A difficult diagnosis of gliomatosis cerebri
Gliomatosis cerebri, a rare condition, requires clinical, radiological and pathological correlation for diagnosis. Mental and personality changes are the most common presenting symptoms with or without focal neurological signs. The widespread nature of the disease is revealed by CT or MRI. The shape...
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Veröffentlicht in: | Neuroradiology 1996-07, Vol.38 (5), p.444-448 |
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description | Gliomatosis cerebri, a rare condition, requires clinical, radiological and pathological correlation for diagnosis. Mental and personality changes are the most common presenting symptoms with or without focal neurological signs. The widespread nature of the disease is revealed by CT or MRI. The shape of the brain may be maintained and pathological gross examination may be unremarkable or show hypertrophy without evident tumour. Microscopic examination reveals infiltration of the brain by variably differentiated neoplastic glial cells. We present a patient with gliomatosis cerebri in whom we experienced difficulties with diagnosis. The literature is reviewed and the diagnostic features summarised. |
doi_str_mv | 10.1007/BF00607270 |
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Mental and personality changes are the most common presenting symptoms with or without focal neurological signs. The widespread nature of the disease is revealed by CT or MRI. The shape of the brain may be maintained and pathological gross examination may be unremarkable or show hypertrophy without evident tumour. Microscopic examination reveals infiltration of the brain by variably differentiated neoplastic glial cells. We present a patient with gliomatosis cerebri in whom we experienced difficulties with diagnosis. The literature is reviewed and the diagnostic features summarised.</description><identifier>ISSN: 0028-3940</identifier><identifier>EISSN: 1432-1920</identifier><identifier>DOI: 10.1007/BF00607270</identifier><identifier>PMID: 8837088</identifier><identifier>CODEN: NRDYAB</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Biological and medical sciences ; Brain - diagnostic imaging ; Brain - pathology ; Brain Neoplasms - diagnosis ; Brain Neoplasms - diagnostic imaging ; Child ; Diagnosis, Differential ; Glioma - diagnosis ; Glioma - diagnostic imaging ; Humans ; Magnetic Resonance Imaging ; Male ; Medical sciences ; Neurology ; Tomography, X-Ray Computed ; Tumors of the nervous system. 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Mental and personality changes are the most common presenting symptoms with or without focal neurological signs. The widespread nature of the disease is revealed by CT or MRI. The shape of the brain may be maintained and pathological gross examination may be unremarkable or show hypertrophy without evident tumour. Microscopic examination reveals infiltration of the brain by variably differentiated neoplastic glial cells. We present a patient with gliomatosis cerebri in whom we experienced difficulties with diagnosis. The literature is reviewed and the diagnostic features summarised.</description><subject>Biological and medical sciences</subject><subject>Brain - diagnostic imaging</subject><subject>Brain - pathology</subject><subject>Brain Neoplasms - diagnosis</subject><subject>Brain Neoplasms - diagnostic imaging</subject><subject>Child</subject><subject>Diagnosis, Differential</subject><subject>Glioma - diagnosis</subject><subject>Glioma - diagnostic imaging</subject><subject>Humans</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Neurology</subject><subject>Tomography, X-Ray Computed</subject><subject>Tumors of the nervous system. 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Phacomatoses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>PYHTINEN, J</creatorcontrib><creatorcontrib>PÄÄKKÖ, E</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Neuroradiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>PYHTINEN, J</au><au>PÄÄKKÖ, E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A difficult diagnosis of gliomatosis cerebri</atitle><jtitle>Neuroradiology</jtitle><addtitle>Neuroradiology</addtitle><date>1996-07-01</date><risdate>1996</risdate><volume>38</volume><issue>5</issue><spage>444</spage><epage>448</epage><pages>444-448</pages><issn>0028-3940</issn><eissn>1432-1920</eissn><coden>NRDYAB</coden><abstract>Gliomatosis cerebri, a rare condition, requires clinical, radiological and pathological correlation for diagnosis. Mental and personality changes are the most common presenting symptoms with or without focal neurological signs. The widespread nature of the disease is revealed by CT or MRI. The shape of the brain may be maintained and pathological gross examination may be unremarkable or show hypertrophy without evident tumour. Microscopic examination reveals infiltration of the brain by variably differentiated neoplastic glial cells. We present a patient with gliomatosis cerebri in whom we experienced difficulties with diagnosis. The literature is reviewed and the diagnostic features summarised.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>8837088</pmid><doi>10.1007/BF00607270</doi><tpages>5</tpages></addata></record> |
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subjects | Biological and medical sciences Brain - diagnostic imaging Brain - pathology Brain Neoplasms - diagnosis Brain Neoplasms - diagnostic imaging Child Diagnosis, Differential Glioma - diagnosis Glioma - diagnostic imaging Humans Magnetic Resonance Imaging Male Medical sciences Neurology Tomography, X-Ray Computed Tumors of the nervous system. Phacomatoses |
title | A difficult diagnosis of gliomatosis cerebri |
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