Microangiopathic antiphospholipid syndrome (MAPS) in the course of undifferentiated connective tissue disease

Authors

  • Bożena Targońska-Stępniak Department of Rheumatology and Connective Tissue Diseases, Medical University of Lublin, Poland
  • Ewa Wielosz Department of Rheumatology and Connective Tissue Diseases, Medical University of Lublin, Poland
  • Maria Majdan Department of Rheumatology and Connective Tissue Diseases, Medical University of Lublin, Poland

DOI:

https://doi.org/10.20883/medical.e49

Keywords:

microangiopathic antiphospholipid syndrome, connective tissue diseases, chronic kidney disease, anticoagulant treatment

Abstract

Introduction. The microangiopathic antiphospholipid syndrome (MAPS) is a subset of APS comprising those patients presenting with thrombotic microangiopathy and demonstrable antiphospholipid antibodies. Renal involvement occurs frequently in the course of MAPS with clinical symptoms of acute renal failure, hypertension, proteinuria and erythrocyturia.
Case report. The report presents the patient with MAPS confirmed by kidney biopsy in the course of undifferentiated connective tissue disease.
Conclusion. The authors emphasize the importance of effective anticoagulant treatment in order to inhibit thrombosis and renal damage in the course of MAPS.

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References

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Published

2014-03-30

Issue

Section

Case Study

How to Cite

1.
Targońska-Stępniak B, Wielosz E, Majdan M. Microangiopathic antiphospholipid syndrome (MAPS) in the course of undifferentiated connective tissue disease. JMS [Internet]. 2014 Mar. 30 [cited 2024 Nov. 17];83(1):81-3. Available from: https://jms.ump.edu.pl/index.php/JMS/article/view/49