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阑尾子宫内膜异位症所致急性阑尾炎:两例报告及文献复习

Acute appendicitis due to appendiceal endometriosis: Two case report and literature review.

作者信息

Bolcatto Abdala, Erina Melisa, Mandojana Facundo Ignacio, Bruera Nicolás, Doniquian Alejandro Marcelo, Viscido German Rodrigo

机构信息

Clinica Universitaria Reina Fabiola, Córdoba, Argentina.

Clinica Universitaria Reina Fabiola, Córdoba, Argentina.

出版信息

Int J Surg Case Rep. 2025 Jan;126:110743. doi: 10.1016/j.ijscr.2024.110743. Epub 2024 Dec 15.

Abstract

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.

摘要

引言

阑尾子宫内膜异位症(AE)是一种罕见病症,在子宫内膜异位症患者中的患病率为0.05%至1.7%。它在急性阑尾炎(AA)病例中所占比例不到1%。

病例展示

我们呈现两例组织学病因是子宫内膜异位症的急性阑尾炎病例。两例患者均为40岁左右,表现为右下腹疼痛。通过腹部计算机断层扫描(CT)诊断为急性阑尾炎,第一例CT显示急性阑尾炎,经腹腔镜阑尾切除术成功治疗。第二例CT显示阑尾蜂窝织炎迹象,最初非手术治疗效果不佳,48小时后进行了探查性腹腔镜检查及脓肿引流。随后在6个月后进行了预定的腹腔镜阑尾切除术。两例的组织病理学诊断均为因阑尾子宫内膜异位症导致的急性阑尾炎,子宫内膜腺体有近期出血,致使阑尾肌层增生。

讨论

子宫内膜异位症的特征是子宫腔外存在子宫内膜组织,很少会累及阑尾,即阑尾子宫内膜异位症。阑尾子宫内膜异位症虽不常见,但由于影像学表现不具特异性且临床表现多样,从无症状病例到急性阑尾炎,给诊断带来了挑战。阑尾切除术后的组织学评估是确诊的关键。阑尾子宫内膜异位症与右侧盆腔受累有关,通常需要手术治疗,阑尾切除术一般可缓解急性症状。然而,盆腔子宫内膜异位症导致的周期性疼痛可能会复发,这凸显了腹腔镜手术期间进行全面评估的重要性。

结论

由阑尾子宫内膜异位症引起的急性阑尾炎是一种罕见病症,仅根据个人病史、临床表现甚至影像学检查进行术前诊断非常困难。对于有相关盆腔子宫内膜异位症的育龄女性,鉴别诊断时应考虑到该病,尽管所有病例推荐的治疗方法都是手术。

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