A Case of Acquired Hemophilia A Following Robot-Assisted Minimally Invasive Esophagectomy.

IF 0.7 Q4 SURGERY
Surgical Case Reports Pub Date : 2026-01-01 Epub Date: 2026-03-04 DOI:10.70352/scrj.cr.25-0797
Shota Eguchi, Yoshio Nagahisa, Kenji Yamaguchi, Yukio Inamura, Michio Okabe, Toshihiko Masui
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Abstract

Introduction: Acquired hemophilia A (AHA) is a rare but potentially fatal bleeding disorder that arises suddenly in individuals without a prior history of bleeding tendency. It is often associated with malignant disease and can present with severe hemorrhagic complications. Reports of AHA occurring in the postoperative course of esophageal cancer surgery are extremely limited, and the safety of immune checkpoint inhibitors (ICIs) in patients with a history of AHA remains uncertain. This case highlights both the diagnostic and therapeutic challenges of AHA and provides novel insight into the safe administration of ICIs in a patient with recurrent esophageal cancer following remission of AHA.

Case presentation: We describe a 77-year-old man with clinical stage II esophageal cancer who received neoadjuvant chemotherapy with docetaxel, cisplatin, and fluorouracil, followed by robot-assisted thoracoscopic and laparoscopic subtotal esophagectomy. Postoperatively, he developed an anastomotic stricture requiring re-anastomosis via median sternotomy. After the second surgery, he experienced uncontrollable wound bleeding, and laboratory testing revealed a markedly prolonged activated partial thromboplastin time. Further evaluation confirmed the diagnosis of AHA, for which medical therapy was initiated, resulting in remission. Subsequently, the patient developed recurrent esophageal cancer and is currently receiving fluorouracil plus cisplatin in combination with pembrolizumab. Notably, no relapse of AHA has been observed during immunotherapy.

Conclusions: This case illustrates that AHA can complicate the postoperative course of esophageal cancer surgery, leading to significant bleeding difficulties. It also suggests that ICIs may be administered relatively safely in patients with recurrent esophageal cancer who have previously developed AHA. Clinicians should remain vigilant for this rare but serious condition when encountering unexplained bleeding in cancer patients, and the findings may provide reassurance regarding the use of immunotherapy in similar clinical contexts.

Abstract Image

Abstract Image

机器人辅助微创食管切除术后获得性血友病A例。
简介:获得性血友病A (AHA)是一种罕见但潜在致命的出血性疾病,在没有出血倾向病史的个体中突然出现。它通常与恶性疾病有关,并可出现严重的出血性并发症。食管癌手术后发生AHA的报道非常有限,免疫检查点抑制剂(ICIs)在有AHA病史的患者中的安全性仍然不确定。本病例强调了AHA的诊断和治疗挑战,并为AHA缓解后食管癌复发患者使用ICIs的安全性提供了新的见解。病例介绍:我们描述了一位77岁的临床II期食管癌患者,他接受了多西紫杉醇、顺铂和氟尿嘧啶的新辅助化疗,随后进行了机器人辅助胸腔镜和腹腔镜食管次全切除术。术后,他出现吻合口狭窄,需要通过正中胸骨切开术重新吻合。在第二次手术后,他经历了无法控制的伤口出血,实验室检查显示部分凝血活酶活化时间明显延长。进一步的评估证实了AHA的诊断,为此开始了药物治疗,导致病情缓解。随后,患者发生食管癌复发,目前正在接受氟尿嘧啶+顺铂联合派姆单抗治疗。值得注意的是,在免疫治疗期间没有观察到AHA复发。结论:本病例说明AHA可使食管癌手术过程复杂化,导致明显的出血困难。研究还表明,对于既往发生AHA的食管癌复发患者,ICIs可以相对安全地使用。当遇到癌症患者不明原因出血时,临床医生应该对这种罕见但严重的情况保持警惕,研究结果可能为在类似临床情况下使用免疫治疗提供保证。
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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