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剖宫产瘢痕处腹壁子宫内膜异位症:一例报告

Abdominal wall endometriosis in a cesarean scar: a case report.

作者信息

Aljbawi Marwa, Redan Lana, Al-Bitar Ahmad, Saghier Ebtihal

机构信息

Faculty of Medicine, Damascus University, Damascus, Syrian Arab Republic.

Department of General Surgery, Faculty of Medicine, Damascus University, Damascus, Syrian Arab Republic.

出版信息

J Med Case Rep. 2025 May 19;19(1):239. doi: 10.1186/s13256-025-05301-3.

Abstract

BACKGROUND

Endometriosis affects 6-15% of reproductive-aged women, with abdominal wall endometriosis occurring in 1-12% of extrapelvic cases. Cesarean scar endometriosis, the most common abdominal wall endometriosis subtype, arises in 0.03-3.5% of post-cesarean patients, often presenting as cyclical pain or a palpable mass near surgical scars. Diagnostic challenges stem from nonspecific symptoms and imaging overlap with granulomas, hernias, or tumors.

CASE PRESENTATION

A 25-year-old female Arab patient presented with a 1.6 cm tender subcutaneous nodule adjacent to her Pfannenstiel scar, worsening during menses. Ultrasound revealed a hypoechoic nodule, while magnetic resonance imaging showed a 15 × 12 mm subcutaneous lesion with low T1 and intermediate T2 signals. Despite imaging favoring granuloma, clinical suspicion for cesarean scar endometriosis prompted wide surgical excision. Histopathology confirmed endometrial glands, stroma, and hemosiderin-laden macrophages, confirming abdominal wall endometriosis. Postoperatively, cyclical pain resolved, with no recurrence at the 2-month follow-up.

CONCLUSION

Cesarean scar endometriosis, though rare, requires high clinical suspicion in patients with prior cesarean sections and cyclical symptoms. Multimodal imaging aids differentiation, but histopathology remains definitive. Surgical excision with clear margins is curative, preventing complications such as malignant transformation. This case highlights the interplay of surgical history, hormonal factors, and anatomical predisposition in cesarean scar endometriosis pathogenesis. Clinicians must prioritize early recognition and intervention to optimize outcomes in this underdiagnosed condition.

摘要

背景

子宫内膜异位症影响6%-15%的育龄女性,腹壁子宫内膜异位症在盆腔外病例中占1%-12%。剖宫产瘢痕子宫内膜异位症是腹壁子宫内膜异位症最常见的亚型,在剖宫产术后患者中发生率为0.03%-3.5%,常表现为手术瘢痕附近的周期性疼痛或可触及的肿块。诊断挑战源于非特异性症状以及与肉芽肿、疝气或肿瘤的影像学表现重叠。

病例介绍

一名25岁的阿拉伯女性患者,在其耻骨联合上横切口瘢痕旁出现一个1.6厘米的压痛性皮下结节,月经期加重。超声显示为低回声结节,而磁共振成像显示一个15×12毫米的皮下病变,T1信号低,T2信号中等。尽管影像学表现倾向于肉芽肿,但对剖宫产瘢痕子宫内膜异位症的临床怀疑促使进行了广泛的手术切除。组织病理学证实存在子宫内膜腺体、间质和含铁血黄素的巨噬细胞,确诊为腹壁子宫内膜异位症。术后,周期性疼痛缓解,2个月随访时无复发。

结论

剖宫产瘢痕子宫内膜异位症虽然罕见,但对于有剖宫产史且有周期性症状的患者需要高度临床怀疑。多模态成像有助于鉴别,但组织病理学仍然是确诊的依据。切缘清晰的手术切除具有治愈性,可预防恶性转化等并发症。本病例突出了手术史、激素因素和解剖易感性在剖宫产瘢痕子宫内膜异位症发病机制中的相互作用。临床医生必须优先考虑早期识别和干预,以优化这种诊断不足疾病的治疗效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/badf/12090436/8446a6b5116b/13256_2025_5301_Fig1_HTML.jpg

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