Open AccessRenal solitary fibrous tumour: A rare pathological entity
Author(s) -
Biao Dong,
Jianjian Zhang,
Gang Wang,
Xiuyu Zhai,
Yue Fu,
Honglan Zhou,
Yuantao Wang
Publication year - 2014
Publication title -
canadian urological association journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.477
H-Index - 38
eISSN - 1920-1214
pISSN - 1911-6470
DOI - 10.5489/cuaj.1854
Subject(s) - solitary fibrous tumor , cd34 , cd99 , cd117 , pathology , immunohistochemistry , desmin , medicine , horseshoe kidney , kidney , renal pelvis , pathological , anatomy , biology , vimentin , genetics , stem cell , endocrinology
A solitary fibrous tumour (SFT) is a rare mesenchymal cell neoplasm that can develop at any site. SFT of the kidney is extremely rare. Recently, we had a case of solitary fibrous tumour involving the left kidney in a 71-year-old female patient. The SFT was incidentally found by imaging modalities at the time of a physical workup. Computed tomography and retrograde pyelography showed a 4 × 3.5 × 4-cm nodular mass in the middle poles of the left kidney adjacent to the renal pelvis. A laparoscopic radical resection of the left kidney was performed. The tumour was well-circumscribed and composed of a mixture of spindle cells; microscopically, we found dense collagenous bands. Immunohistochemical studies showed strong reactions with CD34, bcl-2 and CD99. A nuclear positivity with Ki-67 was observed in less than 1% of cells. The tumour was negative for desmin, SMA and CD117. Histopathological and immunohistochemical studies confirmed the diagnosis of a solitary fibrous tumour.