A Case of Primitive Neuroectodermal Tumor of the Adrenal Gland
Journal of the Korean Pediatric Society
; : 1459-1462, 2001.
Article
ي Ko
| WPRIM
| ID: wpr-117626
المكتبة المسؤولة:
WPRO
ABSTRACT
Primitive neuroectodermal tumors(PNETs) are a group of small round cell tumors that may arise in the central or peripheral nervous system. In the extracranial location, these neoplasms may occur anywhere and at any age group, but most likely in the bone and soft tissue of children and young adults. The incidence of adrenal gland involvement is very rare. This tumor is diagnosed by histopathological, immunohistochemical, and molecular pathological examinations. PNETs are highly aggressive tumors, locally recurrent and rapidly metastasizing to lung, liver, lymph node, and brain. The outcome is poor with a 5 year survival rate below 40% in spite of aggressive combined treatment including surgery, chemotherapy, and radiation therapy. We experienced a case of PNET of adrenal gland, mimicking ruptured Wilms tumor on the US and CT scan.
Key words
النص الكامل:
1
الفهرس:
WPRIM
الموضوع الرئيسي:
Brain
/
Tomography, X-Ray Computed
/
Incidence
/
Survival Rate
/
Peripheral Nervous System
/
Neuroectodermal Tumors, Primitive
/
Adrenal Glands
/
Wilms Tumor
/
Drug Therapy
/
Neural Plate
نوع الدراسة:
Incidence_studies
/
Prognostic_studies
المحددات:
Child
/
Humans
اللغة:
Ko
مجلة:
Journal of the Korean Pediatric Society
السنة:
2001
نوع:
Article