Chromophobe renal cell carcinoma with concomitant sarcomatoid transformation and osseous metaplasia: a case report
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چکیده
منابع مشابه
Chromophobe renal cell carcinoma with concomitant sarcomatoid transformation and osseous metaplasia: a case report
BACKGROUND Chromophobe renal cell carcinoma is the third most common form of adult renal epithelial neoplasm. A sarcomatoid component occurs in approximately 8% of all chromophobe renal cell carcinoma cases, while metaplastic bone formation is extremely rare. CASE PRESENTATION An abdominal computed tomography scan revealed a hypovascular tumor with focal calcification, measuring 2.5 × 2.3 cm,...
متن کاملChromophobe renal cell carcinoma with osseous metaplasia: a case report.
A 60-year-old Japanese male with a chromophobe cell carcinoma of his left kidney is reported. The tumor, 18 x 27 mm in size, was incidentally found by abdominal ultrasonography. Computed tomography and magnetic resonance imaging demonstrated a well-demarcated solid tumor arising from the lower pole of the left kidney. Histopathological examination of the surgically removed tumor revealed that i...
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Clear cellrenal cell carcinoma (RCC) is the most common malignant renal tumor in adults, while chromophobe RCC (CRCC) is the third most common. Any subtypes of RCC can undergo sarcomatoid differentiation, but heterologous differentiation in sarcomatoid area is very rare in RCC. Here a61-year male is presented with hematuria and palpable mass. Clinicoradiologically, RCC was considered and left r...
متن کاملChromophobe Renal Cell Carcinoma with Sarcomatoid Differentiation
We report chromophobe renal cell carcinoma (CRCC) with sarcomatoid dedifferentiation in a sixty-five year old male. CRCC is a prognostically better, distinctive subtype of renal cell carcinoma (RCC), histologically characterized by cells containing translucent and reticulated cytoplasm with distinct cell borders. Sarcomatoid component accompanies 9% of CRCC which alters its prognostic implicati...
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ژورنال
عنوان ژورنال: BMC Urology
سال: 2013
ISSN: 1471-2490
DOI: 10.1186/1471-2490-13-72