Clonal ambiguity of human immunodeficiency virus-associated lymphomas. Similarity to posttransplant lymphomas

S. M. Lippman, J. R. Volk, Catherine S Perry, T. M. Grogan

Research output: Contribution to journalArticle

21 Citations (Scopus)

Abstract

Initial biopsy specimens from two patients with lymphadenopathy and human immunodeficiency virus antibody-positive serum presented considerable difficulty in making specific histologic and immunologic diagnoses, although subsequent biopsy specimens revealed clear progression to acquired immunodeficiency syndrome (AIDS)-associated lymphomas. The initial biopsy specimens revealed multifocal clusters of large blastic lymphoid cells, with some clusters showing a monoclonal λ light chain predominance, whereas other clusters showed a κ predominance, indicating considerable phenotypic ambiguity suggestive of polyclonality. This initial clonal ambiguity was followed within two to three months by overt histologic, phenotypic, and clinical malignant transformation to a diffuse high-grade monoclonal B-cell lymphoma. These data have significant implications for the clonality and pathogenesis of AIDS-associated lymphoproliferative disorders. AIDS-related lymphomas may evolve from an initial multiclonal B-cell expansion similar to that described in other severely immunosuppressed patients (eg, with posttransplantation lymphoma).

Original languageEnglish (US)
Pages (from-to)128-132
Number of pages5
JournalArchives of Pathology and Laboratory Medicine
Volume112
Issue number2
StatePublished - 1988

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Lymphoma
Acquired Immunodeficiency Syndrome
HIV
Biopsy
Immunologic Tests
Lymphoproliferative Disorders
B-Cell Lymphoma
B-Lymphocytes
Lymphocytes
Light
Antibodies
Serum
Lymphadenopathy

ASJC Scopus subject areas

  • Pathology and Forensic Medicine
  • Medical Laboratory Technology

Cite this

Clonal ambiguity of human immunodeficiency virus-associated lymphomas. Similarity to posttransplant lymphomas. / Lippman, S. M.; Volk, J. R.; Perry, Catherine S; Grogan, T. M.

In: Archives of Pathology and Laboratory Medicine, Vol. 112, No. 2, 1988, p. 128-132.

Research output: Contribution to journalArticle

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