Publication:
Extraosseous Ewing Sarcoma in a Pelvic Region: A Case Report

creativeworkseries.issnJNMA Print ISSN: 0028-2715; Online ISSN: 1815-672X
dc.contributor.authorGurung, Sushma
dc.contributor.authorThapa, Sagun
dc.contributor.authorGautam, Shristi
dc.date.accessioned2025-12-12T08:47:05Z
dc.date.available2025-12-12T08:47:05Z
dc.date.issued2022
dc.descriptionSushma Gurung Department of Paediatric Haematology and Oncology, Bhaktapur Cancer Hospital, Dudhpati, Bhaktapur, Nepal Sagun Thapa Department of Paediatric Haematology and Oncology, Bhaktapur Cancer Hospital, Dudhpati, Bhaktapur, Nepal Shristi Gautam Department of Paediatric Haematology and Oncology, Bhaktapur Cancer Hospital, Dudhpati, Bhaktapur, Nepal
dc.description.abstractAbstract Ewing sarcoma is the second most common malignant bone tumour in children. It rarely originates from extraskeletal soft tissue sites such as the upper thigh, buttocks, upper arm and shoulder. Primary extraosseous Ewing sarcoma located in the pelvic region is rare. We report a 17-year-female who had gradual onset of progressive lower abdominal mass and pain. A computed tomography scan revealed well defined lobulated heterogeneously enhancing lesion noted in the pelvic region measuring approximately 12.9 x 9.8 x 9.3 cm. Incisional biopsy showed a small round blue cell tumour which was strongly positive for Cluster of Differentiation 99, vimentin, Friend Leukaemia Integration 1 with 40% Ki-67. Following treatment with chemotherapy, surgery and radiotherapy, there was complete resolution of the tumour. Although extraosseous Ewing sarcoma is rare, it can occur virtually in any soft tissue site. Therefore, clinicians need to distinguish it from soft tissue sarcoma because rapid progression, early diagnosis and timely treatment are crucial for a favourable prognosis.
dc.identifierhttps://doi.org/10.31729/jnma.7523
dc.identifier.urihttps://hdl.handle.net/20.500.14572/3595
dc.language.isoen_US
dc.publisherNepal Medical Association
dc.subjectEwing sarcoma
dc.subjectNeoadjuvant chemotherapy
dc.subjectRadiation therapy
dc.titleExtraosseous Ewing Sarcoma in a Pelvic Region: A Case Report
dc.typeOther
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage640
oaire.citation.startPage638
relation.isJournalIssueOfPublication97a430e0-8e75-4ea0-8404-4f83f1f86a10
relation.isJournalIssueOfPublication.latestForDiscovery97a430e0-8e75-4ea0-8404-4f83f1f86a10
relation.isJournalOfPublicatione6e146a0-0ece-4aba-aa0a-6ccfbd10a12a

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