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A rare cause of precocious puberty: Hepatoblastoma

dc.contributor.authorEren, Erdal
dc.contributor.authorDemirkaya, Metin
dc.contributor.authorPapatya Çakır, Esra D
dc.contributor.authorSevinir, Betül
dc.contributor.authorSağlam, Halil
dc.contributor.authorTarım, Ömer
dc.contributor.buuauthorEREN, ERDAL
dc.contributor.buuauthorDemirkaya, Metin
dc.contributor.buuauthorPapatya Çakır, Esra D
dc.contributor.buuauthorSEVİNİR, BETÜL BERRİN
dc.contributor.buuauthorSAĞLAM, HALİL
dc.contributor.buuauthorTARIM, ÖMER FARUK
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentÇocuk Endokrinolojisi Ana Bilim Dalı
dc.contributor.departmentÇocuk Onkoloji Bilim Dalı
dc.contributor.orcid0000-0002-1684-1053
dc.contributor.scopusid36113153400
dc.contributor.scopusid24331130000
dc.contributor.scopusid37003613900
dc.contributor.scopusid6603199915
dc.contributor.scopusid35612700100
dc.contributor.scopusid6701427186
dc.date.accessioned2025-05-13T10:25:25Z
dc.date.issued2009-12-01
dc.description.abstractHepatoblastoma, an embryonal tumor, is one of the most common primary liver tumors in childhood. It secretes human chorionic gonadotropin (hCG), which can cause precocious puberty (PP). Herein, we present a case with PP who had enlarged penile size noticed during a diagnosis of hepatoblastoma. Laboratory examination revealed increased testosterone, alpha-fetoprotein (AFP), and hCG levels. Serum follicle-stimulating hormone (FSH) and luteinizing hormone (LH) levels were within prepubertal ranges. The diagnosis of hepatoblastoma was made by liver biopsy. Chemotherapy was administered, and the patient was referred to surgery. Ten months later, testis volumes were below 4 ml bilaterally, and penile length was 5.5 cm. Serum testosterone, AFP, and hCG levels decreased. Resection of the tumor and chemotherapy are essential for the treatment of hepatoblastoma and they can eliminate the symptoms of PP. © Journal of Clinical Research in Pediatric Endocrinology, Published by Galenos Publishing. All rights reserved.
dc.identifier.doi10.4274/jcrpe.v1i6.281
dc.identifier.endpage283
dc.identifier.issn1308-5727
dc.identifier.issue6
dc.identifier.scopus2-s2.0-77953469747
dc.identifier.startpage281
dc.identifier.urihttps://hdl.handle.net/11452/52633
dc.identifier.volume1
dc.indexed.scopusScopus
dc.language.isoen
dc.relation.journalJCRPE Journal of Clinical Research in Pediatric Endocrinology
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectPuberty
dc.subjectHepatoblastoma
dc.subjectChorionic gonadotropin
dc.subject.scopusHepatoblastoma Insights in Pediatric Liver Tumors
dc.titleA rare cause of precocious puberty: Hepatoblastoma
dc.typeArticle
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Çocuk Endokrinolojisi Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Çocuk Onkoloji Bilim Dalı
local.indexed.atScopus
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relation.isAuthorOfPublication8d125a37-7601-4609-8cb8-b07ccb1c11a4
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relation.isAuthorOfPublication73e10417-4d1e-4216-b057-4c0a0cf76dc1
relation.isAuthorOfPublication.latestForDiscovery2d1c6521-88a9-4270-9918-92f16f98006c

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