A Case of Wilms Tumor in a Primary Adrenal Mature Teratoma

We report the first known case of an adrenal teratoma containing a Wilms tumor component, in 12-month-old girl with Trisomy 21. Despite teratomas being relatively uncommon, this particular instance raises interesting questions regarding origin, given coexistence both and tumor. Two main theories development have been hypothesized, one which suggests that may develop from primary other proposing could originate Our study leans toward former, as majority displayed characteristics typical mature teratoma, component discovered incidental finding. Successful surgical intervention led to gross total resection Twelve months post-resection, patient remains free recurrence. This contributes our understanding these rare types underlines importance identifying ensure appropriate management treatment.