Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Ovarian Small Cell Carcinoma"'
Publikováno v:
Human Pathology Reports, Vol 28, Iss , Pp 300626- (2022)
We present the first reported case of a 68-year-old woman with an adrenal metastasis from a small cell carcinoma arising in an ovarian teratoma. The patient initially presented with an adrenal small cell carcinoma that was postulated to be a metastas
Externí odkaz:
https://doaj.org/article/2862a93943ef47d8b72ee614930844c8
Autor:
Hirotsugu Hashimoto, MD, Atsushi Kurata, MD, PhD, Koji Fujita, CT, Hideto Shimada, MD, Takeshi Nagai, MD, Hajime Horiuchi, MD, Masahiko Kuroda, MD, PhD
Publikováno v:
Human Pathology: Case Reports, Vol 2, Iss 3, Pp 67-72 (2015)
Ovarian small cell carcinoma of pulmonary type (OSCCPT) is an extremely rare and aggressive disease. The diagnostic significance of cytology of ascites for OSCCPT, however, has not been shown so far. Here, we report the diagnosis of this carcinoma in
Externí odkaz:
https://doaj.org/article/814fe1507eea407697f70fc1ca49fbae
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
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:
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
Autor:
Douglas I. Lin, Yakov Chudnovsky, Bridget Duggan, Deborah Zajchowski, Joel Greenbowe, Jeffrey S. Ross, Laurie M. Gay, Siraj M. Ali, Julia A. Elvin
Publikováno v:
Gynecologic oncology. 147(3)
Small cell carcinoma of the ovary, hypercalcemic-type (SCCOHT) is a rare, extremely aggressive neoplasm that usually occurs in young women and is characterized by deleterious germline or somatic SMARCA4 mutations. We performed comprehensive genomic p
Publikováno v:
Nuclear Medicine and Molecular Imaging. 50:90-92
Publikováno v:
Archives of Gynecology and Obstetrics. 284:1277-1282
Ovarian small cell carcinoma of the hypercalcaemic type is a very rare and highly aggressive malignant disease, mainly affecting young women. Due to the rarity of this tumour entity, prospective randomised trials are unlikely to be conducted, and the
Autor:
W. Glenn McCluggage
Publikováno v:
Diagnostic Histopathology. 14:335-351
With the advent of new antibodies and the discovery of novel applications of established markers, immunohistochemistry is increasingly being used in gynaecological pathology. Most of the applications in the field of ovarian pathology are related to t