[Show abstract][Hide abstract] ABSTRACT: Solitary fibrous tumors are rare mesenchymal spindle cell neoplasms that are usually found in the pleura. The kidneys are an uncommon site and only few cases of renal solitary fibrous tumor exhibit malignant behavior metastasizing to the liver, lung, and bone through the hematogenous pathway.
OncoTargets and Therapy 01/2014; 7:679-85. · 1.34 Impact Factor
[Show abstract][Hide abstract] ABSTRACT: A 49-year-old woman admitted to our hospital with a 3-month history of right flank pain without gross hematuria. Computed tomography scan of the abdomen showed that a 6x6x5 cm, contrast-enhanced mass was localized on the right renal pelvis. Histologically, a tumor composed of small ovoid to spindle shaped nuclei with indistinct cytoplasm was seen. Neoplastic cells showed diffuse immunoreactivity with CD34. It was diagnosed as solitary fibrous tumor. Solitary fibrous tumor of kidney is a very rare spindle cell neoplasm. It can mimic renal malignancy radiographically but almost all of renal solitary fibrous tumors are benign lesions. ÖZET Böbreğin soliter fibröz tümörü: bir olgu sunumu ve literatürün detaylı gözden geçirilmesi Kırk dokuz yaşındaki kadın hasta, gros hematüri olmaksızın 3 aydır süren sağ yan ağrısı şikayeti ile hastanemize başvurdu. Bilgisayarlı tomografide batında, sağ renal pelvis yerleşimli, kontrast tutan 6x6x5 cm boyutlarında kitle görüldü. Histolojik kesitlerde, küçük, iğsi-oval çekirdekli, sitoplazmik sı-nırları net olarak seçilemeyen hücrelerden oluşan tümör görüldü. Neoplastik hücreler CD34 ile kuvvetli immünreaktivite gösterdi. Lezyona soliter fibröz tümör tanısı konuldu. Böbreğin soliter fibröz tümörü, nadir görülen iğsi hüc-reli bir neoplazmdır. Radyolojik olarak renal maligniteleri taklit edebilir, ancak hemen tüm renal soliter fibröz tümörler benign lezyonlardır.
[Show abstract][Hide abstract] ABSTRACT: Renal solitary fibrous tumor (SFT) is a rare, and a large scale study on this topic is lacking to date. In this article, we summarize the previously reported cases. The symptoms and signs resemble those of renal cell carcinoma, including hematuria, flank/abdominal/lumbar pain and palpable abdominal mass. Grossly, the tumor demonstrates a well-circumscribed solid mass. Microscopically, the tumor consists of fusiform or ovoid spindle cells and a various amounts of collagen bundles with patternless, storiform, or fascicular arrangements with an occasional hemangiopericytomatous pattern. Immunohistochemically, CD34, CD99 and bcl-2 are often detected. Ultrastructurally, tumor cells contain irregular nuclei, prominent Golgi apparatus, branching rough endoplasmic reticulum, variable numbers of mitochondria. Surgical resection is considered to be the gold standard therapy. Most of renal SFT are benign, but cases of approximately 10 to 15% behave in an aggressive fashion. All patients need to be on long-term follow-up because clinical behavior is rather unpredictable. As the molecular genetic study of renal SFTs is lacking, a large scale study will be desirable in the future.
International journal of clinical and experimental pathology. 01/2014; 7(6):2737-2742.
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