Post-Transfusion Simultaneous Thrombotic Thrombocytopenic Purpura and Hemolytic Uremic Syndrome: A Rare Occurrence

被引：1

作者：

Patel, Maharshi ^{[1
]}

Pawar, Twinkle ^{[2
]}

Agrawal, Sachin ^{[2
]}

Mudey, Gargi ^{[3
]}

Kumar, Sunil ^{[1
]}

Acharya, Sourya ^{[2
]}

Manuja, Nishtha ^{[1
]}

机构：

[1] Jawaharlal Nehru Med Coll, Dept Med, Wardha, India

[2] Jawaharlal Nehru Med Coll, Datta Meghe Inst Med Sci, Dept Med, Wardha, India

[3] Jawaharlal Nehru Med Coll, Dept Microbiol, Wardha, India

来源：

CUREUS JOURNAL OF MEDICAL SCIENCE | 2022年 / 14卷 / 10期

关键词：

plasmapheresis; acute kidney injury; thrombi; intravascular; endothelial; TRANSFUSION;

D O I：

10.7759/cureus.30181

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Endothelial cell injury, intravascular platelet-fibrin thrombi, and vascular damage are found in hemolytic uremic syndrome (HUS) and thrombotic thrombocytopenic purpura (TTP). The two disorders frequently manifest independently and are the important causes of acute renal damage. Acute kidney injury developed in our patient after blood transfusion and later on, the patient developed neurological complications. The patient was managed symptomatically and conservatively. Plasmapheresis and corticosteroid administration showed improved results.

引用

页数：6

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