Leydig Cell Tumour in a 46,XX Child with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

dc.creatorLazaro, APP
dc.creatorde Lacerda, AM
dc.creatorGhiaroni, J
dc.creatorde Miranda, LCD
dc.creatorVidal, APA
dc.creatorCollett-Solberg, PF
dc.creatorMichelatto, DD
dc.creatorMello, MP
dc.creatorGuimaraes, MM
dc.date2013
dc.date2014-08-01T18:34:04Z
dc.date2015-11-26T17:06:10Z
dc.date2014-08-01T18:34:04Z
dc.date2015-11-26T17:06:10Z
dc.date.accessioned2018-03-28T23:54:35Z
dc.date.available2018-03-28T23:54:35Z
dc.identifierHormone Research In Paediatrics. Karger, v. 79, n. 3, n. 179, n. 184, 2013.
dc.identifier1663-2818
dc.identifierWOS:000318481200008
dc.identifier10.1159/000346899
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/80889
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/80889
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1279779
dc.descriptionCase Report: A 10-year-old male was referred to our institution due to short stature and bilateral cryptorchidism and reported pubic hair development and acne since the age of 4 years. Laboratory and molecular genetic tests indicated congenital adrenal hyperplasia due to 21-hydroxylase deficiency. After treatment with prednisone, adrenal hormones normalised but testosterone remained elevated. Magnetic resonance imaging of the abdomen due to cryptorchidism revealed uterus and adnexal attachments, a prostate and poorly defined nodules on the iliac chains. Upon exploratory laparotomy, a hysterectomy, bilateral oophorectomy and resection of a peri-adnexal nodular lesion on the patient's right side were performed. Histopathology of the nodule mass was compatible with a Leydig cell tumour with a low proliferation rate according to Ki67. Copyright (c) 2013 S. Karger AG, Basel
dc.description79
dc.description3
dc.description179
dc.description184
dc.languageen
dc.publisherKarger
dc.publisherBasel
dc.publisherSuíça
dc.relationHormone Research In Paediatrics
dc.relationHorm. Res. Paediatr.
dc.rightsfechado
dc.rightshttp://www.karger.com/Services/RightsPermissions
dc.sourceWeb of Science
dc.subjectCongenital adrenal hyperplasia
dc.subjectLeydig cell tumour
dc.subjectFemale
dc.subjectChild
dc.subjectHilus Cell
dc.subjectPostmenopausal Woman
dc.subjectOvary
dc.subjectMutations
dc.subjectProstate
dc.titleLeydig Cell Tumour in a 46,XX Child with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
dc.typeArtículos de revistas


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