A Case Study Of Familial Bilateral Adrenal Pheochromocytoma

Objective:In order to analyze the clinical characteristics and treatment of familial bilateral adrenal pheochromocytoma.Methods:Retrospectively analyze one case of familial bilateral adrenal pheochromocytoma,including clinical feature,laboratory findings,pathology,imaging examination and pathological characteristics.To summarize the diagnosis and treatment experience of familial bilateral adrenal pheochromocytoma.Results:1.The patient with familial bilateral adrenal pheochromocytoma presented no clinical manifestations,and his family history of adrenal pheochromocytoma should be noted.2.Family history,laboratory test combined with imaging examination can be confirmed,postoperative pathology confirmed adrenal pheochromocytoma.3.Staging surgery for bilateral adrenal pheochromocytoma is safe and reliable.Suspected familial bilateral adrenal pheochromocytoma should be screened earlier.Attention should be paid to the postoperative follow-up of patients with pheochromocytoma.Conclusion : The clinical manifestations of patients with familial bilateral adrenal pheochromocytoma are atypical,and some patients have no clinical symptoms.The diagnosis of familial bilateral adrenal pheochromocytoma should include screening of suspected patients,qualitative diagnosis of biochemical assays,and localization of anatomy and function.Surgery is the first choice for the treatment of pheochromocytoma.Familial bilateral adrenal pheochromocytoma is an autosomal dominant disease.