A Rare Case of Autoimmune Disorder as a Trigger for Atypical Hemolytic Uremic Syndrome

被引:0
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作者
Pasari, Amit [1 ,2 ]
Balwani, Manish [1 ,2 ]
Gurjar, Prasad [1 ]
Sejpal, Kapil [1 ]
Bawankule, Charulata [2 ]
Tolani, Priyanka [3 ]
Dubey, Shubham [1 ]
Kashiv, Pranjal [1 ]
Bhawane, Amol [4 ]
Malde, Sunny [1 ]
Gupta, Sushrut [1 ]
机构
[1] Datta Meghe Inst Higher Educ & Res, Jawaharlal Nehru Med Coll, Dept Nephrol, Wardha, India
[2] Saraswati Kidney Care Ctr, Dept Nephrol, Nagpur, India
[3] Datta Meghe Inst Higher Educ & Res, Jawaharlal Nehru Med Coll, Dept Internal Med, Wardha, India
[4] All India Inst Med Sci, Dept Nephrol, Nagpur, India
关键词
anca-associated vasculitis; atypical hus; vasculitis; end-stage kidney disease; renal dysfunction; atypical hemolytic uremic syndrome; antineutrophil cytoplasmic antibody; COEXISTENCE; VASCULITIS;
D O I
10.7759/cureus.53126
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Autoimmune diseases may act as a trigger for atypical hemolytic uremic syndrome (aHUS). Triggers for aHUS may include autoimmune diseases, infections, metabolic conditions, pregnancy, and transplants. aHUSmediated injury to various organs, especially kidneys, can be life -threatening. Here, we present the case of a young female who had perinuclear antineutrophil cytoplasmic antibody (p-ANCA)-associated vasculitis and was diagnosed with aHUS. We consider underlying autoimmune p-ANCA-associated vasculitis as a trigger for aHUS in this case.
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页数:3
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