scholarly journals MP17-15 LIPID CELL VARIANT OF UROTHELIAL CARCINOMA - EVALUATION OF TUMOR AGGRESSIVENESS AND DEMONSTRATION OF LIPID COMPONENT

2020 ◽  
Vol 203 ◽  
pp. e231-e232
Author(s):  
Tatsuro Hayashi* ◽  
Go Kimura ◽  
Mikio Shibasaki ◽  
Hiroya Hasegawa ◽  
Naoto Hodotsuka ◽  
...  
2006 ◽  
Vol 13 (11) ◽  
pp. 1448-1450 ◽  
Author(s):  
RYO YAMASHITA ◽  
RAIZOU YAMAGUCHI ◽  
KEIJI YUEN ◽  
MASASHI NIWAKAWA ◽  
KENICHI TOBISU

2018 ◽  
Vol 17 (14) ◽  
pp. e2997
Author(s):  
T. Hayashi ◽  
G. Kimura ◽  
H. Hasegawa ◽  
R. Amakawa ◽  
N. Hodozuka ◽  
...  

2020 ◽  
Vol 33 ◽  
pp. 101331
Author(s):  
Anuj Mahajan ◽  
Prashanth Adiga ◽  
Aaron Fernandes

2010 ◽  
Vol 34 (3) ◽  
pp. 371-376 ◽  
Author(s):  
Antonio Lopez-Beltran ◽  
Mahul B. Amin ◽  
Pedro S. Oliveira ◽  
Rodolfo Montironi ◽  
Ferran Algaba ◽  
...  

Author(s):  
Ioana Mihai ◽  
Sorina Taban ◽  
Alin Cumpanas ◽  
Emilian Gh. Olteanu ◽  
Mihaela Iacob ◽  
...  

The most common histological type of urinary bladder cancer is urothelial carcinoma (UC). In contrast, the clear cell variant of urothelial carcinoma (CCUC) is quite a rare neoplasm. In this study, we report a case of an 81-year-old male, presenting with gross hematuria and acute urinary retention, which was subsequently diagnosed with CCUC at our pathology department. Furthermore, we provide a short systematic review of the literature (PubMed, Scopus, Science Citation Index) for this rare histopathological entity and a brief discussion about its morphological and immunohistochemical (IHC) characteristics.


2019 ◽  
Vol 18 (11) ◽  
pp. e3583
Author(s):  
T. Hayashi ◽  
G. Kimura ◽  
S. Nozaki ◽  
M. Shibasaki ◽  
H. Hasegawa ◽  
...  

Rare Tumors ◽  
2012 ◽  
Vol 4 (4) ◽  
pp. 153-155 ◽  
Author(s):  
Mario W. Kramer ◽  
Mahmoud Abbas ◽  
Stefanie Pertschy ◽  
Jan Ulrich Becker ◽  
Hans-Heinrich Kreipe ◽  
...  

Clear cell variants of transitional cell carcinomas (TCC) of the bladder are extremely rare tumors. Only 6 cases have been reported until now. We report of a 67 year old man who presented with fast growing tumor disease. While initial diagnosis showed localized bladder tumor, final histopathology revealed pT4, G3, L1 urothelial carcinoma with clear cell differentiation. No more than 14 weeks after initial diagnosis the patient died from multi-organ failure after unsuccessful salvage laparotomy which showed massive tumor burden within the pelvis and peritoneal carcinosis. This case demonstrated an extremely fast tumor growth. Therefore, patients with clear cell urothelial carcinoma should be treated vigorously and without time delay. We present a case of clear cell variant of TCC which exhibited an extremely aggressive behavior. To our knowledge this is the fifth report of this rare disease.


2015 ◽  
Vol 8 (3) ◽  
pp. 515-519 ◽  
Author(s):  
Yu Miyama ◽  
Teppei Morikawa ◽  
Tohru Nakagawa ◽  
Yukio Homma ◽  
Masashi Fukayama

We report on a case of urothelial carcinoma (UC) with lipid cell and micropapillary variants in the ureter. A 64-year-old man presented with gross hematuria. Urinary cytology revealed the presence of atypical urothelial cells. Computed tomography and drip infusion/retrograde pyelography identified a mass-occupying lesion in the left mid-ureter, as well as left hydronephrosis. A clinical diagnosis of left ureteral cancer was given and the patient underwent left nephroureterectomy. Microscopically, the major component of the tumor was a conventional high-grade UC. In the invasive region, however, lipid cell and micropapillary variants of UC were also observed. Upon immunohistochemical analysis, all of the components were diffusely positive for cytokeratin 7 and p53. Intense membranous expression of human epidermal growth factor receptor 2 (HER2) was also observed in both the lipid cell and micropapillary variants of UC, whereas weak and incomplete staining was observed in most regions of the conventional UC. The pathological stage was pT3 N2. Multiple times, the patient experienced recurrence of the UC in the urinary bladder and urethra. Although the patient underwent total cystectomy and urethrectomy, 52 months following the initial surgery, signs of local recurrence developed, as well as multiple lymph node and bone metastases. The patient died 75 months following the initial surgery. To the best of our knowledge, this is the first reported case of a lipid cell variant of ureteral UC. The overexpression of HER2 may be associated with both the lipid cell and micropapillary variants of UC.


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