Severe autoimmune pancytopenia after autologous hematopoietic stem cell transplantation for Hodgkin lymphoma.

IF 0.9 Q4 HEMATOLOGY
Yuta Fukui, Akira Honda, Hirofumi Takano, Takafumi Obo, Hideaki Mizuno, Yosuke Masamoto, Mineo Kurokawa
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引用次数: 2

Abstract

Autoimmune pancytopenia is rarely seen with Hodgkin lymphoma, and only one pediatric case of pancytopenia after autologous hematopoietic stem cell transplantation (HSCT) has been reported. We herein report a case of autoimmune pancytopenia that developed after autologous HSCT for nodular lymphocyte predominant Hodgkin lymphoma (NLPHL). A 56-year-old Japanese woman underwent autologous HSCT for NLPHL. She developed autoimmune pancytopenia seven months after autologous HSCT. In this case, PSL was effective, and the blood cell counts normalized completely. However, the patient suffered from a fatal infection, probably because of immunosuppression caused by prolonged administration of PSL, as well as a history of several chemotherapies and autologous HSCT. To our knowledge, this is the first adult case of autoimmune pancytopenia after autologous HSCT for Hodgkin lymphoma. To further validate the optimal treatment strategy for autoimmune cytopenia after autologous HSCT, more cases are necessary.

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自体造血干细胞移植治疗霍奇金淋巴瘤后严重自身免疫性全血细胞减少症。
自身免疫性全血细胞减少症在霍奇金淋巴瘤中很少见,仅报道了一例自体造血干细胞移植(HSCT)后全血细胞减少症的儿童病例。我们在此报告一例自身免疫性全血细胞减少症,在自体造血干细胞移植后发展为结节性淋巴细胞显性霍奇金淋巴瘤(NLPHL)。一名56岁的日本女性因NLPHL接受了自体造血干细胞移植。她在自体造血干细胞移植后7个月出现自身免疫性全血细胞减少症。在这种情况下,PSL是有效的,血细胞计数完全正常化。然而,患者发生了致命的感染,可能是由于长期服用PSL引起的免疫抑制,以及多次化疗和自体造血干细胞移植的历史。据我们所知,这是首例成人霍奇金淋巴瘤自体造血干细胞移植后自身免疫性全血细胞减少症。为了进一步验证自体造血干细胞移植后自身免疫性细胞减少的最佳治疗策略,需要更多的病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.00
自引率
6.70%
发文量
25
审稿时长
11 weeks
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