Pulmonary embolism unmasking concealed Klinefelter syndrome: A case report
Klinefelter syndrome, characterized by the karyotype XXY, is the most common genetic cause of congenital hypogonadism. It commonly presents with under-developed testes, gynaecomastia, and infertility. This condition is associated with impaired fibrinolysis secondary to hypogonadism and other concurrent thrombophilic factors, resulting in a hypercoa-gulable state that predisposes to deep vein thrombosis and thromboembolic events. We report a case of a 21-year-old man who presented with a pulmonary embolism, which subsequently led to the diagnosis of Klinefelter syndrome as the underlying prothrombotic disorder.Future research facilitating a comprehensive understanding of the pathogenesis of venous thromboembolism in the context of Klinefelter syndrome will lead to improved screening and management strategies.
Authors
- Uditha Dassanayake (ORCID: https://orcid.org/0000-0001-6578-4473)
- C. T. W. Malavipathirana (ORCID: https://orcid.org/0009-0007-0886-083X)
- G. G. Liyanarachchi
Publication Details
- Journal
- Journal of the Ceylon College of Physicians
- Published
- 2025-08-13
- DOI
- https://doi.org/10.4038/jccp.v56i1.8105
- Primary Topic
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Type
- article
- Field-Weighted Citation Impact
- 0.00