HIDEJI NAKAMURA, M.D.; MASAFUMI KOGA, M.D.; BUNZO SATO, M.D.; KEIZO NOMA, M.D.; YASUHIKO MORIMOTO, M.D.; SUSUMU KISHIMOTO, M.D.
This content is PDF only. Please click on the PDF icon to access.
To the editor: It is well known that von Recklinghausen's disease is inherited as an autosomal dominant trait and is often associated with various neoplasms, including pheochromocytoma and nonmedullary thyroid cancer (1, 2). Recently, several cases of "nonmedullary" thyroid cancer have been reported in coexistence with pheochromocytoma (3, 4). We report the case of a patient with von Recklinghausen's disease who also had papillary adenocarcinoma of the thyroid gland and pheochromocytoma, which occurred with some familial disposition.
A 58-year-old woman, who had had café au lait spots and neurofibromas since the age of 30 years, was hospitalized with headache and
NAKAMURA H, KOGA M, SATO B, et al. Von Recklinghausen's Disease with Pheochromocytoma and Nonmedullary Thyroid Cancer. Ann Intern Med. 1986;105:796–797. doi: https://doi.org/10.7326/0003-4819-105-5-796_2
Download citation file:
Published: Ann Intern Med. 1986;105(5):796-797.
Copyright © 2020 American College of Physicians. All Rights Reserved.
Print ISSN: 0003-4819 | Online ISSN: 1539-3704
Conditions of Use