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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.
Abstract:
BACKGROUND Hartmann procedure can be necessary for the treatment of rectal cancer and colonic perforation. The distal diverted intestinal tract is usually disregarded, while the proximal colon is diverted with a stoma. Most of the reported complications related to a diverted intestinal tract following Hartmann procedure include inflammation and intestinal tumors; however, there are only a few reports about postoperative anal complications. Herein, we report a rare case of anal atresia following Hartmann procedure. Anal atresia is generally considered as a congenital malformation; therefore, this was an extremely rare case, as there are no previous reports about anal atresia following Hartmann procedure. CASE REPORT An 84-year-old woman presented to our hospital with a persistent feeling of incomplete evacuation. She had undergone Hartmann procedure for diverticular disease of the sigmoid colon, with perforation, 5 years ago and had no major complications after the surgery. She had no history of anal disorders such as hemorrhoids or anal fissures. On examination, her anus was found to be closed by a thin skin, and computed tomography revealed stool retention in the diverted rectum. The anus was surgically opened to remove the stool, after which the feeling of incomplete evacuation resolved with no subsequent recurrence. CONCLUSIONS This is the first report of anal atresia in a patient following Hartmann procedure. The surgical intervention was effective in resolving the blockage and relieving the patient's feeling of incomplete evacuation.
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