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DC Field | Value | Language |
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dc.contributor.author | Vijaylaxmi Gobbur, Anvesha Kumar | - |
dc.date.accessioned | 2019-10-15T11:35:23Z | - |
dc.date.available | 2019-10-15T11:35:23Z | - |
dc.date.issued | 2018-08 | - |
dc.identifier.issn | 24549142 | - |
dc.identifier.uri | http://hdl.handle.net/123456789/1022 | - |
dc.description.abstract | Primary fallopian tube carcinoma is rare and accounts for about 0.3% of all gynaecolgical cancers. Fewer than 2000 cases have been reported in literature. In routine practice, a case of tubal carcinoma is usually diagnosed as an adenxal mass, more commonly as an ovarian tumour. It is usually an intraoperative finding or a histopathological diagnosis. A 45 year old postmenopausal woman, presented with the complaint of pain abdomen since 3 months. On per vaginal examination her uterus was retroverted, 10 to 12 weeks in size and a hard, fixed, nontender, irregular mass of 8 cm x 8 cm, in continuation with the uterus was felt in the left fornix. The clinical and radiological findings with an elevated CA 125 suggested an ovarian tumour with a fibroid uterus. An exploratory laprotomy was done and in the left fallopian tube an exophytic growth 10 cm x 10 cm adherent to the lateral pelvic wall was detected. The left ovary was seen seperate from the mass. Histopathology report confirmed it as a papillary serous adenocarcinoma of the fallopian tube. | en_US |
dc.language.iso | en | en_US |
dc.publisher | BLDE(Deemed to be University) | en_US |
dc.subject | primary fallopian, carcinoma, vaginal | en_US |
dc.title | Primary fallopian tube carcinoma: A case report and literature review. | en_US |
dc.type | Article | en_US |
Appears in Collections: | Faculty of OBG |
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