Title of article :
Peripheral Medulloepithelioma: A Rare Entity to Know
Author/Authors :
Khoubila, N Hematology and Pediatric Oncology Department - Hospital - University Hospital Center Ibn Rochd Casablanca, Morocco , Matrane, W Hematology and Pediatric Oncology Department - Hospital - University Hospital Center Ibn Rochd Casablanca, Morocco , Cherkaoui, S Hematology and Pediatric Oncology Department - Hospital - University Hospital Center Ibn Rochd Casablanca, Morocco , Madani, A Hematology and Pediatric Oncology Department - Hospital - University Hospital Center Ibn Rochd Casablanca, Morocco , Quessar, A. Hematology and Pediatric Oncology Department - Hospital - University Hospital Center Ibn Rochd Casablanca, Morocco , Regragui, M. Pathologic Anatomy and Cytology Laboratory - University Hospital Center Ibn Rochd Casablanca, Morocco , Guebessi, N. Bennani Pathologic Anatomy and Cytology Laboratory - University Hospital Center Ibn Rochd Casablanca, Morocco , Karkouri, M. Pathologic Anatomy and Cytology Laboratory - University Hospital Center Ibn Rochd Casablanca, Morocco , Salam, S. Pediatric Radiology Department - University Hospital Center Ibn Rochd Casablanca, Morocco
Pages :
5
From page :
1
To page :
5
Abstract :
According to the World Health Organization, medulloepithelioma belongs to the embryonal neoplasm entity. It is a very rare,highly malignant tumor typically affecting infants and young children. Usually, the tumor arises in the eye or in the centralnervous system; a peripheral location has been rarely reported without an established treatment. The recognition and separationof this neoplasm from other differential tumors are mandatory for better understanding of its biology and determination ofoptimal treatment. This paper reports a case of an ectopic intrapelvic medulloepithelioma with liver metastasis in a 3-year-old girl.
Keywords :
Peripheral Medulloepithelioma , A Rare Entity to Know , ME
Journal title :
Case Reports in Oncological Medicine
Serial Year :
2020
Full Text URL :
Record number :
2608737
Link To Document :
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