Anal Atresia in a Patient Who Had Undergone Hartmann Procedure

Hiroyuki Sawada1, Kazuhiro Toyota1, Masahiro Ikeda1

  • 1Department of Surgery, National Hospital Organization, Higashihiroshima Medical Center, Hiroshima, Japan.

Insights

A rare case of anal atresia, a congenital condition, developed after a Hartmann procedure for rectal cancer or colonic perforation. Surgical intervention successfully resolved symptoms, marking the first reported instance following this surgery.

Area of Science:

  • Gastroenterology
  • Surgical Oncology
  • Colorectal Surgery

Background:

  • The Hartmann procedure is essential for treating rectal cancer and colonic perforation, involving stoma creation and diversion of the distal bowel.
  • Complications typically involve inflammation or tumors in the diverted tract, with anal complications being rarely reported.
  • Anal atresia, a congenital defect, is exceptionally rare as a postoperative complication.

Observation:

  • An 84-year-old woman experienced persistent incomplete evacuation post-Hartmann procedure.
  • Examination revealed a closed anus with a thin skin layer and rectal stool retention on CT scan.
  • The patient had no prior history of anal disorders.

Findings:

  • This case represents the first documented instance of anal atresia occurring after a Hartmann procedure.
  • Surgical opening of the anus effectively removed retained stool.
  • The patient's symptoms of incomplete evacuation were fully resolved post-surgery.

Implications:

  • This case highlights the potential for rare anal complications following Hartmann procedures.
  • Prompt surgical intervention can effectively manage acquired anal atresia.
  • Further investigation may be warranted into the mechanisms of acquired anal atresia post-colorectal surgery.

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