Right adrenal recurrence of a pheochromocytoma twenty four years after ablation of two ectopic pheochromocytomas

Citation
C. Delplace et al., Right adrenal recurrence of a pheochromocytoma twenty four years after ablation of two ectopic pheochromocytomas, ARCH MAL C, 92(3), 1999, pp. 363-367
Citations number
10
Categorie Soggetti
Cardiovascular & Respiratory Systems
Journal title
ARCHIVES DES MALADIES DU COEUR ET DES VAISSEAUX
ISSN journal
00039683 → ACNP
Volume
92
Issue
3
Year of publication
1999
Pages
363 - 367
Database
ISI
SICI code
0003-9683(199903)92:3<363:RAROAP>2.0.ZU;2-X
Abstract
The classical localisation of chromaffin cell tumours is intra-adrenal. Ect opic or multiple tumours are not rare and are commonly observed in children . The authors report a case of ectopic pheochromocytoma with a double local isation in a 14 year old child (renal pedicle and right retropleural space) , in which surgical ablation resulted in an immediate and sustained correct ion of the hypertension. Hypertension recurred 24 years later and a classical right adrenal pheochro mocytoma was demonstrated by methyl-iodo-benzylguanidine (M.I.B.G.) scintig raphy and abdominal CT scan. Right adrenalectomy resulted in normalisation of the hypertension once again without antihypertensive therapy with a foll ow-up of three years. Regular follow-up is necessary after ablation of a ph eochromocytoma, especially in children, even in the absence of a phacomatos is or multiple endocrine neoplastic syndromes.