Please use this identifier to cite or link to this item:
Full metadata record
DC FieldValueLanguage
dc.contributor.CRUESPUniversidade Estadual de Campinaspt_BR
dc.typeArtigo de periódicopt_BR
dc.titleLeydig Cell Tumour in a 46,XX Child with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiencypt_BR
dc.contributor.authorLazaro, APPpt_BR
dc.contributor.authorde Lacerda, AMpt_BR
dc.contributor.authorGhiaroni, Jpt_BR
dc.contributor.authorde Miranda, LCDpt_BR
dc.contributor.authorVidal, APApt_BR
dc.contributor.authorCollett-Solberg, PFpt_BR
dc.contributor.authorMichelatto, DDpt_BR
dc.contributor.authorMello, MPpt_BR
dc.contributor.authorGuimaraes, MMpt_BR
unicamp.authorPires Lazaro, Ana Paula de Lacerda, Adriano Machado Guimaraes, Marilia Martins Univ Fed Rio de Janeiro, Dept Endocrinol, BR-21941 Rio De Janeiro, Brazilpt_BR
unicamp.authorGhiaroni, Juraci Univ Fed Rio de Janeiro, Dept Gynaecol, BR-21941 Rio De Janeiro, Brazilpt_BR
unicamp.authorDuarte de Miranda, Luiz Carlos Univ Fed Rio de Janeiro, Dept Urol, BR-21941 Rio De Janeiro, Brazilpt_BR
unicamp.authorAguiar Vidal, Ana Paula Univ Fed Rio de Janeiro, Clementino Fraga Filho Univ, Dept Pathol, BR-21941 Rio De Janeiro, Brazilpt_BR
unicamp.authorCollett-Solberg, Paulo Ferrez Univ Estado Rio De Janeiro, Dept Endocrinol, Rio De Janeiro, Brazilpt_BR
unicamp.authorMichelatto, Debora de Paula Mello, Maricilda Palandi Univ Estadual Campinas, Ctr Mol Biol & Genet Engn, Sao Paulo, Brazilpt_BR
dc.subjectCongenital adrenal hyperplasiapt_BR
dc.subjectLeydig cell tumourpt_BR
dc.subject.wosHilus Cellpt_BR
dc.subject.wosPostmenopausal Womanpt_BR
dc.description.abstractCase 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, Baselpt
dc.relation.ispartofHormone Research In Paediatricspt_BR
dc.relation.ispartofabbreviationHorm. Res. Paediatr.pt_BR
dc.identifier.citationHormone Research In Paediatrics. Karger, v. 79, n. 3, n. 179, n. 184, 2013.pt_BR
dc.sourceWeb of Sciencept_BR
dc.description.provenanceMade available in DSpace on 2014-08-01T18:34:04Z (GMT). No. of bitstreams: 0 Previous issue date: 2013en
dc.description.provenanceMade available in DSpace on 2015-11-26T17:06:10Z (GMT). No. of bitstreams: 0 Previous issue date: 2013en
Appears in Collections:Unicamp - Artigos e Outros Documentos

Files in This Item:
There are no files associated with this item.

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.