阑尾子宫内膜异位症1例报告

Taghreed Albalawi, P. Gergi, A. Alotaibi
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摘要

背景:阑尾子宫内膜异位症占所有盆腔子宫内膜异位症病例的不到1%。表现为右髂窝疼痛,与急性阑尾炎相似。只有在切除阑尾的组织病理学检查后才有可能确诊。病例介绍:我们报告一例罕见的阑尾子宫内膜异位症(AE)病例,患者为38岁未婚女性,其他方面健康,以不到24小时的下腹疼痛伴恶心但无呕吐来到急诊室。所有其他的系统评价都不显著。患者无阳性病史或手术史。血液检查正常,腹部超声显示阑尾水肿壁增厚,管腔膨胀12毫米。腹腔镜阑尾切除术时,意外发现盆腔内有血色液体,子宫内有多个突出的肌瘤,阑尾发炎,行阑尾切除术。术后恢复过程顺利。最终的组织病理学检查证实阑尾子宫内膜异位症。结论:AE是一种罕见的实体,几乎都是通过组织病理学检查诊断出来的。急性腹痛,尤其是育龄妇女出现急性阑尾炎临床症状时,应纳入鉴别诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Case Report on Appendicular Endometriosis
Background: Appendicular Endometriosis represents less than 1% of all pelvic endometriosis cases. It manifests with pain in right iliac fossa and bear resemblance to acute appendicitis. Definitive diagnosis is possible only after histopathological examination of excised appendix. Case presentation: We report a rare case of Appendicular Endometriosis (AE) in a 38 years old non-married female, otherwise healthy, came to emergency room with less than 24 hours lower abdominal pain associated with nausea but no vomiting. All other systemic review was unremarkable. Patient has no positive medical or surgical history. Blood investigations were normal and abdominal ultrasound US showed edematous wall thickening of the appendix with 12 mm distended lumen. Laparoscopic appendicectomy was performed with incidental finding of blood-tinged fluid in the pelvis and multiple prominent fibroids of the uterus, the appendix was inflamed, and appendectomy done. Postoperative recovery course was uneventful. The final histopathological examination confirmed endometriosis of appendix. Conclusion: AE is a rare entity and almost always diagnosed after histopathological examination. it should be included in the differential diagnosis of acute abdominal pain, especially when women of childbearing age present with clinical symptoms of acute appendicitis.
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