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Spontaneous Splenic Artery Rupture as the First Symptom of Systemic Amyloidosis

机译:自发性脾动脉破裂作为全身淀粉样蛋白病的第一个症状

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Spontaneous splenic rupture is a life-threatening condition leading to a rapidly progressing hypovolemic shock due to intra-abdominal blood loss, with a mortality rate of about 10%. Spontaneous splenic rupture can be caused by widely different disorders including acute and chronic infections, neoplastic disorders, and inflammatory noninfectious disorders. In this case report, we present a 67-year-old male patient with hemorrhagic shock caused by an acute bleeding from the splenic artery. The patient was massively transfused with blood products and fluids and underwent laparotomy for hemostatic control and clinical stabilization. Multiorgan involvement by amyloid light-chain amyloidosis (AL-amyloidosis) caused by plasma cell dyscrasia, specifically with infiltration of the spleen artery, was found to be the underlying cause of his life-threatening bleeding. Based on this case, we discuss the features of serious spleen bleeding, massive transfusion therapy in the intensive care setting, and AL-amyloidosis pathophysiology and treatment.
机译:自发性脾破裂是一种危及生命的状况导致了快速进展的低血容量性休克由于腹腔内血液损失,其死亡率约为10%。自发性脾破裂可以通过广泛不同的疾病,包括急性和慢性感染,肿瘤性疾病和炎性病症非感染引起的。在这种情况下,报告中,我们提出了一个67岁的男性患者,引起的一种急性从脾动脉大出血失血性休克。病人被大量用血制品和液体和止血控制和临床稳定后行剖腹手术输血。由浆细胞恶液质引起的,特别是与脾动脉的浸润淀粉样蛋白轻链淀粉样变性(AL淀粉样变性)多器官受累,被发现是的潜在病因他的危及生命的出血。基于这种情况,我们讨论了严重的脾出血,在重症监护病房大量输血治疗,而AL-淀粉样变的病理生理学和治疗的功能。

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