Journal
INTERNAL MEDICINE
Volume 59, Issue 13, Pages 1665-1669Publisher
JAPAN SOC INTERNAL MEDICINE
DOI: 10.2169/internalmedicine.4148-19
Keywords
neurofibromatosis type 1; pheochromocytoma; breast cancer
Categories
Ask authors/readers for more resources
A 40-year-old woman presented with a left adrenal incidentaloma. Based on the presence of cafe-au-lait spots, cutaneous neurofibroma, and family history, she was diagnosed with neurofibromatosis type 1 (NF1). Adrenal incidentaloma screening showed an elevated normetanephrine level; the left adrenal mass showed the uptake of 1-123 meta-iodobenzylguanidine. She underwent left adrenalectomy, and pheochromocytoma was diagnosed. One year later, the results of a biopsy of a palpable mass in the left breast suggested invasive ductal carcinoma. The patient underwent neoadjuvant chemotherapy followed by left breast-conserving surgery. We herein report a rare case of an NF1 patient who developed both pheochromocytoma and breast cancer.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available