阑尾子宫内膜异位症致急性阑尾炎2例报告并文献复习。

IF 0.6 Q4 SURGERY International Journal of Surgery Case Reports Pub Date : 2025-01-01 Epub Date: 2024-12-15 DOI:10.1016/j.ijscr.2024.110743
Abdala Bolcatto, Melisa Erina, Facundo Ignacio Mandojana, Nicolás Bruera, Alejandro Marcelo Doniquian, German Rodrigo Viscido
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引用次数: 0

摘要

简介:阑尾子宫内膜异位症(AE)是一种罕见的疾病,在子宫内膜异位症患者中的患病率为0.05%至1.7%。它代表了病例的表现:我们报告了两例AA,其组织学原因是子宫内膜异位症。这两例患者均为40岁左右,表现为右侧髂窝腹痛。通过腹部计算机断层扫描(CT)诊断AA,第一例表现为急性阑尾炎,经腹腔镜阑尾切除术成功治疗。第2例CT显示阑尾粘液征象,最初非手术治疗效果不佳,48 h后行腹腔镜探查及脓肿引流术。随后,6个月后进行腹腔镜阑尾切除术。两例患者的组织病理学诊断均为AE所致AA,伴子宫内膜腺近期出血,引起阑尾肌层增生。讨论:子宫内膜异位症,以子宫腔外存在子宫内膜组织为特征,很少影响阑尾,称为AE。AE虽然不常见,但由于非特异性的影像学表现和不同的表现(从无症状到AA),给诊断带来了挑战。阑尾切除术后的组织学评估对诊断是决定性的。AE与右侧盆腔受累有关,通常需要手术治疗,阑尾切除术通常解决急性症状。然而,盆腔子宫内膜异位症引起的周期性疼痛的复发可能会持续存在,这强调了腹腔镜手术中全面评估的重要性。结论:AE引起的AA是一种罕见的疾病,术前仅根据个人病史、临床表现甚至影像学检查诊断非常困难。对于伴有盆腔子宫内膜异位症的育龄妇女,尽管在所有病例中推荐的治疗方法都是手术,但在鉴别诊断时应考虑到这一点。
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Acute appendicitis due to appendiceal endometriosis: Two case report and literature review.

Introduction: Appendiceal endometriosis (AE) is a rare condition, with a prevalence ranging from 0.05 % to 1.7 % in patients with endometriosis. It represents <1 % of cases of acute appendicitis (AA).

Cases presentation: We present two cases of AA where the histological cause was endometriosis. Both cases involved patients around 40 years old who presented with abdominal pain in the right iliac fossa. AA was diagnosed through abdominal computed tomography (CT), which in the first case showed acute appendicitis, successfully treated with laparoscopic appendectomy. In the second case, the CT showed signs of an appendiceal phlegmon, initially treated non-operatively with poor response, leading to exploratory laparoscopy and abscess drainage 48 h later. Subsequently, a scheduled laparoscopic appendectomy was performed after 6 months. Histopathological diagnosis in both cases was AA due to AE with endometrial glands showing recent bleeding, causing hyperplasia of the appendiceal muscular layer.

Discussion: Endometriosis, characterized by the presence of endometrial tissue outside the uterine cavity, can rarely affect the appendix, termed AE. AE, though uncommon, poses diagnostic challenges due to nonspecific imaging findings and variable presentations, ranging from asymptomatic cases to AA. Histological evaluation post-appendectomy is definitive for diagnosis. AE is associated with right-sided pelvic involvement and often requires surgical management, with appendectomy typically resolving acute symptoms. However, recurrence of cyclical pain due to pelvic endometriosis may persist, underscoring the importance of comprehensive evaluation during laparoscopic procedures.

Conclusion: AA caused by AE is an uncommon condition, with very difficult preoperative diagnosis based solely on personal history, clinical presentation, and even imaging studies. It should be considered in differential diagnoses for women of reproductive age with associated pelvic endometriosis, although the recommended treatment in all cases is surgical.

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