The dilemma of the gender assignment in a Portuguese adolescent with disorder of sex development due to 17 beta-hydroxysteroid-dehydrogenase type 3 enzyme deficiency

被引:7
|
作者
Costa, Carla [1 ]
Castro-Correia, Cintia [1 ]
Mira-Coelho, Alda [2 ]
Monteiro, Bessa [3 ]
Monteiro, Joaquim [3 ]
Hughes, Ieuan [4 ]
Fontoura, Manuel [1 ]
机构
[1] Hosp Sao Joao, Fac Med Porto, Dept Paediat, Paediat Endocrinol & Diabetol Unit, Alameda Prof Hernani Monteiro, P-4202451 Oporto, Portugal
[2] Hosp Sao Joao, Dept Psychiat, Oporto, Portugal
[3] Hosp Sao Joao, Dept Paediat Surg, Oporto, Portugal
[4] Univ Cambridge, Addenbrookes Hosp, Dept Paediat, Endocrinol & Diabetol Unit, Cambridge, England
关键词
D O I
10.1530/EDM-14-0064
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The development of male internal and external genitalia in an XY fetus requires a complex interplay of many critical genes, enzymes, and cofactors. The enzyme 17 beta-hydroxysteroid-dehydrogenase type 3 (17 beta HSD3) is present almost exclusively in the testicles and converts Delta 4-androstenodione (Delta 4) to testosterone. A deficiency in this enzyme is rare and is a frequently misdiagnosed autosomal recessive cause of 46, XY, disorder of sex development. The case report is of a 15-year-old adolescent, who was raised according to female gender. At puberty, the adolescent had a severe virilization and primary amenorrhea. The physical examination showed a male phenotype with micropenis and blind vagina. The Tanner stage was A3B1P4, nonpalpable gonads. The karyotype revealed 46, XY. The endocrinology study revealed: testosterone = 2.38ng/ml, Delta 4> 10.00 ng/ml, and low testosterone/Delta 4 ratio = 0.23. Magnetic resonance imaging of the abdominal-pelvic showed the presence of testicles in inguinal canal, seminal vesicle, prostate, micropenis, and absence of uterus and vagina. The genetic study confirmed the mutation p.Glu215Asp on HSD17B3 gene in homozygosity. The dilemma of sex reassignment was seriously considered when the diagnosis was made. During all procedures the patient was accompanied by a child psychiatrist/psychologist. The teenager desired to continue being a female, so gonadectomy was performed. Estrogen therapy and surgical procedure to change external genitalia was carried out. In this case, there was a severe virilization at puberty. It is speculated to be due to a partial activity of 17bHSD3 in the testicles and/or extratesticular ability to convert D4 to testosterone by 17 beta HSD5. Prenatal exposure of the brain to androgens has increasingly been put forward as a critical factor in gender identity development, but in this case the social factor was more important for the gender assignment.
引用
收藏
页数:4
相关论文
共 26 条
  • [11] AMENORRHEA AND VOICE DEEPENING IN ADOLESCENT FEMALE, FOUND TO HAVE 17-BETA-HYDROXYSTEROID DEHYDROGENASE 3 DEFICIENCY SEX REVERSAL
    Barr, Mary
    Scott, Mary Lauren
    HORMONE RESEARCH IN PAEDIATRICS, 2024, 97 : 122 - 123
  • [12] MALE PSEUDOHERMAPHRODITISM DUE TO 17-BETA-HYDROXYSTEROID DEHYDROGENASE-DEFICIENCY - GENDER REASSIGNMENT IN EARLY INFANCY
    GROSS, DJ
    LANDAU, H
    KOHN, G
    FARKAS, A
    ELRAYYES, E
    ELSHAWWA, R
    LASCH, EE
    ROSLER, A
    ACTA ENDOCRINOLOGICA, 1986, 112 (02): : 238 - 246
  • [13] Guidance for shared decision-making regarding orchiectomy in individuals with differences of sex development due to 17-β-hydroxysteroid dehydrogenase type 3 deficiency
    Yu, Lissa X.
    Johnson, Jodie
    Pennesi, Christine M.
    Ernst, Michelle M.
    Strine, Andrew
    Matheny Antommaria, Armand H.
    Hopkin, Robert J.
    Sandberg, David E.
    Khorashad, Behzad
    Mohnach, Lauren
    Heider, Amer
    Rutter, Meilan M.
    FRONTIERS IN PEDIATRICS, 2025, 13
  • [14] 17β hydroxysteroid dehydrogenase 3 deficiency in 46,XY disorders of sex development: Our experience and a gender role-focused systematic review
    Krishnappa, Brijesh
    Arya, Sneha
    Lila, Anurag R.
    Sarathi, Vijaya
    Memon, Saba S.
    Barnabas, Rohit
    Kumbhar, Bajarang, V
    Bhandare, Vishwambhar V.
    Patil, Virendra
    Shah, Nalini S.
    Kunwar, Ambarish
    Bandgar, Tushar
    CLINICAL ENDOCRINOLOGY, 2022, 97 (01) : 43 - 51
  • [15] FAMILIAL MALE PSEUDOHERMAPHRODITISM WITH GYNECOMASTIA DUE TO 17-BETA-HYDROXYSTEROID DEHYDROGENASE-DEFICIENCY - A REPORT OF 3 CASES
    BALDUCCI, R
    TOSCANO, V
    WRIGHT, F
    BOZZOLAN, F
    DIPIERO, G
    MARODER, M
    PANEI, P
    SCIARRA, F
    BOSCHERINI, B
    CLINICAL ENDOCRINOLOGY, 1985, 23 (04) : 439 - 444
  • [16] MALE PSEUDOHERMAPHRODITISM DUE TO 17-BETA-HYDROXY-STEROID DEHYDROGENASE-DEFICIENCY - EARLY GENDER ASSIGNMENT AND MASCULINIZING GENITOPLASTY
    FARKAS, A
    ROSLER, A
    COHN, G
    JOURNAL OF UROLOGY, 1986, 135 (04): : A132 - A132
  • [17] No genetic mutation in type II 3 beta-hydroxysteroid dehydrogenase gene in patients with biochemical evidence of enzyme deficiency
    Tajima, T
    Nishi, Y
    Takase, A
    Nakae, J
    Murashita, M
    Fujieda, K
    HORMONE RESEARCH, 1997, 47 (02) : 49 - 53
  • [18] Localisation and regulation of 17 beta-hydroxysteroid dehydrogenase type 3 mRNA during development in the mouse testis
    Baker, PJ
    Sha, JH
    OShaughnessy, PJ
    MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1997, 133 (02) : 127 - 133
  • [19] Decision-making regarding orchiectomy in patients with 17-beta-hydroxysteroid dehydrogenase type 3 deficiency: Clinical considerations
    Pennesi, Christine
    Yu, Lissa
    SEXUAL DEVELOPMENT, 2022, 16 (SUPPL 1) : 70 - 71
  • [20] MALE PSEUDOHERMAPHRODITISM (MPH) DUE TO BOTH TESTICULAR 17-KETOREDUCTASE AND PARTIAL ADRENAL 3-BETA-HYDROXYSTEROID-DEHYDROGENASE (3-BETA-HSD) DEFICIENCY
    RODENS, K
    HOMOKI, J
    SCHWEIKERT, HU
    PEDIATRIC RESEARCH, 1988, 24 (04) : 541 - 541