Latent glomerulonephritis often has an insidious onset or may suddenly present with gross hematuria without other urinary system symptoms. Renal function is mostly normal. The main clinical manifestation is urinary abnormalities, which can be divided into the following three forms:
1. Asymptomatic hematuria
Patients are mostly young adults with no clinical symptoms or signs. Sometimes, microscopic glomerular hematuria is found during physical examination, which is persistent or recurrent. Some patients may experience transient gross hematuria after strenuous exercise, high fever, infection, alcohol consumption, etc., which quickly disappears in a short period. During the episode of hematuria, lumbar pain may occur. Due to the recurrent episodes, it is also called benign recurrent hematuria. This type is more common in IgA nephropathy and can also be seen in non-IgA mesangial proliferative glomerulonephritis, focal segmental glomerulonephritis, and thin basement membrane nephropathy.
2. Asymptomatic hematuria and proteinuria
Patients of this type have episodic hematuria, while proteinuria persists. During the episode of hematuria, proteinuria also worsens. After the hematuria subsides, proteinuria decreases accordingly, making the condition more severe than simple hematuria. Due to the absence of hypertension, edema, and renal function decline, patients often fail to seek timely medical attention, leading to early misdiagnosis. This type is more common in mesangial proliferative glomerulonephritis, focal glomerulosclerosis, and IgA nephropathy.
3. Asymptomatic proteinuria
This condition commonly occurs in young males, presenting with persistent proteinuria (although urine protein levels fluctuate with each test, they are always positive). The quantitative urine protein is usually below 2g/d, mainly composed of albumin. Urine sediment is normal, without edema, hypertension, and other clinical manifestations. Renal function is normal, and blood biochemical tests are often normal. The disease can last for many years with a good prognosis. There are no clear pathological changes in histology; it may also be the early manifestation of different types of glomerular diseases, such as membranous nephropathy, mesangial proliferative glomerulonephritis, minimal change nephrotic syndrome, focal segmental glomerulosclerosis, and even early manifestations of certain IgA nephropathy.