Schwannomas limited to the infratemporal fossa : Report of two cases
Schwannomas limited to the infratemporal fossa are rare lesions that may also involve the maxillary sinus, the orbit and the retropharyngeal space. We present two cases of schwannoma arising from the extradural divisions of the trigeminal nerve, with corresponding areas of sensory loss. Both patient...
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Veröffentlicht in: | Journal of neuro-oncology 1998-02, Vol.36 (3), p.269-277 |
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description | Schwannomas limited to the infratemporal fossa are rare lesions that may also involve the maxillary sinus, the orbit and the retropharyngeal space. We present two cases of schwannoma arising from the extradural divisions of the trigeminal nerve, with corresponding areas of sensory loss. Both patients had been operated for spinal canal schwannomas previously. Complete tumor removal was accomplished in both cases. The schwannoma of the maxillary division was excised using an orbitozygomatic extradural approach. The schwannoma of the mandibular division was excised using a subtemporal-infratemporal approach. Trigeminal nerve function was preserved and complete recovery of function was achieved in each patient. Identification of an infratemporal schwannoma should alert the physician to consider the diagnosis of neurofibromatosis. The literature regarding schwannomas limited to the infratemporal fossa is reviewed. |
doi_str_mv | 10.1023/A:1005827010429 |
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K</creator><creatorcontrib>KRISHNAMURTHY, S ; HOLMES, B ; POWERS, S. K</creatorcontrib><description>Schwannomas limited to the infratemporal fossa are rare lesions that may also involve the maxillary sinus, the orbit and the retropharyngeal space. We present two cases of schwannoma arising from the extradural divisions of the trigeminal nerve, with corresponding areas of sensory loss. Both patients had been operated for spinal canal schwannomas previously. Complete tumor removal was accomplished in both cases. The schwannoma of the maxillary division was excised using an orbitozygomatic extradural approach. The schwannoma of the mandibular division was excised using a subtemporal-infratemporal approach. Trigeminal nerve function was preserved and complete recovery of function was achieved in each patient. Identification of an infratemporal schwannoma should alert the physician to consider the diagnosis of neurofibromatosis. The literature regarding schwannomas limited to the infratemporal fossa is reviewed.</description><identifier>ISSN: 0167-594X</identifier><identifier>EISSN: 1573-7373</identifier><identifier>DOI: 10.1023/A:1005827010429</identifier><identifier>PMID: 9524105</identifier><identifier>CODEN: JNODD2</identifier><language>eng</language><publisher>Dordrecht: Springer</publisher><subject>Biological and medical sciences ; Cranial Nerve Neoplasms - diagnosis ; Cranial Nerve Neoplasms - pathology ; Cranial Nerve Neoplasms - surgery ; Disease-Free Survival ; Female ; Humans ; Mandible ; Maxillary sinus ; Medical sciences ; Middle Aged ; Neurilemmoma - diagnosis ; Neurilemmoma - diagnostic imaging ; Neurilemmoma - surgery ; Neurofibromatosis ; Neurology ; Radiography ; Recovery of function ; Schwann cells ; Skull Base Neoplasms - diagnosis ; Skull Base Neoplasms - diagnostic imaging ; Skull Base Neoplasms - surgery ; Temporal Bone - pathology ; Temporal Bone - surgery ; Trigeminal nerve ; Trigeminal Nerve - pathology ; Tumors of the nervous system. 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K</creatorcontrib><title>Schwannomas limited to the infratemporal fossa : Report of two cases</title><title>Journal of neuro-oncology</title><addtitle>J Neurooncol</addtitle><description>Schwannomas limited to the infratemporal fossa are rare lesions that may also involve the maxillary sinus, the orbit and the retropharyngeal space. We present two cases of schwannoma arising from the extradural divisions of the trigeminal nerve, with corresponding areas of sensory loss. Both patients had been operated for spinal canal schwannomas previously. Complete tumor removal was accomplished in both cases. The schwannoma of the maxillary division was excised using an orbitozygomatic extradural approach. The schwannoma of the mandibular division was excised using a subtemporal-infratemporal approach. Trigeminal nerve function was preserved and complete recovery of function was achieved in each patient. Identification of an infratemporal schwannoma should alert the physician to consider the diagnosis of neurofibromatosis. The literature regarding schwannomas limited to the infratemporal fossa is reviewed.</description><subject>Biological and medical sciences</subject><subject>Cranial Nerve Neoplasms - diagnosis</subject><subject>Cranial Nerve Neoplasms - pathology</subject><subject>Cranial Nerve Neoplasms - surgery</subject><subject>Disease-Free Survival</subject><subject>Female</subject><subject>Humans</subject><subject>Mandible</subject><subject>Maxillary sinus</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neurilemmoma - diagnosis</subject><subject>Neurilemmoma - diagnostic imaging</subject><subject>Neurilemmoma - surgery</subject><subject>Neurofibromatosis</subject><subject>Neurology</subject><subject>Radiography</subject><subject>Recovery of function</subject><subject>Schwann cells</subject><subject>Skull Base Neoplasms - diagnosis</subject><subject>Skull Base Neoplasms - diagnostic imaging</subject><subject>Skull Base Neoplasms - surgery</subject><subject>Temporal Bone - pathology</subject><subject>Temporal Bone - surgery</subject><subject>Trigeminal nerve</subject><subject>Trigeminal Nerve - pathology</subject><subject>Tumors of the nervous system. 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K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c309t-97777e0675d82001dc02628732fbdf30452a91b1f9198c0a56e4dfde4f08b44d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Biological and medical sciences</topic><topic>Cranial Nerve Neoplasms - diagnosis</topic><topic>Cranial Nerve Neoplasms - pathology</topic><topic>Cranial Nerve Neoplasms - surgery</topic><topic>Disease-Free Survival</topic><topic>Female</topic><topic>Humans</topic><topic>Mandible</topic><topic>Maxillary sinus</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neurilemmoma - diagnosis</topic><topic>Neurilemmoma - diagnostic imaging</topic><topic>Neurilemmoma - surgery</topic><topic>Neurofibromatosis</topic><topic>Neurology</topic><topic>Radiography</topic><topic>Recovery of function</topic><topic>Schwann cells</topic><topic>Skull Base Neoplasms - diagnosis</topic><topic>Skull Base Neoplasms - diagnostic imaging</topic><topic>Skull Base Neoplasms - surgery</topic><topic>Temporal Bone - pathology</topic><topic>Temporal Bone - surgery</topic><topic>Trigeminal nerve</topic><topic>Trigeminal Nerve - pathology</topic><topic>Tumors of the nervous system. Phacomatoses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>KRISHNAMURTHY, S</creatorcontrib><creatorcontrib>HOLMES, B</creatorcontrib><creatorcontrib>POWERS, S. 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K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Schwannomas limited to the infratemporal fossa : Report of two cases</atitle><jtitle>Journal of neuro-oncology</jtitle><addtitle>J Neurooncol</addtitle><date>1998-02-01</date><risdate>1998</risdate><volume>36</volume><issue>3</issue><spage>269</spage><epage>277</epage><pages>269-277</pages><issn>0167-594X</issn><eissn>1573-7373</eissn><coden>JNODD2</coden><abstract>Schwannomas limited to the infratemporal fossa are rare lesions that may also involve the maxillary sinus, the orbit and the retropharyngeal space. We present two cases of schwannoma arising from the extradural divisions of the trigeminal nerve, with corresponding areas of sensory loss. Both patients had been operated for spinal canal schwannomas previously. Complete tumor removal was accomplished in both cases. The schwannoma of the maxillary division was excised using an orbitozygomatic extradural approach. The schwannoma of the mandibular division was excised using a subtemporal-infratemporal approach. Trigeminal nerve function was preserved and complete recovery of function was achieved in each patient. Identification of an infratemporal schwannoma should alert the physician to consider the diagnosis of neurofibromatosis. The literature regarding schwannomas limited to the infratemporal fossa is reviewed.</abstract><cop>Dordrecht</cop><pub>Springer</pub><pmid>9524105</pmid><doi>10.1023/A:1005827010429</doi><tpages>9</tpages></addata></record> |
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subjects | Biological and medical sciences Cranial Nerve Neoplasms - diagnosis Cranial Nerve Neoplasms - pathology Cranial Nerve Neoplasms - surgery Disease-Free Survival Female Humans Mandible Maxillary sinus Medical sciences Middle Aged Neurilemmoma - diagnosis Neurilemmoma - diagnostic imaging Neurilemmoma - surgery Neurofibromatosis Neurology Radiography Recovery of function Schwann cells Skull Base Neoplasms - diagnosis Skull Base Neoplasms - diagnostic imaging Skull Base Neoplasms - surgery Temporal Bone - pathology Temporal Bone - surgery Trigeminal nerve Trigeminal Nerve - pathology Tumors of the nervous system. Phacomatoses |
title | Schwannomas limited to the infratemporal fossa : Report of two cases |
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