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Latest revision as of 02:34, 25 September 2026
Children presenting with pheochromocytoma should be tested for:
a) von Hipple-Lindau disease
b) Neurofibromatosis type 1
c) Multiple endocrine neoplasia, type 2
d) Succinate dehydrogenase mutations
e) All of the above
Click for Answer
Answer
Answer e. 40% of pheochromocytomas in children are associated with these genetic conditions. All young patients (under 50) should be offered genetic screening, especially as the succinate dehydrogenase mutations are associated with a high risk of malignancy.
Notes
- This question originally printed in the Pediatric Anesthesiology Review Topics kindle book series, and appears courtesy of Naerthwyn Press, LLC.