Pheochromocytoma in children: 15 cases

Y. Révillon, P. Daher, D. Jan, C. Buisson, V. Bonnerot, H. Martelli, C. Nihoul-Fékété

Research output: Contribution to journalArticle

23 Scopus citations

Abstract

Pheochromocytoma is an uncommon tumor in childhood; nevertheless, 20% of all pheochromocytomas are found in the pediatric population. Fifteen children have been treated in our institution from 1962 to 1990. One percent of patients refered over the same period for investigation of high blood pressure were found to have a pheochromocytoma. The majority of patients have hypertension. It varies in intensity and is paroxysmal in about half the patients. Many pediatric cases of unilateral, bilateral, extraadrenal, familial, and recurrent pheochromocytomas have been reported. We reviewed our 28 years experience with this tumor and concentrated on the diagnosis, the preoperative and operative management, and the occurrence of the multiple endocrine neoplasia syndromes.

Original languageEnglish (US)
Pages (from-to)910-911
Number of pages2
JournalJournal of Pediatric Surgery
Volume27
Issue number7
DOIs
StatePublished - Jul 1992

Keywords

  • Pheochromocytoma
  • hypertension
  • multiple endocrine neoplasia

ASJC Scopus subject areas

  • Surgery
  • Pediatrics, Perinatology, and Child Health

Fingerprint Dive into the research topics of 'Pheochromocytoma in children: 15 cases'. Together they form a unique fingerprint.

  • Cite this

    Révillon, Y., Daher, P., Jan, D., Buisson, C., Bonnerot, V., Martelli, H., & Nihoul-Fékété, C. (1992). Pheochromocytoma in children: 15 cases. Journal of Pediatric Surgery, 27(7), 910-911. https://doi.org/10.1016/0022-3468(92)90396-O