医学
血栓性血小板减少性紫癜
微血管病性溶血性贫血
伊库利珠单抗
ADAMTS13号
耐火材料(行星科学)
胰腺炎
血栓性微血管病
急性胰腺炎
胃肠病学
内科学
分裂细胞
病理生理学
血小板
免疫学
疾病
抗体
物理
补体系统
天体生物学
作者
Faizan Malik,Naveed Ali,Irfan Ahsan,Ali Ghani,Christian Fidler
标识
DOI:10.3402/jchimp.v6.32310
摘要
Thrombotic thrombocytopenic purpura (TTP) is a rare multisystem microvascular disorder, which is characterized by pentad of thrombocytopenia, microangiopathic hemolytic anemia, and organ dysfunction due to occlusive thrombi. The proposed pathophysiology involves an imbalance between unusually large von Willebrand factor multimers and the cleaving protease ADAMTS13. Acute pancreatitis is a well-described consequence of TTP, but TTP secondary to acute pancreatitis is a rare phenomenon. We present a patient who developed TTP due to post-ERCP pancreatitis with hematologic, cardiovascular, pulmonary, and renal complications and is the first case of this kind. Despite early initiation of therapy, the patient did not recover making it among the 10% of cases of TTP that prove fatal despite appropriate therapy.
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