Juxtaglomerular Cell Tumour: Case Report and Literature Review
Abstract
Juxtaglomerular tumor cells kidney (reninoma) is an uncommon, mostly benign tumor, characterized by excess secretion of renin, causing a secondary hypertension. The tumor rather seldom meets. In 50 years from the moment of its first description a little more than 100 similar tumors are described in literature. The uncontrollable hypertension leads to endotelial damage and to complications on heart, kidneys and the central nervous system which can be life-threatening. Reception of hypotensive preparations leads to temporary effect. The hypertension is treated by tumor resection or nephrektomy. Clinical case of the women of 29 years old with a juxtaglomerular tumor with the clinical picture of high blood pressure to 160–180 mm Hg within 10 years are presented. Possibilities of ultrasonography (B-mode, duplex scanning, contrast enhancement) at detection of this tumor and the importance of anamnestic data in the differential diagnosis of kidney tumors are shown.
About the Authors
Yulia A. StepanovaRussian Federation
M. D. Med., Senior Research of Department of Radiology Methods of Diagnostics and Treatment
Olesya A. Chekhoeva
Russian Federation
Junior Researcher, Ultrasound Diagnostics of Department
Andrey V. Glotov
Russian Federation
Junior Researcher, Pathology of Department
Aleksandr A. Gritskevich
Russian Federation
Ph. D. Med., Senior Research, the Urology of Department
Sergey S. Pyanikin
Russian Federation
Junior Researcher, Urology of Department
Dmitry V. Kalinin
Russian Federation
Ph. D. Med., Head Pathology of Department
Aleksandr A. Teplov
Russian Federation
M. D. Med., Professor, Deputy Director
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Review
For citations:
Stepanova Yu., Chekhoeva O., Glotov A., Gritskevich A., Pyanikin S., Kalinin D., Teplov A. Juxtaglomerular Cell Tumour: Case Report and Literature Review. Radiology - Practice. 2016;(3):50-63. (In Russ.)