Masui Hideyuki, Kobayashi Hiroyuki, Sakamoto Yusuke, Yagi Shintaro, Kaihara Satoshi
Department of Surgery, Kobe City Medical Center General Hospital, 2-1-1Minatojima-Minamimachi, Chuo-Ku, Kobe, 650-0047, Japan.
Department of Gastrointestinal Surgery, Graduate School of Medicine, Kyoto University, 54 Shogoin-Kawahara-Cho Sakyo-Ku, Kyoto, 606-8507, Japan.
Surg Case Rep. 2024 Jan 2;10(1):2. doi: 10.1186/s40792-023-01795-5.
Anti-coagulant ileus, characterized by intramural hematoma due to excessive anti-coagulant therapy, presents a diagnostic challenge. Although previously considered uncommon, recently, reporting cases of anti-coagulant ileus have become more frequent. Herein, we report a rare surgical case of anti-coagulant ileus mimicking small-bowel tumors.
A 79-year-old man was admitted to our hospital for fatigue. He had been administered warfarin for 5 months for atrial fibrillation. On admission, the patient exhibited mild epigastric tenderness. Laboratory test results revealed anemia (hemoglobin, 8.4 g/dL); unmeasurably prolonged prothrombin time (PT) with international normalized ratio (INR) > 8; and elevated soluble interleukin 2 receptor (sIL-2R) levels (849 IU/mL; normal range, 122-496 IU/mL). Abdominal plain computed tomography (CT) showed a circumferentially thickened intestinal wall at one site in the jejunum and two in the ileum. After hospitalization, bowel obstruction did not improve with conservative treatment. Suspecting small-bowel tumors such as lymphoma, the patient subsequently underwent open surgery on day 3 after admission. No obvious tumor mass was observed intra-operatively. However, only thickened and hemorrhagic segments were identified at the suspected sites. We performed partial jejunal and ileal resections of 12 and 27 cm, respectively. Histopathology confirmed submucosal congestion, edema, and hemorrhage in each area without tumor components, leading to the final diagnosis of intramural hematoma. The postoperative course was uneventful, and he was discharged on postoperative day 9. No recurrence occurred during the 5-year follow-up period.
We encountered a surgical case of anti-coagulant ileus, which was difficult to differentiate from malignant lymphoma based on CT findings and high sIL-2R levels. The possibility of anti-coagulant ileus should always be considered in patients on long-term anticoagulation medication and bowel obstruction with high PT-INR values.
抗凝性肠梗阻以过度抗凝治疗导致的肠壁内血肿为特征,诊断具有挑战性。尽管以前认为不常见,但最近,抗凝性肠梗阻的报告病例变得更加频繁。在此,我们报告一例罕见的模仿小肠肿瘤的抗凝性肠梗阻手术病例。
一名79岁男性因疲劳入院。他因心房颤动接受华法林治疗5个月。入院时,患者表现出轻度上腹部压痛。实验室检查结果显示贫血(血红蛋白,8.4 g/dL);凝血酶原时间(PT)不可测地延长,国际标准化比值(INR)>8;可溶性白细胞介素2受体(sIL-2R)水平升高(849 IU/mL;正常范围,122-496 IU/mL)。腹部平扫计算机断层扫描(CT)显示空肠一处和回肠两处肠壁周向增厚。住院后,保守治疗肠梗阻未改善。怀疑为淋巴瘤等小肠肿瘤,患者随后在入院后第3天接受了开放手术。术中未观察到明显的肿瘤肿块。然而,在疑似部位仅发现增厚和出血的节段。我们分别进行了12 cm和27 cm的部分空肠和回肠切除术。组织病理学证实每个区域均有黏膜下充血、水肿和出血,无肿瘤成分,最终诊断为肠壁内血肿。术后过程顺利,患者于术后第9天出院。在5年随访期内未发生复发。
我们遇到一例抗凝性肠梗阻手术病例,根据CT表现和高sIL-2R水平,难以与恶性淋巴瘤鉴别。对于长期接受抗凝药物治疗且PT-INR值高并伴有肠梗阻的患者,应始终考虑抗凝性肠梗阻的可能性。