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

被引：0

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

来源：

CUREUS JOURNAL OF MEDICAL SCIENCE | 2024年 / 16卷 / 01期

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.

引用

页数：3

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