Microscopic testicular sperm extraction in 46,XY differences in sex development caused by 5-alpha reductase type 2 deficiency

被引:0
|
作者
Cardoso, Joao Paulo Greco [1 ]
Nahas, William Carlos [1 ]
Mendonca, Berenice Bilharinho [2 ]
Cocuzza, Marcello Antonio Signorelli [1 ]
机构
[1] Univ Sao Paulo, Hosp Clin, Fac Med, Div Urol, Av Dr Eneas de Carvalho Aguiar 255,7 Andar,Sala 71, BR-05403000 Sao Paulo, SP, Brazil
[2] Univ Sao Paulo, Disciplina Endocrinol, Fac Med, Sao Paulo, SP, Brazil
来源
关键词
NONOBSTRUCTIVE AZOOSPERMIA; DIAGNOSIS;
D O I
10.20945/2359-4292-2024-0223
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The 46,XY differences in sex development (DSD) caused by 5-alpha reductase type 2 (5ARD2) often presents with bilateral undescended testicles, otherwise normal internal reproductive structures, prostate hypoplasia and undervirilized male genitalia. Notably, as one of the few DSDs where fertility is possible, the clinical presentation of this disease is diverse, and reported cases of assisted reproduction are scarce. The fertility potential, reproductive counseling and treatment depend on the clinical presentation of this DSD, especially the testicular position and urethral anatomy. The influence of the timing and modality of surgery for hypospadias and cryptorchidism should be considered. We aimed to describe the use of microscopic testicular sperm extraction (micro-TESE) in this population. We provide a descriptive analysis of how micro-TESE is a possible potential tool for assisted reproduction in 5ARD2-deficient patients. A 33-year-old male who underwent bilateral orchidopexy, phalloplasty, and urethroplasty at the age of 9 years presented successful sperm retrieval but failed embryo development after intracytoplasmic sperm injection. Testicular histology revealed late spermatogenic arrest. A 28-year-old male with bilateral orchidopexy, phalloplasty, and urethroplasty at age 25 with unsuccessful sperm retrieval. Testicular histology revealed a Sertoli cell-only pattern. 5ARD2-deficient patients are singular patients. The potential impact of the time between atypical genitalia procedures and orchidopexy on fertility should be highly considered. Micro-TESE is a technique that may be used to assist azoospermic patients in this population. Early orchidopexy and penile and urethral corrections should be considered key strategies to preserve the fertility potential of 5ARD2 patients.
引用
收藏
页数:6
相关论文
共 50 条
  • [11] Difficulties in Diagnosis and Treatment of 5α-Reductase Type 2 Deficiency in a Newborn with 46,XY DSD
    Walter, Kerstin N.
    Kienzle, Frederike B.
    Frankenschmidt, Alexander
    Hiort, Olaf
    Wudy, Stefan A.
    van der Werf-Grohmann, Natascha
    Superti-Furga, Andrea
    Schwab, Karl Otfried
    HORMONE RESEARCH IN PAEDIATRICS, 2010, 74 (01): : 67 - 71
  • [12] 46,XY DSD due to 17β-HSD3 Deficiency and 5α-Reductase Type 2 Deficiency
    Inacio, Marlene
    Sircili, Maria Helena P.
    Brito, Vinicius N.
    Domenice, Sorahia
    Oliveira-Junior, Ari Alves
    Arnhold, Ivo J. P.
    Tibor, Francisco D.
    Costa, Elaine M. F.
    Mendonca, Berenice B.
    HORMONAL AND GENETIC BASIS OF SEXUAL DIFFERENTIATION DISORDERS AND HOT TOPICS IN ENDOCRINOLOGY, 2011, 707 : 9 - 14
  • [13] 5 Alpha reductase deficiency: a not so uncommon cause of 46XY DSD
    Rai, Versha Rani
    Rimsha, D. R.
    Khoso, Zubair
    Riaz, Maira
    Chachar, SaadUllah
    Ibrahim, Mohsina Noor
    HORMONE RESEARCH IN PAEDIATRICS, 2023, 96 (SUPPL 2): : 134 - 134
  • [14] Differences in testicular development between 5α-reductase 2 deficiency and isolated bilateral cryptorchidism
    Hadziselimovic, F.
    Dessouky, N.
    JOURNAL OF UROLOGY, 2008, 180 (03): : 1116 - 1120
  • [15] Testicular function of 46,XY subjects with differences of sex development (DSD) due to NR5A1 mutations
    Dallago, Renata T.
    Batista, Rafael Loch
    Guerra-Junior, Gil
    Maciel-Guerra, Andrea Trevas
    El Beck, Mayra S.
    Costa, Elaine M. F.
    Inacio, Marlene
    Nishi, Mirian
    Domenice, Sorahia
    Mendonca, Berenice B.
    HORMONE RESEARCH IN PAEDIATRICS, 2023, 96 (SUPPL 2): : 58 - 58
  • [16] Sex reversal in an infant with Smith-Lemli-Opitz syndrome, type II: Evidence for 5-alpha reductase deficiency
    Salbert, BA
    Schwartz, ID
    Grunt, JA
    JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 1996, 9 (01): : 67 - 69
  • [17] Spectrum of Pathogenic Variants in SRD5A2 in Indian Children with 46,XY Disorders of Sex Development and Clinically Suspected Steroid 5α-Reductase 2 Deficiency
    Kumar, Anil
    Sharma, Rajni
    Faruq, Mohammed
    Suroliya, Varun
    Kumar, Manoj
    Sharma, Shilpa
    Werner, Ralf
    Hiort, Olaf
    Jain, Vandana
    SEXUAL DEVELOPMENT, 2020, 13 (5-6) : 228 - 239
  • [18] COMPARISON OF 2 TESTS TO RECOGNIZE OR EXCLUDE 5-ALPHA REDUCTASE DEFICIENCY IN PREPUBERTAL CHILDREN
    GREENE, S
    ZACHMANN, M
    MANELLA, B
    HESSE, V
    HOEPFFNER, W
    WILLGERODT, H
    PRADER, A
    ACTA ENDOCRINOLOGICA, 1987, 114 (01): : 113 - 117
  • [19] Disorders of sex development (DSD) 46.XY due to type 2 5-α reductase deficiency in three siblings: Case report from a low-resource setting
    Susilo, Artha Falentin Putri
    Tjandraprawira, Kevin Dominique
    Bayu, Patrick
    Bayuaji, Hartanto
    ANNALS OF MEDICINE AND SURGERY, 2022, 82
  • [20] 46 XY disorder of sex development (DSD) due to 5 alpha (SRD5A2) deficiency - Experience from a multidisciplinary Pediatric Gender Clinic
    Bose, Sumona
    Das, Kanishka
    George, Belinda
    Raman, Vijaya
    Shubha, A. M.
    Mahadevappa, Kiran
    Kumar, Prasanna
    Bantwal, Ganapathi
    Ayyar, Vageesh
    Deb, Mainak
    JOURNAL OF PEDIATRIC UROLOGY, 2022, 18 (04) : 492.e1 - 492.e8