Embryonal Carcinoma of the Pineal Gland Developed in an Adolescent Boy with Klinefelter Syndrome / 임상소아혈액종양
Clinical Pediatric Hematology-Oncology
;
: 105-109, 2019.
Article
in English
| WPRIM
| ID: wpr-763513
ABSTRACT
Klinefelter syndrome (KS) is characterized by small testes, gynecomastia, tall stature, and hypergonadotropic hypogonadism. This condition is associated with extra X chromosomes. It is well known that these aneuploidies predispose individuals to the development of several cancers. Moreover, there are many case reports that show KS patients to have a higher relative risk for the development of malignancy. However, incracranial germ cell tumor (ICGCT) associated with KS is very uncommon. Herein, we report delayed diagnosis of KS in a 15-year-old boy with ICGCT, embryonal carcinoma of the pineal gland, after multimodality treatment in Korea.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Pineal Gland
/
Testis
/
X Chromosome
/
Carcinoma, Embryonal
/
Neoplasms, Germ Cell and Embryonal
/
Delayed Diagnosis
/
Gynecomastia
/
Hypogonadism
/
Klinefelter Syndrome
/
Korea
Type of study:
Diagnostic study
/
Etiology study
Limits:
Adolescent
/
Humans
/
Male
Country/Region as subject:
Asia
Language:
English
Journal:
Clinical Pediatric Hematology-Oncology
Year:
2019
Type:
Article
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