Renal transplantation in amyloidosis and MIDD.
نویسندگان
چکیده
Amyloidosis and monoclonal immunoglobulin deposition disease, though rare entities, can wreak havoc on the architecture and functioning of the kidneys. These diseases have a predilection to cause severe renal dysfunction leading to end stage renal disease (ESRD). In recent years, the available treatments for these diseases have expanded and afflicted patients are living longer, but with advanced kidney disease. Because of the complex nature of the pathophysiology and treatment of these diseases, it can be very challenging for a clinician to determine whether or not it is appropriate to refer an affected individual for kidney transplantation.
منابع مشابه
Renal monoclonal immunoglobulin deposition disease: a report of 64 patients from a single institution.
BACKGROUND AND OBJECTIVES To better define the clinical-pathologic spectrum and prognosis of monoclonal immunoglobulin deposition disease (MIDD), this study reports the largest series. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS Characteristics of 64 MIDD patients who were seen at Mayo Clinic are provided. RESULTS Of 64 patients with MIDD, 51 had light chain deposition disease, 7 had heav...
متن کاملScreening and differential diagnosis of renal light chain-associated diseases.
BACKGROUND Renal involvement in the light chain-associated diseases multiple myeloma (MM), amyloidosis (AL) and monoclonal immune position disease (MIDD) is common and differential diagnosis usually requires renal biopsy. The aim of this study was to investigate if noninvasive methods are viable to identify and differentiate between the various types of kidney diseases. PATIENTS AND METHODS A...
متن کاملCombined immunoglobulin G kappa nephropathy: monoclonal immunoglobulin deposition disease and proximal tubulopathy: monoclonal gammopathy of renal significance or smoldering multiple myeloma? Case report and review of literature
Multiple myeloma (MM) is consistently preceded by precursor states of monoclonal gammopathy of undetermined significance (MGUS) and smoldering multiple myeloma (SMM). These represent a continuum of progression of the tumor burden from the absence of symptoms or signs of end-organ damage towards full-blown symptomatic disease. MGUS, by definition presenting by monoclonal gammopathy without end o...
متن کاملAA amyloidosis in the renal allograft: a report of two cases and review of the literature
AA amyloidosis is a disorder characterized by the abnormal formation, accumulation and systemic deposition of fibrillary material that frequently involves the kidney. Recurrent AA amyloidosis in the renal allograft has been documented in patients with tuberculosis, familial Mediterranean fever, ankylosing spondylitis, chronic pyelonephritis and rheumatoid arthritis. De novo AA amyloidosis is ra...
متن کاملHereditary renal amyloidosis associated with a novel mutation in the apolipoprotein AII gene.
Sir, Hereditary amyloidosis is a rare disorder associated with mutations encoding seven proteins: transthyretin, apolipoproteins AI and AII, gelsolina, cystatin C, lysozyme and fibrinogen A. We report a case of renal amyloidosis affecting six members of a family, associated with a novel non-stop mutation in the apolipoprotein AII gene. A 42-year-old Caucasian male with nephrotic syndrome and re...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- Frontiers in bioscience
دوره 7 شماره
صفحات -
تاریخ انتشار 2015