利妥昔单抗一线治疗TAFRO综合征1例报告及文献复习。

IF 3 3区 医学 Q2 HEMATOLOGY
Salar Servati, Ida Mohammadi, Shahryar Rajai Firouzabadi
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引用次数: 0

摘要

TAFRO综合征是Castleman病的一种罕见变体,其特征是血小板减少、贫血、发热、网状蛋白纤维化和器官肿大。一线治疗通常包括免疫抑制疗法,如环孢素A和托珠单抗。然而,利妥昔单抗作为一线治疗药物的使用仍然缺乏报道。在此,我们报告一位38岁的女性患者,她最初表现出淋巴结病变,并在住院期间逐渐发展出与TAFRO综合征相关的全谱症状。利妥昔单抗加强的松龙作为主要治疗。在五个月的随访期间,患者的病情明显改善,表明治疗反应积极。该病例强调了利妥昔单抗作为TAFRO综合征一线治疗的潜在疗效,在标准治疗药物可能不可用、不合适或不有效的情况下提供了一种可能的治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
First-line treatment of TAFRO syndrome with rituximab: a case report and literature review.

TAFRO syndrome, a rare variant of Castleman's disease, is characterized by thrombocytopenia, anasarca, fever, reticulin fibrosis, and organomegaly. First-line treatments typically include immunosuppressive therapies such as cyclosporine A and tocilizumab. However, the use of rituximab as a first-line therapeutic agent remains under-reported. Here, we present the case of a 38-year-old female patient who initially exhibited lymphadenopathy and gradually developed the full spectrum of symptoms associated with TAFRO syndrome during her hospital stay. Rituximab, supplemented by prednisolone, was administered as the primary treatment. Over a follow-up period of five months, the patient's condition improved significantly, suggesting a positive therapeutic response. This case highlights the potential efficacy of rituximab as an alternative first-line therapy for TAFRO syndrome, offering a possible treatment option where standard therapeutic agents may not be available, suitable or effective.

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来源期刊
Annals of Hematology
Annals of Hematology 医学-血液学
CiteScore
5.60
自引率
2.90%
发文量
304
审稿时长
2 months
期刊介绍: Annals of Hematology covers the whole spectrum of clinical and experimental hematology, hemostaseology, blood transfusion, and related aspects of medical oncology, including diagnosis and treatment of leukemias, lymphatic neoplasias and solid tumors, and transplantation of hematopoietic stem cells. Coverage includes general aspects of oncology, molecular biology and immunology as pertinent to problems of human blood disease. The journal is associated with the German Society for Hematology and Medical Oncology, and the Austrian Society for Hematology and Oncology.
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