Diffuse Neurofibromatosis
نویسندگان
چکیده
منابع مشابه
Neurofibromatosis
Neurofibromatosis (NF) is an inherited disorder characterized by the development of a wide variety of clinical manifestations, including characteristic "freckle-like" pigmentations (cafe au lait spots) that develop in infancy, followed by skin tumors that may vary widely in size, number, and distribution. In addition to skin tumors, bone, neurologic, and endocrine abnormalities are common. NF i...
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A 67-year-old Japanese man with neurofibromatosis type 1 underwent right hemicolectomy owing to abscess formation around the cecum. A pathological analysis revealed diffuse intestinal ganglioneuromatosis in the cecum and colon. Colonoscopy performed eight months after hemicolectomy revealed multiple ulcers throughout the colon and rectum. The colorectal ulcers failed to respond to conservative ...
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Segmental neurofibromatosis type I (SNF-I) is a rare variant of neurofibromatosis (NF). It is classified as NF type V and defined as cafe'-au-lait macules and/or neurofibromas in a single ,unilateral segment of the body .We report two cases with SNF-I with striking similar manifestations.
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Introduction:Neurofibromatosis is a genetic disease characterized by multifocal benign tumors of peripheral nerves, called neurofibromas, and pigmented spots on the skin which inherited as autosomal-dominant. The most common form of the disease is neurofibromatosis type 1, also known as von Recklinghausen's disease of the skin. When an individual has small number of lesions in a limited region ...
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WHILST neurofibromatosis, in more or less localised form, is not infrequently seen, most of our knowledge concerning the histological structure of the nodules is gained from biopsy specimens. The following case, illustrating as it does the widespread distribution of the process and the nature of the associated lesions, seemed, therefore, worthy of report. CLINICAL HISTORY. The patient, a man of...
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ژورنال
عنوان ژورنال: Proceedings of the Royal Society of Medicine
سال: 1967
ISSN: 0035-9157
DOI: 10.1177/003591576706000505