CT imaging in adults with neurofibromatosis-1 - Frequent asymptomatic plexiform lesions

被引:114
作者
Tonsgard, JH
Kwak, SM
Short, P
Dachman, AH
机构
[1] Univ Chicago, Dept Pediat, Pritzker Sch Med, Chicago, IL 60637 USA
[2] Univ Chicago, Pritzker Sch Med, Dept Pathol, Chicago, IL 60637 USA
[3] Univ Chicago, Pritzker Sch Med, Dept Radiol, Chicago, IL 60637 USA
[4] Univ Chicago, Pritzker Sch Med, Joseph P Kennedy Jr Mental Retardat Res Ctr, Chicago, IL 60637 USA
关键词
D O I
10.1212/WNL.50.6.1755
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: The authors examined the incidence and radiologic characteristics of plexiform neurofibromas in neurofibromatosis-1 (NF-1) to define a cohort at greatest risk for malignant nerve-sheath tumors. Background: Plexiform neurofibromas are a frequent complication of NF-1. They can impair function, produce disfigurement, and be the site for the development of malignant nerve-sheath tumors. The incidence and natural history of plexiform neurofibromas is unknown, Methods: CT imaging of the chest, abdomen, and pelvis was performed in 91 of 125 consecutive adults (age, greater than or equal to 16 years) with NF-1. Results: Twenty percent of patients had plexiform neurofibromas of the chest in the paraspinal, mediastinal, or supraclavicular area. Approximately 40% of patients had abnormal abdominal/pelvic scans. The paraspinal, sacral plexus, sciatic notch, and perirectal regions were the most common sites. Most plexiform neurofibromas were asymptomatic. Imaging also revealed a number of tumors, including malignant nerve-sheath tumors, adrenal tumors, carcinoids, and schwannomas. Conclusions: The frequency of plexiform lesions and other tumors in NF-1 indicates that clinicians should monitor young adults carefully; however, imaging characteristics alone cannot reliably distinguish benign from malignant lesions.
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页码:1755 / 1760
页数:6
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