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Juxtaglomerular apparatus tumor: a rare, surgically correctable cause of hypertension
Authors:Rubenstein Jonathan N  Eggener Scott E  Pins Michael R  Rosner Karol  Chugh Sumant  Campbell Steven C
Abstract:Although uncommon, presentation of juxtaglomerular cell tumor is distinct and should allow a correct preoperative diagnosis in most patients. Typical clinical presentations include headaches, polyuria, or isolated, asymptomatic, severe hypertension. The diagnosis of a juxtaglomerular apparatus (JGA) tumor typically results from identification of plasma renin levels two- to sevenfold greater than the normal value. Although JGA tumors are considered benign, with no reports of metastases or recurrence, they are potentially lethal if left untreated. Surgical excision is curative.
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