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neurofibromatosis type 2 cases and literature review performance of MRI images
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neurofibromatosis type 2 cases and literature review performance of MRI images
[Keywords:] neural liver fibrosis, MRI
Neurofibromatosis involving multiple organ system, is a autosomal dominant genetic disease. The disease is divided into two types: the type neurofibromatosis (NF1 with neurofibromatosis type (NF2.90% above NF1 type. This paper reports two cases of NF1, this focus on their MRI.
1 Case information
Example 1: Male, 5 years old. The right orbital and temporal large deformities, soft mass in the right upper eyelid, and temporal delay, ptosis, was “S”-type appearance. Head MRI showed: right temporal pachygyria, cranial multiple abnormalities in signal (see Figure 1. the right upper eyelid tumor resection pathological said: plexiform neurofibroma.
Example 2: Male, 12 years old. Right cheek mass, there is hair growth. Childhood systemic multiple skin pigmentation. MRI showed swelling of the right cheek, signaling an exception (see Figure 2. Tumor resection of the pathological results are shown: subcutaneous plexiform neurofibroma.
2 Discussion
Neurofibromatosis is a neurocutaneous syndrome, in addition to clinical with the skin, eye abnormalities, skin milk, coffee stains, but can affect the brain parenchyma, depending on the channel and the peripheral nerves, the brain showed hamartoma, cerebral Liu, depending on the Channel glial Liu and peripheral nerve lesions such as fibroma [1]. According to the National Health Association’s diagnostic criteria for NF1 uniform, including two or more of the following can be diagnosed with NF1: (1 milk or coffee stains 6 6 or more, (2gt; = 2 neurofibromas of any type, orgt; = 1 of plexiform neurofibromas, and (3 axillary or inguinal freckles, (4 optic nerve glioma or other brain parenchymal microglia Liu, (5gt; = 2 hamartomas of iris melanoma, (6 with characteristics of bone damage, (7 first-degree relatives had a family history of NF1. Case 1 right eyelid tumor, caused
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