Clinical Presentation of McCune-Albright Syndrome in Males
- 1 January 2006
- journal article
- research article
- Published by Walter de Gruyter GmbH in Journal of Pediatric Endocrinology and Metabolism
- Vol. 19 (Supplement) , 619-22
- https://doi.org/10.1515/jpem.2006.19.s2.619
Abstract
The aims of this study were: (a) to survey gender prevalence and clinical findings at diagnosis in a series of patients who manifested at the time of this study the classical triad of McCune-Albright syndrome (MAS); (b) to investigate whether clinical presentation of MAS in boys may be different from that in girls; (c) to confirm whether boys with MAS may show a peculiar picture of testicular microlithiasis (TM) by testicular ultrasonography (US). Twenty-six patients (10 boys) with the classical clinical manifestations of MAS were recruited for the present study from the database of the Italian Multicenter Study Group on MAS. Age at diagnosis of MAS was significantly lower in girls than in boys (p < 0.025). Whilst there was no difference in the prevalence of skin and bone fibrous dysplasia for the two groups, a significantly higher prevalence of peripheral precocious puberty (PPP) was found in girls (chi2 = 6.5, p < 0.025). Moreover, PPP onset was earlier in females than in males (2.8 +/- 2.3 vs. 6.9 +/- 2.7 years, p < 0.005). In one boy, aged 2.9 years, the first clinical manifestation of MAS was monolateral testicular enlargement in the context of a picture of classical PPP. US scanning of the testes, at the time of the present study, showed bilateral hyperechogeneic multiple spots, compatible with diagnosis of TM, in 6/10 boys. (a) MAS is slightly more frequent in females. (b) PPP in MAS is significantly more frequent and earlier in girls. (c) PPP in boys with MAS is generally associated with bilateral testicular enlargement, but monolateral macroorchidism may also be seen. (d) TM may be another marker for MAS in males.Keywords
This publication has 9 references indexed in Scilit:
- Testicular microlithiasis: An unreported feature of McCUNE-Albright syndrome in malesThe Journal of Pediatrics, 2004
- Activating Gsα Mutations: Analysis of 113 Patients with Signs of McCune-Albright Syndrome—A European Collaborative StudyJournal of Clinical Endocrinology & Metabolism, 2004
- Does Testicular Microlithiasis Matter? A ReviewClinical Radiology, 2002
- Macroorchidism due to Autonomous Hyperfunction of Sertoli Cells and Gs Gene Mutation: An Unusual Expression of McCune-Albright Syndrome in a Prepubertal BoyJournal of Clinical Endocrinology & Metabolism, 2001
- McCune-Albright Syndrome: A Clinical Longitudinal Study of 32 PatientsJournal of Pediatric Endocrinology and Metabolism, 1999
- Clinical Implications of Genetic Defects in G Proteins: The Molecular Basis of McCune-Albright Syndrome and Albright Hereditary OsteodystrophyMedicine, 1996
- McCune-Albright syndrome in a male child:A clinical and endocrinologic enigmaThe Journal of Pediatrics, 1978
- Growth hormone excess and sexual precocity in polyostotic fibrous dysplasia (McCune-Albright syndrome): Evidence for abnormal hypothalamic functionThe Journal of Pediatrics, 1975
- Sex Precocity and Polyostotic Fibrous DysplasiaAmerican Journal of Diseases of Children, 1966