Scar endometriosis: not a rarity now a day
Scar endometriosis, often linked to increased cesarean sections, presents with cyclical pain and discharge at incision sites, sometimes requiring surgical excision for diagnosis.
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This paper discusses scar endometriosis, focusing on cases occurring at sites of prior surgical scars, which the authors state are rising in frequency alongside increased cesarean sections. Using a single case described in detail, they report greenish discharge from a lesion located below the primary scar site occurring 5 years after the primary surgery, noting that typical presentation may include an underlying mass and cyclical incision-site pain with or without discharge, but that atypical cases may only be diagnosed after surgical excision. The authors aim to discuss the etiology, management, and preventive measures for scar endometriosis, without presenting a larger systematic cohort. This paper is centrally about endometriosis — it specifically reports a case of scar endometriosis following cesarean section and discusses its clinical features and implications.
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References (13)
- Abdominal scar endometriosis after caesarean section: report of five cases. via openalex
- Abdominal wall endometrioma after cesarean section: a preventable complication. via openalex
- Abdominal Wall Endometrioma: Localizing in Rectus Abdominus Sheath via openalex
- Abdominal Wall Endometriosis: An Overlooked but Possibly Preventable Complication via openalex
- Abdominal wall endometriosis: a surgeon's perspective and review of 445 cases via openalex
- Aspiration cytodiagnosis of endometriosis in an abdominal scar after cesarean section. via openalex
- [Endometriosis implant in cesarean section surgical scar]. via openalex
- Intramuscular Abdominal Wall Endometriosis Treated by Ultrasound-Guided Ethanol Injection via openalex
- Scar endometriosis: a clinicopathologic study of 17 cases. via openalex
- Scar Endometriosis: Case Report with Literature Review via openalex
- Scar endometriosis following caesarean section: a rare case report via openalex
- W1906309937 via openalex
- W2339578433 via openalex
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- last seen: 2026-06-10T17:14:06.276822+00:00