Umbilical Hernia as Forerunner of Primary Umbilical Endometriosis: A Case Report
This case report details a rare instance of primary umbilical endometriosis associated with an umbilical hernia, diagnosed via histopathology after surgical repair of the umbilical nodule and abdominal wall defect.
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This paper reports a single 24-year-old woman with spontaneous primary umbilical endometriosis presenting as a painful, enlarging umbilical swelling that darkened and bled during menses, alongside imaging evidence of an umbilical hernia. Diagnosis was based on ultrasound and MRI findings suggesting an endometriotic implant plus a small fascial defect with omental herniation, with fine-needle aspiration showing spindle cells in a hemorrhagic background, and definitive confirmation by histopathology after surgical excision (omphalectomy) and abdominal wall reconstruction with polyester mesh; no intra-abdominal endometriosis was found on imaging or during surgery. The authors note that spontaneous umbilical endometriosis is extremely rare and that the mechanism is unclear, offering several hypotheses such as metaplasia or spread pathways, and they explicitly state that longer follow-up is needed to assess recurrence or malignant transformation. This paper is centrally about endometriosis — it details a case of primary umbilical endometriosis associated with an umbilical hernia and reconstruction after confirmed cutaneous endometriosis.
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References (17)
- CUTANEOUS ENDOMETRIOSIS via openalex
- Endometriosis of the inguinal canal mimicking a hernia. via openalex
- Primary umbilical endometriosis via openalex
- Primary umbilical endometriosis via openalex
- Primary umbilical endometriosis - Diagnosis by fine needle aspiration via openalex
- Spontaneous Cutaneous Endometriosis of the Umbilicus via openalex
- The assessment of immunohistochemical profile of endometriosis implants, a practical method to appreciate the aggressiveness and recurrence risk of endometriosis. via openalex
- The development of the implantation theory for the origin of peritoneal endometriosis via openalex
- Umbilical endometriosis and the Cullen sign; a study of lymphatic transport from the pelvis to the umbilicus in monkeys. via openalex
- Umbilical endometriosis associated with large umbilical hernia. Case report. via openalex
- Umbilical hernia masking primary umbilical endometriosis - a case report. via openalex
- Villar’s nodule: A case report and systematic literature review of endometriosis externa of the umbilicus via openalex
- W2047663393 via openalex
- W2092400809 via openalex
- W1986773747 via openalex
- W6646845415 via openalex
- W6825841344 via openalex
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