Results 201 to 210 of about 9,059 (243)
Excision of large median and ulnar nerve schwannomas: a case series. [PDF]
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Neurilemmoma of the Nasal Cavity and Paranasal Sinuses
Ear, nose, & throat journal, 2021Objectives: Neurilemmoma in the nasal cavity and paranasal sinuses is very rare. The study aimed to improve the understanding of neurilemmoma in the nasal cavity and paranasal sinuses.
Xindi He, Ying Wang
semanticscholar +1 more source
Atypical, Extremely Rapid Growth of Pediatric Orbital Neurilemmoma.
Ophthalmic Plastic and Reconstructive Surgery, 2021Solitary orbital neurilemmoma-a benign tumor of Schwann cells in a peripheral nerve-sheath-are typically very slow growing and present in middle age; in the absence of neurofibromatosis, they are almost never seen in childhood.
K. Vahdani, P. Luthert, G. Rose
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Archives of Otolaryngology - Head and Neck Surgery, 1956
TUMORS of the pharynx are more frequently malignant than benign. Neurilemmomas are relatively uncommon. Not a single case of primary pharyngeal neurilemmoma was encountered among 63 benign tumors of the pharynx and tonsil collected by New and Childrey 1 at the Mayo Clinic over a 13-year period. None has been found by one of us (R. A.
Jose Picó, Raul A. Marcial-Rojas
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TUMORS of the pharynx are more frequently malignant than benign. Neurilemmomas are relatively uncommon. Not a single case of primary pharyngeal neurilemmoma was encountered among 63 benign tumors of the pharynx and tonsil collected by New and Childrey 1 at the Mayo Clinic over a 13-year period. None has been found by one of us (R. A.
Jose Picó, Raul A. Marcial-Rojas
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BJOG: An International Journal of Obstetrics & Gynaecology, 1980
SummaryWe present a case of neurilemmoma of the cervix which is the first to be reported in the English literature. The characteristic histological features are described and its differentiation from a leiomyoma is confirmed by electron microscopic studies.
A. I. Traub, N. J. Gwavava
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SummaryWe present a case of neurilemmoma of the cervix which is the first to be reported in the English literature. The characteristic histological features are described and its differentiation from a leiomyoma is confirmed by electron microscopic studies.
A. I. Traub, N. J. Gwavava
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Journal of Surgical Oncology, 1994
AbstractDiaphragmatic neurilemmomas are rare tumors. We report here such a case and also review five cases from the English‐language medical literature. Neurilemmomas of the diaphragm are benign tumors that display slow, progressive growth. They remain encapsulated and do not invade adjacent structures.
Hiroshi Takita +2 more
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AbstractDiaphragmatic neurilemmomas are rare tumors. We report here such a case and also review five cases from the English‐language medical literature. Neurilemmomas of the diaphragm are benign tumors that display slow, progressive growth. They remain encapsulated and do not invade adjacent structures.
Hiroshi Takita +2 more
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Archives of Dermatology, 1959
A neurilemmoma or Schwann cell tumor is a distinctive nerve sheath tumor, characterized histologically by the regimentation of its cells. It is probably seen more commonly by surgeons than by dermatologists. While dermatology texts refer to it, no original article was found in the American dermatologic literature of the past 20 years.
Edward S. Mercantini, Coleman Mopper
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A neurilemmoma or Schwann cell tumor is a distinctive nerve sheath tumor, characterized histologically by the regimentation of its cells. It is probably seen more commonly by surgeons than by dermatologists. While dermatology texts refer to it, no original article was found in the American dermatologic literature of the past 20 years.
Edward S. Mercantini, Coleman Mopper
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Archives of Otolaryngology - Head and Neck Surgery, 1966
A SPECIFIC tumor of nerve sheath origin was first described in 1908 by Verocay. 1 He christened this tumor "neurinoma" in 1910. Two opposing views of its cellular origin immediately arose: first, that it could only arise from cells of mesodermal origin, namely, the perineural or endoneural components of the nerve sheath, since it contained considerable
Howard W. Smith, Seth Thaler
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A SPECIFIC tumor of nerve sheath origin was first described in 1908 by Verocay. 1 He christened this tumor "neurinoma" in 1910. Two opposing views of its cellular origin immediately arose: first, that it could only arise from cells of mesodermal origin, namely, the perineural or endoneural components of the nerve sheath, since it contained considerable
Howard W. Smith, Seth Thaler
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Skeletal Radiology, 1999
Intraosseous neurilemmoma is rare, representing less than 1% of benign primary bone tumors. The site most commonly involved is the mandible. We report on a neurilemmoma of the mandible in a 30-year-old woman. A panoramic radiograph of the mandible showed a well-defined unilocular osteolytic lesion with a thin uniform sclerotic margin located in the ...
Young-Euy Park +4 more
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Intraosseous neurilemmoma is rare, representing less than 1% of benign primary bone tumors. The site most commonly involved is the mandible. We report on a neurilemmoma of the mandible in a 30-year-old woman. A panoramic radiograph of the mandible showed a well-defined unilocular osteolytic lesion with a thin uniform sclerotic margin located in the ...
Young-Euy Park +4 more
openaire +3 more sources