Collagenofibrotic glomerulopathy in a kidney transplant recipient: A first report
| dc.contributor.author | Jdiaa, Sara S. | |
| dc.contributor.author | Moeckel, Gilbert W. | |
| dc.contributor.author | K̈foury, Hala Kassouf | |
| dc.contributor.author | Medawar, Walid A. | |
| dc.contributor.author | Abu-Alfa, Ali K. | |
| dc.contributor.department | Internal Medicine | |
| dc.contributor.department | Pathology and Laboratory Medicine | |
| dc.contributor.department | Division of Nephrology and Hypertension | |
| dc.contributor.faculty | Faculty of Medicine (FM) | |
| dc.contributor.institution | American University of Beirut | |
| dc.date.accessioned | 2025-01-24T11:43:11Z | |
| dc.date.available | 2025-01-24T11:43:11Z | |
| dc.date.issued | 2021 | |
| dc.description.abstract | Collagenofibrotic glomerulopathy (CG) is a rare disease characterized by the deposition of collagen type 3 fibrils in the glomeruli. Patients may have proteinuria, hematuria, and/or renal dysfunction. CG is considered a progressive disease with variable rates of progression. The definitive diagnosis is made by electron microscopy with the presence of characteristic subendothelial and mesangial curved, comma-like, banded collagen type 3 fibers of 40–65 nm periodicity. We are reporting the first case of CG in a kidney transplant recipient with kidney disease of unknown cause. © 2020 The American Society of Transplantation and the American Society of Transplant Surgeons | |
| dc.identifier.doi | https://doi.org/10.1111/ajt.16399 | |
| dc.identifier.eid | 2-s2.0-85097957933 | |
| dc.identifier.pmid | 33206467 | |
| dc.identifier.uri | http://hdl.handle.net/10938/30227 | |
| dc.language.iso | en | |
| dc.publisher | Blackwell Publishing Ltd | |
| dc.relation.ispartof | American Journal of Transplantation | |
| dc.source | Scopus | |
| dc.subject | Clinical research/practice | |
| dc.subject | Genetics | |
| dc.subject | Kidney transplantation/nephrology | |
| dc.subject | Recurrent disease | |
| dc.subject | Collagen type iii | |
| dc.subject | Humans | |
| dc.subject | Kidney diseases | |
| dc.subject | Kidney glomerulus | |
| dc.subject | Kidney transplantation | |
| dc.subject | Proteinuria | |
| dc.subject | Azathioprine | |
| dc.subject | Calcineurin inhibitor | |
| dc.subject | Collagen type 3 | |
| dc.subject | Collagen type 4 | |
| dc.subject | Creatinine | |
| dc.subject | Cyclosporine | |
| dc.subject | Dipeptidyl carboxypeptidase inhibitor | |
| dc.subject | Mycophenolate mofetil | |
| dc.subject | Prednisone | |
| dc.subject | Tacrolimus | |
| dc.subject | Adult | |
| dc.subject | Albuminuria | |
| dc.subject | Article | |
| dc.subject | Capillary basement membrane | |
| dc.subject | Case report | |
| dc.subject | Clinical article | |
| dc.subject | Collagen fiber | |
| dc.subject | Collagen fibril | |
| dc.subject | Collagenofibrotic glomerulopathy | |
| dc.subject | Creatinine blood level | |
| dc.subject | Cytoplasm | |
| dc.subject | Diabetes mellitus | |
| dc.subject | Drug substitution | |
| dc.subject | Endothelium cell | |
| dc.subject | Epithelium cell | |
| dc.subject | Fibrosing alveolitis | |
| dc.subject | Follow up | |
| dc.subject | Glomerulopathy | |
| dc.subject | Glomerulus capillary | |
| dc.subject | Glucosuria | |
| dc.subject | Graft recipient | |
| dc.subject | Hematuria | |
| dc.subject | Human | |
| dc.subject | Hyaline degeneration | |
| dc.subject | Hypertension | |
| dc.subject | Immunohistochemistry | |
| dc.subject | Immunosuppressive treatment | |
| dc.subject | Iraqi | |
| dc.subject | Kidney biopsy | |
| dc.subject | Kidney cortex | |
| dc.subject | Leg edema | |
| dc.subject | Lymphocyte | |
| dc.subject | Male | |
| dc.subject | Mesangium | |
| dc.subject | Microscopy | |
| dc.subject | Plasma cell | |
| dc.subject | Priority journal | |
| dc.subject | Sclerosis | |
| dc.subject | Adverse event | |
| dc.subject | Glomerulus | |
| dc.subject | Kidney disease | |
| dc.title | Collagenofibrotic glomerulopathy in a kidney transplant recipient: A first report | |
| dc.type | Article |
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