ABSTRACT
We assessed the predictive value of anatomical findings and karyotype for establishing a diagnostic orientation in patients with disorders of sex development (DSD). We performed a retrospective chart analysis of 228 patients, grouped into 4 categories: 46,XX DSD, non-dysgenetic testicular DSD, dysgenetic testicular DSD and ovotesticular DSD. Degree of virilisation, presence of vagina, presence of palpable gonads, size of gonads and a plain karyotype was available for all cases. 46,XX DSD due to congenital adrenal hyperplasia counted for 59.2% of the cases, non-dysgenetic testicular DSD for 13.6%, dysgenetic testicular DSD for 21.5% and ovotesticular DSD for 5.7%. Excluding congenital adrenal hyperplasia (CAH), a karyotype with at least one 46,XX cell line had a high diagnostic efficiency for ovotesticular DSD. In these patients, anatomical findings were not as useful to predict the gonadal phenotype. The existence of a 45,X cell line predicted with very high efficiency dysgenetic testicular DSD. Genital palpation was only partially helpful to predict the existence of testicular tissue. Non-dysgenetic testicular DSD could be ruled out with high efficiency in patients with an abnormal karyotype. Anatomical findings were helpful in 46,XY patients: palpated masses predicted non-dysgenetic testes with high accuracy. In all cases assessment of gonadal volume was less useful.
Subject(s)
Disorders of Sex Development/diagnosis , Disorders of Sex Development/genetics , Adrenal Hyperplasia, Congenital/complications , Chromosomes, Human, Y/genetics , Disorders of Sex Development/etiology , Female , Gonadal Dysgenesis, 46,XX/diagnosis , Gonadal Dysgenesis, 46,XX/etiology , Gonadal Dysgenesis, 46,XX/genetics , Gonadal Dysgenesis, 46,XY/diagnosis , Gonadal Dysgenesis, 46,XY/etiology , Gonadal Dysgenesis, 46,XY/genetics , Humans , Infant, Newborn , Karyotyping/methods , Male , Ovary/metabolism , Ovary/pathology , Testis/metabolism , Testis/pathologyABSTRACT
La disgenesia gonodal pura 46XY (Síndrome de Swyer) es una entidad rara, caracterizada por la presencia de estrías gonodales indiferenciadas en una paciente de fenotipo femenino que posee genitales femeninos hipoplásticos. La etiología no está muy clara, pero con frecuencia involucra trastornos genéticos a nivel de la región determinante del sexo del cromosoma Y. Se reporta el caso de una paciente abordada por amenorrea primaria a quien se le diagnosticó el sindrome de Swyer y se incluye una breve revisión bibliográfica