血管内淋巴瘤表现为多发性内分泌衰竭,转化为噬血细胞变异,并复发为血栓性微血管病。

IF 0.7 Q4 HEMATOLOGY
Case Reports in Hematology Pub Date : 2025-09-17 eCollection Date: 2025-01-01 DOI:10.1155/crh/5560781
Nigel P Murray, Cinthia Escobar, Enrique Ramos, Claudia Perez, Dan Hartman
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引用次数: 0

摘要

血管内大b细胞淋巴瘤(IVLCBL)是一种罕见的非霍奇金淋巴瘤,其特征是大b细胞在血管和骨髓窦内生长。一个55岁的男性提出了多发性内分泌衰竭,并进展为全血细胞减少症。骨髓活检显示窦状窦弥漫性大b细胞浸润,符合血管内淋巴瘤。经过6个周期的R-CHOP后,完全缓解。6个月后,患者复发,表现为血栓性微血管病变,并发展为多器官衰竭和死亡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intravascular Lymphoma Presenting as Multiple Endocrine Failure, Transforming Into the Hemophagocytic Variant, and Relapsing as a Thrombotic Microangiopathy.

Intravascular large B-cell lymphoma (IVLCBL) is a rare form of non-Hodgkin's lymphoma and is characterized by the growth of large B-cells within blood vessels and bone marrow sinusoids. A 55-year-old man presented with a multiple endocrine failure which progressed to a pancytopenia. A bone marrow biopsy revealed a diffuse infiltration by large B-cells in the sinusoids consistent with intravascular lymphoma. After 6 cycles of R-CHOP, complete remission was achieved. Six months later, the patient relapsed presenting with a thrombotic microangiopathy which progressed to multiple organ failure and death.

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