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Mediastinal germ cell tumor in a child with precocious puberty and Klinefelter syndrome.
Bebb, G G; Grannis, F W; Paz, I B; Slovak, M L; Chilcote, R.
Affiliation
  • Bebb GG; Department of General and Oncologic Surgery, City of Hope National Medical Center, Duarte, California 91010, USA.
Ann Thorac Surg ; 66(2): 547-8, 1998 Aug.
Article in En | MEDLINE | ID: mdl-9725401
ABSTRACT
An 8-year-old boy presented with precocious puberty and a mediastinal mass. A computer search showed that this rare presentation is most common with germ cell tumor of the mediastinum in children with Klinefelter syndrome. The tumor was completely resected after preoperative chemotherapy, and the patient is well 2 years after the operation. In patients with Klinefelter syndrome, germ cell tumors are 50 times more common than in patients without Klinefelter syndrome, usually contain nonseminomatous elements, present at an earlier age, and are seldom testicular in location.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Puberty, Precocious / Germinoma / Klinefelter Syndrome / Mediastinal Neoplasms Limits: Child / Humans / Male Language: En Journal: Ann Thorac Surg Year: 1998 Document type: Article Affiliation country: United States
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Collection: 01-internacional Database: MEDLINE Main subject: Puberty, Precocious / Germinoma / Klinefelter Syndrome / Mediastinal Neoplasms Limits: Child / Humans / Male Language: En Journal: Ann Thorac Surg Year: 1998 Document type: Article Affiliation country: United States