J Korean Soc Radiol.  2023 Sep;84(5):1181-1184. 10.3348/jksr.2023.0025.

Swyer Syndrome: A Case Report

• Choi HG
• Park S

• KMID: 2546661
• DOI: http://doi.org/10.3348/jksr.2023.0025

Abstract

Swyer syndrome is a rare form of primary amenorrhea resulting from gonadal dysgenesis. It is characterized by the presence of a female phenotype with a 46, XY karyotype. In our case, CT scans revealed the absence of the uterus and bilateral ovaries of the 16-year-old female patient. Calcific nodules were found in both inguinal areas, which were suspected to be calcified atrophic testes. A chromosomal study confirmed the diagnosis of Swyer syndrome. Herein, we report a rare case of Swyer syndrome.

Keyword

Swyer Syndrome; Computed Tomography, X-Ray; Karyotype