scholarly journals Bilateral well differentiated paratesticular liposarcoma: A rare case report

2018 ◽  
Vol 2 (4) ◽  
Author(s):  
Funda Bozkurt ◽  
Hamide Sayar ◽  
Tuba Kara ◽  
Mehmet Ozgur OT
2013 ◽  
Vol 4 (3) ◽  
pp. 272-274
Author(s):  
Shubha P. Bhat ◽  
Kishan H. L. Prasad ◽  
Rohan Shetty ◽  
Rajesh Ballal ◽  
Sunil Y. Kumar ◽  
...  

2009 ◽  
Vol 2009 ◽  
pp. 1-2 ◽  
Author(s):  
Toshihiro Matsuo ◽  
Takashi Sugita ◽  
Shoji Shimose ◽  
Tadahiko Kubo ◽  
Yuji Yasunaga ◽  
...  

Liposarcoma is categorized as a soft tissue sarcoma and most commonly appears in the lower extremities and rarely in the foot during adulthood. We present a very rare case report of a primary well-differentiated liposarcoma arising in the foot on a 60-year-old female. Marginal resection of the tumor with metatarsal ray amputation was eventually performed. The patient's postoperative course was uneventful without recurrence 5 years after the original operation. The authors review the literature and also report on the low incidence of this tumor arising in the foot.


2014 ◽  
Vol 6 (1) ◽  
pp. 15 ◽  
Author(s):  
HagadurGurureddy Vinay ◽  
Mohammed Raza ◽  
Mirzeeshan Ali ◽  
Gurubasappa Siddesh

2004 ◽  
Vol 61 (5) ◽  
pp. 565-568 ◽  
Author(s):  
Zorica Stojsic ◽  
Dragoljub Bacetic ◽  
Bozina Radevic ◽  
Jovan Vasiljevic

Background. The coexistence of a well-differentiated liposarcoma (atypical lipomatous tumor) and benign smooth muscle component in a single soft tissue neoplasm is extremely rare. Case report. Histologic and immunohistochemical characteristics of tumor, which represented the reccurence of a retroperitoneal atypical lipoma in a 50-year-old female patient are presented in this paper. The tumor represented the recurrence of a retroperitoneal atypical lipoma. Lipomatous component consisted of a mixture of lipoma-like and sclerosing variant of well-differentiated liposarcoma. Characteristically, the heterologous smooth muscle differentiation was manifested as a macroscopically visible nodular growth in the form of a leiomyoma within the adipocytic component. It consisted of intersecting fascicles of spindle cells, which lacked mitoses and significant atypia, and were immunopositive for smooth muscle markers. Conclusion. This case of well-differentiated liposarcoma with benign smooth muscle is the first reported tumor of retroperitoneal localization. It is also the first one to exhibit the heterologous smooth muscle component as a distinct leiomyoma.


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