Combined Tumors in Hematolymphoid Neoplasms: Case Series of Histiocytic and Langerhans Cell Sarcomas Arising From Low-Grade B-Cell Lymphoma

Author:

Skala Stephanie L1ORCID,Ye Jing C2,Stumph Jennifer3,Macon William R4,Quinones Frances R3,Khachaturov Vadim3,Ketterling Rhett P4,Dewar Rajan1

Affiliation:

1. Department of Pathology, Michigan Medicine, University of Michigan, Ann Arbor, MI, USA

2. Division of Hematology and Oncology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI, USA

3. Michigan Pathology Specialists, Spectrum Health, Grand Rapids, MI, USA

4. Department of Laboratory Medicine and Pathology, Mayo Clinic College of Medicine, Rochester, MN, USA

Abstract

We report an index case of histiocytic sarcoma arising in a 70-year-old patient with long-standing chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL). The patient presented in 2017 with painful, enlarging swelling of the left neck. He had remote history of cutaneous squamous cell carcinoma with no sign of recurrence, and his CLL/SLL was thought to be in remission. Computed tomography showed mild splenomegaly and multifocal lymphadenopathy including a 3-cm left neck mass. Biopsy of the left neck mass showed CLL/SLL with associated histiocytic sarcoma. Flow cytometry demonstrated a B cell neoplasm with CLL/SLL phenotype. Despite radiation therapy, he expired 3 months after presentation. Two similar cases (CLL/SLL and histiocytic sarcoma, follicular lymphoma and Langerhans cell sarcoma) from another institution are also illustrated. The pathological features of combined tumors in lymphoid neoplasms, a general framework to the work-up to determine interrelatedness of tumor components, and the clinical relevance are discussed.

Publisher

SAGE Publications

Subject

Microbiology (medical),Histology,Pathology and Forensic Medicine

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