孤立性输卵管缺血合并扭转及小肠扭转1例

Medical Reports Pub Date : 2025-04-01 Epub Date: 2025-03-03 DOI:10.1016/j.hmedic.2025.100183
Oussama lamzouri , R. Rhazi , Bellejdel Ibtissam , Hafsa Taheri , Hanane Saadi , Ahmed Mimouni
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引用次数: 0

摘要

孤立性输卵管缺血是一种极其罕见的情况,特别是小肠扭转的结果。虽然小肠扭转是一种公认的外科急症,但其与继发性妇科并发症的关系仍未得到充分报道。我们描述了一个前所未有的病例,术后粘连导致肠梗阻和随后的压迫引起的输卵管扭转,最终导致缺血和坏死。一位30岁女性,阑尾切除术后两个月,表现为急性下胃疼痛和呕吐。腹部骨盆增强CT显示小肠扭转伴漩涡征,提示肠扭转。急诊腹腔镜检查发现广泛的术后粘连引起小肠梗阻。肠扭转的机械牵引力导致右输卵管的扭转和缺血。术中发现包括梗死,扭曲的右输卵管和保留的卵巢。手术干预包括粘连松解、右侧输卵管切除术和小肠切除术并原发回肠吻合术。术后过程顺利,1个月完全恢复。小肠扭转主要由先天性或后天的解剖异常引起,包括术后粘连。本病例的病理生理机制涉及继发性肠扭转对邻近结构施加压缩力,促使输卵管扭转。由此造成的血管损伤导致缺血性坏死,需要进行不可逆转的输卵管切除术。虽然卵巢扭转是一种典型的实体,孤立的输卵管扭转仍然是一个诊断挑战,特别是在肠梗阻的背景下。本病例强调了术后粘连、肠梗阻和妇科缺血并发症之间的重要相互作用。对于怀疑小肠扭转的病例,尤其是术后患者,早期手术干预是至关重要的,以减轻涉及邻近盆腔结构的缺血性并发症的风险。本病例强调需要提高临床对输卵管扭转的认识,这是严重粘连疾病和肠梗阻的潜在后果。多学科的方法是必不可少的,以确保及时诊断和优化手术结果。
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Isolated tubal ischemia due to combined torsion and small bowel volvulus: A rare case report
Isolated fallopian tube ischemia is an extremely rare condition, particularly as a consequence of small bowel volvulus. While small bowel volvulus is a well-recognized surgical emergency, its association with secondary gynecological complications remains underreported. We describe an unprecedented case in which postoperative adhesions led to intestinal obstruction and subsequent compression-induced torsion of the fallopian tube, culminating in ischemia and necrosis. A 30-year-old woman, two months post-appendectomy, presented with acute hypogastric pain and vomiting. Abdominopelvic contrast-enhanced computed tomography (CT) revealed a small bowel volvulus with a whirlpool sign, indicative of intestinal torsion. Emergency laparoscopy identified extensive postoperative adhesions causing small bowel obstruction. The mechanical traction exerted by the volvulized bowel led to the torsion and subsequent ischemia of the right fallopian tube. Intraoperative findings included an infarcted, twisted right fallopian tube with a preserved ovary. Surgical intervention involved adhesiolysis, right salpingectomy, and small bowel resection with primary ileal anastomosis. The postoperative course was uneventful, with full recovery at one month. Small bowel volvulus primarily results from congenital or acquired anatomical anomalies, including postoperative adhesions. The pathophysiological mechanism in this case involved secondary bowel volvulus exerting compressive forces on adjacent structures, precipitating fallopian tube torsion. The resultant vascular compromise led to ischemic necrosis, necessitating irreversible tubal resection. While ovarian torsion is a well-characterized entity, isolated tubal torsion remains a diagnostic challenge, particularly in the context of intestinal obstruction. This case highlights the critical interplay between post-surgical adhesions, bowel obstruction, and gynecological ischemic complications. Early surgical intervention is paramount in cases of suspected small bowel volvulus, particularly in post-surgical patients, to mitigate the risk of ischemic complications involving adjacent pelvic structures. This case underscores the need for heightened clinical awareness of fallopian tube torsion as a potential consequence of severe adhesive disease and bowel obstruction. A multidisciplinary approach is essential to ensure prompt diagnosis and optimize surgical outcomes.
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