腎球旁細(xì)胞瘤1例并文獻(xiàn)復(fù)習(xí)
[Abstract]:Objective To study the clinical features and methods of diagnosis and treatment of subrenal cell tumor (JGCT). Methods The clinical data of 1 case of JGCT were retrospectively analyzed. Results The patient was a 26-year-old female, with high blood pressure as the first symptom, the blood potassium was normal, and the CT and MRI examination showed the possibility of renal cell carcinoma. The left and right partial nephrectomy of the renal unit was left after general anesthesia, and the postoperative pathological diagnosis was JGCT. The blood renin activity, angiotensin I and aldosterone decreased significantly after 1 week after operation, and the blood pressure returned to normal. Conclusion JGCT is a rare benign tumor. It is mainly characterized by high renin activity and high blood pressure. The combined CT scan of MRI is helpful to the diagnosis of this disease.
【作者單位】: 南京中醫(yī)藥大學(xué)附屬?gòu)埣腋坩t(yī)院;
【分類號(hào)】:R737.11
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