Two cases of gonad retention in adolescent patients with complete androgen insensitivity syndrome (CAIS)
- PMID: 32864333
- PMCID: PMC7453803
- DOI: 10.1016/j.epsc.2019.101332
Two cases of gonad retention in adolescent patients with complete androgen insensitivity syndrome (CAIS)
Abstract
Bilateral gonadectomy was the historical recommendation for patients diagnosed with complete androgen insensitivity syndrome (CAIS) due to the perceived risk of malignancy in the gonads. However, new shared-decision making approaches are allowing patients to explore the option to defer surgery. Here we report two patients who presented with primary amenorrhea to their primary care provider (PCP). After imaging and karyotyping, these patients were diagnosed with CAIS. They underwent exams under anesthesia and diagnostic laparoscopies in which the gonads did not present any immediate concerns or indications for removal. After discussing their options using the shared-decision making approach with the differences in sex development (DSD) team, they opted to defer gonadectomy and follow up annually with imaging to monitor the gonads.
Keywords: Complete androgen insensitivity syndrome; Gonadectomy; Shared-decision making.
Conflict of interest statement
Declaration of competing interest The following authors have no financial disclosures: SMN, EMW, KVL.
References
-
- Oakes M, Eyvazzadeh A, Quint E, Smith Y. Complete androgen insensitivity syndrome – a review. J Pediatr Adolesc Gynecol 2008;21:305–10. - PubMed
-
- Bangsboll S, Qvist I, Lebech PE, Lewinsky M. Testicular feminization syndrome and associated gonadal tumors in Denmark. Acta Obstet Gynecol Scand 1992;71:63–6. - PubMed
-
- Boehmer AL, Brinkmann O, Brüggenwirth H, et al. Genotype versus phenotype in families with androgen insensitivity syndrome. J Clin Endocrinol Metab 2001;86: 4151–60. - PubMed
Grants and funding
LinkOut - more resources
Full Text Sources