Journal List > J Korean Rheum Assoc > v.16(3) > 1003680

Kang, Kim, Jang, Shin, and Kim: Renal Artery Thrombosis in a Patient with Systemic Lupus Erythematosus without Antiphospholipid Antibody Syndrome: A Case Study

Abstract

Systemic lupus erythematosus (SLE) is a multisystemic inflammatory autoimmune disease caused by various autoantibodies and immune complexes. SLE and antiphospholipid antibodies are associated with thrombotic manifestations. However, renal artery thrombosis which causes renal artery occlusion is uncommon even in SLE patients with antiphospholipid antibodies. A 27-year-old woman with SLE suddenly developed left flank pain and generalized edema. From the laboratory workup, the woman was negative for antiphospholipid antibody and nephrotic-range proteinuria was detected. Computed tomography revealed renal artery thromboembolism and multiple renal infarctions with parenchymal perfusion defects in the left kidney. Renal biopsy showed WHO classification III and V lupus nephritis. Left flank pain, generalized edema and proteinuria were resolved and the thromboembolism resolved itself after a high dose of steroid and anticoagulation therapy. In SLE patients, sudden onset of unexplained flank pain is considered as a possible symptom of renal vessel thromboembolism even if the antiphospholipid antibody is negative.

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Fig. 1.
27-year-old woman with multiple left renal infarctions. (A) Contrast-enhanced computed tomography image during corticomedullary phase shows multiple parenchymal perfusion defects in the left kidney compatible with renal infarctions. Multiple filling defects (arrows) in left main and segmental renal arteries suggest the thromboembolism. (B) Follow-up contrast-enhanced maximal intensity projection image obtained one week later shows the thromboembolism is no longer present in the left main and segmental renal arteries as well as a decreased extent of parenchymal loss.
jkra-16-248f1.tif
Fig. 2.
27-year-old woman with lupus nephritis WHO class III+V. (A) Light microscopy shows moderate hypercellular mesangial tissue and focal endocapillary proliferation. Capillary loops are focally thickened with subendothelial deposition (H&E stain, ×400). (B) Electron microscopy shows diffuse effacement of epithelial foot processes and wide spread subepithelial electron-dense deposition (×5,000).
jkra-16-248f2.tif
Table 1.
Comparison of previous renal infarction cases of SLE patients negative for antiphospholipid antibodies to the current case
  A B C
Sex Male Female Female
Race Asian Asian Asian
Age 13-year old 42-year-old 27-year-old
SLE duration 11-month 8-year 4-year
Symptom Hypertension, fever, seizure, abdominal pain Right abdominal pain Left flank pain, generalized edema
Drug history Prednisolone, mizoribine, dilazep dihydrochloride Prednisolone, azathioprine Prednisolone, hydroxychloroquine
Other complication CNS lupus, lupus nephritis Lupus nephritis Lupus nephritis

Tsugawa K, Tanaka H, Kudo M, Nakahata T. Renal artery thrombosis in a pediatric case of systemic lupus

Suwabe H, Moriuchi J, erythematosus without antiphospholipid antibodies. Pediatr Nephrol 2005; 20(11):1648–50., Hoshina Y. Renal and cerebral infarctions in a patient with systemic lupus erythematosus without antiphospholipid antibodies. Ryumachi 1993;33(4):335–40.,

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