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İKİ OLGU NEDENİYLE KRESENTÎK NEKROTÎZAN GLOMERULONEFRİTLÎ HASTALARDA AYIRT EDİCİ TANI

DIFFERENTIAL DIAGNOSIS IN TWO PATIENTS WITH CRESENTIC GLOMERULONEPHRITIS

Journal Name:

  • Türk Nefroloji, Diyaliz ve Transplantasyon Dergisi

Publication Year:

  • 1999

Key Words:

Keywords (Original Language):

Author NameUniversity of AuthorFaculty of Author
Abstract (2. Language): 
Microscopic polyangiitis is small vessel necrotizing vasculitis involving the kidney, sometimes skin, and lung. This disease is characterized by the presence of an ANCA and few or no immune deposits in involved vessels. We reviewed the different features of MPA due to our two patients.
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Abstract (Original Language): 
Mikroskopik Polianjitis (MPA) böbreği, cildi ve akciğerleri tutan küçük damarların nekrotizan vaskülitidir. Bu hastalık ANCA pozitifliği ve biyopsilerde immundepozitlerin bulunmaması ile karekterizedir. Bu yazıda MPA' in özellikleri iki olgumuz nedeniyle gözden geçirildi.
FULL TEXT (PDF): 
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  • 1
33-35
  • Turkish

REFERENCES

References: 

1. Savage COS, Harper L, Adu L: Primary systemic vasculitis. Lancet 1997; 349: 552-8.
2. Scot DGI, Watts RA. Classification and epidemiology of systemic vasculitis (editorial). Br J Rheomatol 1994;33:897-900.
3. Penas PF, Porras JI, Fraga J et al. Mikroscopic polyangitis. A systemic vasculitis with a positive
P-ANCA. Br J Dermatol 1996;134:542-547.
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