Umbilical reconstruction for endometriosis: A case report

IF 0.7 Q4 SURGERY
Amine Sebai, Aida Zaiem, Souhaib Atri, Ahmed Ben Mahmoud, Aida Khadhar, Montassar Kacem
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Abstract

Introduction

Umbilical endometriosis is a rare form of cutaneous endometriosis characterized by the presence of ectopic endometrial tissue in the umbilical skin. This condition may arise spontaneously or secondary to surgical procedures.

Case presentation

A 30-year-old nulliparous woman presented with a three-month history of a painful, hyperpigmented umbilical nodule that worsened during menstruation, following laparoscopic resection of a urachal cyst one year earlier. Physical examination revealed a 2 cm firm nodule, and imaging confirmed a subcutaneous umbilical mass without evidence of pelvic endometriosis. Given the cyclical nature of symptoms, umbilical endometriosis was suspected, and surgical excision with a 1 cm margin was performed, followed by immediate umbilical reconstruction using a modified purse-string technique. Histopathological analysis confirmed endometriosis with no signs of malignancy, and the patient was started on GnRH agonist therapy postoperatively. At 3- and 12-month follow-ups, the patient had no recurrence, and the reconstructed umbilicus maintained a satisfactory aesthetic result.

Clinical discussion

Umbilical endometriosis is a rare form of cutaneous endometriosis, typically presenting as a painful, hyperpigmented umbilical nodule with cyclical symptoms tied to menstruation. Diagnosis relies on clinical suspicion, imaging, and is confirmed by histopathology. Surgical excision remains the definitive treatment, often followed by immediate umbilical reconstruction using techniques such as the purse-string method for optimal aesthetic outcomes. Adjunctive hormonal therapy may help manage residual symptoms and reduce recurrence risk.

Conclusion

This case highlights the importance of including umbilical endometriosis in the differential diagnosis of umbilical masses and demonstrates effective management through surgical excision and reconstruction.
子宫内膜异位症脐重建1例。
简介:脐带子宫内膜异位症是一种罕见的皮肤子宫内膜异位症,其特征是在脐带皮肤中存在异位子宫内膜组织。这种情况可能自发发生或继发于外科手术。病例介绍:一名30岁的未生育妇女,在一年前腹腔镜切除尿管囊肿后,在月经期间出现疼痛,色素沉着的脐结节,三个月的病史。体格检查显示一个2厘米的坚固结节,影像学证实皮下脐肿块,无盆腔子宫内膜异位症的证据。考虑到症状的周期性,怀疑脐带子宫内膜异位症,手术切除1厘米边缘,随后立即使用改良的荷包线技术重建脐带。组织病理学分析证实子宫内膜异位症,无恶性肿瘤迹象,患者术后开始接受GnRH激动剂治疗。在3个月和12个月的随访中,患者没有复发,重建的脐部保持了令人满意的美观效果。临床讨论:脐带子宫内膜异位症是一种罕见的皮肤子宫内膜异位症,典型表现为疼痛、色素沉着的脐带结节,伴有周期性月经症状。诊断依赖于临床怀疑,影像学,并由组织病理学证实。手术切除仍然是最终的治疗方法,通常随后使用诸如钱包线方法等技术立即进行脐带重建,以获得最佳的美学效果。辅助激素治疗可能有助于控制残留症状并降低复发风险。结论:本病例强调了将脐带子宫内膜异位症纳入脐带肿块鉴别诊断的重要性,并通过手术切除和重建展示了有效的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.10
自引率
0.00%
发文量
1116
审稿时长
46 days
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