单中心25例获得性A型血友病临床分析

Q4 Medicine
Yu-Jie Guo, Huan Han, Xiao Li, Zhi-Yun Niu, Jing-Yu Zhang, Yan Wang
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引用次数: 0

摘要

目的:通过分析获得性血友病A (AHA)的临床资料,探讨其诊断和治疗方法。方法:回顾性分析25例在河北医科大学第二医院确诊为AHA的患者的临床表现、实验室特征、治疗及转归。结果:11例患者有继发因素,其中自身免疫性疾病5例,妊娠相关疾病3例,类天疱疮1例,Graves病1例,未知意义单克隆γ球蛋白血症(MGUS) 1例。出血部位包括皮肤、粘膜、肌肉、关节腔和脑组织。23例患者采用泼尼松联合环磷酰胺治疗(CP方案),1例患者因股骨头坏死采用利妥昔单抗联合环磷酰胺治疗,1例患者因泼尼松治疗后消化道出血采用利妥昔单抗治疗。其中完全缓解(CR) 23例,部分缓解(PR) 2例,CR后复发8例,10例患者均采用利妥昔单抗治疗,其中2例为PR, 8例为CR后复发。最终8例患者达到CR, 2例患者(均为首次CR后复发患者)达到PR。这2例患者均达到PR,均采用小剂量利妥昔单抗联合硼替佐米(RB方案)治疗。1例患者在4个疗程后达到CR,另1例患者在6个疗程后达到CR。CR后,10例接受利妥昔单抗治疗的患者中有4例接受了利妥昔单抗维持治疗,持续1.5 ~ 2年,无复发。未接受维持治疗的6例患者中,4例CR后复发,中位复发时间为15个月。8例接受CP方案治疗的患者出现常见感染,2例接受利妥昔单抗治疗的患者出现严重肺炎。25例患者均存活至随访结束。结论:皮肤瘀斑、黏膜出血和肌肉血肿是AHA最常见的出血表现,也可发生关节出血和脑出血。CP方案是AHA一线治疗的首选方案。利妥昔单抗可用于类固醇禁忌症或上述治疗无效或有效治疗后复发的患者,建议维持治疗以降低复发风险。同时,应密切关注利妥昔单抗治疗过程中感染事件的发生。利妥昔单抗联合硼替佐米也可用于难治性或复发性AHA患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Clinical Analysis of 25 Cases of Acquired Hemophilia A in a Single Center].

Objective: To explore the diagnosis and treatment of acquired hemophilia A (AHA) based on the analysis of clinical data.

Methods: A retrospective analysis was conducted on the clinical manifestations, laboratory characteristics, treatment, and outcomes of 25 patients diagnosed with AHA who were admitted to the Second Hospital of Hebei Medical University.

Results: Among all patients, 11 cases had secondary factors, including 5 cases of autoimmune diseases, 3 cases of pregnancy-related disease, 1 case of pemphigoid, 1 case of Graves' disease, and 1 case of monoclonal gammaglobulinemia of unknown significance (MGUS). The bleeding sites include the skin, mucous membrane, muscle, joint cavity and brain tissue. Twenty-three patients were treated with prednisone combined with cyclophosphamide (CP regimen), one patient with rituximab combined with cyclophosphamide because of femoral head necrosis, and one case with rituximab monotherapy because of gastrointestinal bleeding after prednisone treatment. Among them, 23 cases achieved complete remission (CR), 2 cases were partial remission (PR), and 8 cases relapsed after CR. All of 10 patients including 2 cases with PR and 8 relapsed cases after CR were treated with rituximab. At last, 8 patients achieved CR, and 2 patients (both were patients with recurrence after first CR) achieved PR. These two patients achieving PR were treated with low-dose rituximab combined with bortezomib (RB regimen). One patient reached CR after 4 cycles and the other reached CR after 6 cycles of RB regimen. After CR, 4 of the 10 patients treated with rituximab received maintenance therapy with rituximab monotherapy for 1.5 to 2 years, in which, none of them relapsed. Among the 6 patients who did not receive maintenance therapy, 4 patients relapsed after CR, and the median time to relapse was 15 months. Eight patients treated with CP regimen developed common infections, and two patients treated with rituximab developed severe pneumonia. All 25 patients survived until the end of follow-up.

Conclusion: Skin ecchymosis, mucous hemorrhage and muscle hematoma are the most common hemorrhagic manifestations in AHA, and joint hemorrhage and cerebral hemorrhage can also occur. CP regimen is the preferred option of first-line therapy for AHA. Rituximab can be used for patients with steroid contraindication or who failed to respond to the above therapy or relapsed after effective treatment, and maintenance therapy is recommended to reduce the risk of recurrence. Meanwhile, close attention should be paid to the occurrence of infection events during rituximab treatment. Rituximab in combination with bortezomib can also be used in patients with refractory or relapsing AHA.

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中国实验血液学杂志
中国实验血液学杂志 Medicine-Medicine (all)
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