Hemophagocytic lymphohistiocytosis complicating a T-cell rich B-cell lymphoma

Background Hemophagocytic lymphohistiocytosis in adults is often secundary to an infection or a neoplasm. In this last case, T cell lymphomas are the most frequent causes. Hemophagocytic lymphohistiocytosis secundary to a B cell lymphoma has been rarely reported. Case presentation We describe a case...
Ausführliche Beschreibung

Gespeichert in:

Autor*in:	Mahtat, El Mehdi [verfasserIn] Zine, Maryem Allaoui, Mohamed Kerbout, Malika Messaoudi, Nezha Doghmi, Kamal Mikdame, Mohamed

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2016

Schlagwörter:	Epstein Barr Virus Hodgkin Lymphoma Epstein Barr Virus Infection Hemophagocytic Lymphohistiocytosis Epstein Barr Virus Reactivation

Anmerkung:	© The Author(s). 2016

Übergeordnetes Werk:	Enthalten in: BMC hematology - London : BioMed Central, 2013, 16(2016), 1 vom: 24. Nov.
Übergeordnetes Werk:	volume:16 ; year:2016 ; number:1 ; day:24 ; month:11

Links:	Volltext

DOI / URN:	10.1186/s12878-016-0065-5

Katalog-ID:	SPR027652203

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520			\|a Background Hemophagocytic lymphohistiocytosis in adults is often secundary to an infection or a neoplasm. In this last case, T cell lymphomas are the most frequent causes. Hemophagocytic lymphohistiocytosis secundary to a B cell lymphoma has been rarely reported. Case presentation We describe a case of a hemophagocytic lymphohistiocytosis complicating a T-cell rich B-cell lymphoma treated with conventionnal chemotherapy leading to a complete remission. Conclusion Prompt etiologic diagnosis and treatment of hemophagocytic lymphohistiocytosis leads to satisfactory outcome.
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allfields	10.1186/s12878-016-0065-5 doi (DE-627)SPR027652203 (SPR)s12878-016-0065-5-e DE-627 ger DE-627 rakwb eng Mahtat, El Mehdi verfasserin aut Hemophagocytic lymphohistiocytosis complicating a T-cell rich B-cell lymphoma 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s). 2016 Background Hemophagocytic lymphohistiocytosis in adults is often secundary to an infection or a neoplasm. In this last case, T cell lymphomas are the most frequent causes. Hemophagocytic lymphohistiocytosis secundary to a B cell lymphoma has been rarely reported. Case presentation We describe a case of a hemophagocytic lymphohistiocytosis complicating a T-cell rich B-cell lymphoma treated with conventionnal chemotherapy leading to a complete remission. Conclusion Prompt etiologic diagnosis and treatment of hemophagocytic lymphohistiocytosis leads to satisfactory outcome. Epstein Barr Virus (dpeaa)DE-He213 Hodgkin Lymphoma (dpeaa)DE-He213 Epstein Barr Virus Infection (dpeaa)DE-He213 Hemophagocytic Lymphohistiocytosis (dpeaa)DE-He213 Epstein Barr Virus Reactivation (dpeaa)DE-He213 Zine, Maryem aut Allaoui, Mohamed aut Kerbout, Malika aut Messaoudi, Nezha aut Doghmi, Kamal aut Mikdame, Mohamed aut Enthalten in BMC hematology London : BioMed Central, 2013 16(2016), 1 vom: 24. Nov. (DE-627)773473114 (DE-600)2744433-8 2052-1839 nnns volume:16 year:2016 number:1 day:24 month:11 https://dx.doi.org/10.1186/s12878-016-0065-5 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 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_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 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 16 2016 1 24 11
spelling	10.1186/s12878-016-0065-5 doi (DE-627)SPR027652203 (SPR)s12878-016-0065-5-e DE-627 ger DE-627 rakwb eng Mahtat, El Mehdi verfasserin aut Hemophagocytic lymphohistiocytosis complicating a T-cell rich B-cell lymphoma 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s). 2016 Background Hemophagocytic lymphohistiocytosis in adults is often secundary to an infection or a neoplasm. In this last case, T cell lymphomas are the most frequent causes. Hemophagocytic lymphohistiocytosis secundary to a B cell lymphoma has been rarely reported. Case presentation We describe a case of a hemophagocytic lymphohistiocytosis complicating a T-cell rich B-cell lymphoma treated with conventionnal chemotherapy leading to a complete remission. Conclusion Prompt etiologic diagnosis and treatment of hemophagocytic lymphohistiocytosis leads to satisfactory outcome. Epstein Barr Virus (dpeaa)DE-He213 Hodgkin Lymphoma (dpeaa)DE-He213 Epstein Barr Virus Infection (dpeaa)DE-He213 Hemophagocytic Lymphohistiocytosis (dpeaa)DE-He213 Epstein Barr Virus Reactivation (dpeaa)DE-He213 Zine, Maryem aut Allaoui, Mohamed aut Kerbout, Malika aut Messaoudi, Nezha aut Doghmi, Kamal aut Mikdame, Mohamed aut Enthalten in BMC hematology London : BioMed Central, 2013 16(2016), 1 vom: 24. Nov. (DE-627)773473114 (DE-600)2744433-8 2052-1839 nnns volume:16 year:2016 number:1 day:24 month:11 https://dx.doi.org/10.1186/s12878-016-0065-5 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 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_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 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 16 2016 1 24 11
allfields_unstemmed	10.1186/s12878-016-0065-5 doi (DE-627)SPR027652203 (SPR)s12878-016-0065-5-e DE-627 ger DE-627 rakwb eng Mahtat, El Mehdi verfasserin aut Hemophagocytic lymphohistiocytosis complicating a T-cell rich B-cell lymphoma 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s). 2016 Background Hemophagocytic lymphohistiocytosis in adults is often secundary to an infection or a neoplasm. In this last case, T cell lymphomas are the most frequent causes. Hemophagocytic lymphohistiocytosis secundary to a B cell lymphoma has been rarely reported. Case presentation We describe a case of a hemophagocytic lymphohistiocytosis complicating a T-cell rich B-cell lymphoma treated with conventionnal chemotherapy leading to a complete remission. Conclusion Prompt etiologic diagnosis and treatment of hemophagocytic lymphohistiocytosis leads to satisfactory outcome. Epstein Barr Virus (dpeaa)DE-He213 Hodgkin Lymphoma (dpeaa)DE-He213 Epstein Barr Virus Infection (dpeaa)DE-He213 Hemophagocytic Lymphohistiocytosis (dpeaa)DE-He213 Epstein Barr Virus Reactivation (dpeaa)DE-He213 Zine, Maryem aut Allaoui, Mohamed aut Kerbout, Malika aut Messaoudi, Nezha aut Doghmi, Kamal aut Mikdame, Mohamed aut Enthalten in BMC hematology London : BioMed Central, 2013 16(2016), 1 vom: 24. Nov. (DE-627)773473114 (DE-600)2744433-8 2052-1839 nnns volume:16 year:2016 number:1 day:24 month:11 https://dx.doi.org/10.1186/s12878-016-0065-5 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 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_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 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 16 2016 1 24 11
allfieldsGer	10.1186/s12878-016-0065-5 doi (DE-627)SPR027652203 (SPR)s12878-016-0065-5-e DE-627 ger DE-627 rakwb eng Mahtat, El Mehdi verfasserin aut Hemophagocytic lymphohistiocytosis complicating a T-cell rich B-cell lymphoma 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s). 2016 Background Hemophagocytic lymphohistiocytosis in adults is often secundary to an infection or a neoplasm. In this last case, T cell lymphomas are the most frequent causes. Hemophagocytic lymphohistiocytosis secundary to a B cell lymphoma has been rarely reported. Case presentation We describe a case of a hemophagocytic lymphohistiocytosis complicating a T-cell rich B-cell lymphoma treated with conventionnal chemotherapy leading to a complete remission. Conclusion Prompt etiologic diagnosis and treatment of hemophagocytic lymphohistiocytosis leads to satisfactory outcome. Epstein Barr Virus (dpeaa)DE-He213 Hodgkin Lymphoma (dpeaa)DE-He213 Epstein Barr Virus Infection (dpeaa)DE-He213 Hemophagocytic Lymphohistiocytosis (dpeaa)DE-He213 Epstein Barr Virus Reactivation (dpeaa)DE-He213 Zine, Maryem aut Allaoui, Mohamed aut Kerbout, Malika aut Messaoudi, Nezha aut Doghmi, Kamal aut Mikdame, Mohamed aut Enthalten in BMC hematology London : BioMed Central, 2013 16(2016), 1 vom: 24. Nov. (DE-627)773473114 (DE-600)2744433-8 2052-1839 nnns volume:16 year:2016 number:1 day:24 month:11 https://dx.doi.org/10.1186/s12878-016-0065-5 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 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_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 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 16 2016 1 24 11
allfieldsSound	10.1186/s12878-016-0065-5 doi (DE-627)SPR027652203 (SPR)s12878-016-0065-5-e DE-627 ger DE-627 rakwb eng Mahtat, El Mehdi verfasserin aut Hemophagocytic lymphohistiocytosis complicating a T-cell rich B-cell lymphoma 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s). 2016 Background Hemophagocytic lymphohistiocytosis in adults is often secundary to an infection or a neoplasm. In this last case, T cell lymphomas are the most frequent causes. Hemophagocytic lymphohistiocytosis secundary to a B cell lymphoma has been rarely reported. Case presentation We describe a case of a hemophagocytic lymphohistiocytosis complicating a T-cell rich B-cell lymphoma treated with conventionnal chemotherapy leading to a complete remission. Conclusion Prompt etiologic diagnosis and treatment of hemophagocytic lymphohistiocytosis leads to satisfactory outcome. Epstein Barr Virus (dpeaa)DE-He213 Hodgkin Lymphoma (dpeaa)DE-He213 Epstein Barr Virus Infection (dpeaa)DE-He213 Hemophagocytic Lymphohistiocytosis (dpeaa)DE-He213 Epstein Barr Virus Reactivation (dpeaa)DE-He213 Zine, Maryem aut Allaoui, Mohamed aut Kerbout, Malika aut Messaoudi, Nezha aut Doghmi, Kamal aut Mikdame, Mohamed aut Enthalten in BMC hematology London : BioMed Central, 2013 16(2016), 1 vom: 24. Nov. (DE-627)773473114 (DE-600)2744433-8 2052-1839 nnns volume:16 year:2016 number:1 day:24 month:11 https://dx.doi.org/10.1186/s12878-016-0065-5 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 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_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 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 16 2016 1 24 11
language	English
source	Enthalten in BMC hematology 16(2016), 1 vom: 24. Nov. volume:16 year:2016 number:1 day:24 month:11
sourceStr	Enthalten in BMC hematology 16(2016), 1 vom: 24. Nov. volume:16 year:2016 number:1 day:24 month:11
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institution	findex.gbv.de
topic_facet	Epstein Barr Virus Hodgkin Lymphoma Epstein Barr Virus Infection Hemophagocytic Lymphohistiocytosis Epstein Barr Virus Reactivation
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author	Mahtat, El Mehdi
spellingShingle	Mahtat, El Mehdi misc Epstein Barr Virus misc Hodgkin Lymphoma misc Epstein Barr Virus Infection misc Hemophagocytic Lymphohistiocytosis misc Epstein Barr Virus Reactivation Hemophagocytic lymphohistiocytosis complicating a T-cell rich B-cell lymphoma
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topic_title	Hemophagocytic lymphohistiocytosis complicating a T-cell rich B-cell lymphoma Epstein Barr Virus (dpeaa)DE-He213 Hodgkin Lymphoma (dpeaa)DE-He213 Epstein Barr Virus Infection (dpeaa)DE-He213 Hemophagocytic Lymphohistiocytosis (dpeaa)DE-He213 Epstein Barr Virus Reactivation (dpeaa)DE-He213
topic	misc Epstein Barr Virus misc Hodgkin Lymphoma misc Epstein Barr Virus Infection misc Hemophagocytic Lymphohistiocytosis misc Epstein Barr Virus Reactivation
topic_unstemmed	misc Epstein Barr Virus misc Hodgkin Lymphoma misc Epstein Barr Virus Infection misc Hemophagocytic Lymphohistiocytosis misc Epstein Barr Virus Reactivation
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title	Hemophagocytic lymphohistiocytosis complicating a T-cell rich B-cell lymphoma
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author_browse	Mahtat, El Mehdi Zine, Maryem Allaoui, Mohamed Kerbout, Malika Messaoudi, Nezha Doghmi, Kamal Mikdame, Mohamed
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title_sort	hemophagocytic lymphohistiocytosis complicating a t-cell rich b-cell lymphoma
title_auth	Hemophagocytic lymphohistiocytosis complicating a T-cell rich B-cell lymphoma
abstract	Background Hemophagocytic lymphohistiocytosis in adults is often secundary to an infection or a neoplasm. In this last case, T cell lymphomas are the most frequent causes. Hemophagocytic lymphohistiocytosis secundary to a B cell lymphoma has been rarely reported. Case presentation We describe a case of a hemophagocytic lymphohistiocytosis complicating a T-cell rich B-cell lymphoma treated with conventionnal chemotherapy leading to a complete remission. Conclusion Prompt etiologic diagnosis and treatment of hemophagocytic lymphohistiocytosis leads to satisfactory outcome. © The Author(s). 2016
abstractGer	Background Hemophagocytic lymphohistiocytosis in adults is often secundary to an infection or a neoplasm. In this last case, T cell lymphomas are the most frequent causes. Hemophagocytic lymphohistiocytosis secundary to a B cell lymphoma has been rarely reported. Case presentation We describe a case of a hemophagocytic lymphohistiocytosis complicating a T-cell rich B-cell lymphoma treated with conventionnal chemotherapy leading to a complete remission. Conclusion Prompt etiologic diagnosis and treatment of hemophagocytic lymphohistiocytosis leads to satisfactory outcome. © The Author(s). 2016
abstract_unstemmed	Background Hemophagocytic lymphohistiocytosis in adults is often secundary to an infection or a neoplasm. In this last case, T cell lymphomas are the most frequent causes. Hemophagocytic lymphohistiocytosis secundary to a B cell lymphoma has been rarely reported. Case presentation We describe a case of a hemophagocytic lymphohistiocytosis complicating a T-cell rich B-cell lymphoma treated with conventionnal chemotherapy leading to a complete remission. Conclusion Prompt etiologic diagnosis and treatment of hemophagocytic lymphohistiocytosis leads to satisfactory outcome. © The Author(s). 2016
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title_short	Hemophagocytic lymphohistiocytosis complicating a T-cell rich B-cell lymphoma
url	https://dx.doi.org/10.1186/s12878-016-0065-5
remote_bool	true
author2	Zine, Maryem Allaoui, Mohamed Kerbout, Malika Messaoudi, Nezha Doghmi, Kamal Mikdame, Mohamed
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up_date	2024-07-03T14:14:36.664Z
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Hemophagocytic lymphohistiocytosis complicating a T-cell rich B-cell lymphoma

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