Pregnancy-Associated Isolated Fallopian Tube Torsion With a True Knot Managed by Laparoscopic Salpingectomy: A Case Report.

IF 0.8 Q4 OBSTETRICS & GYNECOLOGY
Case Reports in Obstetrics and Gynecology Pub Date : 2026-09-11 eCollection Date: 2026-01-01 DOI:10.1155/crog/8852614
Ahmed Abdeltawab
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Abstract

Isolated torsion of the fallopian tube is a rare cause of acute abdomen in women of reproductive age, with an estimated annual incidence of approximately one per 1.5 million women. Its occurrence during pregnancy is rarer still, with fewer than 50 cases published. We present a 25-year-old primigravida at 27+6 weeks of gestation who was admitted to Farwaniya Hospital, Kuwait, with persistent right iliac fossa pain refractory to conservative management, associated with nausea and dysuria, on a background of recurrent urinary tract infection. Laboratory investigations showed leucocytosis and mild anaemia. Transabdominal ultrasound with colour Doppler identified a small simple right adnexal cystic lesion with preserved ovarian vascularity, and pelvic magnetic resonance imaging demonstrated an encysted fluid collection in the right iliac fossa of probable adnexal origin, together with a nondistended, normal-appearing appendix showing no features of inflammation. Following failure of conservative treatment and after counselling of the patient and her husband, diagnostic laparoscopy was performed. The right fallopian tube was gangrenous, twisted repeatedly upon itself and configured as a true knot, and salpingectomy was performed. Both ovaries and the appendix were macroscopically normal. Histopathology confirmed haemorrhagic infarction with epithelial necrosis of the tubal mucosa. The postoperative course was uneventful and the pregnancy continued to term, with spontaneous vaginal delivery of a healthy female neonate at 40+3 weeks of gestation. This case illustrates the diagnostic difficulty of isolated tubal torsion in pregnancy, in which urinary symptoms and non-specific imaging readily divert attention towards pyelonephritis, and supports laparoscopy as a safe and definitive diagnostic and therapeutic option in the second trimester. The intraoperative finding of a true knot is unusual and is documented here with annotated operative imaging.

腹腔镜输卵管切除术治疗妊娠相关孤立输卵管扭转伴真结一例报告。
孤立性输卵管扭转是育龄妇女急腹症的罕见病因,估计年发病率约为150万妇女中有1例。它在怀孕期间的发生更为罕见,发表的病例不到50例。我们报告了一位25岁的妊娠27+6周的初孕妇女,她在科威特Farwaniya医院住院,因持续的右髂窝疼痛,保守治疗难治性,伴有恶心和排尿困难,背景为复发性尿路感染。实验室检查显示白细胞增多和轻度贫血。经腹彩色多普勒超声发现单纯性右附件囊性病变,卵巢血管保留;盆腔磁共振成像显示右侧髂窝有囊状积液,可能起源于附件,同时有一个未膨胀的、外观正常的阑尾,未显示炎症特征。保守治疗失败后,经患者及其丈夫咨询,行诊断性腹腔镜检查。右输卵管坏疽,反复缠绕,形成真结,行输卵管切除术。卵巢和阑尾宏观上正常。组织病理学证实出血性梗死伴输卵管粘膜上皮坏死。术后过程平稳,妊娠持续足月,妊娠40+3周时阴道自然分娩一名健康女性新生儿。本病例说明了妊娠期孤立性输卵管扭转的诊断困难,其中泌尿系统症状和非特异性影像学很容易将注意力转移到肾盂肾炎,并支持腹腔镜作为妊娠中期安全和明确的诊断和治疗选择。术中发现真正的结是不寻常的,在这里有注释的手术影像记录。
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来源期刊
Case Reports in Obstetrics and Gynecology
Case Reports in Obstetrics and Gynecology Medicine-Obstetrics and Gynecology
CiteScore
1.30
自引率
0.00%
发文量
64
审稿时长
12 weeks
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