远端胆管癌胰十二指肠切除术后发生获得性血友病A例。

IF 2.3 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Makoto Takahashi, Yasuhiro Morita, Tatsuya Hayashi, Taku Higashihara, Keishi Kawasaki, Shunsuke Sato, Shota Yokose, Shu Sasaki, Kaoruko Funakoshi, Takayoshi Sasaki, Daren Zhou, Akinori Ichinose, Hideo Ohtsuka, Yuji Ishibasi, Fumihiko Hatao, Keiki Shimizu, Nobuo Isono, Naomi Sasaki, Yasuji Kozai, Haruka Okada, Yushi Chikasawa
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引用次数: 0

摘要

获得性血友病A (AHA)是一种罕见的疾病,由因子VIII抑制剂引起凝血异常引起,某些病例可能在高侵入性手术后发生。本病例报告一名68岁男性患者,因远端胆管癌行保胃胰十二指肠次全切除术后发生AHA。患者术后出现并发症,术后第5天(PD)因Braun氏肠造口破裂需要再次手术。PD 6在空肠肢体发现出血后行血管造影,但检查时自发止血。PD 8再次出血,直接手术结扎。PD 14时,空肠肢体出血复发,行血管造影栓塞第二空肠动脉周围。在手术过程中,凝血酶原时间正常,但只有活化的部分凝血活酶时间延长。凝血系统的仔细检查显示因子VIII水平下降和因子VIII抑制剂的存在,导致AHA的诊断。在PD 15开始给药类固醇,除了每日输血外,还给予活化的凝血酶原复合物浓缩物以实现止血。患者于PD 36出院,但后来由于胃空肠吻合术部位缝合失败而出现难治性唇瘘。尽管给予类固醇治疗,但仍继续使用因子VIII抑制剂,在PD 58时增加了环磷酰胺(CPA)脉冲治疗。然而,CPA无效,在PD 98开始给予利妥昔单抗。在12个疗程的利妥昔单抗治疗后,患者PD 219的因子VIII抑制剂检测呈阴性。在PD 289时,持续更换因子VIII进行唇瘘关闭,患者在PD 342时出院。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A case of acquired hemophilia A after pancreaticoduodenectomy for distal cholangiocarcinoma.

A case of acquired hemophilia A after pancreaticoduodenectomy for distal cholangiocarcinoma.

A case of acquired hemophilia A after pancreaticoduodenectomy for distal cholangiocarcinoma.

A case of acquired hemophilia A after pancreaticoduodenectomy for distal cholangiocarcinoma.

Acquired hemophilia A (AHA) is a rare disease that results from factor VIII inhibitors causing abnormal coagulation, and certain cases may develop after highly invasive surgery. The present case study reports on a 68-year-old male patient who developed AHA after undergoing a subtotal stomach-preserving pancreatoduodenectomy for distal cholangiocarcinoma. The patient experienced complications after surgery, requiring reoperation on postoperative day (PD) 5 due to rupture of the Braun's enterostomy. On PD 6, angiography was performed after bleeding was detected in the jejunal limb, but hemostasis occurred spontaneously during the examination. Bleeding was observed again on PD 8 and direct surgical ligation was performed. On PD 14, bleeding recurred in the jejunal limb and angiography was performed to embolize the periphery of the second jejunal artery. During the procedure, the prothrombin time was normal, but only the activated partial thromboplastin time was prolonged. A close examination of the coagulation system revealed a decrease in factor VIII levels and the presence of factor VIII inhibitors, resulting in the diagnosis of AHA. Administration of steroids was initiated on PD 15 and, in addition to daily blood transfusions, activated prothrombin complex concentrate was administered to achieve hemostasis. The patient was discharged from the intensive care unit on PD 36 but later developed an intractable labial fistula due to suture failure at the gastrojejunostomy site. As the use of factor VIII inhibitors continued despite the administration of steroids, cyclophosphamide (CPA) pulse therapy was added at PD 58. However, CPA was ineffective and the administration of rituximab was initiated on PD 98. After 12 courses of rituximab, the patient tested negative for factor VIII inhibitors on PD 219. On PD 289, labial fistula closure was performed with continuous replacement of factor VIII and the patient was discharged on PD 342.

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来源期刊
Biomedical reports
Biomedical reports MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
4.10
自引率
0.00%
发文量
86
期刊介绍: Biomedical Reports is a monthly, peer-reviewed journal, dedicated to publishing research across all fields of biology and medicine, including pharmacology, pathology, gene therapy, genetics, microbiology, neurosciences, infectious diseases, molecular cardiology and molecular surgery. The journal provides a home for original research, case reports and review articles.
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