Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Ovarian Small Cell Carcinoma"'
Autor:
Mark Gruppetta, Annalisa Montebello
Publikováno v:
BMJ case reports. 14(7)
A 37-year-old woman presented with a few days’ history of lower abdominal pain and an incidental finding of hypercalcaemia. A thorough workup ensued, and the cause was found to be an exceptionally rare ovarian tumour—ovarian small cell carcinoma
Autor:
Andrew L. Folpe, Brooke E. Howitt
Publikováno v:
Genes, Chromosomes and Cancer. 60:190-209
Our knowledge regarding the role of genes encoding the chromatin remodeling switch/sucrose non-fermenting (SWI/SNF) complex in the initiation and progression of gynecologic malignancies continues to evolve. This review focuses on gynecologic tumors i
Autor:
Audrey LeFormal, Sebastien Gouy, Félix Blanc-Durand, Ariane Dunant, E. Bentivegna, Alexandra Leary, A Maulard, Mojgan Devouassoux-Shisheboran, Aurélie Auguste, Jean-Yves Scoazec, Patricia Pautier, Philippe Morice, Catherine Genestie
Publikováno v:
British Journal of Cancer
Background Ovarian small cell carcinoma, hypercalcaemic type (SCCOHT) is a rare and lethal disease affecting young women. As histological diagnosis is challenging and urgent, there is a clear need for a robust diagnostic test. While mutations in the
Publikováno v:
Medicine
Rationale: Ovarian small cell carcinoma of hypercalcemic type (OSCCHT) is a relatively rare and highly fatal gynecological malignancy of unknown histogenesis, affecting mainly girls and young women. OSCCHT occurring during pregnancy is an uncommon ev
Autor:
Steffen Albrecht, Donato Callegaro-Filho, Javad Nadaf, Nelly Sabbaghian, Somayyeh Fahiminiya, William D. Foulkes
Publikováno v:
Familial Cancer. 18:161-163
One of a pair of monozygous twins was diagnosed and died of small cell carcinoma of the ovary of hypercalcemic type (SCCOHT) at the age of 30 years. Her sister remained unaffected and was very concerned about her risk for developing SCCOHT. By perfor
Publikováno v:
International Journal of Gynecologic Cancer. 31:152-153
Small cell carcinoma of the ovary, hypercalcemic type, is a rare undifferentiated carcinoma which characteristically presents in women over 40 years of age with abdominal fullness, unilateral tumor, and hypercalcemia.[1][1] It is an aggressive cancer
Publikováno v:
Iranian Journal of Pathology
Iranian Journal of Pathology, Vol 13, Iss 1, Pp 99-102 (2018)
Iranian Journal of Pathology, Vol 13, Iss 1, Pp 99-102 (2018)
Ovarian small cell carcinoma is a rare and highly malignant tumor with poor prognosis. It usually presents in younger females with features of hypercalcemia. The exact histogenesis of the tumor is unclear and it may present as an undifferentiated tum
Publikováno v:
Gynecologic Oncology Reports
Background Ovarian small cell carcinoma is a rare, aggressive neoplasm that occurs in young women and has a poor long-term prognosis. Treatment involves surgical resection and chemotherapy. The required radicality of surgery is uncertain, balancing c
Publikováno v:
Case Reports in Oncology
Case Reports in Oncology, Vol 9, Iss 2, Pp 305-311 (2016)
Case Reports in Oncology, Vol 9, Iss 2, Pp 305-311 (2016)
We present a rare case of malignant rhabdoid tumor (ovarian small cell carcinoma of hypercalcemic type) in a 24-year-old female with fulminant course. Clinically, hypercalcemia was not found at the time of primary diagnosis. However, it appeared late
Publikováno v:
Medicine. 97(23)
Rationale Small cell carcinoma of the ovary (SCCO) is a rare and aggressive extra-pulmonary variant of small cell tumors of uncertain histogenesis. The pathogenesis and optimal treatment of SCCO is unclear. We present a very rare case of a synchronou