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Rare disease
Case report
Pheochromocytoma and gastrointestinal stromal tumours in an adult neurofibromatosis type 1 patient: a rare co-occurrence

Authors

  • Nuttawut Vongsumran Endocrine and Metabolism Unit, Internal Medicine Department, Faculty of Medicine, Chiang Mai University, Muang Chiang Mai, Chiang Mai, Thailand PubMed articlesGoogle scholar articles
  • Sarawut Kongkarnka Department of Pathology, Faculty of Medicine, Chiang Mai University, Muang Chiang Mai, Chiang Mai, Thailand PubMed articlesGoogle scholar articles
  • Pittaporn Watanawittawas Endocrine and Metabolism Unit, Internal Medicine Department, Faculty of Medicine, Chiang Mai University, Muang Chiang Mai, Chiang Mai, ThailandEndocrine and Metabolism Unit, Sriphat Medical Center, Faculty of Medicine, Chiang Mai University, Muang Chiang Mai, Chiang Mai, Thailand PubMed articlesGoogle scholar articles
  • Worapaka Manosroi Endocrine and Metabolism Unit, Internal Medicine Department, Faculty of Medicine, Chiang Mai University, Muang Chiang Mai, Chiang Mai, Thailand PubMed articlesGoogle scholar articles
  1. Correspondence to Worapaka Manosroi; worapaka.m{at}gmail.com
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Citation

Vongsumran N, Kongkarnka S, Watanawittawas P, et al
Pheochromocytoma and gastrointestinal stromal tumours in an adult neurofibromatosis type 1 patient: a rare co-occurrence
BMJ Case Reports CP 2020;13:e235129.

Publication history

  • Accepted May 25, 2020
  • First published June 28, 2020.
Online issue publication 
June 28, 2020

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