2000
DOI: 10.1258/0022215001906318
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Cerebellopontine angle lymphoma presenting as chronic mastoiditis

Abstract: Middle-ear tumours are not uncommonly mistaken for mastoiditis on presentation. We report a case of cerebellopontine angle non-Hodgkin's B-cell lymphoma originally presenting as a middle-ear inflammatory process. In mastoiditis not resolving with conventional treatment it is important to look for an underlying cause.

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Cited by 6 publications
(5 citation statements)
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“…And clinical manifestations are related to the anatomical structures surrounding the lesion and volumes of the tumors. PCNSLs of the CPA typically present with trigeminal, facial, audio vestibular and cerebellar dysfunction, including hearing loss, tinnitus, facial palsy, vertigo and ataxia [7,11,18]. Other neurological symptoms include headache, nausea, vomiting, hoarseness and nystagmus [18,15,16].…”
Section: Discussionmentioning
confidence: 99%
“…And clinical manifestations are related to the anatomical structures surrounding the lesion and volumes of the tumors. PCNSLs of the CPA typically present with trigeminal, facial, audio vestibular and cerebellar dysfunction, including hearing loss, tinnitus, facial palsy, vertigo and ataxia [7,11,18]. Other neurological symptoms include headache, nausea, vomiting, hoarseness and nystagmus [18,15,16].…”
Section: Discussionmentioning
confidence: 99%
“…Primary central nervous system lymphoma is a rare and aggressive extranodal non-Hodgkin lymphoma that restricted entirely to the brain, leptomeninges, spinal cord or eyes, without systemic involvement [9,29]. PCNSL accounts for approximately 1-4% of all primary brain tumors [2,24], but its incidence has been increasing over the past 20 years in both immunocompetent and immunocompromised individuals [10,12]. Diffuse large B-Cell Lymphomas are the most common type (~ 90%), while the remaining 10% are poorly characterized by Burkitt's lymphomas, T-Cell lymphomas and low-grade lymphomas [29][30][31][32].…”
Section: Discussionmentioning
confidence: 99%
“…Clinical manifestations of the PCNSLs of the CPA are related to the anatomical structures surrounding the lesion and volumes of the tumors. PCNSLs of the CPA typically present with trigeminal, facial, audiovestibular and cerebellar dysfunction, including hearing loss, tinnitus, facial palsy, vertigo and ataxia [7,10,14,29]. Other neurological symptoms include headache, nausea, vomiting, hoarseness and nystagmus [18,23,24].…”
Section: Discussionmentioning
confidence: 99%
“…Primary central nervous system lymphoma is a rare and aggressive extranodal non-Hodgkin lymphoma that restricted entirely to the brain, leptomeninges, spinal cord or eyes, without systemic involvement [28,33]. PCNSL accounts for approximately 1-4% of all primary brain tumors [32,40], but its incidence has been increasing over the past 20 years in both immunocompetent and immunocompromised individuals [14,36]. Diffuse large B-Cell Lymphomas are the most common type (~90%), while the remaining 10% are poorly characterized by Burkitt's lymphomas, T-Cell lymphomas and low-grade lymphomas [5,12,15,33].…”
Section: Discussionmentioning
confidence: 99%
“…Clinical manifestations of the PCNSLs of the CPA are related to the anatomical structures surrounding the lesion and volumes of the tumors. PCNSLs of the CPA typically present with trigeminal, facial, audiovestibular and cerebellar dysfunction, including hearing loss, tinnitus, facial palsy, vertigo and ataxia [14,19,33,38]. Other neurological symptoms include headache, nausea, vomiting, hoarseness and nystagmus [18,31,32].…”
Section: Discussionmentioning
confidence: 99%