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[Multiple familial pheochromocytomas: sonographic demonstration of multiple adrenal, celiac and bladder localizations
J M Arroja1, F Gudinchet, P Maeder
1Département de radiologie, Centre hospitalier universitaire vaudois, Lausanne.
Praxis
|October 24, 1995
Abstract:
Familial pheochromocytoma is an uncommon form of this neoplasia. It is characterized by an autosomal dominant inheritance and multicentric locations. It is more frequently encountered in children, but with a smaller risk of malignant transformation than in adults. The familial form may be associated with other disorders, particularly with multiple endocrine neoplasia (MEN), Von Hippel-Lindau's disease and Von Recklinghausen's disease. We report the case of a nine-year-old boy with multiple familial pheochromocytoma in whom sonography allowed to demonstrate five localizations.