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What Can We Do When All Collapses? Fatal Outcome of Collapsing Glomerulopathy and Systemic Lupus Erythematosus With Diffuse Alveolar Hemorrhage: Case Report

dc.contributor.authorPinto, H
dc.contributor.authorLeal, R
dc.contributor.authorRodrigues, L
dc.contributor.authorSantos, L
dc.contributor.authorRomãozinho, C
dc.contributor.authorMacário, F
dc.contributor.authorAlves, R
dc.contributor.authorPratas, J
dc.contributor.authorSousa, V
dc.contributor.authorMarinho, C
dc.contributor.authorPrado E Castro, L
dc.contributor.authorCosta, F
dc.contributor.authorCampos, M
dc.contributor.authorMota, A
dc.contributor.authorFigueiredo, A
dc.date.accessioned2020-03-30T13:55:11Z
dc.date.available2020-03-30T13:55:11Z
dc.date.issued2017-05
dc.description.abstractNTRODUCTION: Collapsing glomerulopathy (CG) is a rare form of glomerular injury. Although commonly associated with human immunodeficiency virus (HIV) infection, it can occur in association with systemic lupus erythematosus (SLE). CASE REPORT: We present the case of a 50-year-old man, with chronic kidney disease secondary to focal and segmental glomerulosclerosis, who received a cadaveric kidney transplant in 2007. There were no relevant intercurrences until May 2015, when he presented with nephrotic range proteinuria (± 4 g/d). A graft biopsy was performed and it did not show any significant pathological changes. In September, he developed a full nephrotic syndrome (proteinuria 19 g/d) and a graft biopsy was repeated. CG features were evident with a rich immunofluorescence. Antinuclear antibodies (ANA) and anti-double-stranded DNA (anti-dsDNA) antibodies were positive; the remaining immunologic study was normal. Viral markers for HIV, hepatitis C virus (HCV), and hepatitis B virus (HBV) were negative. The patient was treated with corticosteroid pulses and plasmapheresis (seven treatments). A rapid deterioration of kidney function was seen and he became dialysis dependent. He was discharged with a low-dose immunosuppressive treatment. In October, he was hospitalized with diffuse alveolar hemorrhage (DAH). The auto-immune study was repeated, revealing complement consumption and positive titers of ANA and Anti-dsDNA antibodies. Anti-neutrophil cytoplasmic antibodies (ANCAs) and antiglomerular basement membrane antibody (anti-GBM) were negative. Treatment with intravenous corticosteroids, plasmapheresis, and human immunoglobulin was ineffective and the outcome was fatal. CONCLUSION: This case report highlights the possible association of CG and SLE. To our knowledge, it is the first case of SLE presenting with CG and DAH, with the singularity of occurring in a kidney transplant recipient receiving immunosuppression.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationTransplant Proc. 2017 May;49(4):913-915.pt_PT
dc.identifier.doi10.1016/j.transproceed.2017.03.007pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.4/2279
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.subjectHemorragiapt_PT
dc.subjectLupus Eritematoso Sistémicopt_PT
dc.subjectNefrite Lúpicapt_PT
dc.subjectComplicações Pós-operatóriaspt_PT
dc.titleWhat Can We Do When All Collapses? Fatal Outcome of Collapsing Glomerulopathy and Systemic Lupus Erythematosus With Diffuse Alveolar Hemorrhage: Case Reportpt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage915pt_PT
oaire.citation.issue4pt_PT
oaire.citation.startPage913-915pt_PT
oaire.citation.titleTransplantation proceedingspt_PT
oaire.citation.volume49pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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