نتایج جستجو برای: ovarian adenocarcinoma

تعداد نتایج: 142001  

2006
YASUSHI MABUCHI MAREO YAMOTO SAWAKO MINAMI NAOHIKO UMESAKI

Our purpose was to examine the immunolocalization of inhibin, activin and the activin signaling system in ovarian clear cell adenocarcinoma tissue. Tissue samples of ovarian clear cell adenocarcinoma were collected from ten women. The patients' ages ranged from 41 to 71 years (mean ± standard deviation; 53.4±9.9). Their surgicopathological staging was based on the criteria of the International ...

2013
Takashi Yamada Takayoshi Kanda Hiroshi Mori Kaname Shimokawa Mitsuo Kagawa Yuro Shibayama

UNLABELLED BACKGROUND Cell lines are very useful for clinical and basic research. Thus far, only 11 reports have documented the characteristics of ovarian endometrioid adenocarcinoma cell lines in the literature. Due to the scarcity of information, the establishment of an ovarian malignant tumor cell line with distinctive characteristics is particularly important to study this disease. Thus,...

2014
Fangfang Chen Ping Ren Ye Feng Haiyan Liu Yang Sun Zhonghui Liu Jingyan Ge Xueling Cui

BACKGROUND Follistatin (FST), a single chain glycoprotein, is originally isolated from follicular fluid of ovary. Previous studies have revealed that serum FST served as a biomarker for pregnancy and ovarian mucinous tumor. However, whether FST can serve as a biomarker for diagnosis in lung adenocarcinoma of humans remains unclear. METHODS AND RESULTS The study population consisted of 80 pati...

Journal: :Oncology reports 2016
Takashi Takeda Kouji Banno Ryuichiro Okawa Megumi Yanokura Moito Iijima Haruko Irie-Kunitomi Kanako Nakamura Miho Iida Masataka Adachi Kiyoko Umene Yuya Nogami Kenta Masuda Yusuke Kobayashi Eiichiro Tominaga Daisuke Aoki

The AT-rich interacting domain‑containing protein 1A gene (ARID1A) encodes ARID1A, a member of the SWI/SNF chromatin remodeling complex. Mutation of ARID1A induces changes in expression of multiple genes (CDKN1A, SMAD3, MLH1 and PIK3IP1) via chromatin remodeling dysfunction, contributes to carcinogenesis, and has been shown to cause transformation of cells in association with the PI3K/AKT pathw...

2011
Irma Virant-Klun Thomas Skutella Branko Cvjeticanin Martin Stimpfel Jasna Sinkovec

INTRODUCTION The presence of oocytes in the ovarian surface epithelium has already been confirmed in the fetal ovaries. We report the presence of SSEA-4, SOX-2, VASA and ZP2-positive primitive oocyte-like cells in the adult ovarian surface epithelium of a patient with serous papillary adenocarcinoma. CASE PRESENTATION Ovarian tissue was surgically retrieved from a 67-year old patient. Histolo...

2012
Abdul Hakeem Attar Zeenath Begum

Background: A 54 year female presented with distension of abdomen, and weight loss. Abdominal ultrasonography revealed Bilateral Ovarian carcinoma. Patient was operated and specimen received to the department of Pathology. The resected specimen showed two large ovarian masses, on cut open solid and cystic areas seen. Histologically tubular pattern of tumor tissue seen with no endometriotic (end...

2014
Bhavith Remalayam Santhosh Kuriakose Prathapan Valiya Kambarath Ramachandran Thazhath Mavali

Peutz-Jeghers syndrome (PJS) is an hereditary syndrome characterized by gastrointestinal polyposis and mucocutaneous pigmentation. PJS patients are at increased risk of developing various cancers, especially of the gastrointestinal and gynaecological tracts. Colonic adenocarcinoma is one of the more common tumours that occur in PJS. We report a young lady presenting with a large ovarian tumour,...

Journal: :Japanese journal of clinical oncology 1988
K Niwa N Yoshimi S Sugie H Sakamoto T Tanaka K Kato H Kaneko H Mori

A case of double cancer (pancreatic and ovarian adenocarcinomas) in a woman suggested by exfoliative and fine needle aspiration (FNA) cytology is reported. Exfoliative cytology, including immunohistochemical findings of the biliary juice and those of clinical image examinations indicated tubular adenocarcinoma of the pancreatic body. FNA cytologic findings with immunohistochemical observation a...

2017
Sarah P. Huepenbecker Laura Divine Christina S. Chu David G. Mutch

BACKGROUND Mayer-Rokitansky-Küster-Hauser syndrome is a rare entity with proposed genetic underpinnings. Ovarian carcinoma has well-described genetic associations and syndromes, although much of the etiology of the disease remains unknown. CASES Two sisters present in the 1970s with primary amenorrhea, 46, XX karyotypes, and absent uteri consistent with MRKH syndrome. In the 2010s, both siste...

2015
Laura Anne Rebecca Laura Anne Rebecca Lockwood Rachel Airley

Background: The genetic control of tumour progression presents the opportunity for bioinformatics and gene expression data to be used as a basis for tumour grading. The development of a genetic signature based on microarray data allows for the development of personalised chemotherapeutic regimes. Method: ONCOMINE was utilised to create a genetic signature for ovarian serous adenocarcinoma and t...

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