본문 바로가기
KERD
논문KCI 등재

Complete androgen insensitivity syndrome and risk of gonadal malignancy: systematic review

2

조회

0

다운로드

1

인용

0

참고문헌

키워드

주제분류소아과학

초록

Complete androgen insensitivity syndrome (CAIS) is a rare condition characterized by 46,XY karyotype, female external genitalia, absence of uterus, and testes located intra-abdominally, in the inguinal ring or in the labia majora. In the present study, the frequency of testicular malignancy in prepubertal and pubertal patients with CAIS who underwent gonadectomy or gonadal biopsy were evaluated. Systematic review was performed using electronic databases according to the PRISMA-P (Preferred Reporting Items for Systematic Review and Meta-Analysis Protocols) guidelines. The samples included 15 articles published between 1998 and 2019. From a total of 456 patients who underwent gonadectomy or gonadal biopsy, 6.14% had a premalignant lesion and most were postpubertal (82.14%). A malignant lesion was found in 1.3% and all were postpubertal. Because the risk of malignancy is very low in prepubertal patients with CAIS, gonadectomy may be delayed until puberty is complete, allowing it to progress naturally; however, close follow-up of the patient is required.

Abstract

Complete androgen insensitivity syndrome (CAIS) is a rare condition characterized by 46,XY karyotype, female external genitalia, absence of uterus, and testes located intra-abdominally, in the inguinal ring or in the labia majora. In the present study, the frequency of testicular malignancy in prepubertal and pubertal patients with CAIS who underwent gonadectomy or gonadal biopsy were evaluated. Systematic review was performed using electronic databases according to the PRISMA-P (Preferred Reporting Items for Systematic Review and Meta-Analysis Protocols) guidelines. The samples included 15 articles published between 1998 and 2019. From a total of 456 patients who underwent gonadectomy or gonadal biopsy, 6.14% had a premalignant lesion and most were postpubertal (82.14%). A malignant lesion was found in 1.3% and all were postpubertal. Because the risk of malignancy is very low in prepubertal patients with CAIS, gonadectomy may be delayed until puberty is complete, allowing it to progress naturally; however, close follow-up of the patient is required.

참고문헌 (30)

  1. Oakes MB, "Complete androgen insensitivity syndrome – a review", J Pediatr Adolesc Gynecol, 21, pp.305~310 (2008)
  2. Mongan NP, "Androgen Insensitivity Syndrome", Best Pract Res Clin Endocrinol Metab, 29, pp.569~580 (2015)
  3. Hannema SE, "Testis development in the complete androgen insensitivity syndrome", J Pathol, 208, pp.518~527 (2006)
  4. Cools M, "Germ cell tumors in the intersex gonad : old paths, new directions, moving frontiers", Endocr Rev, 27, pp.468~484 (2006)
  5. Chaudhry S, "Frequency of gonadal tumours in complete androgen insensitivity syndrome(CAIS) : a retrospective case-series analysis", J Pediatr Urol, 13, pp.498~ (2017)
  6. Gidekel S, "Oct-3", 4 is a dose-dependent oncogenic fate determinant, 2003, pp.4, 361~370
  7. Deans R, "Timing of gonadectomy in adult women with complete androgen insensitivity syndrome(CAIS) : patient preferences and clinical evidences", Clin Endocrinol, 76, pp.894~898 (2012)
  8. Döhnert U, "Gonadectomy in complete androgen insensitivity syndrome : why and when", Sex Dev, 11, pp.171~174 (2017)
  9. Lee PA, "Global disorders of sex development update since 2006 : perceptions, approach and care", Horm Res Paediatr, 85, pp.158~180 (2016)
  10. Moher D, "The PRISMA Group. Preferred Reporting Items for Systematic Reviews and Meta-Analyses: the PRISMA statement", PLoS Med, 6, pp.e1000097~ (2009)
  11. Kriplani A, "L aparos copic gonadectomy in male pseudohermaphrodites", Eur J Obstet Gynecol Reprod Biol, 81, pp.37~41 (1998)
  12. Ahmed SF, "Phenotypic features, androgen receptor binding, and mutational analysis in 278 clinical cases reported as androgen insensitivity syndrome", J Clin Endocrinol Metab, 85, pp.658~665 (2000)
  13. Yalinkaya A, "Laparoscopy-assisted transinguinal extracorporeal gonadectomy in six patients with Androgen Insensitivity Syndrome", Fertil Steril, 80, pp.429~433 (2003)
  14. Cools M, "Morphological and immunohistochemical differences between gonadal maturation delay and early germ cell neoplasia in patients with undervirilization syndromes", J Clin Endocrinol Metab, 90, pp.5295~5303 (2005)
  15. Cheikhelard A, "Long-term follow-up and comparison between genotype and phenotype in 29 cases of Complete Androgen Insensitivity Syndrome", J Urol, 180, pp.1496~1501 (2008)
  16. Purves JT, "Complete androgen insensitivity : the role of the surgeon", J Urol, 180, pp.1716~1719 (2008)
  17. Kravarusic D, "Androgen insensitivity syndrome : risk of malignancy and timing of surgery in a paediatric and adolescent population", Afr J Paediatr Surg, 8, pp.194~198 (2011)
  18. Dobanovacki D, "Complete androgen insensitivity syndrome : review of four cases", Cent Eur J Med, 7, pp.729~732 (2012)
  19. Wünsch L, "Patients with disorders of sex development(DSD)at risk of gonadal tumour development : management based on laparoscopic biopsy and molecular diagnosis", BJU Int, 110, pp.E958~E965 (2012)
  20. Esposito C, "Risk of malignancy and need of surgery in pediatric patients with Morris or Y-chromosome Turner : a multicenter survey", J Pediatr Adolesc Gynecol, 28, pp.333~336 (2015)
  21. Liu AX, "Increased risk of gonadal malignancy and prophylactic gonadectomy : a study of 102 phenotypic female patients with Y chromosome or Y-derived sequences", Hum Reprod, 29, pp.1413~1419 (2014)
  22. Wang Z, "Complete Androgen Insensitivity Syndrome in juveniles and adults with female phenotypes", J Obstet Gynaecol Res, 40, pp.2044~2050 (2014)
  23. Huang, H, "Gonadal tumour risk in 292 phenotypic female patients with Disorders of Sex Development containing Y chromosome or Y-derived sequence", Clin Endocrinol, 86, pp.621~627 (2017)
  24. Countant R, "Divergent effect of endogenous and exogenous sex steroids on the insulin like growth factor response to growth hormone in short normal adolescents", J Clin Endocrinol Metab, 89, pp.6185~6192 (2004)
  25. Perry RJ, "The role of sex steroids in controlling pubertal growth", Clin Endocrinol, 68, pp.4~15 (2008)
  26. Ferlin A, "Testicular function and bone metabolism – beyond testosterone", Nat Rev Endocrinol, 9, pp.548~554 (2013)
  27. Tack LJW, "Management of gonads in adults with androgen insensitivity : an International survey", Horm Res Paediatr, 90, pp.236~246 (2018)
  28. Wisniewski AB, "Complete androgen insensitivity syndrome : long-term medical, surgical, and psychosexual outcome", J Clin Endocrinol Metab, 85, pp.2664~2669 (2000)
  29. Slowikowska-Hilczer J, "Neoplastic potential of germ cells in relation to disturbances of gonadal organogenesis and changes in karyotype", J Androl, 24, pp.270~278 (2013)
  30. Jones TD, "OCT4 staining in testicular tumors : a sensitive and specific marker for seminoma and embryonal carcinoma", Am J Surg Pathol, 28, pp.935~940 (2004)

관련 논문AI추천

Clinical outcomes and genotype-phenotype correlations in patients with complete and partial androgen insensitivity syndromesChoi Jin-Ho, Hwang Soojin, Kim Gu-Hwan, Kim Ja Hye, Lee Nae-yun, Yoo Han-Wook, Yoon Ji-Hee대한소아내분비학회 · Annals of Pediatric Endocrinology & Metabolism2023 · 제28권 제3호Two Korean girls with complete androgen insensitivity syndrome diagnosed in infancy고정민, 김만진, 박성섭, 신충호, 양세원, 이영아, 허유정대한소아내분비학회 · Annals of Pediatric Endocrinology & Metabolism2018 · 제23권 제4호Phenotypic spectrum and long-term outcomes of patients with 46,XX disorders of sex developmentChoi Jin-Ho, Kim Dohyung, Kim Ja Hye, Yoo Han-Wook, Yoon Heeyon대한소아내분비학회 · Annals of Pediatric Endocrinology & Metabolism2025 · 제30권 제2호악성혼합성선세포종양을 동반한 완전 안드로겐 무감응증후군 1예김규래, 김미성, 김종혁, 박정열, 이경희, 이종심, 임유진, 조정현대한산부인과학회 · Obstetrics & Gynecology Science2011 · 제54권 제11호Pubertal outcomes and sex of rearing of patients with ovotesticular disorder of sex development and mixed gonadal dysgenesis김건석, 김윤명, 오아름, 유한욱, 최진호대한소아내분비학회 · Annals of Pediatric Endocrinology & Metabolism2019 · 제24권 제4호LAPAROSCOPIC GONADECTOMY OF STREAK GONADS WITHIN THE INGUINAL CANALS IN A PATIENT WITH XY PARTIAL GONADAL DYSGENESIS김혜경, 송미현, 안별님, 오훈규, 이태성, 최윤석대한산부인과학회 · Obstetrics & Gynecology Science2012 · 제55권 제03호

이 간행물의 다른 논문 (9건)