Successful Surgical Treatment of a Recurrent Pelvic Solitary Fibrous Tumor of Uterine Origin Accompanied by Doege-Potter Syndrome: A Case Report

Yasunori Deguchi; Wataru Komuta; Tomokazu Watanabe; Kazuho Saiga; Koki Kurahashi; Kazuo Otsuka; Koji Hirata; Masaki Mizumoto; Akihiro Kitaoka; Masazumi Zaima

doi:10.12659/AJCR.936806

13 October 2022 : Case report Japan

Successful Surgical Treatment of a Recurrent Pelvic Solitary Fibrous Tumor of Uterine Origin Accompanied by Doege-Potter Syndrome: A Case Report

Mistake in diagnosis, Rare disease

Yasunori Deguchi^1ABCDEF*, Wataru Komuta^1BCDEF, Tomokazu Watanabe^2BCD, Kazuho Saiga^3BCD, Koki Kurahashi^1B, Kazuo Otsuka^1B, Koji Hirata^1B, Masaki Mizumoto^1B, Akihiro Kitaoka^1B, Masazumi Zaima^1ABE

DOI: 10.12659/AJCR.936806

Am J Case Rep 2022; 23:e936806

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Figure 1. Computed tomography (CT) and magnetic resonance imaging (MRI) at presentation. (A) Contrast-enhanced CT showed a heterogeneously enhanced mass occupying the pelvic space that compressed the bladder (yellow arrows) and the rectum (yellow arrow heads) to the right. (B) T1-weighted MRI showed a low-intensity mass. (C) T2-weighed MRI showed a heterogenous iso- to high-intensity mass.

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Successful Surgical Treatment of a Recurrent Pelvic Solitary Fibrous Tumor of Uterine Origin Accompanied by Doege-Potter Syndrome: A Case Report

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