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Article: Coincidence of intracranial myoepithelioma and adrenocortical carcinoma in a young man

TitleCoincidence of intracranial myoepithelioma and adrenocortical carcinoma in a young man
Authors
KeywordsAdrenocortical carcinoma
brain neoplasms
myoepithelioma
Issue Date2021
PublisherMedknow Publications and Media Pvt. Ltd. The Journal's web site is located at http://www.asianjns.org
Citation
Asian Journal of Neurosurgery, 2021, v. 16 n. 3, p. 598-602 How to Cite?
AbstractMyoepithelial tumors are rare neoplasms that develop from myoepithelial cells in glandular structures and soft tissues. Primary intracranial myoepithelial neoplasms are even rarer with around ten cases reported. On the other hand, adrenocortical carcinoma (ACC) is also uncommon with an annual incidence of 0.7–2 per million and carries a poor prognosis. It is known to have an association with certain familial cancer syndromes. Even in sporadic cases, a significant portion of them had other malignancies before and after diagnosis of ACC. We reported a 34‑year‑old gentleman who was diagnosed to have ACC without known familial cancer syndrome. After that, he was also found to have right occipital myoepithelioma that was confirmed by excisional biopsy. There was no known association between these two pathologies. This is the first report of coincidence of ACC and intracranial myoepithelioma.
Persistent Identifierhttp://hdl.handle.net/10722/304021
ISSN
PubMed Central ID

 

DC FieldValueLanguage
dc.contributor.authorLi, LF-
dc.contributor.authorHo, SLR-
dc.contributor.authorTsang, COA-
dc.date.accessioned2021-09-23T08:54:08Z-
dc.date.available2021-09-23T08:54:08Z-
dc.date.issued2021-
dc.identifier.citationAsian Journal of Neurosurgery, 2021, v. 16 n. 3, p. 598-602-
dc.identifier.issn1793-5482-
dc.identifier.urihttp://hdl.handle.net/10722/304021-
dc.description.abstractMyoepithelial tumors are rare neoplasms that develop from myoepithelial cells in glandular structures and soft tissues. Primary intracranial myoepithelial neoplasms are even rarer with around ten cases reported. On the other hand, adrenocortical carcinoma (ACC) is also uncommon with an annual incidence of 0.7–2 per million and carries a poor prognosis. It is known to have an association with certain familial cancer syndromes. Even in sporadic cases, a significant portion of them had other malignancies before and after diagnosis of ACC. We reported a 34‑year‑old gentleman who was diagnosed to have ACC without known familial cancer syndrome. After that, he was also found to have right occipital myoepithelioma that was confirmed by excisional biopsy. There was no known association between these two pathologies. This is the first report of coincidence of ACC and intracranial myoepithelioma.-
dc.languageeng-
dc.publisherMedknow Publications and Media Pvt. Ltd. The Journal's web site is located at http://www.asianjns.org-
dc.relation.ispartofAsian Journal of Neurosurgery-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectAdrenocortical carcinoma-
dc.subjectbrain neoplasms-
dc.subjectmyoepithelioma-
dc.titleCoincidence of intracranial myoepithelioma and adrenocortical carcinoma in a young man-
dc.typeArticle-
dc.identifier.emailLi, LF: lfrandom@hku.hk-
dc.identifier.emailHo, SLR: hsl388@hku.hk-
dc.identifier.emailTsang, COA: acotsang@hku.hk-
dc.identifier.authorityTsang, COA=rp01519-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.4103/ajns.AJNS_502_20-
dc.identifier.pmid34660377-
dc.identifier.pmcidPMC8477820-
dc.identifier.hkuros325721-
dc.identifier.volume16-
dc.identifier.issue3-
dc.identifier.spage598-
dc.identifier.epage602-
dc.publisher.placeIndia-

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