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 4. Pathological findings of the resected specimens. (A, B) Hematoxylin and eosin staining with a (A) low-power view and a (B) high-power view. (C–E) Immunohistochemistry (IHC) showed positive staining for CD34 (C), STAT6 (D), and IGF-II (E). (F) IHC study of Ki67 (Scale bars: 100 µm).

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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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