Results 171 to 180 of about 25,703 (229)
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The American Journal of Surgery, 1948
Abstract 1. 1. A general review of neurofibroma of the stomach is presented. 2. 2. Certain points deemed helpful in differentiating between malignancy and benignancy of gastric neoplasm are offered for consideration. 3. 3. A plea is made to make every effort to bring patients with gastric neoplasms within physiologic balance so that they ...
R W, TATE, W J, FUSARO
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Abstract 1. 1. A general review of neurofibroma of the stomach is presented. 2. 2. Certain points deemed helpful in differentiating between malignancy and benignancy of gastric neoplasm are offered for consideration. 3. 3. A plea is made to make every effort to bring patients with gastric neoplasms within physiologic balance so that they ...
R W, TATE, W J, FUSARO
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Archives of Otolaryngology - Head and Neck Surgery, 1950
IN SPEAKING of "benign tumors" of the larynx it is necessary to remember that the majority of so-called tumors are not true neoplasms at all. They are, rather, inflammatory swellings or hyper-plastic growths which originate as physiologic responses to some form of irritation.
S J, PEARLMAN, E A, FRIEDMAN, M, APPEL
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IN SPEAKING of "benign tumors" of the larynx it is necessary to remember that the majority of so-called tumors are not true neoplasms at all. They are, rather, inflammatory swellings or hyper-plastic growths which originate as physiologic responses to some form of irritation.
S J, PEARLMAN, E A, FRIEDMAN, M, APPEL
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Trametinib Induces Neurofibroma Shrinkage and Enables Surgery
Neuropediatrics, 2019Plexiform neurofibromas are congenital peripheral nerve sheath tumors characteristic of neurofibromatosis type 1 (NF1)—a frequent neurocutaneous disorder caused by mutations of the NF1 tumor suppressor gene.
P. Vaassen +4 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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Histopathology, 1977
At rare intervals in the literature, reports have appeared of a skin tumour containing structures resembling Pacinian corpuscles. Four such tumours collected over the course of 20 years are described and the literature reviewed.
D M, MacDonald, E, Wilson-Jones
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At rare intervals in the literature, reports have appeared of a skin tumour containing structures resembling Pacinian corpuscles. Four such tumours collected over the course of 20 years are described and the literature reviewed.
D M, MacDonald, E, Wilson-Jones
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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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The British Journal of Radiology, 1952
This case is reported because of the rarity of the condition, and the unusual size of the tumour. The radiological findings were subsequently confirmed at operation. Mrs. B.G., aged 71, was admitted to the Bristol Royal Infirmary on 18.11.1950, one month after a small haematemesis.
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This case is reported because of the rarity of the condition, and the unusual size of the tumour. The radiological findings were subsequently confirmed at operation. Mrs. B.G., aged 71, was admitted to the Bristol Royal Infirmary on 18.11.1950, one month after a small haematemesis.
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Annals of Plastic Surgery, 1986
Neurofibromas cause unsightly and crippling deformities. These locally destructive tumors arise along the distribution of peripheral and cranial nerves. The 2 patients presented here had neurofibromas of the external ear. In one patient, the lesion was limited to the auricle.
T R, Stevenson +2 more
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Neurofibromas cause unsightly and crippling deformities. These locally destructive tumors arise along the distribution of peripheral and cranial nerves. The 2 patients presented here had neurofibromas of the external ear. In one patient, the lesion was limited to the auricle.
T R, Stevenson +2 more
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