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Surgical Case Reports
Fig. 5 | Surgical Case Reports

Fig. 5

From: A giant pelvic solitary fibrous tumor with Doege–Potter syndrome successfully treated with transcatheter arterial embolization followed by surgical resection: a case report

Fig. 5

Pathological findings. Hematoxylin and eosin staining of the tumor showed monotonous spindle cell proliferation without atypia. The mitosis rate was low (2/10 high-power fields). Immunohistochemical staining demonstrated that the tumor cells were positive for CD34, CD99, Bcl-2, STAT6, and vimentin, consistent with a diagnosis of solitary fibrous tumor

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