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Archives of Ophthalmology, 1997
Neurilemoma (schwannoma) of the conjunctiva is a rare ocular tumor. We report 3 cases of benign conjunctival neurilemoma occurring in women without other ocular or systemic disease. Two of these tumors arose from the bulbar conjunctiva and 1 from the tarsal conjunctiva. Immunoperoxidase staining for S-100 protein was positive in each case.
N C, Charles +4 more
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Neurilemoma (schwannoma) of the conjunctiva is a rare ocular tumor. We report 3 cases of benign conjunctival neurilemoma occurring in women without other ocular or systemic disease. Two of these tumors arose from the bulbar conjunctiva and 1 from the tarsal conjunctiva. Immunoperoxidase staining for S-100 protein was positive in each case.
N C, Charles +4 more
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Intraoral Plexiform (Multinodular) Neurilemoma
Pediatric Pathology, 1991An intraoral (buccal) mass in a 6-year-old child was found to be a benign plexiform (multinodular) neurilemoma by fine-needle aspiration (FNA) biopsy cytology and histologic examination of the excised specimen. Clinical and pathological features of these rare tumors are reviewed, and the capacity of FNA to guide surgical planning in the pediatric ...
S A, Heifetz +3 more
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Degenerated Neurilemoma (Ancient Schwannoma)
The Journal of Dermatology, 2001AbstractWe report a case of degenerated neurilemoma in a 65‐year‐old Japanese woman. A tumor in the right thigh histopathologically showed a mixture of Antoni type A and B patterns, and contained prominent blood vessels with hyalinized walls, but no calcification. The tumor cell nuclei of middle areas were large, hyperchromatic and often multilobed but
T, Ishihara, T, Ono
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Archives of Otolaryngology - Head and Neck Surgery, 1979
Neurilemomas of the tracheobronchial tree are exceedingly rare. In this article we report what is, to our knowledge, the 12th case--the third such case of tracheal origin. Clinical features are referable to airway obstruction and local pressure effects. The gross appearance is of an encapsulated lesion.
R L, Nass, N L, Cohen
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Neurilemomas of the tracheobronchial tree are exceedingly rare. In this article we report what is, to our knowledge, the 12th case--the third such case of tracheal origin. Clinical features are referable to airway obstruction and local pressure effects. The gross appearance is of an encapsulated lesion.
R L, Nass, N L, Cohen
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Neurilemoma of the retroperitoneum
Klinische Wochenschrift, 1991A case is presented in which suprarenal neurilemoma was associated with paroxysmal attacks of hypertension, headache and sweating with elevated plasma and urinary catecholamines. Pheochromocytoma was excluded using an overnight clonidine suppression test. Ultrasonography, computed tomography and magnetic resonance imaging, which showed cystic mass with
M, Kihara +8 more
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Intracerebral and Intracerebellar Neurilemoma
Southern Medical Journal, 1988Neurilemomas (schwannomas) within the brain substance and not associated with a peripheral nerve are rare. We have presented two such cases, one with a prominent angiomatous component. Neither patient had neurofibromatosis. Both patients had headache and focal neurologic signs, and surgical excision was curative in both cases.
A M, Schwartz, A, Sotrel
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Urology, 1996
Neurilemomas are neoplasms that originate from Schwann cells of the central and peripheral nervous systems. Thirteen case reports of neurilemomas involving the kidney have been described in the English literature. We report the fifth case of a neurilemoma within the renal sinus and review the previous cases of renal neurilemoma.
A J, Singer, K H, Anders
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Neurilemomas are neoplasms that originate from Schwann cells of the central and peripheral nervous systems. Thirteen case reports of neurilemomas involving the kidney have been described in the English literature. We report the fifth case of a neurilemoma within the renal sinus and review the previous cases of renal neurilemoma.
A J, Singer, K H, Anders
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Archivos espanoles de urologia, 2002
To present a case of preputial neurilemoma.A 23-year-old man presented with a small, nodular, preputial mass that he had noted three years earlier.The tumor was excised under local anesthesia without complications. Currently, no evidence of tumor recurrence has been observed.Preputial nuerilemoma is rare.
Francisco Javier, Madrid García +4 more
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To present a case of preputial neurilemoma.A 23-year-old man presented with a small, nodular, preputial mass that he had noted three years earlier.The tumor was excised under local anesthesia without complications. Currently, no evidence of tumor recurrence has been observed.Preputial nuerilemoma is rare.
Francisco Javier, Madrid García +4 more
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Archives of Orthopaedic and Traumatic Surgery, 1988
A case of familial multiple neurilemoma is reported. A 59-year-old man with five neurilemomas was treated. Fifteen of his 22 family members had had soft-tissue tumors. Ten neurilemomas had been diagnosed microscopically in five members of the family. There were no symptoms related to von Recklinghausen's disease. This case seems to be a forme fruste or
F, Yamazaki +6 more
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A case of familial multiple neurilemoma is reported. A 59-year-old man with five neurilemomas was treated. Fifteen of his 22 family members had had soft-tissue tumors. Ten neurilemomas had been diagnosed microscopically in five members of the family. There were no symptoms related to von Recklinghausen's disease. This case seems to be a forme fruste or
F, Yamazaki +6 more
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Annals of ophthalmology, 1978
The diagnosis of orbital tumors is a challenging one. Neurilemomas are among the rarer causes of lesions in this location and usually are curable by local excision. The results of tests used in diagnosing orbital tumors are inconsistent in patients with this disease entity. Four patients with orbital neurilemoma are reported.
M I, Allman, W C, Frayer, T R, Hedges
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The diagnosis of orbital tumors is a challenging one. Neurilemomas are among the rarer causes of lesions in this location and usually are curable by local excision. The results of tests used in diagnosing orbital tumors are inconsistent in patients with this disease entity. Four patients with orbital neurilemoma are reported.
M I, Allman, W C, Frayer, T R, Hedges
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