Presenting signs and symptoms of pheochromocytoma in pediatric-aged patients

Janet Sullivan1, Ted Groshong, Joseph D Tobias

  • 1University of Missouri School of Medicine, Columbia, Missouri 65212, USA.

Clinical Pediatrics
|October 8, 2005
PubMed

Insights

Pediatric pheochromocytoma often presents with central nervous system (CNS) symptoms, not just hypertension. Early diagnosis can be delayed, highlighting the need for awareness of diverse signs in children.

Area of Science:

  • Pediatric Endocrinology
  • Pediatric Oncology
  • Pediatric Nephrology

Background:

  • Pheochromocytoma is a rare neuroendocrine tumor.
  • Presentation in children can be atypical and delayed.

Purpose of the Study:

  • To detail the diverse presenting signs and symptoms of pediatric pheochromocytoma.
  • To review the clinical course following surgical excision.

Main Methods:

  • Retrospective chart review of 7 pediatric patients.
  • Analysis of presenting signs, symptoms, and clinical course post-surgery.

Main Results:

  • Most patients (6/7) had central nervous system (CNS) symptoms, including altered mental status.
  • Hypertension was present initially in 2 patients and developed later in 5.
  • Diagnosis was delayed (≥5 months) in 4 patients, despite elevated urinary catecholamines in all.

Conclusions:

  • Pediatric pheochromocytoma frequently manifests with CNS symptoms, not solely hypertension.
  • Diverse presentations and diagnostic delays underscore the need for heightened clinical suspicion.

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