Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14356/1795
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dc.contributor.authorShakya, B-
dc.date.accessioned2023-05-23T05:49:08Z-
dc.date.available2023-05-23T05:49:08Z-
dc.date.issued2014-
dc.identifier.citationShakyaB. (2014). Intestinal Type Borderline Mucinous OvarianTumour. Journal of Nepal Health Research Council. https://doi.org/10.33314/jnhrc.v0i0.442en_US
dc.identifier.issnPrint ISSN: 1727-5482; Online ISSN: 1999-6217-
dc.identifier.urihttp://103.69.126.140:8080/handle/20.500.14356/1795-
dc.descriptionCase Reporten_US
dc.description.abstractAbstract A 26 years old para 4 lady presented with abdominal distension following a home delivery 18 months back and lactationalamenorrhoea following since. Examination and investigation findings revealed a large ovarian tumour(28X28 cm) occupying the whole of the abdomen. Tumour markers were normal except for a slightly raised lactate dehydrogenase enzyme. Patient underwent staging laparotomy- left salpingoophorectomy, right tubal ligation with omental biopsy and peritoneal fluid cytology. Histopathology report revealed borderline mucinous ovarian tumour of intestinal type. Her postoperative period was uneventful and she was advised for follow-up. Borderline ovarian tumours are uncommon tumours. In the younger age with stage I, fertility sparing surgery is enough and has excellent prognosis, but follow up is important. Â Keywords: borderline ovarian tumour; follow-up, prognosisen_US
dc.language.isoenen_US
dc.publisherNepal Health Research Councilen_US
dc.relation.ispartofseriesJan-April, 2014;442-
dc.subjectBorderline ovarian tumouren_US
dc.subjectFollow-upen_US
dc.subjectPrognosisen_US
dc.titleIntestinal Type Borderline Mucinous OvarianTumouren_US
dc.typeJournal Articleen_US
local.journal.categoryCase Report-
Appears in Collections:Vol. 12 No. 1 Issue 26 Jan - Apr, 2014

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