scholarly journals Bladder perivascular epithelioid cell neoplasm: The importance of immunohistochemistry in the diagnosis of an unusual neoplasm

2021 ◽  
Vol 9 ◽  
pp. 2050313X2110008
Author(s):  
Solange De Noon ◽  
Benjamin Ayres ◽  
Uday Patel ◽  
Rami Issa ◽  
Colan Maxwell Ho-Yen

Perivascular epithelioid cell neoplasms represent a group of uncommon mesenchymal tumours with as yet undiscovered benign counterpart. Although perivascular epithelioid cell neoplasms have been described arising in most organ systems as well as in soft tissue and bone, only a small number of perivascular epithelioid cell neoplasms have been reported in the bladder. To date, there is no agreed system for predicting the behaviour of these tumours. We describe a case of a perivascular epithelioid cell neoplasm of the bladder arising in a 57-year-old male and initially diagnosed on biopsy and present a review of the literature focussing on the pathological differential diagnosis and the importance of key histological features in conjunction with a broad immunohistochemical panel. This case report highlights the key features of bladder perivascular epithelioid cell neoplasms that distinguishes these rare neoplasms from other bladder lesions.

2012 ◽  
Vol 41 (11) ◽  
pp. 1469-1474 ◽  
Author(s):  
Nicholas M. Desy ◽  
Mitchell Bernstein ◽  
Ayoub Nahal ◽  
Mohamed Aziz ◽  
Samuel Kenan ◽  
...  

2020 ◽  
Vol 13 (12) ◽  
pp. e236288
Author(s):  
Michaela Janks ◽  
Amelia Heaford ◽  
Maesha Deheragoda ◽  
Nedim Dino Hadzic

Perivascular epithelioid cell tumours are a novel histological description of mesenchymal tumours consisting of perivascular and epithelioid cells. Angiomyolipomas are one of the commoner types of this tumour group. They are typically associated with the inherited condition tuberous sclerosis (TS). In TS they are often seen arising in the kidneys and brain, although much more rarely can be seen in the liver. While usually thought of as benign tumours there is little evidence to predict whether they will progress to malignancy. Currently, there is no recommended best management strategy between resection and surveillance. We report two patients with TS seen in our centre with these described PEComa liver lesions histologically, however only one required a resection. On review of the literature, features such as increased size, rapid growth and vascular invasion would be concerning for possible malignant potential and therefore merit resection, as well as significant symptoms.


2021 ◽  
Vol 05 (13) ◽  
Author(s):  
Anic K ◽  
Karch K ◽  
Straub BK ◽  
Hönig A ◽  
Soder S ◽  
...  

2015 ◽  
Vol 19 ◽  
pp. 1-5 ◽  
Author(s):  
Angela Musella ◽  
Francesca De Felice ◽  
A. Kyriacos Kyriacou ◽  
Francesco Barletta ◽  
Filippo Maria Di Matteo ◽  
...  

2014 ◽  
Vol 38 (2) ◽  
pp. 176-188 ◽  
Author(s):  
John Kenneth Schoolmeester ◽  
Brooke E. Howitt ◽  
Michelle S. Hirsch ◽  
Paola Dal Cin ◽  
Bradley J. Quade ◽  
...  

2014 ◽  
Vol 57 (5) ◽  
pp. 409 ◽  
Author(s):  
Hyun-Jung Cho ◽  
Mi-Kyung Lee ◽  
Byung-Moon Kang ◽  
Sung-Hoon Kim ◽  
Hee-Dong Chae ◽  
...  

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