[Multiple familial pheochromocytomas: sonographic demonstration of multiple adrenal, celiac and bladder localizations in a child]

Détails

ID Serval
serval:BIB_9875DAABA66C
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Etude de cas (case report): rapporte une observation et la commente brièvement.
Collection
Publications
Institution
Titre
[Multiple familial pheochromocytomas: sonographic demonstration of multiple adrenal, celiac and bladder localizations in a child]
Périodique
Schweizerische Rundschau für Medizin Praxis
Auteur(s)
Arroja  J. M., Gudinchet  F., Maeder  P., Fournier  D.
ISSN
1013-2058
Statut éditorial
Publié
Date de publication
10/1995
Volume
84
Numéro
43
Pages
1231-1234
Notes
Case Reports English Abstract Arroja, J M Gudinchet, F Maeder, P Fournier, D Switzerland Schweizerische Rundschau fur Medizin Praxis = Revue suisse de medecine Praxis Schweiz Rundsch Med Prax. 1995 Oct 24;84(43):1231-4. --- Old month value: Oct 24
Résumé
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.
Mots-clé
Adrenal Gland Neoplasms/*genetics/radionuclide imaging/ultrasonography Child Humans Male Multiple Endocrine Neoplasia/*genetics/radionuclide imaging/ultrasonography Pheochromocytoma/*genetics/radionuclide imaging/ultrasonography Retroperitoneal Neoplasms/radionuclide imaging/ultrasonography
Pubmed
Création de la notice
08/04/2008 15:38
Dernière modification de la notice
20/08/2019 16:00
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