Endothelial lesion and complement activation in patients with Scleroderma Renal Crisis

Bibliographic Details
Main Author: Pérez,Ney Arencibia
Publication Date: 2019
Other Authors: Morales,María Luisa Agüera, Sánchez,Rafael Sánchez, Salas,Rosa María Ortega, Puebla,Rafael Ángel Fernández de la, Hernández,Mario Espinosa
Format: Article
Language: eng
Source: Jornal Brasileiro de Nefrologia
Download full: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002019000400580
Summary: Abstract In kidney biopsies reviews, scleroderma renal crisis (SRC) is characterized by vascular endothelial injuries, C4d deposits on peritubular vessels, and acute and chronic injuries coexisting on the same biopsy. The clinical signs of thrombotic microangiopathy (TMA) are described in systemic sclerosis (SSc), nevertheless, it has not been related to acute injuries described on kidney biopsies. We report a case of SRC in a patient with scleroderma-dermatomyositis overlap syndrome, which also showed clinical and histopathological data of TMA. On fundus examination, a severe acute hypertensive retinopathy was found. The kidney biopsy showed severe endothelial damage with widening of mucoid cells at the level of the intima, focal concentric proliferation on most small arterioles, and C3, C4d, and IgM deposits along the capillary walls. The genetic study of complement only showed the presence of membrane cofactor protein (MCP) risk haplotypes, without other genetic complement disorders. We understand that in a patient with TMA and SSc, the kidney damage would be fundamentally endothelial and of an acute type; moreover, we would observe clear evidence of complement activation. Once further studies correlate clinical-analytical data with anatomopathological studies, it is likely that we will be forced to redefine the SRC concept, focusing on the relationship between acute endothelial damage and complement activation.
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spelling Endothelial lesion and complement activation in patients with Scleroderma Renal CrisisScleroderma, LocalizedThrombotic MicroangiopathySystemic SclerosisHypertensive RetinopathyEndotheliumComplement ActivationAbstract In kidney biopsies reviews, scleroderma renal crisis (SRC) is characterized by vascular endothelial injuries, C4d deposits on peritubular vessels, and acute and chronic injuries coexisting on the same biopsy. The clinical signs of thrombotic microangiopathy (TMA) are described in systemic sclerosis (SSc), nevertheless, it has not been related to acute injuries described on kidney biopsies. We report a case of SRC in a patient with scleroderma-dermatomyositis overlap syndrome, which also showed clinical and histopathological data of TMA. On fundus examination, a severe acute hypertensive retinopathy was found. The kidney biopsy showed severe endothelial damage with widening of mucoid cells at the level of the intima, focal concentric proliferation on most small arterioles, and C3, C4d, and IgM deposits along the capillary walls. The genetic study of complement only showed the presence of membrane cofactor protein (MCP) risk haplotypes, without other genetic complement disorders. We understand that in a patient with TMA and SSc, the kidney damage would be fundamentally endothelial and of an acute type; moreover, we would observe clear evidence of complement activation. Once further studies correlate clinical-analytical data with anatomopathological studies, it is likely that we will be forced to redefine the SRC concept, focusing on the relationship between acute endothelial damage and complement activation.Sociedade Brasileira de Nefrologia2019-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002019000400580Brazilian Journal of Nephrology v.41 n.4 2019reponame:Jornal Brasileiro de Nefrologiainstname:Sociedade Brasileira de Nefrologia (SBN)instacron:SBN10.1590/2175-8239-jbn-2018-0202info:eu-repo/semantics/openAccessPérez,Ney ArencibiaMorales,María Luisa AgüeraSánchez,Rafael SánchezSalas,Rosa María OrtegaPuebla,Rafael Ángel Fernández de laHernández,Mario Espinosaeng2020-01-16T00:00:00Zoai:scielo:S0101-28002019000400580Revistahttp://www.bjn.org.br/ONGhttps://old.scielo.br/oai/scielo-oai.php||jbn@sbn.org.br2175-82390101-2800opendoar:2020-01-16T00:00Jornal Brasileiro de Nefrologia - Sociedade Brasileira de Nefrologia (SBN)false
dc.title.none.fl_str_mv Endothelial lesion and complement activation in patients with Scleroderma Renal Crisis
title Endothelial lesion and complement activation in patients with Scleroderma Renal Crisis
spellingShingle Endothelial lesion and complement activation in patients with Scleroderma Renal Crisis
Pérez,Ney Arencibia
Scleroderma, Localized
Thrombotic Microangiopathy
Systemic Sclerosis
Hypertensive Retinopathy
Endothelium
Complement Activation
title_short Endothelial lesion and complement activation in patients with Scleroderma Renal Crisis
title_full Endothelial lesion and complement activation in patients with Scleroderma Renal Crisis
title_fullStr Endothelial lesion and complement activation in patients with Scleroderma Renal Crisis
title_full_unstemmed Endothelial lesion and complement activation in patients with Scleroderma Renal Crisis
title_sort Endothelial lesion and complement activation in patients with Scleroderma Renal Crisis
author Pérez,Ney Arencibia
author_facet Pérez,Ney Arencibia
Morales,María Luisa Agüera
Sánchez,Rafael Sánchez
Salas,Rosa María Ortega
Puebla,Rafael Ángel Fernández de la
Hernández,Mario Espinosa
author_role author
author2 Morales,María Luisa Agüera
Sánchez,Rafael Sánchez
Salas,Rosa María Ortega
Puebla,Rafael Ángel Fernández de la
Hernández,Mario Espinosa
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Pérez,Ney Arencibia
Morales,María Luisa Agüera
Sánchez,Rafael Sánchez
Salas,Rosa María Ortega
Puebla,Rafael Ángel Fernández de la
Hernández,Mario Espinosa
dc.subject.por.fl_str_mv Scleroderma, Localized
Thrombotic Microangiopathy
Systemic Sclerosis
Hypertensive Retinopathy
Endothelium
Complement Activation
topic Scleroderma, Localized
Thrombotic Microangiopathy
Systemic Sclerosis
Hypertensive Retinopathy
Endothelium
Complement Activation
description Abstract In kidney biopsies reviews, scleroderma renal crisis (SRC) is characterized by vascular endothelial injuries, C4d deposits on peritubular vessels, and acute and chronic injuries coexisting on the same biopsy. The clinical signs of thrombotic microangiopathy (TMA) are described in systemic sclerosis (SSc), nevertheless, it has not been related to acute injuries described on kidney biopsies. We report a case of SRC in a patient with scleroderma-dermatomyositis overlap syndrome, which also showed clinical and histopathological data of TMA. On fundus examination, a severe acute hypertensive retinopathy was found. The kidney biopsy showed severe endothelial damage with widening of mucoid cells at the level of the intima, focal concentric proliferation on most small arterioles, and C3, C4d, and IgM deposits along the capillary walls. The genetic study of complement only showed the presence of membrane cofactor protein (MCP) risk haplotypes, without other genetic complement disorders. We understand that in a patient with TMA and SSc, the kidney damage would be fundamentally endothelial and of an acute type; moreover, we would observe clear evidence of complement activation. Once further studies correlate clinical-analytical data with anatomopathological studies, it is likely that we will be forced to redefine the SRC concept, focusing on the relationship between acute endothelial damage and complement activation.
publishDate 2019
dc.date.none.fl_str_mv 2019-12-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002019000400580
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002019000400580
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/2175-8239-jbn-2018-0202
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Nefrologia
publisher.none.fl_str_mv Sociedade Brasileira de Nefrologia
dc.source.none.fl_str_mv Brazilian Journal of Nephrology v.41 n.4 2019
reponame:Jornal Brasileiro de Nefrologia
instname:Sociedade Brasileira de Nefrologia (SBN)
instacron:SBN
instname_str Sociedade Brasileira de Nefrologia (SBN)
instacron_str SBN
institution SBN
reponame_str Jornal Brasileiro de Nefrologia
collection Jornal Brasileiro de Nefrologia
repository.name.fl_str_mv Jornal Brasileiro de Nefrologia - Sociedade Brasileira de Nefrologia (SBN)
repository.mail.fl_str_mv ||jbn@sbn.org.br
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