Natural History and Prognostic Factors of IgA Nephropathy Presented with Isolated Microscopic Hematuria in Chinese Patients

2007 ◽  
Vol 106 (4) ◽  
pp. c157-c161 ◽  
Author(s):  
Peicheng Shen ◽  
Liqun He ◽  
Yi Li ◽  
Yunman Wang ◽  
May Chan
Keyword(s):  
Prognostic Factors ◽  
Natural History ◽  
Iga Nephropathy ◽  
Microscopic Hematuria ◽  
Chinese Patients ◽  
Isolated Microscopic Hematuria

Etiologies of asymptomatic microscopic hematuria in children – systematic review of 1092 subjects

Diagnosis ◽  
2015 ◽  
Vol 2 (4) ◽  
pp. 211-216 ◽  
Author(s):  
Michelle Clark ◽  
Stephen Aronoff ◽  
Michael Del Vecchio
Keyword(s):  
Systematic Review ◽  
Differential Diagnosis ◽  
Basement Membrane ◽  
Iga Nephropathy ◽  
Microscopic Hematuria ◽  
Data Bases ◽  
Multiple Data ◽  
Thin Basement Membrane Disease ◽  
Isolated Microscopic Hematuria ◽  
Evidenced Based

AbstractAsymptomatic microscopic hematuria is common in children. No systematic review providing an evidence based approach for the differential diagnosis of these children has been performed.Multiple data bases were search. The PRISMA criteria were followed. Data regarding the etiology of the hematuria were extracted using a standardized extraction tool. Seven studies encompassing 1092 children (857 with isolated microscopic hematuria and 235 with combined microscopic hematuria and proteinuria), comprise this review. A total 42.4% of isolated microscopic and 81.3% of microscopic hematuria and proteinuria subjects had identified etiologies. Thin basement membrane nephritis (15.2%), IgA nephropathy (10.4%), and hypercalciuria without nephrolithiasis (7.7%), were the most common etiologies among children with isolated microscopic hematuria. IgA nephropathy (44.3%), thin basement membrane disease (12.8%), and mesangial proliferative glomerulosclerosis (8.9%) were the most common etiologies among children with combined microscopic hematuria and proteinuria.The present study provides an evidenced based resource, based on a systematic review, for the differential diagnosis of asymptomatic hematuria in children. Additionally, these observations suggest that children with isolated microscopic hematuria should be followed for persistence of hematuria or the development of proteinuria. Children with combined microscopic hematuria and proteinuria should be comprehensively evaluated.

scholarly journals Natural History and Renal Pathology in Patients with Isolated Microscopic Hematuria

2009 ◽  
Vol 24 (4) ◽  
pp. 356 ◽  
Author(s):  
Byung Soo Kim ◽  
Yong Kyun Kim ◽  
Young Shin Shin ◽  
Young Ok Kim ◽  
Ho Cheol Song ◽  
...  
Keyword(s):  
Natural History ◽  
Renal Pathology ◽  
Microscopic Hematuria ◽  
Isolated Microscopic Hematuria

Prevalence of isolated microscopic hematuria and IgA nephropathy in asymptomatic pregnant women

2004 ◽  
Vol 6 (2) ◽  
pp. A5
Author(s):  
K.Y. Chung ◽  
C.C. Szeto ◽  
K.F. To ◽  
F.M. Lai ◽  
K.M. Chow ◽  
...  
Keyword(s):  
Pregnant Women ◽  
Iga Nephropathy ◽  
Microscopic Hematuria ◽  
Isolated Microscopic Hematuria

Epidemiology and risk factors for progression in Chinese patients with IgA nephropathy

2020 ◽  
Author(s):  
Yang Liu ◽  
Wei Wei ◽  
Chengyuan Yu ◽  
Li Xing ◽  
Mingao Wang ◽  
...  
Keyword(s):  
Risk Factors ◽  
Iga Nephropathy ◽  
Chinese Patients

scholarly journals A novel prognostic model for angioimmunoblastic T-cell lymphoma: A retrospective study of 55 cases

2021 ◽  
Vol 49 (5) ◽  
pp. 030006052110132
Author(s):  
Jie Sun ◽  
Sha He ◽  
Hong Cen ◽  
Da Zhou ◽  
Zhe Li ◽  
...  
Keyword(s):  
Prognostic Factors ◽  
T Cell ◽  
Prognostic Model ◽  
Proportional Hazards Model ◽  
Cell Lymphoma ◽  
Initial Diagnosis ◽  
Cox Proportional Hazards Model ◽  
T Cell Lymphoma ◽  
Chinese Patients ◽  
Angioimmunoblastic T Cell Lymphoma

Objective To explore prognostic factors and develop an accurate prognostic prediction model for angioimmunoblastic T-cell lymphoma (AITL). Methods Clinical data from Chinese patients with newly diagnosed AITL were retrospectively analysed. Overall survival (OS) and progression-free survival (PFS) were estimated using Kaplan-Meier method survival curves; prognostic factors were determined using a Cox proportional hazards model. The sensitivity and specificity of the predicted survival rates were compared using area under the curve (AUC) of receiver operating characteristic (ROC) curves. Results The estimated 5-year OS and PFS of 55 eligible patients with AITL were 22% and 3%, respectively. Multivariate analysis showed that the presence of pneumonia, and serous cavity effusions at initial diagnosis were significant prognostic factors for OS. Based on AUC ROC values, our novel prognostic model was superior to IPI and PIT based models and suggested better diagnostic accuracy. Conclusions Our prognostic model based on pneumonia, and serous cavity effusions at initial diagnosis enabled a balanced classification of AITL patients into different risk groups.

Clinical Features and Prognosis of Adult-onset Still’s Disease: 61 Cases from China

2009 ◽  
Vol 36 (5) ◽  
pp. 1026-1031 ◽  
Author(s):  
TING ZENG ◽  
YU-QIONG ZOU ◽  
MEI-FANG WU ◽  
CHENG-DE YANG
Keyword(s):  
Prognostic Factors ◽  
Clinical Features ◽  
Chinese Patients ◽  
Adult Onset Still’S Disease ◽  
Disease Course ◽  
Adult Onset ◽  
Still’S Disease ◽  
Laboratory Findings ◽  
Still's Disease ◽  
Adult Onset Still's Disease

Objective.To describe the onset, clinical features, prognostic factors, and treatment of adult-onset Still’s disease (AOSD) in cases from China.Methods.Sixty-one Chinese patients with AOSD were analyzed retrospectively.Results.Common clinical features were fever (100.0%), rash (88.5%), and arthritis (82.0%). The laboratory findings were as follows: leukocytosis (83.6%), increased erythrocyte sedimentation rate (100.0%), elevated transaminase concentrations (23.0%), elevated ferritin levels (79.6%), negative antinuclear antibody (88.5%), and negative rheumatoid factor (88.5%). Of the 61 patients, 44.3% exhibited a monocyclic disease pattern, 29.5% experienced disease relapse at least once, 16.4% exhibited chronic articular course, and 9.8% died; most deaths were due to pulmonary infection and respiratory failure. Based on the disease course, we divided the 61 patients into 2 groups: those with favorable outcome (cyclic disease course, n = 45) and unfavorable outcome (chronic disease course or death, n = 16). We analyzed the prognostic factors for the 2 groups, and found that pleuritis, interstitial pneumonia, elevated ferritin levels, and failure of fever to subside after 3 days of prednisolone at 1 mg/kg/day were unfavorable prognostic factors for patients with AOSD.Conclusion.Patients with AOSD had complex symptoms with no specific laboratory findings. Our results indicate that AOSD is not a relatively benign disease, especially in cases that are refractory to high doses of prednisone.

scholarly journals Renal Pathology in Two Chinese Patients with Concomitant IgG4-Related Disease (IgG4-RD) and IgA Nephropathy (IgAN)

2015 ◽  
Vol 17 (2) ◽  
pp. S36
Author(s):  
C.K.Y. Poon ◽  
H.L. Tang ◽  
Y.F. Mak ◽  
H.M. Cheng ◽  
L.Y. Wong ◽  
...  
Keyword(s):  
Iga Nephropathy ◽  
Renal Pathology ◽  
Chinese Patients ◽  
Related Disease ◽  
Igg4 Related Disease

scholarly journals Guillain-Barré Syndrome: Natural history and prognostic factors: a retrospective review of 106 cases

BMC Neurology ◽  
2013 ◽  
Vol 13 (1) ◽  
Author(s):  
Inés González-Suárez ◽  
Irene Sanz-Gallego ◽  
Francisco Javier Rodríguez de Rivera ◽  
Javier Arpa
Keyword(s):  
Prognostic Factors ◽  
Natural History ◽  
Retrospective Review ◽  
Guillain Barre Syndrome ◽  
Guillain Barré Syndrome ◽  
Guillain Barré
Sign in / Sign up

Export Citation Format

Share Document