Reversible hypertensive retinopathy in a child with bilateral pheochromocytoma after tumor resection

T. Y. Chen, C. D. Liang*, C. S. Shieh, S. F. Ko, M. L. Kao

*Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

8 Scopus citations

Abstract

Pheochromocytoma is very rare in children. We report a case of bilateral pheochromocytoma in a 12-year-old boy who had blurred vision due to hypertensive retinopathy. Abdominal ultrasound and computed tomography revealed bilateral suprarenal tumors. Resection of the bilateral tumors along with right total and left subtotal adrenalectomy were performed. Blood pressure and visual acuity returned to normal after surgery.

Original languageEnglish
Pages (from-to)945-947
Number of pages3
JournalJournal of the Formosan Medical Association
Volume99
Issue number12
StatePublished - 2000
Externally publishedYes

Keywords

  • Child
  • Hypertensive retinopathy
  • Pheochromocytoma

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