Neurolymphomatosis mimicking neurosarcoidosis: a case report

<p>Abstract</p> <p>Introduction</p> <p>Both neurosarcoidosis and central nervous system lymphoma can be very difficult to diagnose. We describe the case of a patient in whom neurosarcoidosis was strongly suspected, but who was eventually found to have lymphoma. We belie...

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Main Authors: Scolding Neil J, Santos Ernestina
Format: Article
Language:English
Published: BMC 2010-01-01
Series:Journal of Medical Case Reports
Online Access:http://www.jmedicalcasereports.com/content/4/1/5
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spelling doaj-066a6cdd0e6d41eab5602ffad1475ef92020-11-25T00:25:00ZengBMCJournal of Medical Case Reports1752-19472010-01-0141510.1186/1752-1947-4-5Neurolymphomatosis mimicking neurosarcoidosis: a case reportScolding Neil JSantos Ernestina<p>Abstract</p> <p>Introduction</p> <p>Both neurosarcoidosis and central nervous system lymphoma can be very difficult to diagnose. We describe the case of a patient in whom neurosarcoidosis was strongly suspected, but who was eventually found to have lymphoma. We believe the case to be of interest and practical value to neurologists, oncologists and internists with an interest in inflammatory diseases.</p> <p>Case presentation</p> <p>A diagnosis of neurosarcoidosis was considered in a 49-year-old Caucasian man on the basis of the following symptoms and indications: a cough, bilateral hilar lymphadenopathy confirmed by thoracic computed tomography, the development of an S1 radiculopathy, cerebrospinal fluid abnormalities (raised protein level), bilateral lung hilar and lachrymal gland uptake on a gallium scan, and erythema nodosum confirmed with skin biopsy. These were followed by the development of multiple cranial neuropathies, including seventh nerve palsy. Exhaustive further investigations yielded no evidence for an alternative diagnosis. Treatments with steroids, cyclophosphamide, intravenous immunoglobulin and finally infliximab were of no benefit. He eventually developed cutaneous nodules, a biopsy of which revealed lymphoma that proved resistant to therapy.</p> <p>Conclusion</p> <p>Constant diagnostic vigilance is required in disorders such as neurosarcoidosis.</p> http://www.jmedicalcasereports.com/content/4/1/5
collection DOAJ
language English
format Article
sources DOAJ
author Scolding Neil J
Santos Ernestina
spellingShingle Scolding Neil J
Santos Ernestina
Neurolymphomatosis mimicking neurosarcoidosis: a case report
Journal of Medical Case Reports
author_facet Scolding Neil J
Santos Ernestina
author_sort Scolding Neil J
title Neurolymphomatosis mimicking neurosarcoidosis: a case report
title_short Neurolymphomatosis mimicking neurosarcoidosis: a case report
title_full Neurolymphomatosis mimicking neurosarcoidosis: a case report
title_fullStr Neurolymphomatosis mimicking neurosarcoidosis: a case report
title_full_unstemmed Neurolymphomatosis mimicking neurosarcoidosis: a case report
title_sort neurolymphomatosis mimicking neurosarcoidosis: a case report
publisher BMC
series Journal of Medical Case Reports
issn 1752-1947
publishDate 2010-01-01
description <p>Abstract</p> <p>Introduction</p> <p>Both neurosarcoidosis and central nervous system lymphoma can be very difficult to diagnose. We describe the case of a patient in whom neurosarcoidosis was strongly suspected, but who was eventually found to have lymphoma. We believe the case to be of interest and practical value to neurologists, oncologists and internists with an interest in inflammatory diseases.</p> <p>Case presentation</p> <p>A diagnosis of neurosarcoidosis was considered in a 49-year-old Caucasian man on the basis of the following symptoms and indications: a cough, bilateral hilar lymphadenopathy confirmed by thoracic computed tomography, the development of an S1 radiculopathy, cerebrospinal fluid abnormalities (raised protein level), bilateral lung hilar and lachrymal gland uptake on a gallium scan, and erythema nodosum confirmed with skin biopsy. These were followed by the development of multiple cranial neuropathies, including seventh nerve palsy. Exhaustive further investigations yielded no evidence for an alternative diagnosis. Treatments with steroids, cyclophosphamide, intravenous immunoglobulin and finally infliximab were of no benefit. He eventually developed cutaneous nodules, a biopsy of which revealed lymphoma that proved resistant to therapy.</p> <p>Conclusion</p> <p>Constant diagnostic vigilance is required in disorders such as neurosarcoidosis.</p>
url http://www.jmedicalcasereports.com/content/4/1/5
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