Cellular angiofibroma arising from the rectocutaneous fistula in an adult: A case report.

World J Clin Cases

Division of Colon and Rectal Surgery, Department of Surgery, Tri-Service General Hospital Songshan Branch, National Defense Medical Center, Taipei 105, Taiwan.

Published: April 2024

AI Article Synopsis

  • Rectocutaneous fistulae develop from infections in anal glands and can lead to perineal masses, as seen in a rare case of cellular angiofibroma (CAF) associated with such a fistula.
  • A 52-year-old male with a 2-year history of a painful perineal mass underwent imaging that revealed its connection to a rectocutaneous fistula, leading to surgical excision and diagnosis of CAF.
  • The case illustrates that CT imaging is effective for diagnosing perineal lesions, and CAFs can be successfully removed even when linked to cutaneous fistulas.

Article Abstract

Background: Rectocutaneous fistulae are common. The infection originates within the anal glands and subsequently extends into adjacent regions, ultimately resulting in fistula development. Cellular angiofibroma (CAF), also known as an angiomyofibroblastoma-like tumor, is a rare benign soft tissue neoplasm predominantly observed in the scrotum, perineum, and inguinal area in males and in the vulva in females. We describe the first documented case CAF that developed within a rectocutaneous fistula and manifested as a perineal mass.

Case Summary: In the outpatient setting, a 52-year-old male patient presented with a 2-year history of a growing perineal mass, accompanied by throbbing pain and minor scrotal abrasion. Physical examination revealed a soft, well-defined, non-tender mass at the left buttock that extended towards the perineum, without a visible opening. The initial assessment identified a soft tissue tumor, and the laboratory data were within normal ranges. Abdominal and pelvic computed tomography (CT) revealed swelling of the abscess cavity that was linked to a rectal cutaneous fistula, with a track-like lesion measuring 6 cm × 0.7 cm in the left perineal region and attached to the left rectum. Rectoscope examination found no significant inner orifices. A left medial gluteal incision revealed a thick-walled mass, which was excised along with the extending tract, and curettage was performed. Histopathological examination confirmed CAF diagnosis. The patient achieved total resolution during follow-up assessments and did not require additional hospitalization.

Conclusion: CT imaging supports perineal lesion diagnosis and management. Perineal angiofibromas, even with a cutaneous fistula, can be excised transperineally.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11036466PMC
http://dx.doi.org/10.12998/wjcc.v12.i10.1778DOI Listing

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