Page 967 - Clinical Immunology_ Principles and Practice ( PDFDrive )
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CHaPter 68  Immunological Renal Diseases             933.e1


              MUL t IPL e -CHOIC e  QU e S t IO n S

           1.  A 45-year-old woman presented to the emergency department   was afebrile, and his blood pressure was 140/80 mm Hg. The
             (ED) with swelling in both ankles, 15-lb weight gain over the   catheter site was clean, and the remainder of the examination
             past 3 months and shortness of breath. During a physical   was unremarkable. There was trace edema. Laboratory findings
             examination 1 year prior, 1+ protein was noted on dipstick   were notable for mild hypoalbuminemia (serum albumin of
             urinalysis, but no further workup was done. There was no   3.1 g/dL), serum creatinine of 2.1 mg/dL, hypocomplement-
             family history of renal disease. The patient has blood pressure   emia (C3, 4 mg/dL, C4, 5 mg/dL, and CH50, 10 U/mL).
             of 120/80 mm Hg, elevated respiratory rate of 25, and oxygen   Urinalysis was notable for proteinuria 2+, and urine microscopy
             saturation of 90%. Physical examination was notable for pitting   revealed 15 acanthocytes per high-power field. The spot urine
             edema in her legs up to the mid-thighs. Lungs were clear.   protein/creatinine ratio was 1.8 g/g. Human immunodeficiency
             Laboratory testing revealed a hemoglobin level of 14 g/dL,   virus (HIV), antinuclear antibody (ANA), and hepatitis B
             hematocrit of 42%, serum creatinine level of 1.0 mg/dL, blood   and C screen results were negative. Renal biopsy was performed
             urea nitrogen (BUN) of 28 mg/dL, albumin level of 1.6 g/  after admission. Light microscopy (LM) revealed diffuse
             dL, serum total cholesterol level of 350 mg/dL (normal,   mesangial and endocapillary hypercellularity, lobulation in
             <200 mg/dL), and serum triglyceride level of 800 mg/dL   the glomeruli, and double contours in the glomerular capillary.
             (normal, <150 mg/dL). Serum complement levels were within   Two of 18 glomeruli had segmental crescents. Immunofluo-
             normal limits. Urinalysis demonstrated 4+ protein on dipstick.   rescence microscopy revealed staining for IgG (3+) and C3
             Urine microscopy revealed 0–2 nondysmorphic red blood   (3+) along the capillary and mesangial regions in a granular
             cells per high-power field, oval fat bodies, and fatty casts. A   pattern. Electron microscopy (EM) revealed subendothelial
             spot protein/creatinine ratio was 8 g/g. The chest radiography   and mesangial electron-dense deposits. What further workup
             result was negative. Computed tomography (CT) angiography   is indicated?
             revealed multiple pulmonary emboli, and therapeutic anti-   A. ANCAs testing
             coagulation was immediately initiated. Renal biopsy was    B. Anti–glomerular basement membrane (GBM) antibody
             deferred because of the need for urgent anticoagulation. What    C. Blood culture
             would have been the most likely biopsy finding if biopsy had    D. Evaluation for genetic mutations of complement regulatory
             been done?                                                proteins, including complement factor H (CFH), CFI, and
              A. Acute post infectious glomerulonephritis              Membrane cofactor protein (MCP).
              B. Alport syndrome                                  3.  A 60-year-old male with new diagnosis of Hodgkin lymphoma
              C. Antineutrophil cytoplasmic antibodies (ANCAs)–associated   was noted to have 3+ edema on examination by his oncologist.
               crescentic glomerulonephritis                        Serum creatinine was 1.1 mg/dL. Serum albumin was 2.5 g/
              D. Membranous nephropathy (MN)
                                                                    dL.  Urinary protein  excretion  revealed  6 g/24 hr.  Urine
           2.  A 20-year-old male with history of short bowel syndrome   microscopy showed fatty casts but no cellular elements. Kidney
             was admitted to the hospital with elevated creatinine, mac-  biopsy result was consistent with minimal change disease
             roscopic hematuria and proteinuria, and renal insufficiency.   (MCD). What is the appropriate treatment?
             He had been on long-term peripheral nutrition via a central    A. High-dose prednisone
             venous catheter for 4 years. He was admitted 6 months ago    B. Cyclosporine with prednisone
             with a line infection and was given antibiotics for 7 days, but    C. Mycophenolate mofetil
             the line was not removed. He was noted to have trace pro-   D. Chemotherapy
             teinuria and hematuria 6 months ago. Upon admission, he
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