Publication:
Paediatric Ovarian Dysgerminoma: A Case Report

creativeworkseries.issnJNMA Print ISSN: 0028-2715; Online ISSN: 1815-672X
dc.contributor.authorAdhikari, Siddhant
dc.contributor.authorJoti, Santosh
dc.contributor.authorChhetri, Parvat Kuwar
dc.date.accessioned2025-11-06T06:51:18Z
dc.date.available2025-11-06T06:51:18Z
dc.date.issued2022
dc.descriptionSiddhant Adhikari Motherland Hospital, Pepsicola, Kathmandu, Nepal. Santosh Joti TMSS Medical College, Dhaka-Rangpur Highway, Gokul, Bangladesh Parvat Kuwar Chhetri TMSS Medical College, Dhaka-Rangpur Highway, Gokul, Bangladesh
dc.description.abstractAbstract Dysgerminoma is the most common malignant germ cell tumour of the ovary. Abdominal pain, abdominal distention, and the presence of a palpable mass are common symptoms at presentation. This is usually detected in youth, before the age of 20 years. Ovarian or adnexal tumours are very rare in patients below the age of 18 years, most of them being functional cysts, only 10% being malignant. Here is a rare case of an 8 years old girl with dysgerminoma who underwent right-sided salpingo-oophorectomy for unilateral involvement with conservation of fertility and now the patient is on chemotherapy as the tumour metastasized to the pre-aortic lymph node.
dc.identifierhttps://doi.org/10.31729/jnma.7894
dc.identifier.urihttps://hdl.handle.net/20.500.14572/3074
dc.language.isoen_US
dc.publisherNepal Medical Association
dc.subjectCase reports
dc.subjectDysgerminoma
dc.subjectMetastasis
dc.subjectPaediatrics
dc.titlePaediatric Ovarian Dysgerminoma: A Case Report
dc.typeOther
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage988
oaire.citation.startPage985
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relation.isJournalIssueOfPublication.latestForDiscoverye2f2f036-234f-4302-8cf3-16306564c925
relation.isJournalOfPublicatione6e146a0-0ece-4aba-aa0a-6ccfbd10a12a

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