| Autor: |
Singh, Aditya Pratap, Tanger, Ramesh, Ansari, Maryem, Gupta, Arun Kumar, Barolia, Dinesh Kumar |
| Předmět: |
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| Zdroj: |
APSP Journal of Case Reports; 2018, Vol. 9 Issue 3, p1-4, 4p |
| Abstrakt: |
Background: Teratoma is a germ cell tumor (GCT) arising from totipotent stem cells that differentiate into the tissues that are foreign to the anatomic site. Teratoma at the suprarenal location is extremely rare. The association with the Down syndrome also makes it unusual. Case Report: We are presenting here a case of one-year-old female infant with Down syndrome who had an antenatal diagnosis of right suprarenal mass. Laparotomy revealed a large cystic mass in the right suprarenal location which was completely excised. Right adrenal gland could not be seen separately from the mass. The histological diagnosis was a mature cystic teratoma. Conclusion: Adrenal teratoma is rare and may be considered in the differential diagnosis of antenatally diagnosed suprarenal lesion. Its association with Down syndrome is rare finding. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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