**Core Concept**
This question tests the recognition of **HCV-associated membranoproliferative glomerulonephritis (MPGN)**, a classic renal complication of chronic hepatitis C infection. Key features include subnephrotic proteinuria, hematuria, low complement levels, and skin/vascular manifestations like purpura or ulcers due to cryoglobulinemia.
**Why the Correct Answer is Right**
HCV-induced MPGN (Type II) is characterized by immune complex deposition in glomeruli, leading to complement activation and C3 consumption. The triad of **hepatitis C positivity**, **low serum complement (C3)**, and **renal pathology with subnephrotic proteinuria/microhematuria** is diagnostic. Skin ulceration and vasculitis (e.g., cryoglobulinemic vasculitis) further support this diagnosis, as HCV drives mixed cryoglobulinemia.
**Why Each Wrong Option is Incorrect**
- **Option A:** IgA nephropathy typically presents with gross hematuria post-infection and normal complement; no skin ulcers or HCV association.
- **Option B:** Lupus nephritis would show systemic lupus features (e.g., malar rash, ANA positivity), not HCV antibodies.
- **Option C:** Diabetic nephropathy causes nephrotic-range proteinuria (>3.5g) and hypertension, with normal complement.
**Clinical Pearl / High-Yield Fact**
HCV-related MPGN is a **complement-mediated** disease. Remember the **"HCV triad"**: hepatitis C infection, low C3, and renal biopsy showing MPGN. Skin ulcers and cryoglobulinemia are red flags for HCV-associated vasculitis. Always check for HCV in patients with unexplained glomerulonephritis and complement abnormalities.
**Correct Answer: C. Membranoproliferative glomerulonephritis (MPGN) associated with hepatitis C**
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