Paratesticular Solitary Fibrous Pseudotumor and a Brief Literature Review
نویسندگان
چکیده
منابع مشابه
Paratesticular fibrous pseudotumor arising from tunica vaginalis.
Intrascrotal benign fibrous proliferations are uncommon and mostly arise from paratesticular region falling into the category of fibrous pseudotumor which is characterized by nodular growth composed of probably reactive proliferation of fibroblasts and inflammatory cells. Although benign, this often clinically mimics intrascrotal malignancy and usually remains undiagnosed preoperatively. Here, ...
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Solitary fibrous tumor (SFT) is a rare spindle cell neoplasm that usually arising from the pleura, but has been reported in diverse extrapleural sites. Urogenital localization is rare, and only several cases of paratesticular SFT have been reported. In the present report, we present the case of a 61-year-old male suffering from a paratesticular SFT. A surgical excision of the lesion was perform...
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A 78-year-old male patient presented with an inguinoscrotal nodule that had lasted for 3 years. The patient reported a past medical history of hydrocele formation. The final diagnosis was fibrous pseudotumor of the paratesticular region, which was based on a histopathological examination and immunohistochemical findings. The aim of this case report is to spread awareness and recognition of neop...
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Tumors arising in the spermatic cord are very rare. The common benign tumors of the spermatic cord include adenomatoid tumor, lipoma, neurofibroma, and leiomyoma. We report a rare case of fibrous pseudotumor of the spermatic cord presenting clinically as a hydrocele. A 28-year-old male presented with the complaint of swelling in the left scrotum, which gradually progressed in size over four yea...
متن کاملParatesticular Fibrous Pseudotumors
Paratesticular fibrous pseudotumors (PFPs) are rare pathologies with quite wide and variable topographic-morphological features. It is difficult to distinguish PFPs from malignant masses. Treatment can be done by resection of the mass. We reported a young patient's findings about this rare pathology.
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ژورنال
عنوان ژورنال: Journal of Urological Surgery
سال: 2019
ISSN: 2148-9580
DOI: 10.4274/jus.galenos.2019.2649