T-cell lymphoma with von Hippel-Lindau disease: a rare case report and review of literature

Int J Clin Exp Pathol. 2015 May 1;8(5):5837-43. eCollection 2015.

Abstract

von Hippel-Lindau disease (VHLD) comprises a series of complicated clinical manifestations. We hereby described a unique case of co-existing T-cell lymphoma (TCL) and confirmed VHLD. The symptoms in this 42-year-old male included fever and pancytopenia. Overall tests and examination made an infectious process unlikely. The results of bone marrow biopsy confirmed the diagnosis. The purposes we described this case were to probe into the relationship between TCL and VHLD, which was not mentioned in previously literature. Combination of clinical, radiological, immunophenotypic, pathological, and genetic data plays an important role in improving the rate of diagnosis, particularly in the challenge for diagnosis of T cell non-Hodgkin lymphoma.

Keywords: T-cell lymphoma; hematological neoplasm; von Hippel-Lindau disease.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adult
  • Biopsy
  • Bone Marrow Examination
  • Flow Cytometry
  • Humans
  • Immunohistochemistry
  • Immunophenotyping
  • Lymphoma, T-Cell / complications*
  • Lymphoma, T-Cell / diagnosis
  • Lymphoma, T-Cell / genetics
  • Lymphoma, T-Cell / therapy
  • Male
  • Predictive Value of Tests
  • Tomography, X-Ray Computed
  • von Hippel-Lindau Disease / complications*
  • von Hippel-Lindau Disease / diagnosis
  • von Hippel-Lindau Disease / genetics
  • von Hippel-Lindau Disease / therapy