Chronic Glomerulonephritis Clinical Presentation
- Author: Moro O Salifu, MD, MPH, FACP; Chief Editor: Vecihi Batuman, MD, FACP, FASN more...
History
The history should focus on cause-specific symptoms to determine the causes of CKD (if unknown) and on symptoms related to uremia to determine if renal replacement therapy is needed.
- Cause-specific history: Obtain a cause-specific history so that further workup and management of the disease (if systemic) can be planned.
- Uremia-specific history
- The following symptoms suggest uremia:
- Weakness and fatigue
- Loss of energy, appetite, and weight
- Pruritus
- Early morning nausea and vomiting
- Change in taste sensation
- Reversal in sleep pattern (ie, sleepiness in daytime, wakefulness at night)
- Peripheral neuropathy
- Seizures
- Tremors
- The presence of edema and hypertension suggests volume retention.
- Dyspnea or chest pain that varies with position suggests fluid overload and pericarditis, respectively.
- Leg cramps may suggest hypocalcemia or other electrolyte abnormalities.
- Weakness, lethargy, and fatigue may be due to anemia.
- The following symptoms suggest uremia:
Physical
Cause-specific physical examination findings are discussed in articles on the specific causes. See Causes for links to such articles.
- Uremia-specific findings
- Hypertension
- Jugular venous distension (if severe volume overload is present)
- Pulmonary rales (if pulmonary edema is present)
- Pericardial friction rub in pericarditis
- Tenderness in the epigastric region or blood in the stool (possible indicators for uremic gastritis or enteropathy)
- Decreased sensation and asterixis (indicators for advanced uremia)
Causes
The progression from acute glomerulonephritis to chronic glomerulonephritis is variable. Whereas complete recovery of renal function is the rule for patients with poststreptococcal glomerulonephritis, several other glomerulonephritides, such as immunoglobulin A (IgA) nephropathy, often have a relatively benign course and many do not progress to ESRD.
- Rapidly progressive glomerulonephritis or crescentic glomerulonephritis: Approximately 90% of patients progress to ESRD within weeks or months.
- Focal segmental glomerulosclerosis: Approximately 80% of patients progress to ESRD in 10 years. Patients with the collapsing variant, which is termed malignant focal segmental glomerulosclerosis, have a more rapid progression. This form may be idiopathic or related to HIV infection.
- Membranous nephropathy: Approximately 20-30% of patients with membranous nephropathy progress to chronic renal failure (CRF) and ESRD in 10 years.
- Membranoproliferative glomerulonephritis: Approximately 40% of patients with membranoproliferative glomerulonephritis progress to CRF and ESRD in 10 years.[2]
- IgA nephropathy: Approximately 10% of patients with IgA nephropathy progress to CRF and ESRD in 10 years.[3]
- Poststreptococcal glomerulonephritis: Approximately 1-2% of patients with poststreptococcal glomerulonephritis progress to CRF and ESRD. Older children who present with crescentic glomerulonephritis are at greatest risk.
- Lupus nephritis: Overall, approximately 20% of patients with lupus nephritis progress to CRF and ESRD in 10 years; however, patients with certain histologic variants (eg, class IV) may have a more rapid decline.
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