Hepatosplenic Gamma Delta T cell Lymphoma in a Young Male with Visceral Leishmaniasis
Hepatosplenic gamma delta T-cell lymphoma (HSTCL) is a rare peripheral T-cell lymphoma of cytotoxic T-cell origin with an aggressive clinical course. It is characterized by hepatosplenomegaly without significant lymphadenopathy, with clinically significant cytopenias. Chronic immunosuppression has...
Ausführliche Beschreibung
Autor*in: |
Deepti Mutreja [verfasserIn] Mrinalini Kotru [verfasserIn] Mukul Aggarwal [verfasserIn] Narendra Tejwani [verfasserIn] Rahul Kumar Sharma [verfasserIn] HaraPrasad Pati [verfasserIn] |
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Englisch |
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2014 |
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In: Mediterranean Journal of Hematology and Infectious Diseases - Mattioli1885, 2010, 1(2014) |
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Übergeordnetes Werk: |
volume:1 ; year:2014 |
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Katalog-ID: |
DOAJ015249875 |
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(DE-627)DOAJ015249875 (DE-599)DOAJ62eee0fd54af40c1a79ec9965811bda2 DE-627 ger DE-627 rakwb eng RC633-647.5 Deepti Mutreja verfasserin aut Hepatosplenic Gamma Delta T cell Lymphoma in a Young Male with Visceral Leishmaniasis 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Hepatosplenic gamma delta T-cell lymphoma (HSTCL) is a rare peripheral T-cell lymphoma of cytotoxic T-cell origin with an aggressive clinical course. It is characterized by hepatosplenomegaly without significant lymphadenopathy, with clinically significant cytopenias. Chronic immunosuppression has been proposed as a possible pathogenetic mechanism in HSTCL. No association of HSTCL with visceral leishmaniasis has been described in the past. We describe a case of an adolescent male patient with HSTCL with leukemic presentation, who was diagnosed to have visceral leishmaniasis, nine months prior to presentation at our centre. Leishmaniasis Hepatosplenic gamma delta T cell lymphoma leukemic presentation immunophenotyping Diseases of the blood and blood-forming organs Mrinalini Kotru verfasserin aut Mukul Aggarwal verfasserin aut Narendra Tejwani verfasserin aut Rahul Kumar Sharma verfasserin aut HaraPrasad Pati verfasserin aut In Mediterranean Journal of Hematology and Infectious Diseases Mattioli1885, 2010 1(2014) (DE-627)721581978 (DE-600)2674750-9 20353006 nnns volume:1 year:2014 https://doaj.org/article/62eee0fd54af40c1a79ec9965811bda2 kostenfrei https://mjhid.org/index.php/mjhid/article/view/1895 kostenfrei https://doaj.org/toc/2035-3006 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ 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_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 1 2014 |
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(DE-627)DOAJ015249875 (DE-599)DOAJ62eee0fd54af40c1a79ec9965811bda2 DE-627 ger DE-627 rakwb eng RC633-647.5 Deepti Mutreja verfasserin aut Hepatosplenic Gamma Delta T cell Lymphoma in a Young Male with Visceral Leishmaniasis 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Hepatosplenic gamma delta T-cell lymphoma (HSTCL) is a rare peripheral T-cell lymphoma of cytotoxic T-cell origin with an aggressive clinical course. It is characterized by hepatosplenomegaly without significant lymphadenopathy, with clinically significant cytopenias. Chronic immunosuppression has been proposed as a possible pathogenetic mechanism in HSTCL. No association of HSTCL with visceral leishmaniasis has been described in the past. We describe a case of an adolescent male patient with HSTCL with leukemic presentation, who was diagnosed to have visceral leishmaniasis, nine months prior to presentation at our centre. Leishmaniasis Hepatosplenic gamma delta T cell lymphoma leukemic presentation immunophenotyping Diseases of the blood and blood-forming organs Mrinalini Kotru verfasserin aut Mukul Aggarwal verfasserin aut Narendra Tejwani verfasserin aut Rahul Kumar Sharma verfasserin aut HaraPrasad Pati verfasserin aut In Mediterranean Journal of Hematology and Infectious Diseases Mattioli1885, 2010 1(2014) (DE-627)721581978 (DE-600)2674750-9 20353006 nnns volume:1 year:2014 https://doaj.org/article/62eee0fd54af40c1a79ec9965811bda2 kostenfrei https://mjhid.org/index.php/mjhid/article/view/1895 kostenfrei https://doaj.org/toc/2035-3006 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ 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_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 1 2014 |
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RC633-647.5 Hepatosplenic Gamma Delta T cell Lymphoma in a Young Male with Visceral Leishmaniasis Leishmaniasis Hepatosplenic gamma delta T cell lymphoma leukemic presentation immunophenotyping |
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Hepatosplenic Gamma Delta T cell Lymphoma in a Young Male with Visceral Leishmaniasis |
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Hepatosplenic gamma delta T-cell lymphoma (HSTCL) is a rare peripheral T-cell lymphoma of cytotoxic T-cell origin with an aggressive clinical course. It is characterized by hepatosplenomegaly without significant lymphadenopathy, with clinically significant cytopenias. Chronic immunosuppression has been proposed as a possible pathogenetic mechanism in HSTCL. No association of HSTCL with visceral leishmaniasis has been described in the past. We describe a case of an adolescent male patient with HSTCL with leukemic presentation, who was diagnosed to have visceral leishmaniasis, nine months prior to presentation at our centre. |
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Hepatosplenic gamma delta T-cell lymphoma (HSTCL) is a rare peripheral T-cell lymphoma of cytotoxic T-cell origin with an aggressive clinical course. It is characterized by hepatosplenomegaly without significant lymphadenopathy, with clinically significant cytopenias. Chronic immunosuppression has been proposed as a possible pathogenetic mechanism in HSTCL. No association of HSTCL with visceral leishmaniasis has been described in the past. We describe a case of an adolescent male patient with HSTCL with leukemic presentation, who was diagnosed to have visceral leishmaniasis, nine months prior to presentation at our centre. |
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Hepatosplenic gamma delta T-cell lymphoma (HSTCL) is a rare peripheral T-cell lymphoma of cytotoxic T-cell origin with an aggressive clinical course. It is characterized by hepatosplenomegaly without significant lymphadenopathy, with clinically significant cytopenias. Chronic immunosuppression has been proposed as a possible pathogenetic mechanism in HSTCL. No association of HSTCL with visceral leishmaniasis has been described in the past. We describe a case of an adolescent male patient with HSTCL with leukemic presentation, who was diagnosed to have visceral leishmaniasis, nine months prior to presentation at our centre. |
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Hepatosplenic Gamma Delta T cell Lymphoma in a Young Male with Visceral Leishmaniasis |
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https://doaj.org/article/62eee0fd54af40c1a79ec9965811bda2 https://mjhid.org/index.php/mjhid/article/view/1895 https://doaj.org/toc/2035-3006 |
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|
score |
7.4010916 |