MKSAP: 38-year-old woman with primary membranous glomerulopathy

By | November 16, 2019

Test your medicine knowledge with the MKSAP challenge, in partnership with the American College of Physicians.

A 38-year-old woman is evaluated during a follow-up visit for primary membranous glomerulopathy. Diagnosis was made by kidney biopsy 4 months ago, and she was found to be positive for anti–phospholipase A2 receptor (PLA2R) antibodies. Medications are furosemide, losartan, and simvastatin. Recent age- and sex-appropriate cancer screening tests were normal.

On physical examination, vital signs are normal. There is pitting lower extremity edema to the mid shins bilaterally.

Laboratory studies:

Albumin2.1 g/dL (21 g/L)
Total cholesterol288 mg/dL (7.5 mmol/L)
Creatinine1.1 mg/dL (97.2 µmol/L)
Urine protein-creatinine ratio9135 mg/g

Which of the following complications is this patient at greatest risk for developing?

A. Gout
B. Malignancy
C. Renal cell carcinoma
D. Venous thromboembolism

MKSAP Answer and Critique

The correct answer is D.

The nephrotic syndrome can be complicated by clotting manifestations due to a secondary hypercoagulable state. Of all the nephrotic syndromes, membranous glomerulopathy carries the greatest risk for clotting abnormalities, with some series reporting thrombotic complications in up to 35% of the most severe membranous glomerulopathy cases. The etiology for the hypercoagulable state in membranous glomerulopathy and other forms of heavy nephrosis is multifactorial. In response to the hypoalbuminemia induced by nephrotic-range proteinuria, the liver overproduces proteins. This is most classically seen in the form of hyperlipidemia. In addition, hepatic overproduction of proteins in response to hypoalbuminemia can also lead to increased levels of procoagulant proteins such as factor V, factor VIII, and fibrinogen. Urinary loss of albumin in high volume is also accompanied by similar urinary losses of low-molecular-weight anticoagulants (notably, antithrombin III and protein S) and fibrinolytics (such as plasminogen). In a large retrospective cohort of clotting complications in membranous glomerulopathy, >70% of the clots occurred within 2 years of diagnosis, and the risk of clotting markedly increased once albumin levels dropped below 2.8 g/dL (28 g/L) (OR, 2.53; P = 0.02, compared with albumin ≥2.8 g/dL [28 g/L]).

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Chronic kidney disease is a risk factor for hyperuricemia and acute gout due to underexcretion of urate by the kidneys. In these patients, hyperuricemia may be due to impaired glomerular filtration and/or defects of urate handling in the renal proximal tubule. This patient’s current kidney function does not place her at increased risk for gout.

Patients with membranous glomerulopathy have an increased risk of malignancy. Most cancers are diagnosed in men ≥65 years of age and are often solid tumors of the prostate, lung, or gastrointestinal tract. The risk for malignancy seems to be reduced in patients with anti-phospholipase A2 receptor (PLA2R) antibody. Taking into account her negative age- and sex-appropriate cancer screening, young age, and anti-PLA2R antibody status, this patient’s risk of malignancy is low.

Patients with end-stage kidney disease have a markedly increased risk for renal cell carcinoma. Although current guidelines do not support routine screening for renal cell carcinoma in all patients with chronic kidney disease, a high level of suspicion is warranted in patients with symptoms such as new-onset gross hematuria or unexplained flank pain. In the absence of end-stage kidney disease, this patient is not at increased risk for renal cell carcinoma.

Key Point

  • The nephrotic syndrome can be complicated by clotting manifestations due to a secondary hypercoagulable state, and risk is related to the degree of hypoalbuminemia.

This content is excerpted from MKSAP 18 with permission from the American College of Physicians (ACP). Use is restricted in the same manner as that defined in the MKSAP 18 Digital license agreement. This material should never be used as a substitute for clinical judgment and does not represent an official position of ACP. All content is licensed to on an “AS IS” basis without any warranty of any nature. The publisher, ACP, shall not be liable for any damage or loss of any kind arising out of or resulting from use of content, regardless of whether such liability is based in tort, contract or otherwise.

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