ALK-Positive Anaplastic Large Cell Lymphoma in a Patient With Chronic Lymphocytic Leukemia

Author:

Ting Liu 1,Mai He 2,Carlson Diane L.2,Hedvat Cyrus2,Teruya-Feldstein Julie3

Affiliation:

1. Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, New York, Department of Pathology, Huntsman Cancer Hospital, University of Utah, Salt Lake City, Utah

2. Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, New York

3. Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, New York,

Abstract

This article reports the case of a 59-year-old patient with an 8-year history of chronic lymphocytic leukemia (CLL), prostate carcinoma, and squamous cell carcinoma who developed an ALK-positive anaplastic large cell lymphoma (ALCL). Lymph node and bone marrow biopsies showed 2 distinct morphologic populations: ( a) the CLL component showing a diffuse monomorphous infiltrate of small lymphocytes with the typical immunophenotype showing positive CD20, CD5, CD23, and κ light chain restriction and ( b) the ALCL component showing large anaplastic pleomorphic cells positive for CD30, CD45, ALK, CD45Ro, CD4, and vimentin. Polymerase chain reaction performed on the lymph node for immunoglobulin heavy chain and T-cell receptor γ and β showed gene rearrangements after macrodissection of morphologically distinct populations, indicating confirmed genetically distinct populations. Despite intensive chemotherapy, the patient died. This case represents the rare occurrence of an ALK-positive ALCL developing in a patient with CLL.

Publisher

SAGE Publications

Subject

Pathology and Forensic Medicine,Surgery,Anatomy

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