Tīmeklis2016. gada 15. dec. · Reninoma, jukstaglomeruler hucrelerden koken alan nadir bir tumordur. Bu calismamizda sekonder hipertansiyon ve yan agrisi ile uroloji poliklinigine basvuran 17 yasinda bir erkek hastayi ve ardindan literaturde reninoma ile ilgili bilgileri sunmayi amacladik. Hastanin yapilan degerlendirmesinde hipokalemik oldugu … TīmeklisConclusion: Renin-secreting juxtaglomerular tumor of the kidney (reninoma) is a very rare but curable cause of severe hypertension. The syndrome of “primary hyperreninism” is characterized by severe hypertension, hypokalemia, secondary hyperaldosteronism and a renal mass in sonography. Download to read the full article text.
Juxtaglomerular Cell Tumor With Atypical Pathological Features: Report ...
TīmeklisA 25-year-old lady presented with hypertensive encephalopathy. She also had chronic refractory hypertension for the past 7 years. Workup revealed persistent hypokalaemia with metabolic alkalosis … TīmeklisReninoma should be suspected in young hypertensives (especially females) with significant hypokalaemia and high PRA or direct renin concentration after renovascular hypertension has been excluded. CT imaging and carefully performed RVRRs provide the highest likelihood of locating these tumours. jennifer lopez and daughter
Juxtaglomerular cell tumor - Wikipedia
Juxtaglomerular cell tumor (JCT, JGCT, also reninoma) is an extremely rare kidney tumour of the juxtaglomerular cells, with less than 100 cases reported in literature. This tumor typically secretes renin, hence the former name of reninoma. It often causes severe hypertension that is difficult to control, in adults … Skatīt vairāk By hypersecretion of renin, JCT causes hypertension, often severe and usually sustained but occasionally paroxysmal, and secondary hyperaldosteronism inducing hypokalemia, though the later can be mild despite … Skatīt vairāk JCT often is described as benign, however one case of metastasis has been reported, so its malignant potential is uncertain. In most cases the tumor is encapsulated. Skatīt vairāk Juxtaglomerular cell tumor was first described in 1967 in a paper by Robertson et al., and first named by Kihara et al. in 1968. Since then, approximately 100 case reports have been published. Karyotyping of a small number of these tumors revealed a … Skatīt vairāk JCT is morphologically characterized by multiple foci malignant mesenchymal epithelioid cells with, often with admixed necrosis, … Skatīt vairāk Clinically, hypertension, especially when severe or poorly controlled, combined with evidence of a kidney tumor via imaging or gross examination suggest … Skatīt vairāk Tīmeklis2024. gada 2. janv. · Hiperaldosteronizm jest stanem patologicznym spowodowanym zwiększoną produkcją aldosteronu, głównego hormonu mineralokortykoidowego kory mózgowej. TīmeklisReninoma is a tumor of the renal juxtaglomerular cell apparatus that causes hypertension and hypokalemia via hypersecretion of renin. We describe a case of … pac http区别