scholarly journals A case report of small round cell tumor of palm: A difficult code to decipher on cytology

2021 ◽  
Vol 89 ◽  
pp. 106659
Author(s):  
Alka Yadav ◽  
Aarzoo Jahan ◽  
Shakti Kumar Yadav ◽  
Sonam Kumar Pruthi ◽  
Sompal Singh ◽  
...  
2015 ◽  
Vol 10 (5) ◽  
pp. 2991-2995 ◽  
Author(s):  
YUAN CAO ◽  
YING CHEN ◽  
LI YANG ◽  
ZI-HUA QIAN ◽  
SHU-GAO HAN ◽  
...  

Health ◽  
2012 ◽  
Vol 04 (04) ◽  
pp. 207-211 ◽  
Author(s):  
Hafida Benhammane ◽  
Leila Chbani ◽  
Abdelmalek Ousadden ◽  
Ouadii Mouquit ◽  
Siham Tizniti ◽  
...  

2014 ◽  
Vol 8 (5) ◽  
pp. 1986-1992 ◽  
Author(s):  
HEE-JEONG LEE ◽  
JIN-SOO HYUN ◽  
HOE-SOO JANG ◽  
HYOUNG SUL ◽  
SANG-GON PARK

Author(s):  
Goran Vujić ◽  
Mislav Mikuš ◽  
Luka Matak ◽  
Aleksandra Bonevski ◽  
Ivan Babić ◽  
...  

Abstract Objective Desmoplastic small round cell tumor (DSRCT) is a rare intraabdominal neoplasm that grows along serosal surfaces and is primarily found in young men. To date, only 16 cases of ovarian DSRCT have been previously reported in women in the English literature, and no large population-based studies on this topic exist. Case Report We report the case of a 19-year-old virgo with unremarkable past medical history, initially presented with abdominal fullness. After being treated with the optimal treatment modality (primary and secondary surgical debulking, unique chemotherapy, protocol and adjuvant radiotherapy), the patient has remained without tumor disease for 40 months. Conclusion Although the best therapy for patients with DSRCT has yet to be determined, combining complete surgical resection, adjuvant chemotherapy, and radiotherapy is required to prolong survival and to achieve proper quality of life.


2014 ◽  
Vol 7 (5) ◽  
pp. 1464-1468 ◽  
Author(s):  
JIRO SHIMAZAKI ◽  
GYO MOTOHASHI ◽  
KIYOTAKA NISHIDA ◽  
TAKANOBU TABUCHI ◽  
HIDEYUKI UBUKATA ◽  
...  

2021 ◽  
pp. 7-8
Author(s):  
Bhuwan Kumar ◽  
Rajde Singh ◽  
Anurag Mishra

Desmoplastic small round cell tumor is a rare, highly malignant neoplasm originating from mesenchymal tissue which was initially described in 1 1991 by Gerald and Rosai. It is composed of small round tumor cells of uncertain histogenesis associated with prominent stromal desmoplasia and 2 polyphenotypic differentiation. It typically occurs in adolescents and young adults. Usually presents with widespread abdominal, serosal, and mesenteric involvement with poor prognosis.


2015 ◽  
Vol 2 (1) ◽  
pp. 9-15 ◽  
Author(s):  
Vadim Khachaturov ◽  
Roth W. Christopher ◽  
Jacob R. Hodge ◽  
John Joseph Doyle ◽  
Darren J. Leitao ◽  
...  

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