Zobrazeno 1 - 10
of 100
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:
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
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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
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Publikováno v:
Endocrine Abstracts.
BACKGROUND: Hypercalcaemia is commonly encountered during clinical practice. SCCOHT is a rare ovarian malignancy typically found in young women. In two thirds of patients, it causes a paraneoplastic hypercalcaemia which is usually asymptomatic.
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
Publikováno v:
ePoster.
Introduction/Background Small cell carcinoma of the ovary of pulmonary type, is a rare, aggressive tumor with poor prognosis and its optimal management is unclear. Methodology Case presentation: A 55 - year - old Caucasian woman presented with abdomi