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Perforated jejunal duplication cyst in an adult: diagnosis and management
Vikram Saini1, Parshant Kumar2, Ujwal Chander3
1Department of Surgical Discipline, All India Institute of Medical Sciences Bathinda, Bathinda, Punjab, India vikramsaini2006@hotmail.com.
Insights
Enteric duplication cysts, rare congenital anomalies, can occur in the jejunum. This case highlights a perforated jejunal duplication cyst in an adult, requiring surgical resection and anastomosis.
Area of Science:
- Gastroenterology
- Surgical Pathology
Background:
- Enteric duplication cysts are rare congenital gastrointestinal anomalies.
- They are typically diagnosed in children, with adult cases being infrequent.
Purpose of the Study:
- To report a rare case of jejunal duplication cyst perforation in an adult.
- To emphasize the importance of recognizing this anomaly for surgical planning.
Main Methods:
- Case report of a male in his 50s presenting with acute abdomen.
- Emergency exploratory laparotomy revealing perforated jejunal duplication cysts.
- Surgical resection of the affected jejunal segment with end-to-end anastomosis.
Main Results:
- Identification and surgical management of two communicating jejunal duplication cysts, one perforated.
- Successful resection and anastomosis performed.
- Histological examination confirmed the diagnosis.
Conclusions:
- Adult presentation of enteric duplication cysts, particularly with perforation, is uncommon.
- Multimodality imaging can aid preoperative diagnosis, but intraoperative diagnosis is frequent.
- Increased clinical awareness is crucial for timely recognition and surgical intervention.
Abstract:
Enteric duplication cysts are an uncommon congenital anomaly that can occur anywhere along the gastrointestinal tract. These rare abnormalities are predominantly diagnosed in children and seldom reported in adults. We report a case of a male in his 50s who presented with an acute abdomen due to perforation peritonitis. Emergency exploratory laparotomy revealed two communicating jejunal duplication cysts, one of which was perforated. The involved jejunal segment was resected, and a primary end-to-end anastomosis was performed. Ultrasonography, CT and MRI can assist in making a preoperative diagnosis; however, intraoperative diagnosis is common and histological examination is required for confirmation. In this case, the congenital anomaly was identified intraoperatively and managed surgically. Increased awareness of this rare congenital entity among clinicians can aid in early recognition and appropriate surgical planning.
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