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Postoperative pathology confirmed perianal plexiform neurofibroma: a case report. [PDF]
Front Med (Lausanne)Wu ZB +5 more
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American Journal of Medical Genetics, Part A, 1999
Plexiform neurofibromas are among the most common and debilitating complications of neurofibromatosis type 1 (NF1). They account for substantial morbidity, including disfigurement, functional impairment, and may even be life threatening. Plexiform neurofibromas are also subject to transformation into malignant peripheral nerve sheath tumor (MPNST), a ...
Bruce R. Korf
exaly +3 more sources
Plexiform neurofibromas are among the most common and debilitating complications of neurofibromatosis type 1 (NF1). They account for substantial morbidity, including disfigurement, functional impairment, and may even be life threatening. Plexiform neurofibromas are also subject to transformation into malignant peripheral nerve sheath tumor (MPNST), a ...
Bruce R. Korf
exaly +3 more sources
Insight - the Journal of the American Society of Ophthalmic Registered Nurses, 1996
Although neurofibroma is a rare orbital tumor, ophthalmic nurses may have the first opportunity to observe patients with this tumor. These patients may first be seen with normal visual acuity, proptosis, or affected ocular motility. An interesting patient who was diagnosed with an orbital neurofibroma is presented.
C A, Servodidio +2 more
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Although neurofibroma is a rare orbital tumor, ophthalmic nurses may have the first opportunity to observe patients with this tumor. These patients may first be seen with normal visual acuity, proptosis, or affected ocular motility. An interesting patient who was diagnosed with an orbital neurofibroma is presented.
C A, Servodidio +2 more
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Collagens in Neurofibromas and Neurofibroma Cell Cultures
Annals of the New York Academy of Sciences, 1986Neurofibromas contain approximately 30-50% collagen of their lipid-free dry weight, which is about half of the value of skin but approximately twice that described for peripheral nerve endoneurium. Immunohistochemical stainings indicate that neurofibromas contain types I, III, IV, and V collagens and fibronectin. Most of the neurofibroma cells are type
J, Peltonen +3 more
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New England Journal of Medicine, 1953
PRIMARY tumors of the diaphragm are rare, less than 40 cases having been reported in the literature.
R H, SWEET, T, GEPHART
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PRIMARY tumors of the diaphragm are rare, less than 40 cases having been reported in the literature.
R H, SWEET, T, GEPHART
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The Journal of Laryngology & Otology, 1992
AbstractThis paper is a retrospective study of 15 patients with parapharyngeal neurofibromas operated over a six year period. No patient presented with a neurological deficit. CT scans revealed a well encapsulated moderately enhancing mass in ten cases.
D A, Tandon +4 more
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AbstractThis paper is a retrospective study of 15 patients with parapharyngeal neurofibromas operated over a six year period. No patient presented with a neurological deficit. CT scans revealed a well encapsulated moderately enhancing mass in ten cases.
D A, Tandon +4 more
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American Journal of Medical Genetics, 1999
Unless omitted and underreported, penile neurofibromas are rare. Between January 2, 1982 and December 31, 1997 through the USF Regional Genetics Program we evaluated 566 propositi with suspected or clinically diagnosed neurofibromatosis (NF1, NF2, segmental NF=NF5, NF/Noonan syndrome, familial café-au-lait macules, and solitary neurofibroma, NF). These
B G, Kousseff, D L, Hoover
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Unless omitted and underreported, penile neurofibromas are rare. Between January 2, 1982 and December 31, 1997 through the USF Regional Genetics Program we evaluated 566 propositi with suspected or clinically diagnosed neurofibromatosis (NF1, NF2, segmental NF=NF5, NF/Noonan syndrome, familial café-au-lait macules, and solitary neurofibroma, NF). These
B G, Kousseff, D L, Hoover
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Southern Medical Journal, 1983
We have described a unique example of intratracheal neurofibroma in a patient with neurofibromatosis. Although tracheal neoplasms are rare, they should be considered in the presence of obstructive respiratory symptoms. Careful scrutiny of plain roentgenograms with special views should be undertaken for optimal evaluation.
J N, Rutledge, J A, Harolds
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We have described a unique example of intratracheal neurofibroma in a patient with neurofibromatosis. Although tracheal neoplasms are rare, they should be considered in the presence of obstructive respiratory symptoms. Careful scrutiny of plain roentgenograms with special views should be undertaken for optimal evaluation.
J N, Rutledge, J A, Harolds
openaire +2 more sources