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非常漂亮的电镜照片,从电镜照片上看病变轻微,光镜及免疫荧光无明显病变,需要考虑的诊断有:
1.薄基底膜病,尽管薄基底膜病常发生在儿童及青年,但也有成人患者的报道,临床主要表现为血尿,本例电镜感觉基底膜有点薄,需要进行测量有无薄基底膜病的可能
2。肾小球微小病变,不支持点,临床主要 以血尿为主,电镜下足突只是局灶性融合,未见弥漫性融合。
3.轻度系膜增生性肾小球肾炎,不支持点,电镜系膜细胞和基质增生不明显,荧光无免疫复合物的沉积
肾小球轻微病变是在实际工作中经常遇到,也是很难诊断的,希望能多得到QU老师指导!
Thank you for your comment. This is the case of thin basement membrane disease (薄基底膜病). There is mild subendothelial space widening ( I interpret it as chronic ischemic change), which makes GBM look thicker. I measured the thickness of GBM. The average glomerular basement membrane thickness is 218 nm, supporting the diagnosis of thin basement membrane nephropathy, though I routinely use 200 nm as cut-off point (mostly in young patients). In this case, I factored in the patient age and history of hypertension. Therefore, I lower down the threshold.
Your differential diagnosis is nice. The effacement of foot process is patchy, not enough for minimal change disease. I want to see diffuse effacement for that diagnosis. Why is the foot process focally effaced? Honestly, I don't know. If patient has no proteinuria, I ignore it. IF a patient has proteinuria, I MAY stretch the finding a little bit, suggesting to clinician that this could be unsampled focal segmental glomerulosclerosis (FSGS). But we have to keep it in mind that FSGS is a diagnosis of exclusion.
The other differential diagnosis is IgA nephropathy. A negative immunofluorescence and absence of dense deposits rule it out. Thank you again for your comment.