X-Linked
  • Humans
  • Intracellular Signaling Peptides and Proteins / genetics
  • Lymphatic Vessels / pathology*
  • Lymphoproliferative Disorders / complications*
  • Lymphoproliferative Disorders / immunology
  • Lymphoproliferative Disorders / pathology
  • Male
  • Signaling Lymphocytic Activation Molecule Associated Protein
  • T-Lymphocytes / pathology
  • Vasculitis / etiology*

Substances

  • Intracellular Signaling Peptides and Proteins
  • SH2D1A protein, human
  • Signaling Lymphocytic Activation Molecule Associated Protein