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.
CITATION STYLE
Choi, H. G., & Park, S. (2023). Swyer Syndrome: A Case Report. Journal of the Korean Society of Radiology, 84(5), 1181–1184. https://doi.org/10.3348/jksr.2023.0025
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