Approach to the Patient with Glomerular Disease

2018 ◽  
Author(s):  
Richard J. Glassock ◽  
An S De Vriese ◽  
Fernando C. Fervenza

Glomerular diseases of the kidneys are associated with a limited array of clinical syndromes, including asymptomatic hematuria and/or proteinuria, acute nephritis, nephrotic syndrome, rapidly progressive glomerulonephritis, and chronic glomerulonephritis. The specific diseases that underlie these syndromes are numerous and heterogeneous. Broadly, they may be divided into primary and secondary disorders depending on whether the kidneys are the sole organs affected or whether other organ systems are also involved in the disease processes. A systematic approach involving a careful history, physical examination, assessment of renal function, and urinalysis (composition and microscopy) and protein excretion, combined with biochemical and serologic testing, can provide important clues to diagnosis and prognosis. Renal biopsy is often required for a complete and accurate diagnosis as well as a prognosis and therapeutic decision making. This review contains 4 figures, 6 tables and 92 references Key words: glomerular filtration rate, glomerulonephritis, hematuria, nephrotic syndrome, proteinuria, renal biopsy, serum complement

2018 ◽  
Author(s):  
Richard J. Glassock ◽  
An S De Vriese ◽  
Fernando C. Fervenza

Glomerular diseases of the kidneys are associated with a limited array of clinical syndromes, including asymptomatic hematuria and/or proteinuria, acute nephritis, nephrotic syndrome, rapidly progressive glomerulonephritis, and chronic glomerulonephritis. The specific diseases that underlie these syndromes are numerous and heterogeneous. Broadly, they may be divided into primary and secondary disorders depending on whether the kidneys are the sole organs affected or whether other organ systems are also involved in the disease processes. A systematic approach involving a careful history, physical examination, assessment of renal function, and urinalysis (composition and microscopy) and protein excretion, combined with biochemical and serologic testing, can provide important clues to diagnosis and prognosis. Renal biopsy is often required for a complete and accurate diagnosis as well as a prognosis and therapeutic decision making. This review contains 4 figures, 6 tables and 92 references Key words: glomerular filtration rate, glomerulonephritis, hematuria, nephrotic syndrome, proteinuria, renal biopsy, serum complement


2002 ◽  
Vol 130 (9-10) ◽  
pp. 323-328 ◽  
Author(s):  
Radovan Bogdanovic ◽  
Milos Kuzmanovic ◽  
Jasmina Markovic-Lipkovski ◽  
Milos Ognjanovic ◽  
Dragan Micic ◽  
...  

Several reports have documented various forms of glomerular diseases in adults with myelodysplastic syndromes (MDS), but similar reports in children are lacking. We describe two children with MDS-associated with steroid-responsive nephrotic syndrome (NS). Patient 1, who had MDS with myelofibrosis, presented also hepatosplenomegaly, pancytopenia, chronic hepatitis, moderate proteinuria, hypocomplementemia and elevated ANA titer. During initial prednisone treatment proteinuria markedly diminished and partial but transient haematological improvement occurred. Relapse subsequently occurred that was manifested by overt NS and pancytopenia. High doses of prednisolone led to remission of the renal disease but haematological remission did not occur. Persisting pancytopenia and repeated infections terminated in sepsis, two years after the onset of MDS. Patient 2, who had refractory anemia with clonal monosomy 19, manifested bowel disease, hepatospleno- megaly, anaemia and non-organic specific autoantibodies. Prednisone led to both clinical and haematological remission. Haematologic disease relapsed 12 months later, when nephrotic-range proteinuria, haematuria and mild azotaemia were also found. Corticosteroid treatment led to long-lasting renal and haematologic remission, maintained by a small dosage of prednisone. In both patients renal biopsy findings were consistent with those seen in idiopathic NS. A Medline search disclosed 16 cases of glomerulopathy in the course of MDS in adult patients. Clinical features included NS, usually accompanied by renal insufficiency with either acute, chronic, or rapidly progressive glomerulonephritis. On biopsy, membranous nephropathy, crescentic or mesangial proliferative glomerulonephritis and AL amyloidosis, were found. We conclude: (1) that glomerular disease may be present and should be searched for in patients with MDS; (2) that MDS can be added to the list of rare conditions associated with corticosteroid-responsive NS in children.


2018 ◽  
Vol 2018 ◽  
pp. 1-9 ◽  
Author(s):  
Mayerly Prada Rico ◽  
Carmen Inés Rodríguez Cuellar ◽  
Monica Fernandez Hernandez ◽  
Luz Stella González Chaparro ◽  
Olga Lucía Prado Agredo ◽  
...  

Introduction. Renal biopsy is the principal instrument to evaluate the diagnosis and prognosis of children with kidney disease. There are relatively few studies establishing epidemiology of its findings in the pediatric population. Methods. A descriptive study was conducted to describe characteristics of pediatric patients who had undergone a renal biopsy over the last 10 years in a national reference center, trying to accomplish an etiopathogenic approach of biopsy findings. Results. 241 patients were included. Most frequent indications were nephrotic syndrome (34.1%) and systemic disease with renal involvement (30.2%). The most prevalent biopsy diagnosis was glomerulonephritis (44%) and among these patients, glomerulonephritis mediated by immune complexes was the most frequent pathogenic type (90.5%). When the biopsy was indicated for proteinuria plus hematuria and systemic disease with renal involvement, the most frequent biopsy diagnosis was glomerulonephritis (60 and 85%, respectively). For isolated hematuria, the predominant biopsy diagnosis was inherited diseases of the glomerular basement membrane (70%) and for nephrotic syndrome, podocytopathy (82%). Glomerulonephritis was more frequent in patients older than 10 yrs (65%) and the rate of postbiopsy major complications was low (1.2%). Conclusion. Immune complex glomerulonephritis was the most frequent histological finding, differing from previous reports. To our knowledge this is the first description that classifies biopsy findings according to the probable pathogenic mechanism.


2020 ◽  
Vol 21 (1) ◽  
Author(s):  
Gaofei Yan ◽  
Guanzhi Liu ◽  
Xuefei Tian ◽  
Lifang Tian ◽  
Hao Wang ◽  
...  

Abstract Background Minimal change disease (MCD) is one of the major causes of nephrotic syndrome (NS). A confirmed MCD diagnosis mainly depends on renal biopsy at present, which is an invasive procedure with many potential risks. The overall incidence of complications caused by renal biopsy procedures has been reported as approximately 11 and 6.6% outside and within China, respectively. Unfortunately, there is currently no noninvasive procedure or practical classification method for distinguishing MCD from other primary glomerular diseases available. Method A total of 1009 adult patients who underwent renal biopsy between January 2017 and November 2019 were enrolled in this study. Twenty-five parameters extracted from patient demographics, clinical manifestations, and laboratory test results were statistically analysed. LASSO regression analysis was further performed on these parameters. The parameters with the highest area under the curve (AUC) were selected and used to establish a logistic diagnostic prediction model. Results Of the 25 parameters, 14 parameters were significantly different (P < 0.05). MCD patients were mostly younger (36 (22, 55) vs. 41 (28.75, 53)) and male (59% vs. 52%) and had lower levels of diastolic blood pressure (DBP) (79 (71, 85.5) vs. 80 (74, 89)) and IgG (5.42 (3.17, 6.36) vs. 9.38 (6.79, 12.02)) and higher levels of IgM (1.44 (0.96, 1.88) vs. 1.03 (0.71, 1.45)) and IgE (160 (46.7, 982) vs. 47.3 (19, 126)) than those in the non-MCD group. Using the LASSO model, we established a classifier for adults based on four parameters: DBP and the serum levels of IgG, IgM, IgE. We were able to clinically classify adult patients with NS into MCD and non-MCD using this model. The validation accuracy of the logistic regression model was 0.88. A nomogram based on these four classifiers was developed for clinical use that could predict the probability of MCD in adult patients with NS. Conclusions A LASSO model can be used to distinguish MCD from other primary glomerular diseases in adult patients with NS. Combining the model and the nomogram potentially provides a novel and valuable approach for nephrologists to diagnose MCD, avoiding the complications caused by renal biopsy.


2021 ◽  
Vol 22 (1) ◽  
Author(s):  
Shuai-Shuai Shi ◽  
Xian-Zu Yang ◽  
Xiao-Ye Zhang ◽  
Hui-Dan Guo ◽  
Wen-Feng Wang ◽  
...  

Abstract Background Horseshoe kidney (HSK) is a common congenital defect of the urinary system. The most common complications are urinary tract infection, urinary stones, and hydronephrosis. HSK can be combined with glomerular diseases, but the diagnosis rate of renal biopsy is low due to structural abnormalities. There are only a few reports on HSK with glomerular disease. Here, we have reported a case of PLA2R-positive membranous nephropathy occurring in a patient with HSK. Case presentation After admission to the hospital due to oedema of both the lower extremities, the patient was diagnosed with nephrotic syndrome due to abnormal 24-h urine protein (7540 mg) and blood albumin (25 g/L) levels. Abdominal ultrasonography revealed HSK. The patient’s brother had a history of end-stage renal disease due to nephrotic syndrome. Therefore, the patient was diagnosed with PLA2R-positive stage II membranous nephropathy through renal biopsy under abdominal ultrasonography guidance. He was administered adequate prednisone and cyclophosphamide, and after 6 months of treatment, urinary protein excretion levels significantly decreased. Conclusion The risk and difficulty of renal biopsy in patients with HSK are increased due to structural abnormalities; however, renal biopsy can be accomplished through precise positioning with abdominal ultrasonography. In the literature, 20 cases of HSK with glomerular disease have been reported thus far. Because of the small number of cases, estimating the incidence rate of glomerular diseases in HSK is impossible, and the correlation between HSK and renal pathology cannot be stated. Further studies should be conducted and cases should be accumulated to elucidate this phenomenon.


Nephrology is the study of the kidney and its diseases. This chapter describes the aetiology, presentation, and management of the main clinical syndromes of acute kidney injury, chronic kidney disease, glomerular diseases causing nephrotic syndrome, and glomerulonephritis, and the different modalities of renal replacement therapy: haemodialysis, peritoneal dialysis, renal transplantation, and conservative care. Practical skills of fluid assessment and intravenous fluid administration are discussed, as well as procedures including renal biopsy, dialysis line insertion, and arteriovenous fistula creation. Key components of the ‘renal examination’ and renal investigations are summarized. Renal diseases in the setting of multisystem disorders such as myeloma, rhabdomyolysis, and liver disease are also described.


2020 ◽  
Vol 154 (Supplement_1) ◽  
pp. S68-S69
Author(s):  
L Ding ◽  
J Tomaszewski ◽  
L Liu ◽  
B Murray

Abstract Introduction/Objective Lupus podocytopathy (LP), featured by nephrotic syndrome, is a unique subtype of lupus nephritis that mimics minimal change disease or primary focal segmental glomerulosclerosis (FSGS) on renal biopsy with diffuse podocyte foot process effacement and no capillary-loop immune deposits. LP usually presents on a background of ISN/RPS class I or class II lupus nephritis, and very rarely may present without immune deposits. Diagnosis of LP, when confounded by other glomerular diseases associated with nephrotic syndrome, can be very challenging and requires thorough clinical and pathology correlations. Methods Here we report a case of LP in a patient with nephrotic syndrome and multiple comorbidities affecting kidneys. A 24-year-old female with type-I diabetes, psoriasis, and intermittent arthritis/rash of unknown etiology, presented with abrupt onset of nephrotic proteinuria attributed to recent low dose prednisone therapy, and renal insufficiency. A renal biopsy showed nodular glomerulosclerosis and FSGS. No immune deposits were identified by immunofluorescence or electron microscopy. Ultrastructurally there was also diffuse glomerular basement membrane thickening and over 90% podocyte foot process effacement. With no established systemic lupus erythematosus (SLE), the case was initially diagnosed as diabetic nephropathy with coexistent FSGS as the etiologies for nephrotic proteinuria, and the patient was put on ACEI and diuretics. However, massive proteinuria persisted, and the patient also developed pancytopenia. Serology concurrent with the biopsy came out later showing positive autoantibodies against dsDNA, Smith, and Histone. With continued worsening of creatinine, a renal biopsy was repeated revealing essentially similar findings to the first biopsy. Results Integrating the serology results and clinical presentation, SLE was favored. The pathology findings were re- evaluated and considered to be most consistent with LP and coexistent diabetic nephropathy, with FSGS either a component of LP or an independent lesion secondary to diabetes or hypertension. The patient was started with high dose prednisone at 60 mg/day. One month later, her proteinuria, serum creatinine, pancytopenia, skin rash, and arthritis were all significantly improved. Conclusion LP can be easily masked by coexistent glomerular diseases. Sufficient awareness of the entity is necessary for the appropriate diagnosis and treatment.


1977 ◽  
Author(s):  
T. Abe

Coagulation and fibrinolysis system have been imagined to have some pathogenic influence on various kinds of nephropathy. Our study group on the clinical effect of urokinase (UK) administration to nephropathies applied this material to 106 patients with acute and chronic glomerulonephritis, nephrotic syndreome with different causes and renal failure together with 25 control subjects. From 120×104 to 900×104 units of UK was given in ten to twenty-two days solely or together with corticosteroid, dipyridamole, Clofibrate, furosemide, spironolactone, -methyl-dopa, indomethacine, cyclophosphamide, azathiopurine and so on. Heparin was also employed to some control or comparison cases in daily doses of five to fifteen thousand units.Daily amounts of urine, urinary protein, phenolsulphon-phthalein excretion, creatinine clearance were found responsive to UK administration and their beneficial changes were realized statistically in cases of chronic glomerulonephritis (22 cases in 47), rapidly progressive glomerulonephritis (2 in 5), nephrotic syndrome (5 in 35) and some others showed only decrease of urinary protein. As for the cases of renal failure, no definite coclusion was drawn. Only a few cases gave some clues of side effect such as headache, nausea and aggravated hematuria. Histological classification was also tried to find that the proliferative type was most responsive to this treatment.


2020 ◽  
Vol 35 (Supplement_3) ◽  
Author(s):  
Vincenzo L'Imperio ◽  
Gisella Vischini ◽  
Fabio Pagni ◽  
Pietro Manuel Ferraro

Abstract Background and Aims ANCA-associated vasculitis is the most common cause of rapidly progressive glomerulonephritis (GN) and can lead to ESRD or death, even after aggressive immunosuppressive therapies (Jones et al, N Engl J Med, 363(2010), 211-220). The histological assessment of renal tissue can help in predicting the outcome and a 4-tiered classification based on glomerular lesions has been proposed to stratify these cases (Berden et al, J Am Soc Nephrol, 21(2010), 1628-1636). Subsequent studies, however, failed to confirm its predictive value (Tanna et al, Nephrol Dial Transplant, 30(2015), 1185-1192), stressing the need of new prognostic markers of the disease. The present study investigates whether additional histological features can improve the performance of the current classification in predicting the outcome of these patients. Method A retrospective series of biopsy-proven paucimmune crescentic GN has been collected between January 2012 and June 2018 from two Italian centers (San Gerardo Hospital, Monza and Fondazione Policlinico Universitario A. Gemelli IRCCS, Roma). After the exclusion of patients with negative/unavailable serum ANCA testing, lacking clinical data, less than 12 months of follow-up, less than 5 glomeruli per biopsy and coexisting glomerular diseases, a final cohort of 52 cases was selected. Demographic and clinical data at the time of the diagnosis are reported in Figure, panel A. Renal biopsies have been reviewed by two experts in renal pathology and scored for multiple glomerular, tubulointerstitial and vascular lesions, as well as classified following the 4-tiered schema. The outcome of interest was time to need for RRT or death, whatever occurred first. Cox proportional hazards regression models were constructed with time to composite event, loss to follow-up or censoring (06/30/2019). Time at risk started at the date of renal biopsy. Histologic predictors were collapsed into binary variables (0-1 = low; 2-3 = high) and tested in univariate models, with the association expressed as hazard ratios (HRs) and 95% confidence intervals (CI); those showing a significant association with the outcome ( Figure, panel B) were included in a multivariable model together with a variable representing the Berden class. The prognostic performance of models including only the Berden class or the Berden class plus additional predictors was assessed using Harrell’s c-statistic. Results During a follow-up of 1,828 person-months, 13 composite events developed (8 deaths, 5 RRT), corresponding to an incidence rate of 7.1 (95% CI 4.2, 12.2) per 1,000 person-months. Of the tested predictors, Bowman’s capsule rupture (BCR, Figure, panel C) was significantly associated with the outcome (p = 0.023). Compared with a model including only Berden class (c = 0.67), the addition of this parameter significantly improved the prognostic performance (c = 0.76). In the multivariable model including Berden class, BCR remained significantly associated with the outcome (HR 3.61, 95% CI 1.15, 11.34; p = 0.028). Conclusion The present study demonstrated an improved performance of Berden classification in predicting patients’ outcome after the implementation of BCR. This can allow a better stratification of these cases, leading to tailored therapeutic approaches. Further investigations on a larger prospective cohort are required to confirm these results.


1970 ◽  
Vol 10 (1) ◽  
pp. 34-35
Author(s):  
Md Julhash Uddin ◽  
Kazi Monjurul Alam ◽  
Fazle Rabbi Mohammed ◽  
Md Billal Alam

Hypothyroidism may coexist with different renal pathologies. Several cases of glomerular diseases have been associated with thyroid diseases of which the most frequent lesion described is membranous glomerulopathy, presented as a nephrotic syndrome. Although pseudohypothyroidism is well-known in nephrotic pathophysiology, actual hypothyroidism are uncommon. We report here an unusual association of hypothyroidism due to Hashimoto's disease with nephrotic syndrome due to membranoproliferative glumerulonephritis which were revealed by hormone & antibody assay and renal biopsy respectively.   doi:10.3329/jom.v10i1.2003 J Medicine 2009; 10: 34-35


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