Publication:
Hemangioblastoma: An Uncommon Cause of Polycythemia in a Child

creativeworkseries.issn1999-6217
dc.contributor.authorAryal, Surabhi
dc.contributor.authorSharma, Arun Kumar
dc.date.accessioned2025-08-01T05:10:09Z
dc.date.available2025-08-01T05:10:09Z
dc.date.issued2023
dc.descriptionSurabhi Aryal Department of Pediatrics, Tribhuvan University Teaching Hospital, Maharajgunj, Kathmandu, Nepal Arun Kumar Sharma Department of Pediatrics, Tribhuvan University Teaching Hospital, Maharajgunj, Kathmandu, Nepal
dc.description.abstractAbstract Polycythemia is a rare condition in children. Myeloproliferative neoplasms, including polycythemia vera although rare, is an important cause of childhood primary polycythemia. Secondary polycythemia is more common in children due to conditions causing hypoxia or due to pathologic erythropoietin production in malignancies like renal cell carcinoma, Wilms tumor or Hepatocellular carcinoma. Central nervous system hemangioblastoma is one of the rare causes of polycythemia. We report a 13-year-old girl with primarily neurological symptoms identified to be polycythemic during routine evaluation. Clinical examination and neuroimaging subsequently confirmed an intracranial space occupying lesion which was excised. Hemoglobin level normalized after tumor excision. This case report emphasizes the need for thorough systemic evaluation including central nervous system examination in children identified to be polycythemic. Keywords: CNS tumor; hemangioblastoma; polycythemia
dc.identifierhttps://doi.org/10.33314/jnhrc.v21i3.4160
dc.identifier.urihttps://hdl.handle.net/20.500.14572/1106
dc.language.isoen_US
dc.publisherNepal Health Research Council
dc.titleHemangioblastoma: An Uncommon Cause of Polycythemia in a Child
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage537
oaire.citation.startPage534
relation.isJournalIssueOfPublication5e202d37-79c9-4a3f-8d30-c812f7d72775
relation.isJournalIssueOfPublication.latestForDiscovery5e202d37-79c9-4a3f-8d30-c812f7d72775
relation.isJournalOfPublication40bd2739-8b19-447c-be60-723a1bdd1dcd

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