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Xanthogranulomatous pyelonephritis (XGPN) is a rare, severe chronic renal inflammation causing diffuse parenchymal destruction.
肾内科Nonobstructive chronic pyelonephritis (N11.801) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Metabolic-abnormality-related chronic interstitial nephritis (N11.800x003) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being
Immune-related chronic interstitial nephritis (N11.800x002) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Chronic tubulointerstitial nephritis, other (N11.800) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Chronic obstructive pyelonephritis (N11.100) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Reflux pyelonephritis (N11.000x001) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Nonobstructive chronic pyelonephritis related to reflux (N11.000) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Acute pyelonephritis is acute pyogenic inflammation of the renal pelvis, calyces and parenchyma caused by bacteria, course under 6 months. Two routes: ① ascending infection, bacteria from ureter to pelvis then parenchyma; 70% arise this way. ② hematogenou
肾内科Acute interstitial nephritis (N10.x01) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Acute infectious interstitial nephritis (N10.x00x003) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Acute pyelitis (N10.x00x002) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Acute tubulointerstitial nephritis (N10.x00) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Dent disease (N07.900x002) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Hereditary nephritis (Alport syndrome, AS) is a hereditary glomerular basement membrane disease mainly presenting as hematuria, progressive renal decline, sensorineural deafness and ocular abnormalities, caused by mutation of the gene encoding type IV col
肾内科Hereditary nephropathy, unclassifiable elsewhere (N07.900) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Hereditary nephropathy, other, unclassifiable elsewhere (N07.800) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introduction is being compiled.
Hereditary nephropathy with diffuse crescentic glomerulonephritis, unclassifiable elsewhere (N07.700) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed patholog
Hereditary nephropathy with dense deposit disease, unclassifiable elsewhere (N07.600) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed pathological introductio
Hereditary nephropathy with diffuse mesangiocapillary glomerulonephritis, unclassifiable elsewhere (N07.500) is a disease included in the National Health Commission's 'Disease Classification and Codes, National Clinical Version 2.0' standard; a detailed p
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