The patient, a 48-year-old man, presents with facial puffiness, frothy urine, and hypertension. He has a history of hepatitis B infection and microscopic hematuria is noted on urine examination. The kidney biopsy shows a spike and dome pattern histologically. These clinical and pathological findings suggest Membranous nephropathy as the correct diagnosis.
Here is the rationale:
- Facial puffiness, frothy urine, and hypertension: These symptoms are commonly associated with nephrotic syndrome, characterized by significant proteinuria, hypoalbuminemia, and often hyperlipidemia.
- History of hepatitis B infection: Membranous nephropathy is linked with hepatitis B virus infection, among other causes.
- Microscopic hematuria: While not exclusive to membranous nephropathy, it can be present in this condition.
- Histopathological finding: The 'spike and dome' appearance is characteristic of membranous nephropathy, arising from subepithelial immune complex deposits that lead to thickening of the glomerular basement membrane.
Other options consideration:
- Minimal change disease: Typically presents with nephrotic syndrome but without hypertension or microscopic hematuria and there's no spike and dome pattern.
- Focal segmental glomerulosclerosis (FSGS): May present with hypertension and nephrotic syndrome, but histology would show segmental sclerosis and collapsing lesions, not spike and dome.
- PSGN (Post-Streptococcal Glomerulonephritis): Often occurs after streptococcal infections with a different histological presentation of subepithelial 'humps'.
In conclusion, the combination of clinical presentation, history of hepatitis B infection, and the distinctive biopsy findings indicate that the diagnosis is membranous nephropathy.