CASE REPORT UROTHELIAL CARCINOMA OF BLADDER WITH SARCOMATOID FEATURES AND GIANT CELL COMPONENT
نویسندگان
چکیده
Around 0.3 percent of all primary tumors the urinary bladder are sarcomatoid carcinomas, a rare aggressive tumor with poor prognosis. Histological diagnosis for urothelialcarcinoma plays significant role but is challenging in several ways. Making foundational relies heavily on immunohistochemistry. We present case high-grade urothelial cancer characteristics and having components giant cells. The discusses an 80-year-old male who had been referred because painless intermittent hematuria. A 32 m mass at posterior lateral walls without perivesical fat infiltration was detected during computed tomography urography. Histopathology results from transurethral resection patient showed pTa malignant carcinoma spindle cell tumor. Due to recurrence, underwent Re-TURBT twice our institution BCG re-induction intravenously. Given that it contained mesenchymal markers such as EMA, IHC corroborated final cancer. It crucial recognize unusual variations they have impact prognosis general care. largely determined by For variants, radical cystectomy standard treatment however, intravenous may be beneficial patients not fit surgery.
منابع مشابه
Urinary bladder carcinoma with triplicate differentiations into giant cell sarcomatoid carcinoma, squamous cell carcinoma, and papillary urothelial transitional cell carcinoma: a case report
The author reports a very rare and very unique urinary bladder carcinoma. This carcinoma occurred in a 68-year-old Japanese patient who underwent cystectomy for bladder tumor. The tumor was large polypoid and ulcerated one. Histologically, the tumor consisted of the following three elements: giant cell sarcomatoid carcinoma (70% in area), squamous cell carcinoma (20% in area), and papillary uro...
متن کاملSarcomatoid Chromophobe Renal Cell Carcinoma with Heterologous Component
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 کاملSynchronous papillary urothelial carcinoma of the bladder and squamous cell carcinoma with sarcomatoid differentiation: A case report.
The incidence rate of multiple primary tumors is 37% in all types of cancer. A patient diagnosed with primary cancer is 1.29 times more likely to develop an additional primary cancer when compared with the general population. Furthermore, in patients diagnosed with primary cancer, the possibility of a secondary malignancy in the same or different organ is increased. Following the identification...
متن کاملSarcomatoid carcinoma with small cell carcinoma component of the urinary bladder: a case report with review of the literature.
Sarcomatoid carcinoma of the urinary bladder is an uncommon neoplasm characterized histopathologically by the presence of malignant spindle cell and epithelial components. Albeit extremely rare, sarcomatoid carcinoma with small cell carcinoma has been reported. Herein, we describe an additional case of sarcomatoid carcinoma with small cell carcinoma and squamous cell carcinoma of the urinary bl...
متن کاملGiant sarcomatoid carcinoma of the breast - a rare case report.
Metaplastic breast carcinoma breast is rare entity having mixture of epithelial and mesenchymal elements which contains overtly sarcoma-like elements on light microscopy and its clinical behaviour is not well documented. We are presenting a case in a 50 - year old female presented with a large swelling over the left side of the breast. On histopathology, diagnosis made as metaplastic carcinoma ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: International journal of advanced research
سال: 2022
ISSN: ['2707-7802', '2707-7810']
DOI: https://doi.org/10.21474/ijar01/15297