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Title: Asymptomatic pheochromocytoma in the posterior mediastinum. Author: Bouhouch A, Hendriks JM, Lauwers PR, De Raeve HR, Van Schil PE. Journal: Acta Chir Belg; 2007; 107(4):465-7. PubMed ID: 17966552. Abstract: A 66-year-old female patient was treated for a posterior mediastinal tumour with unknown histology. During thoracotomy, repetitive hypertensive crises had to be treated. The tumour was completely resected. Pathology revealed an extra-adrenal pheochromocytoma. Diagnosis of pheochromocytoma is usually made on the basis of clinical presentation and elevated catecholamine levels in serum or urine. Imaging is used primarily for localizing tumours prior to surgery. Complete surgical excision is the primary treatment. The only absolute indicator of malignancy is the identification of distant metastases to bone, liver, lung or lymph nodes.[Abstract] [Full Text] [Related] [New Search]