Autor: |
Dakshit, Debashis, Chakraborty, Prithvijit, Ramakrishnan, Karthik Krishna, Basu, Nupur, Ghosh, Suhas, Bhadra, Ashok |
Předmět: |
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Zdroj: |
Pakistan Journal of Radiology; Jan-Mar2018, Vol. 28 Issue 1, p64-68, 5p |
Abstrakt: |
Primitive neuroectodermal tumor of adrenal gland is a rare malignant neoplasm. It is categorised under peripheral primitive neuroectodermal tumors (pPNET). They have aggressive course with very poor prognosis. A 10-year old male patient was being evaluated for left loin pain. Ultrasonography showed a large mass in left lumber region with heterogenous echotexture and increased vascularity on colour Doppler. Computed tomography showed the mass was arising from left suprarenal gland. PET-CT scan reveald the mass was metabolically active. Biopsy from that mass showed histopathological features consistent with primitive neuroectodermal tumor of adrenal origin. [ABSTRACT FROM AUTHOR] |
Databáze: |
Complementary Index |
Externí odkaz: |
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