INTRODUCTION Neurofibromatosis type-1 is a common genetic disorder which often affects the skeleton. Skeletal manifestations of neurofibromatosis type-1 include scoliosis, congenital pseudarthrosis of the tibia and intraosseous cystic lesions. Dislocation of the hip associated with neurofibromatosis type-1 is a rare occurrence and is underreported in the literature. CASE PRESENTATION We repor...

STUDY OBJECTIVES To reassess the association between neurofibromatosis and pulmonary fibrosis. DESIGN Retrospective single-center study with analysis of patients' chest radiographs, CT scans, and medical records. SETTING Tertiary care, referral medical center. PATIENTS One hundred fifty-six adult patients with neurofibromatosis seen over a 6-year period between 1997 and 2002. RESULTS A ...

neurofibromatosis type 1, also known as von recklinghausen disease, is an autosomal dominant disorder with an incidence of 1 per 4000. neurofibromas are benign, heterogeneous tumors arising from the connective tissue of peripheral nerve sheaths, especially the endoneurium. visceral involvement in disseminated neurofibromatosis is rare. neurofibroma occurs most frequently in the stomach and jeju...

provided the original work is properly cited. CC Type 1 neurofibromatosis, also referred to as von Recklinghausen's disease, is characterized by café-au-lait spots and benign cutaneous neurofibromas and is more common than type 2 neurofibromatosis [1,2]. In contrast, type 2 neurofibromatosis affects the central nervous system (CNS) via spinal cord tumors and bilateral vestibular schwannomas [1-...