Pleocytosis in a patient with relapsing polychondritis accompanied by meningoencephalitis: a case report

Background Relapsing polychondritis (RP) is an uncommon immune-related disease with unknown causes. It is characterized by inflammation of cartilaginous or non-cartilaginous structures, such as the ears, nose, respiratory tract, eyes, and joints. Neurological involvement is rare in RP. Case presenta...
Ausführliche Beschreibung

Gespeichert in:

Autor*in:	Cao, Jie [verfasserIn] Zhang, Min

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2018

Schlagwörter:	Cerebrospinal fluid Meningoencephalitis Relapsing polychondritis

Anmerkung:	© The Author(s). 2018

Übergeordnetes Werk:	Enthalten in: BMC neurology - London : BioMed Central, 2001, 18(2018), 1 vom: 25. Apr.
Übergeordnetes Werk:	volume:18 ; year:2018 ; number:1 ; day:25 ; month:04

Links:	Volltext

DOI / URN:	10.1186/s12883-018-1059-7

Katalog-ID:	SPR027554783

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520			\|a Background Relapsing polychondritis (RP) is an uncommon immune-related disease with unknown causes. It is characterized by inflammation of cartilaginous or non-cartilaginous structures, such as the ears, nose, respiratory tract, eyes, and joints. Neurological involvement is rare in RP. Case presentation We report a case of pleocytosis in a 64-year-old man diagnosed as having RP with meningoencephalitis. The patient’s condition markedly improved following methylprednisolone treatment. Conclusions To our knowledge, this is the first report of recurrent pleocytosis in a patient with RP accompanied by meningoencephalitis. Steroid pulse therapy is effective in most cases, and early diagnosis is of importance.
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allfields	10.1186/s12883-018-1059-7 doi (DE-627)SPR027554783 (SPR)s12883-018-1059-7-e DE-627 ger DE-627 rakwb eng Cao, Jie verfasserin aut Pleocytosis in a patient with relapsing polychondritis accompanied by meningoencephalitis: a case report 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s). 2018 Background Relapsing polychondritis (RP) is an uncommon immune-related disease with unknown causes. It is characterized by inflammation of cartilaginous or non-cartilaginous structures, such as the ears, nose, respiratory tract, eyes, and joints. Neurological involvement is rare in RP. Case presentation We report a case of pleocytosis in a 64-year-old man diagnosed as having RP with meningoencephalitis. The patient’s condition markedly improved following methylprednisolone treatment. Conclusions To our knowledge, this is the first report of recurrent pleocytosis in a patient with RP accompanied by meningoencephalitis. Steroid pulse therapy is effective in most cases, and early diagnosis is of importance. Cerebrospinal fluid (dpeaa)DE-He213 Meningoencephalitis (dpeaa)DE-He213 Relapsing polychondritis (dpeaa)DE-He213 Zhang, Min aut Enthalten in BMC neurology London : BioMed Central, 2001 18(2018), 1 vom: 25. Apr. (DE-627)326643664 (DE-600)2041347-6 1471-2377 nnns volume:18 year:2018 number:1 day:25 month:04 https://dx.doi.org/10.1186/s12883-018-1059-7 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 18 2018 1 25 04
spelling	10.1186/s12883-018-1059-7 doi (DE-627)SPR027554783 (SPR)s12883-018-1059-7-e DE-627 ger DE-627 rakwb eng Cao, Jie verfasserin aut Pleocytosis in a patient with relapsing polychondritis accompanied by meningoencephalitis: a case report 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s). 2018 Background Relapsing polychondritis (RP) is an uncommon immune-related disease with unknown causes. It is characterized by inflammation of cartilaginous or non-cartilaginous structures, such as the ears, nose, respiratory tract, eyes, and joints. Neurological involvement is rare in RP. Case presentation We report a case of pleocytosis in a 64-year-old man diagnosed as having RP with meningoencephalitis. The patient’s condition markedly improved following methylprednisolone treatment. Conclusions To our knowledge, this is the first report of recurrent pleocytosis in a patient with RP accompanied by meningoencephalitis. Steroid pulse therapy is effective in most cases, and early diagnosis is of importance. Cerebrospinal fluid (dpeaa)DE-He213 Meningoencephalitis (dpeaa)DE-He213 Relapsing polychondritis (dpeaa)DE-He213 Zhang, Min aut Enthalten in BMC neurology London : BioMed Central, 2001 18(2018), 1 vom: 25. Apr. (DE-627)326643664 (DE-600)2041347-6 1471-2377 nnns volume:18 year:2018 number:1 day:25 month:04 https://dx.doi.org/10.1186/s12883-018-1059-7 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 18 2018 1 25 04
allfields_unstemmed	10.1186/s12883-018-1059-7 doi (DE-627)SPR027554783 (SPR)s12883-018-1059-7-e DE-627 ger DE-627 rakwb eng Cao, Jie verfasserin aut Pleocytosis in a patient with relapsing polychondritis accompanied by meningoencephalitis: a case report 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s). 2018 Background Relapsing polychondritis (RP) is an uncommon immune-related disease with unknown causes. It is characterized by inflammation of cartilaginous or non-cartilaginous structures, such as the ears, nose, respiratory tract, eyes, and joints. Neurological involvement is rare in RP. Case presentation We report a case of pleocytosis in a 64-year-old man diagnosed as having RP with meningoencephalitis. The patient’s condition markedly improved following methylprednisolone treatment. Conclusions To our knowledge, this is the first report of recurrent pleocytosis in a patient with RP accompanied by meningoencephalitis. Steroid pulse therapy is effective in most cases, and early diagnosis is of importance. Cerebrospinal fluid (dpeaa)DE-He213 Meningoencephalitis (dpeaa)DE-He213 Relapsing polychondritis (dpeaa)DE-He213 Zhang, Min aut Enthalten in BMC neurology London : BioMed Central, 2001 18(2018), 1 vom: 25. Apr. (DE-627)326643664 (DE-600)2041347-6 1471-2377 nnns volume:18 year:2018 number:1 day:25 month:04 https://dx.doi.org/10.1186/s12883-018-1059-7 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 18 2018 1 25 04
allfieldsGer	10.1186/s12883-018-1059-7 doi (DE-627)SPR027554783 (SPR)s12883-018-1059-7-e DE-627 ger DE-627 rakwb eng Cao, Jie verfasserin aut Pleocytosis in a patient with relapsing polychondritis accompanied by meningoencephalitis: a case report 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s). 2018 Background Relapsing polychondritis (RP) is an uncommon immune-related disease with unknown causes. It is characterized by inflammation of cartilaginous or non-cartilaginous structures, such as the ears, nose, respiratory tract, eyes, and joints. Neurological involvement is rare in RP. Case presentation We report a case of pleocytosis in a 64-year-old man diagnosed as having RP with meningoencephalitis. The patient’s condition markedly improved following methylprednisolone treatment. Conclusions To our knowledge, this is the first report of recurrent pleocytosis in a patient with RP accompanied by meningoencephalitis. Steroid pulse therapy is effective in most cases, and early diagnosis is of importance. Cerebrospinal fluid (dpeaa)DE-He213 Meningoencephalitis (dpeaa)DE-He213 Relapsing polychondritis (dpeaa)DE-He213 Zhang, Min aut Enthalten in BMC neurology London : BioMed Central, 2001 18(2018), 1 vom: 25. Apr. (DE-627)326643664 (DE-600)2041347-6 1471-2377 nnns volume:18 year:2018 number:1 day:25 month:04 https://dx.doi.org/10.1186/s12883-018-1059-7 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 18 2018 1 25 04
allfieldsSound	10.1186/s12883-018-1059-7 doi (DE-627)SPR027554783 (SPR)s12883-018-1059-7-e DE-627 ger DE-627 rakwb eng Cao, Jie verfasserin aut Pleocytosis in a patient with relapsing polychondritis accompanied by meningoencephalitis: a case report 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s). 2018 Background Relapsing polychondritis (RP) is an uncommon immune-related disease with unknown causes. It is characterized by inflammation of cartilaginous or non-cartilaginous structures, such as the ears, nose, respiratory tract, eyes, and joints. Neurological involvement is rare in RP. Case presentation We report a case of pleocytosis in a 64-year-old man diagnosed as having RP with meningoencephalitis. The patient’s condition markedly improved following methylprednisolone treatment. Conclusions To our knowledge, this is the first report of recurrent pleocytosis in a patient with RP accompanied by meningoencephalitis. Steroid pulse therapy is effective in most cases, and early diagnosis is of importance. Cerebrospinal fluid (dpeaa)DE-He213 Meningoencephalitis (dpeaa)DE-He213 Relapsing polychondritis (dpeaa)DE-He213 Zhang, Min aut Enthalten in BMC neurology London : BioMed Central, 2001 18(2018), 1 vom: 25. Apr. (DE-627)326643664 (DE-600)2041347-6 1471-2377 nnns volume:18 year:2018 number:1 day:25 month:04 https://dx.doi.org/10.1186/s12883-018-1059-7 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 18 2018 1 25 04
language	English
source	Enthalten in BMC neurology 18(2018), 1 vom: 25. Apr. volume:18 year:2018 number:1 day:25 month:04
sourceStr	Enthalten in BMC neurology 18(2018), 1 vom: 25. Apr. volume:18 year:2018 number:1 day:25 month:04
format_phy_str_mv	Article
institution	findex.gbv.de
topic_facet	Cerebrospinal fluid Meningoencephalitis Relapsing polychondritis
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container_title	BMC neurology
authorswithroles_txt_mv	Cao, Jie @@aut@@ Zhang, Min @@aut@@
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It is characterized by inflammation of cartilaginous or non-cartilaginous structures, such as the ears, nose, respiratory tract, eyes, and joints. Neurological involvement is rare in RP. Case presentation We report a case of pleocytosis in a 64-year-old man diagnosed as having RP with meningoencephalitis. The patient’s condition markedly improved following methylprednisolone treatment. Conclusions To our knowledge, this is the first report of recurrent pleocytosis in a patient with RP accompanied by meningoencephalitis. 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author	Cao, Jie
spellingShingle	Cao, Jie misc Cerebrospinal fluid misc Meningoencephalitis misc Relapsing polychondritis Pleocytosis in a patient with relapsing polychondritis accompanied by meningoencephalitis: a case report
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topic_title	Pleocytosis in a patient with relapsing polychondritis accompanied by meningoencephalitis: a case report Cerebrospinal fluid (dpeaa)DE-He213 Meningoencephalitis (dpeaa)DE-He213 Relapsing polychondritis (dpeaa)DE-He213
topic	misc Cerebrospinal fluid misc Meningoencephalitis misc Relapsing polychondritis
topic_unstemmed	misc Cerebrospinal fluid misc Meningoencephalitis misc Relapsing polychondritis
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title	Pleocytosis in a patient with relapsing polychondritis accompanied by meningoencephalitis: a case report
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title_full	Pleocytosis in a patient with relapsing polychondritis accompanied by meningoencephalitis: a case report
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title_sort	pleocytosis in a patient with relapsing polychondritis accompanied by meningoencephalitis: a case report
title_auth	Pleocytosis in a patient with relapsing polychondritis accompanied by meningoencephalitis: a case report
abstract	Background Relapsing polychondritis (RP) is an uncommon immune-related disease with unknown causes. It is characterized by inflammation of cartilaginous or non-cartilaginous structures, such as the ears, nose, respiratory tract, eyes, and joints. Neurological involvement is rare in RP. Case presentation We report a case of pleocytosis in a 64-year-old man diagnosed as having RP with meningoencephalitis. The patient’s condition markedly improved following methylprednisolone treatment. Conclusions To our knowledge, this is the first report of recurrent pleocytosis in a patient with RP accompanied by meningoencephalitis. Steroid pulse therapy is effective in most cases, and early diagnosis is of importance. © The Author(s). 2018
abstractGer	Background Relapsing polychondritis (RP) is an uncommon immune-related disease with unknown causes. It is characterized by inflammation of cartilaginous or non-cartilaginous structures, such as the ears, nose, respiratory tract, eyes, and joints. Neurological involvement is rare in RP. Case presentation We report a case of pleocytosis in a 64-year-old man diagnosed as having RP with meningoencephalitis. The patient’s condition markedly improved following methylprednisolone treatment. Conclusions To our knowledge, this is the first report of recurrent pleocytosis in a patient with RP accompanied by meningoencephalitis. Steroid pulse therapy is effective in most cases, and early diagnosis is of importance. © The Author(s). 2018
abstract_unstemmed	Background Relapsing polychondritis (RP) is an uncommon immune-related disease with unknown causes. It is characterized by inflammation of cartilaginous or non-cartilaginous structures, such as the ears, nose, respiratory tract, eyes, and joints. Neurological involvement is rare in RP. Case presentation We report a case of pleocytosis in a 64-year-old man diagnosed as having RP with meningoencephalitis. The patient’s condition markedly improved following methylprednisolone treatment. Conclusions To our knowledge, this is the first report of recurrent pleocytosis in a patient with RP accompanied by meningoencephalitis. Steroid pulse therapy is effective in most cases, and early diagnosis is of importance. © The Author(s). 2018
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title_short	Pleocytosis in a patient with relapsing polychondritis accompanied by meningoencephalitis: a case report
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