Dwyre Denis M, Dursteler Bryce, Nashelsky Marcus, Friedman Kenneth D, Raife Thomas J
Department of Pathology, University of California Davis Medical Center, Sacramento, California 95817, USA.
J Clin Apher. 2009;24(3):106-10. doi: 10.1002/jca.20196.
Thrombotic thrombocytopenic purpura (TTP) is a clinical diagnosis that can be difficult to establish in severely ill patients. We report a case of fulminant TTP in a woman who died before receiving plasma exchange. An autopsy plasma sample was analyzed for ADAMTS13 activity and inhibitor for correlation with the diagnosis of TTP. Recognizing that hemolysis in postmortem blood samples could interfere with ADAMTS13 activity, plasma samples from four additional decedents not suspected of having TTP were analyzed and correlated with their autopsy results. The purpose of this study was to assess whether testing postmortem samples for ADAMTS13 is useful in the postmortem diagnosis of TTP.
Plasma samples from the index case and four non-TTP decedents were analyzed for ADAMTS13 activity, ADAMTS13 inhibitor levels, and plasma free hemoglobin (PFH). Autopsy tissues were evaluated for evidence of platelet microthrombi in all five cases.
The ADAMTS13 activity level in the index patient was <4%, and the inhibitor level was 1.0 inhibitor unit. Microthrombi were prominent in the heart, kidneys, pancreas, and adrenal glands, consistent with the clinical diagnosis of TTP. ADAMTS13 activity levels in the four non-TTP decedents ranged from 4 to 82% (3/4 < or = 26%), and inhibitor was present in two of the four samples. Postmortem PFH levels in the four non-TTP decedents ranged from 64 to 3,917 mg/dL. No microthrombi were observed.
Low postmortem ADAMTS13 activity and evidence of inhibitor can occur in decedents without clinical or histologic evidence of TTP. Postmortem ADAMTS13 activity levels may not be valid in establishing a diagnosis of TTP, and high inhibitor levels in this setting may be related to elevated PFH. Caution must be used in the interpretation of ADAMTS13 testing in the presence of hemolysis.
血栓性血小板减少性紫癜(TTP)是一种临床诊断,在重症患者中可能难以确诊。我们报告一例暴发性TTP女性病例,该患者在接受血浆置换前死亡。对一份尸检血浆样本进行ADAMTS13活性和抑制剂分析,以与TTP诊断相关联。认识到死后血样中的溶血可能干扰ADAMTS13活性,对另外四名未怀疑患有TTP的死者的血浆样本进行分析,并将其与尸检结果相关联。本研究的目的是评估检测死后样本中的ADAMTS13在TTP死后诊断中是否有用。
对索引病例和四名非TTP死者的血浆样本进行ADAMTS13活性、ADAMTS13抑制剂水平和血浆游离血红蛋白(PFH)分析。对所有五例尸检组织进行血小板微血栓证据评估。
索引患者的ADAMTS13活性水平<4%,抑制剂水平为1.0抑制剂单位。心脏、肾脏、胰腺和肾上腺中微血栓明显,与TTP临床诊断一致。四名非TTP死者的ADAMTS13活性水平为4%至82%(3/4≤26%),四个样本中有两个存在抑制剂。四名非TTP死者的死后PFH水平为64至3917mg/dL。未观察到微血栓。
在没有TTP临床或组织学证据的死者中,可能出现死后ADAMTS13活性低和抑制剂证据。死后ADAMTS13活性水平在TTP诊断中可能无效,在此情况下高抑制剂水平可能与PFH升高有关。在存在溶血的情况下,对ADAMTS13检测结果的解释必须谨慎。