Síndrome de Klinefelter diagnosticado en un adulto a raíz del estudio de infección respiratoria recurrente y masa mediastínica.

Autores/as

  • Jorge Carriel Mancilla Hospital Universitario Clínico San Carlos
  • Antonio Leone Hospital Clínico San Carlos
  • Encarnación Borreguero Martínez Hospital Clínico San Carlos
  • Pedro Ruiz Artacho Hospital Clínico San Carlos
  • Fernando Tornero Romero Hospital Clínico San Carlos
  • Elpidio Calvo Manuel Hospital Clínico San Carlos

Palabras clave:

Genetics, Medical, Klinefelter Syndrome, Mediastinal Diseases, Neoplasms, Germ Cell and Embryonal

Resumen

Klinefelter syndrome (47, XXY in most cases) is a frequently underdiagnosed chromosomal anomaly associated with multiple comorbidities in adult life. Patients with Klinefelter syndrome have a higher risk of cancer. Specifically, these patients have a higher risk for mediastinal germ cell tumors. It is estimated that 8% of male patients with mediastinal tumors have Klinefelter. We report a 42-years-old male who suffered recurrent respiratory infections. During the study, a mediastinal mass was found, whose pathological study disclosed a type B thymoma. The patient had a history of infertility, high stature, gynecomastia, obesity with gynecoid distribution of body fat and testicular atrophy. A karyotype was requested (47, XXY), confirming the diagnosis of Klinefelter syndrome.

Biografía del autor/a

Jorge Carriel Mancilla, Hospital Universitario Clínico San Carlos

Servicio de Medicina Interna

Descargas

Publicado

2019-04-30

Cómo citar

Carriel Mancilla, J., Leone, A., Borreguero Martínez, E., Ruiz Artacho, P., Tornero Romero, F., & Calvo Manuel, E. (2019). Síndrome de Klinefelter diagnosticado en un adulto a raíz del estudio de infección respiratoria recurrente y masa mediastínica. Revista Médica De Chile, 147(4). Recuperado a partir de https://www.revistamedicadechile.cl/index.php/rmedica/article/view/6539

Número

Sección

Reporte de Caso Clínico