Results 141 to 150 of about 12,175 (184)
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Gastroenterology, 1950
Summary 1.Three cases of solitary neurofibroma of the stomach which came to operation are reported. 2.As a group they demonstrated all of the clinical features which may characterize the onset and subsequent course of such tumors. 3.The pathologic data are recorded and amplified with a discussion of other available information on the gross and ...
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Summary 1.Three cases of solitary neurofibroma of the stomach which came to operation are reported. 2.As a group they demonstrated all of the clinical features which may characterize the onset and subsequent course of such tumors. 3.The pathologic data are recorded and amplified with a discussion of other available information on the gross and ...
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Current Opinion in Neurology, 2002
Neurofibromas and schwannomas are benign peripheral nerve sheath tumours that occur as isolated sporadic lesions, but have their major clinical impact on the neurocutaneous diseases neurofibromatosis 1 and neurofibromatosis 2. The gene products neurofibromin and merlin (schwannomin), respectively, are thought to act as tumour suppressors.
Ferner, R E, O'Doherty, M J
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Neurofibromas and schwannomas are benign peripheral nerve sheath tumours that occur as isolated sporadic lesions, but have their major clinical impact on the neurocutaneous diseases neurofibromatosis 1 and neurofibromatosis 2. The gene products neurofibromin and merlin (schwannomin), respectively, are thought to act as tumour suppressors.
Ferner, R E, O'Doherty, M J
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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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Otolaryngology–Head and Neck Surgery, 1980
A neurofibroma in the larynx is quite unusual and is more likely to appear as a solitary, isolated lesion rather than a concomitant finding in von Recklinghausen's disease. A case is presented of a patient with residual endolaryngeal neurofibroma despite eight attempts at removal.
J S, Supance, D J, Quenelle, J, Crissman
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A neurofibroma in the larynx is quite unusual and is more likely to appear as a solitary, isolated lesion rather than a concomitant finding in von Recklinghausen's disease. A case is presented of a patient with residual endolaryngeal neurofibroma despite eight attempts at removal.
J S, Supance, D J, Quenelle, J, Crissman
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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
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The Annals of Thoracic Surgery, 1997
Benign esophageal tumors occur infrequently, with leiomyomas accounting for approximately 70% of cases. Benign neural tumors of the esophagus account for 200 cases reported in the literature and rarely require operative resection. The case of a 58-year-old woman with a 4-month history of progressive dysphagia and odynophagia is presented.
R, Lee, W A, Williamson
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Benign esophageal tumors occur infrequently, with leiomyomas accounting for approximately 70% of cases. Benign neural tumors of the esophagus account for 200 cases reported in the literature and rarely require operative resection. The case of a 58-year-old woman with a 4-month history of progressive dysphagia and odynophagia is presented.
R, Lee, W A, Williamson
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Urology, 1987
A periurethral neurofibroma presenting as a midline perineal mass was removed in a three-year-old boy. An immunohistochemical study of S-100 protein distribution within the tumor tissue was performed.
Selli C +4 more
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A periurethral neurofibroma presenting as a midline perineal mass was removed in a three-year-old boy. An immunohistochemical study of S-100 protein distribution within the tumor tissue was performed.
Selli C +4 more
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American Journal of Medical Genetics, 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 ...
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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 ...
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Endotracheobronchial neurofibromas
The Annals of Thoracic Surgery, 2002Among benign tracheobronchial neoplasms, neurofibromas of neurogenic origin are exceedingly rare. In a search world literature, only 23 cases of endotracheobronchial neurofibromas in 21 series were found. We report another case of a 52-year-old man who presented to our hospital with the symptoms of intermittent productive cough and fever.
Han-Shui, Hsu +3 more
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Glycosaminoglycans in Neurofibromas
The Journal of Dermatology, 1990AbstractGlycosaminoglycan (GAG) contents in neurofibromas (NFs) were examined to clarify how well they corresponded to their histological features. Eight cutaneous NFs and three plexiform NFs from five patients with Recklinghausen's (R) disease, two senile NFs, and control dermis were subjected to the isolation of GAGs.
T, Sasaki, S, Onodera
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