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Murine Mesenteric Lymphadenectomy for Selective Disruption of Lymphatic Communication with Region-Specific Gut

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Mesenteric lipoblastoma presenting as a segmental volvulus.

David C Yu¹, Patrick J Javid, Kudakwashe R Chikwava

¹Department of Pediatric Surgery, Children's Hospital Boston, Harvard Medical School, Boston, MA 02115, USA. david.yu@childrens.harvard.edu

Journal of Pediatric Surgery

|February 24, 2009

Summary

A rare mesenteric lipoblastoma caused a rare case of bowel obstruction and midgut volvulus in a child. Surgical resection was successful, with no signs of recurrence.

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A Mouse Model of Intestinal Partial Obstruction

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Published on: March 5, 2018

Area of Science:

Pediatric Surgery
Surgical Oncology
Gastroenterology

Background:

Mesenteric lipoblastoma is a rare pediatric tumor.
Bowel obstruction and midgut volvulus are serious surgical emergencies.

Observation:

A 7-year-old girl presented with symptoms of nausea and vomiting.
Initial examination suggested possible malrotation with midgut volvulus.

Findings:

Emergency laparotomy revealed a large mesenteric lipoblastoma causing segmental small bowel volvulus.
The tumor was successfully resected with a segment of small bowel.
Resection margins were clear of tumor.

Implications:

This case highlights the importance of considering rare tumors in pediatric surgical emergencies.
Early diagnosis and surgical intervention are crucial for favorable outcomes.
Complete resection offers a good prognosis for mesenteric lipoblastoma.