Neurofibroma of the Breast Detected on Positron Emission Tomography-CT in a Patient with Neurofibromatosis Type 1: A Case Report
Author(s) -
Ho Seok Lee,
Hye Jung Kim,
Bora Yang,
So Mi Lee,
Ji Yun Jeong
Publication year - 2016
Publication title -
journal of the korean society of radiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.126
H-Index - 3
eISSN - 2288-2928
pISSN - 1738-2637
DOI - 10.3348/jksr.2016.74.2.128
Subject(s) - medicine , neurofibromatosis , neurofibroma , mammography , radiology , positron emission tomography , breast cancer , neurofibromatosis type i , nuclear medicine , cancer
Neurofibromas are slow-growing, painless, benign nervesheath tumors. They occur most commonly in the dermis and subcutis, and are rarely found in the breast (1). Breast neurofibromas may develop as a result of inherited autosomal dominant neurofibromatosis type 1 (NF1) or randomly at a later time due to genetic mutations (2). They usually appear as well-circumscribed oval masses on both mammography and ultrasonography (US), and are usually located on the nipple-areolar area (2-4). We report a case of neurofibroma secondary to NF1 in the retromammary space resulting from endometrial cancer, which was detected on positron emission tomography-computed tomography (PET-CT) after hysterectomy. CASE REPORT
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