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Rare, Yet Emerging Cause of Graft Dysfunction—ALECT 2 Amyloidosis
Amyloidosis is characterized by pathological deposition of abnormal protein aggregates in various tissues, AL protein being the commonest. Amyloidosis derived from leukocyte cell-derived chemotaxin 2 (LECT2) is a recently recognized form of amyloidosis in the United States with predominant involveme...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7470195/ https://www.ncbi.nlm.nih.gov/pubmed/33013073 http://dx.doi.org/10.4103/ijn.IJN_258_19 |
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author | Singh, Kulwant Sethi, Jasmine Duggal, Rajan Joshi, Kusum Bains, Arjinder S. |
author_facet | Singh, Kulwant Sethi, Jasmine Duggal, Rajan Joshi, Kusum Bains, Arjinder S. |
author_sort | Singh, Kulwant |
collection | PubMed |
description | Amyloidosis is characterized by pathological deposition of abnormal protein aggregates in various tissues, AL protein being the commonest. Amyloidosis derived from leukocyte cell-derived chemotaxin 2 (LECT2) is a recently recognized form of amyloidosis in the United States with predominant involvement of kidney and liver. We present a case of ALECT2 renal amyloid in a transplant recipient who presented with gradual worsening of graft function and subnephrotic proteinuria. To our knowledge, this is first case of LECT2 amyloidosis from Northern India in a transplant recipient. There is no effective therapy for amyloidosis derived from leukocyte cell-derived chemotaxin 2. |
format | Online Article Text |
id | pubmed-7470195 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-74701952020-10-02 Rare, Yet Emerging Cause of Graft Dysfunction—ALECT 2 Amyloidosis Singh, Kulwant Sethi, Jasmine Duggal, Rajan Joshi, Kusum Bains, Arjinder S. Indian J Nephrol Case Report Amyloidosis is characterized by pathological deposition of abnormal protein aggregates in various tissues, AL protein being the commonest. Amyloidosis derived from leukocyte cell-derived chemotaxin 2 (LECT2) is a recently recognized form of amyloidosis in the United States with predominant involvement of kidney and liver. We present a case of ALECT2 renal amyloid in a transplant recipient who presented with gradual worsening of graft function and subnephrotic proteinuria. To our knowledge, this is first case of LECT2 amyloidosis from Northern India in a transplant recipient. There is no effective therapy for amyloidosis derived from leukocyte cell-derived chemotaxin 2. Wolters Kluwer - Medknow 2020 2020-02-11 /pmc/articles/PMC7470195/ /pubmed/33013073 http://dx.doi.org/10.4103/ijn.IJN_258_19 Text en Copyright: © 2020 Indian Journal of Nephrology http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Singh, Kulwant Sethi, Jasmine Duggal, Rajan Joshi, Kusum Bains, Arjinder S. Rare, Yet Emerging Cause of Graft Dysfunction—ALECT 2 Amyloidosis |
title | Rare, Yet Emerging Cause of Graft Dysfunction—ALECT 2 Amyloidosis |
title_full | Rare, Yet Emerging Cause of Graft Dysfunction—ALECT 2 Amyloidosis |
title_fullStr | Rare, Yet Emerging Cause of Graft Dysfunction—ALECT 2 Amyloidosis |
title_full_unstemmed | Rare, Yet Emerging Cause of Graft Dysfunction—ALECT 2 Amyloidosis |
title_short | Rare, Yet Emerging Cause of Graft Dysfunction—ALECT 2 Amyloidosis |
title_sort | rare, yet emerging cause of graft dysfunction—alect 2 amyloidosis |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7470195/ https://www.ncbi.nlm.nih.gov/pubmed/33013073 http://dx.doi.org/10.4103/ijn.IJN_258_19 |
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