Results 131 to 140 of about 5,711 (179)
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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.
N J, Gwavava, A I, Traub
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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.
N J, Gwavava, A I, Traub
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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.
J D, Urschel, J G, Antkowiak, H, Takita
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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.
J D, Urschel, J G, Antkowiak, H, Takita
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International Urology and Nephrology, 1978
A rare case of benign pelvic neurilemmoma with bladder infiltration and ureteral obstruction is presented. This neurally originated tumor may occur anywhere in the body, but involvement of the urinary tract is rare. Management depends upon location and other clinical findings, and in this case, since complete removal was impossible, urinary derivation ...
F T, Dénes +3 more
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A rare case of benign pelvic neurilemmoma with bladder infiltration and ureteral obstruction is presented. This neurally originated tumor may occur anywhere in the body, but involvement of the urinary tract is rare. Management depends upon location and other clinical findings, and in this case, since complete removal was impossible, urinary derivation ...
F T, Dénes +3 more
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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
S U, Thaler, H W, Smith
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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
S U, Thaler, H W, Smith
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Urology, 1978
The clinical and pathologic features of benign and malignant retroperitoneal neurilemmoma are reviewed, and the pertinence of this tumor to the urologist is stressed. Two additional case reports are added to the literature.
P L, Miller +3 more
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The clinical and pathologic features of benign and malignant retroperitoneal neurilemmoma are reviewed, and the pertinence of this tumor to the urologist is stressed. Two additional case reports are added to the literature.
P L, Miller +3 more
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The Laryngoscope, 1981
AbstractBenign facial nerve neurilemmomas are frequently misdiagnosed tumors due to subtle and variable clinical presentation. Three cases treated recently at the University of California — San Francisco are presented to demonstrate the clinical features, diagnostic evaluation, and surgical treatment.
K L, Horn, R L, Crumley, R A, Schindler
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AbstractBenign facial nerve neurilemmomas are frequently misdiagnosed tumors due to subtle and variable clinical presentation. Three cases treated recently at the University of California — San Francisco are presented to demonstrate the clinical features, diagnostic evaluation, and surgical treatment.
K L, Horn, R L, Crumley, R A, Schindler
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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 ...
Y, 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 ...
Y, Park +4 more
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British Journal of Oral and Maxillofacial Surgery, 1989
Parapharyngeal neurilemmomas are uncommon benign tumours. Two patients are reported with one tumour arising from the vagus and the other from the hypoglossal nerve. Access to the vagal tumour was accomplished with the aid of an osteotomy at the angle of the mandible.
N, Bradley, J E, Bowerman
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Parapharyngeal neurilemmomas are uncommon benign tumours. Two patients are reported with one tumour arising from the vagus and the other from the hypoglossal nerve. Access to the vagal tumour was accomplished with the aid of an osteotomy at the angle of the mandible.
N, Bradley, J E, Bowerman
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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.
E S, MERCANTINI, C, 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.
E S, MERCANTINI, C, MOPPER
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Neurilemmomas of the Forearm and Hand
Clinical Orthopaedics and Related Research, 1975Neurilemmoma is the most common tumor arising from peripheral nerves. Although infrequently encountered, it must be included in the differential diagnosis of soft tissue tumors. Because of its cystic consistency, a neurilemmoma in the hand or wrist may be mistaken for a ganglion. In this series of 17 neurilemmomas, 6 were present in the forearm, and 11
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