Primary desmoplastic small round cell tumor in the left orbit: a case report and literature review

2018 ◽  
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pp. 471-475 ◽  
Author(s):  
Xue-Rui He ◽  
Zheng Liu ◽  
Jing Wei ◽  
Wan-Jun Li ◽  
Tao Liu
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Ana Pando-Sandoval ◽  
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Pere Casan

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JIN-SOO HYUN ◽  
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HYOUNG SUL ◽  
SANG-GON PARK

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Goran Vujić ◽  
Mislav Mikuš ◽  
Luka Matak ◽  
Aleksandra Bonevski ◽  
Ivan Babić ◽  
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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.


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.


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