2005
DOI: 10.1148/rg.254045207
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Idiopathic Tumefactive Hypertrophic Pachymeningitis

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Cited by 26 publications
(16 citation statements)
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“…MRI shows either linear or nodular dural enhancement at anatomical sites corresponding to clinical findings [1]. Cerebral oedema or parenchymal involvement are rarely seen in IHP, and in our case appears to be associated with seizures, which has been encountered in half of cases (three of six) with it [1–6].…”
mentioning
confidence: 63%
“…MRI shows either linear or nodular dural enhancement at anatomical sites corresponding to clinical findings [1]. Cerebral oedema or parenchymal involvement are rarely seen in IHP, and in our case appears to be associated with seizures, which has been encountered in half of cases (three of six) with it [1–6].…”
mentioning
confidence: 63%
“…56 Histopathologically, there is fibrosis with inflammatory cell infiltration. Mass-like presentations have been described (tumefactive pachymeningitis).…”
Section: Idiopathic Pachymeningitismentioning
confidence: 99%
“…(c) Sarcoidosis: P(Sarcoidosis, KLH clinical, radiological, LP profile) ¼ Reasonably High. Isolated neurosarcoidosis is possible and presents as a chronic meningitis [13]. Silent pulmonary involvement can be screened using a CT Chest with Contrast.…”
Section: Sub-eventmentioning
confidence: 99%
“…(d) Sjogren's Syndrome: P(Sjogren's Syndrome, KLH clinical, radiological, LP profile) is reasonably high. This can be tested using anti-SSA and -SSB antibodies for initial screening [13]. (e) Temporal Arteritis: P(Temporal Arteritis, KLH clinical, radiological, LP profile) is lower than the rest given poor response to steroids in the past, continued preservation of vision untreated.…”
Section: Sub-eventmentioning
confidence: 99%
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