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Recurrence of kala‐azar after PKDL: role of co‐factors
Recurrence of kala‐azar after post kala‐azar dermal leishmaniasis (PKDL) has remained uncommon. We report here two patients with recurrence of kala‐azar (KA) after development of PKDL. In one case the second attack of KA was preceded by repeated attacks of malaria and tuberculosis, and in the other...
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Published in: | Tropical medicine & international health 1998-01, Vol.3 (1), p.76-78 |
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creator | Nandy, A. Addy, M. Maji, A. K. Guha, S. K. Banerjee, D. Chaudhuri, D. |
description | Recurrence of kala‐azar after post kala‐azar dermal leishmaniasis (PKDL) has remained uncommon. We report here two patients with recurrence of kala‐azar (KA) after development of PKDL. In one case the second attack of KA was preceded by repeated attacks of malaria and tuberculosis, and in the other the recurrence of KA followed an attack of measles. While measles has earlier been suggested as co‐factor in inducing transformation from sub‐clinical to clinical kala‐azar, malaria was demonstrated to enhance the virulence and invasiveness of Leishmania in an experimental model as well as under natural condition. We propose that in our cases, measles and repeated attacks of malaria or tuberculosis led to immunosuppression and recurrence of visceral leishmaniasis (VL). |
doi_str_mv | 10.1046/j.1365-3156.1998.00176.x |
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K.</creatorcontrib><creatorcontrib>Guha, S. K.</creatorcontrib><creatorcontrib>Banerjee, D.</creatorcontrib><creatorcontrib>Chaudhuri, D.</creatorcontrib><title>Recurrence of kala‐azar after PKDL: role of co‐factors</title><title>Tropical medicine & international health</title><addtitle>Trop Med Int Health</addtitle><description>Recurrence of kala‐azar after post kala‐azar dermal leishmaniasis (PKDL) has remained uncommon. We report here two patients with recurrence of kala‐azar (KA) after development of PKDL. In one case the second attack of KA was preceded by repeated attacks of malaria and tuberculosis, and in the other the recurrence of KA followed an attack of measles. While measles has earlier been suggested as co‐factor in inducing transformation from sub‐clinical to clinical kala‐azar, malaria was demonstrated to enhance the virulence and invasiveness of Leishmania in an experimental model as well as under natural condition. We propose that in our cases, measles and repeated attacks of malaria or tuberculosis led to immunosuppression and recurrence of visceral leishmaniasis (VL).</description><subject>Adolescent</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>co‐factors</subject><subject>Human protozoal diseases</subject><subject>Humans</subject><subject>Immune Tolerance</subject><subject>Infectious diseases</subject><subject>Leishmaniasis, Cutaneous - complications</subject><subject>Leishmaniasis, Cutaneous - etiology</subject><subject>Leishmaniasis, Visceral - complications</subject><subject>Leishmaniasis, Visceral - etiology</subject><subject>Leishmaniasis, Visceral - immunology</subject><subject>Leshmaniasis</subject><subject>Malaria, Vivax - complications</subject><subject>Malaria, Vivax - immunology</subject><subject>Male</subject><subject>Measles - complications</subject><subject>Measles - immunology</subject><subject>Medical sciences</subject><subject>Parasitic diseases</subject><subject>PKDL</subject><subject>Protozoal diseases</subject><subject>Recurrence</subject><subject>recurrent kala‐azar</subject><subject>re‐visceralization</subject><subject>Tropical medicine</subject><subject>Tuberculosis, Lymph Node - complications</subject><subject>Tuberculosis, Lymph Node - immunology</subject><subject>Tuberculosis, Pulmonary - complications</subject><subject>Tuberculosis, Pulmonary - immunology</subject><issn>1360-2276</issn><issn>1365-3156</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNqNkMtKw0AUhgdRqlYfQchC3CWeuWQuxY3UW7GiSF0P08kEUtOmzjTYuvIRfEafxKQtXbs6B77_nB8-hCIMCQbGLycJpjyNKU55gpWSCQAWPFnuoaMd2F_vEBMi-CE6DmECAIylvIM6ikmmBDtCvVdna-_dzLqoyqN3U5rf7x_zZXxk8oXz0cvjzbAX-apcc1s1NDd2Uflwgg5yUwZ3up1d9HZ3O-o_xMPn-0H_ehhbxgiPMRdjSA2nqcPOQUqIksAlzYSSDSMgM0YIwdmYcSWNkQyE4Biks2CtobSLLjZ_5776qF1Y6GkRrCtLM3NVHbRQAmjT1ATlJmh9FYJ3uZ77Ymr8SmPQrTY90a0d3drRrTa91qaXzenZtqMeT122O9x6avj5lptgTZl7M7NF2MUIpkoq0sSuNrHPonSrf9fr0dOgWegfsEWGog</recordid><startdate>199801</startdate><enddate>199801</enddate><creator>Nandy, A.</creator><creator>Addy, M.</creator><creator>Maji, A. 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K. ; Banerjee, D. ; Chaudhuri, D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4426-167b05a635e1ee0522980683d798167208d42221db4698aa840776108ec0cca33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Adolescent</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>co‐factors</topic><topic>Human protozoal diseases</topic><topic>Humans</topic><topic>Immune Tolerance</topic><topic>Infectious diseases</topic><topic>Leishmaniasis, Cutaneous - complications</topic><topic>Leishmaniasis, Cutaneous - etiology</topic><topic>Leishmaniasis, Visceral - complications</topic><topic>Leishmaniasis, Visceral - etiology</topic><topic>Leishmaniasis, Visceral - immunology</topic><topic>Leshmaniasis</topic><topic>Malaria, Vivax - complications</topic><topic>Malaria, Vivax - immunology</topic><topic>Male</topic><topic>Measles - complications</topic><topic>Measles - immunology</topic><topic>Medical sciences</topic><topic>Parasitic diseases</topic><topic>PKDL</topic><topic>Protozoal diseases</topic><topic>Recurrence</topic><topic>recurrent kala‐azar</topic><topic>re‐visceralization</topic><topic>Tropical medicine</topic><topic>Tuberculosis, Lymph Node - complications</topic><topic>Tuberculosis, Lymph Node - immunology</topic><topic>Tuberculosis, Pulmonary - complications</topic><topic>Tuberculosis, Pulmonary - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nandy, A.</creatorcontrib><creatorcontrib>Addy, M.</creatorcontrib><creatorcontrib>Maji, A. K.</creatorcontrib><creatorcontrib>Guha, S. K.</creatorcontrib><creatorcontrib>Banerjee, D.</creatorcontrib><creatorcontrib>Chaudhuri, D.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Tropical medicine & international health</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nandy, A.</au><au>Addy, M.</au><au>Maji, A. K.</au><au>Guha, S. K.</au><au>Banerjee, D.</au><au>Chaudhuri, D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Recurrence of kala‐azar after PKDL: role of co‐factors</atitle><jtitle>Tropical medicine & international health</jtitle><addtitle>Trop Med Int Health</addtitle><date>1998-01</date><risdate>1998</risdate><volume>3</volume><issue>1</issue><spage>76</spage><epage>78</epage><pages>76-78</pages><issn>1360-2276</issn><eissn>1365-3156</eissn><abstract>Recurrence of kala‐azar after post kala‐azar dermal leishmaniasis (PKDL) has remained uncommon. We report here two patients with recurrence of kala‐azar (KA) after development of PKDL. In one case the second attack of KA was preceded by repeated attacks of malaria and tuberculosis, and in the other the recurrence of KA followed an attack of measles. While measles has earlier been suggested as co‐factor in inducing transformation from sub‐clinical to clinical kala‐azar, malaria was demonstrated to enhance the virulence and invasiveness of Leishmania in an experimental model as well as under natural condition. We propose that in our cases, measles and repeated attacks of malaria or tuberculosis led to immunosuppression and recurrence of visceral leishmaniasis (VL).</abstract><cop>Oxford BSL</cop><pub>Blackwell Science Ltd</pub><pmid>9484974</pmid><doi>10.1046/j.1365-3156.1998.00176.x</doi><tpages>3</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Biological and medical sciences Child co‐factors Human protozoal diseases Humans Immune Tolerance Infectious diseases Leishmaniasis, Cutaneous - complications Leishmaniasis, Cutaneous - etiology Leishmaniasis, Visceral - complications Leishmaniasis, Visceral - etiology Leishmaniasis, Visceral - immunology Leshmaniasis Malaria, Vivax - complications Malaria, Vivax - immunology Male Measles - complications Measles - immunology Medical sciences Parasitic diseases PKDL Protozoal diseases Recurrence recurrent kala‐azar re‐visceralization Tropical medicine Tuberculosis, Lymph Node - complications Tuberculosis, Lymph Node - immunology Tuberculosis, Pulmonary - complications Tuberculosis, Pulmonary - immunology |
title | Recurrence of kala‐azar after PKDL: role of co‐factors |
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