Q2 Medicine
BMC Hematology Pub Date : 2018-08-10 eCollection Date: 2018-01-01 DOI:10.1186/s12878-018-0100-9
Jean Uwingabiye, Hafid Zahid, Mohamed El Amrani, Fayçal Labrini, Abdelhak Elkhazraji, Driss El Kabbaj, Mohammed Benyahia, Anass Yahyaoui, Rachid Hadef, Nezha Messaoudi
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引用次数: 1

摘要

背景:获得性凝血抑制剂已经在非常罕见的单克隆伽玛病病例中被观察到。病例介绍:男性,59岁,无病理史,因肾功能不全及贫血综合征入住肾脏病科。病史和体格检查显示出出血综合征的印记,包括血胸和咯血。止血评估显示孤立的活化部分凝血活素时间延长(APTT), APTT比值= 2.0。循环抗凝血指标(37.2%)显示存在循环抗凝血。标准化稀释罗素毒蛇毒液的时间比为0.99,强调了狼疮抗凝血剂的缺失。此外,血球计数显示双氧体减少症合并非再生正红细胞正色贫血和血小板减少症。血液涂片显示浆细胞计数为49% (2842/mm3),提示PCL。骨髓被营养不良的浆细胞侵袭高达90%。生化评估提示轻链生成旺盛引起的下游肾脏和电解质紊乱,异常包括高尿酸血症、高钙血症、乳酸脱氢酶升高、非肾范围蛋白尿和高水平C反应蛋白。血清蛋白电泳显示存在单克隆峰。血清免疫固定试验检测单克隆游离λ轻链的存在。他接受了维凯德、沙利度胺和地塞米松治疗。患者经治疗2周后死亡。单克隆γ病变伴有出血表现的患者应怀疑因子抑制剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rare and unusual case of anti-factor XI antibodies in patient with plasma cell leukemia.

Background: The acquired inhibitors of coagulation have been observed in very rare cases of monoclonal gammopathies. We report a very rare case of anti-factor XI antibodies in patient with plasma cell leukemia (PCL).

Case presentation: This is a 59-year-old male patient without pathological history, admitted to the nephrology department for management of renal insufficiency and anemia syndrome. The history and physical examination revealed stigmata of hemorrhagic syndrome including hemothorax and hemoptysis. The hemostasis assessment showed an isolated prolonged activated partial thromboplastin time (APTT) with APTT ratio = 2.0.The index of circulating anticoagulant (37.2%) revealed the presence of circulating anticoagulants. The normalized dilute Russell viper venom time ratio of 0.99 has highlighted the absence of lupus anticoagulants. The coagulation factors assay objectified the decrease of the factor XI activity corrected by the addition of the control plasma confirming the presence of anti-factor XI autoantibodies. In addition, the blood count showed bicytopenia with non-regenerative normocytic normochromic anemia and thrombocytopenia. The blood smear demonstrated a plasma cell count of 49% (2842/mm3) evoking PCL. The bone marrow was invaded up to 90% by dystrophic plasma cells. The biochemical assessment suggested downstream renal and electrolyte disturbances from exuberant light chain production with abnormalities including hyperuricemia, hypercalcemia, elevated lactate dehydrogenase, non nephrotic-range proteinuria and high level of C reactive protein. The serum protein electrophoresis showed the presence of a monoclonal peak. The serum immunofixation test detects the presence of monoclonal free lambda light chains. He was treated with velcade, thalidomide and dexamethasone. The patient died after 2 weeks despite treatment.

Conclusion: Both PCL and anti-factor XI inhibitors are two very rare entities. To the best of our knowledge, this is the first reported case of a factor XI inhibitor arising in the setting of PCL. Factor inhibitors should be suspected in patients whose monoclonal gammopathies are accompanied by bleeding manifestations.

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来源期刊
BMC Hematology
BMC Hematology Medicine-Hematology
CiteScore
4.10
自引率
0.00%
发文量
0
期刊介绍: BMC Hematology is an open access, peer-reviewed journal that considers articles on basic, experimental and clinical research related to hematology. The journal welcomes submissions on non-malignant and malignant hematological diseases, hemostasis and thrombosis, hematopoiesis, stem cells and transplantation.
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