Diffuse Large B‐Cell Lymphoma Transdifferentiating Into Histiocytic Sarcoma: Case Report + Systematic Review

A 68-year-old man with a history of diffuse large B-cell lymphoma (DLBCL) with cutaneous involvement presented with a new, rapidly growing, exophytic, bleeding tumor. Histopathologic and immunophenotypic characterization was consistent with a diagnosis of histiocytic sarcoma (HS). A subsequent lymph node biopsy also yielded a diagnosis of HS. Genetic analysis of this patient's original DLBCL bone marrow specimen and subsequent lymph node HS specimen identified identical p.G13D KRAS mutations. This case highlights, to our knowledge, the first case of systemic DLBCL with cutaneous involvement linked to transdifferentiated cutaneous HS by identical KRAS mutations. We also include a systematic review of cutaneous HS cases, identifying only two cases with underlying hematologic transdifferentiation. The distinct clinical morphology, histopathologic characteristics, and immunohistochemical markers associated with each of these entities highlight a very rare and unique example of histiocytic transdifferentiation in the context of a hematologic malignancy.

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Journal
Journal of Cutaneous Pathology
Published
2025-12-26
DOI
https://doi.org/10.1111/cup.70051
Primary Topic
Histiocytic Disorders and Treatments
Type
article
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article

Diffuse Large B‐Cell Lymphoma Transdifferentiating Into Histiocytic Sarcoma: Case Report + Systematic Review

Sagun D. Goyal, Sino Mehrmal, Friederike Kreisel, Nicole M. Burkemper et al.
Journal of Cutaneous Pathology
Histiocytic Disorders and Treatments
article

Diffuse Large B‐Cell Lymphoma Transdifferentiating Into Histiocytic Sarcoma: Case Report + Systematic Review

Sagun D. Goyal, Sino Mehrmal, Friederike Kreisel, Nicole M. Burkemper, Patricia K. Mansfield, Gillian Heinecke, Emily H. Smith, Kristin Smith, Alexander B. Aria, M. Yadira Hurley
article en

Abstract

A 68-year-old man with a history of diffuse large B-cell lymphoma (DLBCL) with cutaneous involvement presented with a new, rapidly growing, exophytic, bleeding tumor. Histopathologic and immunophenotypic characterization was consistent with a diagnosis of histiocytic sarcoma (HS). A subsequent lymph node biopsy also yielded a diagnosis of HS. Genetic analysis of this patient's original DLBCL bone marrow specimen and subsequent lymph node HS specimen identified identical p.G13D KRAS mutations. This case highlights, to our knowledge, the first case of systemic DLBCL with cutaneous involvement linked to transdifferentiated cutaneous HS by identical KRAS mutations. We also include a systematic review of cutaneous HS cases, identifying only two cases with underlying hematologic transdifferentiation. The distinct clinical morphology, histopathologic characteristics, and immunohistochemical markers associated with each of these entities highlight a very rare and unique example of histiocytic transdifferentiation in the context of a hematologic malignancy.

Journal of Cutaneous PathologyVol. 53(4)
SSM Health Care (US), Baylor University Medical Center (US), Saint Louis University (US)
Good health and well-being
Openalex Percentile: Top 33%
Histiocytic Disorders and Treatments
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Diffuse Large B‐Cell Lymphoma Transdifferentiating Into Histiocytic Sarcoma: Case Report + Systematic Review — Sagun D. Goyal, Sino Mehrmal, et al. · Journal of Cutaneous Pathology (2025) | TGRS Research Map | TGRS