复合血管免疫母细胞t细胞淋巴瘤和弥漫性大b细胞淋巴瘤表现为分布性休克。

IF 1.1 Q4 HEMATOLOGY Hematology Reports Pub Date : 2023-11-16 DOI:10.3390/hematolrep15040064
Nisha Hariharan, Alisha Kabadi, Michelle Don, Mazen Odish, Benjamin Heyman
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引用次数: 0

摘要

弥漫性大b细胞淋巴瘤(DLBCL)和血管免疫母细胞t细胞淋巴瘤(AITL)是非霍奇金淋巴瘤(NHL)的两种亚型。复合淋巴瘤同时发生DLBCL和AITL是非常罕见的,目前还没有确定的治疗方案。我们报告一例85岁男性患者,因分布性休克、淋巴细胞增多和淋巴结病被送入重症监护室,随后被诊断为混合性AITL和DLBCL,并接受brentuximab vedotin (BV)和rituximab治疗。据我们所知,这是第一例以分布性休克为表现的复合性淋巴瘤,经BV和利妥昔单抗治疗,休克得到了成功的解决。
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Composite Angioimmunoblastic T-Cell Lymphoma and Diffuse Large B-Cell Lymphoma Presenting with Distributive Shock.

Diffuse large B-cell lymphoma (DLBCL) and angioimmunoblastic T-cell lymphoma (AITL) are two subtypes of non-Hodgkin lymphoma (NHL). The simultaneous occurrence of DLBCL and AITL in a composite lymphoma is very rare, and there are no established treatment regimens. We present the case of an 85-year-old male admitted to the intensive care unit with distributive shock, lymphocytosis, and lymphadenopathy, who was subsequently diagnosed with composite AITL and DLBCL, and treated with brentuximab vedotin (BV) and rituximab. To our knowledge, this is the first case of composite lymphoma presenting with distributive shock and treated with BV and rituximab, with successful resolution of shock.

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来源期刊
Hematology Reports
Hematology Reports HEMATOLOGY-
CiteScore
0.90
自引率
0.00%
发文量
47
审稿时长
10 weeks
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