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J Korean Soc Radiol. 2016 Nov;75(5):410-414. English. Case Report. https://doi.org/10.3348/jksr.2016.75.5.410
Yoo HW , Lee KT , Lee SM .
Department of Radiology, Soonchunhyang University Cheonan Hospital, Cheonan, Korea.
Department of Internal Medicine, Soonchunhyang University Cheonan Hospital, Cheonan, Korea.
Department of Nuclear Medicine, Soonchunhyang University Cheonan Hospital, Cheonan, Korea. c91300@schmc.ac.kr
Abstract

Desmoid tumors are rare benign tumors with aggressive fibroblastic proliferation. Although desmoid tumors do not metastasize, they have locally aggressive features and can cause a urinary fistula. Here, we report a case of a 35-year-old woman with Gardner syndrome who was diagnosed with an intra-abdominal desmoid tumor 1 year previously and who presented with a newly developed cystic mass lesion on a computed tomography scan. The cystic mass lesion was clinically diagnosed as an urinoma from the right ureterotumoral fistula; thus, surgical resection of the mass lesion was planned. However, Tc-99m diethylenetriamine pentaacetic acid renal scintigraphy revealed bilateral ureterotumoral fistulas; hence, the treatment plan was changed to conservative management.

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