scholarly journals Desmoplastic Small Round Cell Tumor of the Ovary: A Case Report with a New Modality of Treatment and Review of the Literature

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.

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

2014 ◽  
Vol 2014 ◽  
pp. 1-5 ◽  
Author(s):  
Christina K. Lettieri ◽  
Pamela Garcia-Filion ◽  
Pooja Hingorani

Desmoplastic small round cell tumor (DSRCT) is a rare but highly fatal malignancy. Due to the rarity of this neoplasm, no large population based studies exist.Procedure. This is a retrospective cohort analysis. Incidence rates were calculated based on sex and ethnicity and compared statistically. Gender-, ethnicity-, and treatment- based survival were calculated using the Kaplan-Meier method.Results. A total of 192 cases of DSRCT were identified. Peak incidence age was between 20 and 24 years. Age-adjusted incidence rate for blacks was 0.5 cases/million and for whites was 0.2 cases/million (P=0.037). There was no statistically significant difference in survival based on gender or ethnicity. When adjusted for age, there was no statistically significant difference in survival amongst patients who received radiation therapy compared to those who did not (HRadj = 0.73; 95% CI 0.49, 1.11). There was a statistically significant survival advantage for patients who received radiation after surgery compared to those who did not (HR 0.49; 95% CI 0.30, 0.79).Conclusion. DSRCT is more common in males and in people of African-American descent. Although overall survival remains poor, radiation therapy following surgery seems to improve outcome in these patients.


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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