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1.
Tuberculosis and Respiratory Diseases ; : 117-122, 1999.
Artigo em Coreano | WPRIM | ID: wpr-154911

RESUMO

Primary germ cell tumors of the mediastinum are rare, accounting 1-5% among all germ cell tumors and 10% of all neoplasms in this area. Approximately 85% of these tumors occur in men with a mean age 29 years. These tumors are mainly found in the anterior mediastinum and appear grossly as large lobulated masses. They are frequently invasive at the time of diagnosis and almost 90% of patients are symptomatic. Primary nonseminomatous germ cell tumor arising in the posterior mediastinum is very rare. We report a case of 37- year old male arising from the posterior mediastinum. Serum tumors markers including alpha-fetoprotein and beta-hCG which are usually elevated in germ cell tumor were not elevated. He was found to have a primary mediastinal embryonal carcinoma with pulmonary metastasis at open exploration. He was treated with debulking surgery and cisplatin-based chemotherapy, died of sepsis after 15 months postoperatively.


Assuntos
Humanos , Masculino , alfa-Fetoproteínas , Carcinoma Embrionário , Diagnóstico , Tratamento Farmacológico , Mediastino , Metástase Neoplásica , Neoplasias Embrionárias de Células Germinativas , Sepse
2.
Tuberculosis and Respiratory Diseases ; : 1035-1041, 1996.
Artigo em Coreano | WPRIM | ID: wpr-50153

RESUMO

Klinefelter's syndrome is characterized by small testes, azoospermia, gynecomastia, and elevated levels of plasma gonadotropins in men with two or more X chromosomes. Previous investigators reported that patients with Klinefelter's syndrome are predisposed to the development of a non-seminomatous germ cell tumor in the mediastinum. It is suggested that this linkage may be due to the hormonal imbalance in Klinefelter's syndrome and consequently, the formation of dysgenetic germ cell and/or abnomal migration of germ cell. We report here a case of Klinefelter's syndrome in a 24-years-old man who was presented with anterior mediastinal mass. The clinical and laborarotory findings were compatible with Klinefelter's syndrome and he was found to have 47 XXY karyotype. Pathological findings for mediastinal mass revealed mixed germ cell tumor composed of mature cystic teratoma and endodermal sinus tumor. He was treated with cis-platin containing chemotherapy and followed up in partial remission.


Assuntos
Humanos , Masculino , Azoospermia , Tratamento Farmacológico , Tumor do Seio Endodérmico , Células Germinativas , Gonadotropinas , Ginecomastia , Cariótipo , Síndrome de Klinefelter , Mediastino , Neoplasias Embrionárias de Células Germinativas , Plasma , Pesquisadores , Teratoma , Testículo , Cromossomo X
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