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Published on: August 21, 2017
Ileal angiomyolipoma manifested by small intestinal intussusception
Chang Ho Lee1, Jong Hun Kim, Doo Hyun Yang
1Department of Surgery, Chonbuk National University Medical School, Jeonbuk 561-180, South Korea.
World Journal of Gastroenterology
|March 19, 2009
Summary
This study reports an exceedingly rare case of an ileal angiomyolipoma (AML) causing intussusception in a 28-year-old man. The findings highlight the importance of considering rare small intestinal tumors in diagnosis.
Area of Science:
- Gastroenterology
- Oncology
- Pathology
Background:
- Angiomyolipomas (AMLs) are benign mesenchymal hamartomas typically found in the kidneys, often associated with tuberous sclerosis.
- Extra-renal AMLs are uncommon, with the liver being the most frequent site.
- Small intestinal AMLs are exceptionally rare.
Observation:
- A case of a 28-year-old male presenting with ileal intussusception is described.
- The intussusception was caused by an ileal angiomyolipoma.
- Clinicopathological and immunohistochemical features of this rare entity were analyzed.
Findings:
- The study details the case of a rare ileal angiomyolipoma.
- It discusses the clinicopathological and immunohistochemical characteristics of small intestinal AMLs.
- A review of the existing literature on small intestinal AMLs is presented.
Implications:
- This case underscores the rarity of small intestinal angiomyolipomas.
- It emphasizes the need for considering unusual diagnoses in cases of intussusception.
- Further research into the pathogenesis and management of extra-renal AMLs is warranted.
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