CLINICAL CASE OF SECONDARY ANTIPHOSPHOLIPID SYNDROME IN A NEPHROLOGICAL PATIENT

Authors

  • Skosyreva O.V
  • Khasanov A. A
  • Babazhanova N.R ORCID: 0000-0002-6955-7064, Tashkent State Dental Institute Tashkent , Uzbekistan

Keywords:

Antiphospholide syndrome, chronic glomerulonephritis, arterial hypertension.

Abstract

The article describes a clinical case of late diagnosis of secondary aPL with multiinflammatory syndrome in a patient with chronic glomerulonephritis. The experience of Covid-19 led to the launch of systemic homeostasiological disorders, which manifested as thrombosis in the inferior vena cava, renal vein, and lower lobe pulmonary artery. In this case, the onset of the disease was “varicocele,” which most likely was a manifestation of thrombosis of the spermatic cord vein. The addition of arterial hypertension, anasarca, massive proteinuria with active urinary sediment, hypoproteinemia , hypercreatininemia was regarded as manifestations of clinical and laboratory signs of a mixed form of CGN with impaired renal function, which required pulse therapy with a glucocorticosteroid and a cytostatic in combination with combined nephroprotective therapy against the background of anticoagulants and antiplatelet agents .

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Published

2024-02-08

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