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Acute Splenic Infarction at an Academic General Hospital Over 10 Years: Presentation, Etiology, and Outcome

机译:一家学术综合医院十年来的急性脾梗塞:表现,病因和结果

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Few case series provide a current, comprehensive, and detailed description of splenic infarction (SI), an uncommon condition. Retrospective chart review complemented by imaging evaluation and patient follow-up. All adult patients with a confirmed diagnosis of acute SI discharged over 10 years from a single academic center were studied. A systematic literature review was done to compile a complete list of SI etiologies. SI was found in 32 patients, 0.016% of admissions. Ages ranged from 18 to 86 (median 64) years. Cardiogenic emboli were the predominant etiology (20/32, 62.5%) and atrial fibrillation was frequent. Other patients had autoimmune disease (12.5%), associated infection (12.5%), or hematological malignancy (6%). Nine of the patients (28%) had been previously healthy or with no recognized morbidity predisposing to SI. In 5 of 9 hitherto silent antiphospholipid syndrome or mitral valve disease had been identified. Two remained cryptogenic. Most patients presented with abdominal pain (84%), often felt in the left upper quadrant or epigastrium. Associated symptoms, leukocytosis or increased serum lactate dehydrogenase occurred inconsistently (~25% each). Chest X-ray showed suggestive Lt. supra-diaphragmatic findings in 22%. Thus, the typical predisposing factors and/or clinical presentation should suggest SI to the clinician and be followed by early imaging by computed tomography (CT), highly useful also in atypical presentations. Complications were rare and patients were discharged after 6.5 days (median) on anticoagulant treatment. The systematic literature review revealed an extensive list of conditions underlying SI. In some, SI may be the first and presenting manifestation. SI is a rare event but should be considered in predisposed patients or those with any combination of suggestive clinical features, especially abdominal pain CT evaluation is diagnostic and the outcome is good.
机译:很少有病例系列能够对脾梗塞(SI)(一种罕见的情况)进行最新,全面而详细的描述。回顾性图表检查辅以影像学评估和患者随访。研究人员对从单一学术中心出院超过10年的确诊为急性SI的所有成人患者进行了研究。进行了系统的文献综述以汇编出SI病因的完整列表。在32例患者中发现SI,占入院率的0.016%。年龄从18岁到86岁(中位数64岁)不等。心源性栓塞是主要病因(20 / 32,62.5%),并且心房颤动频繁。其他患者患有自身免疫性疾病(12.5%),相关感染(12.5%)或血液系统恶性肿瘤(6%)。 9名患者(28%)以前是健康的,或没有易患SI的已知发病。迄今为止,在9个中的5个中,已经确定了沉默的抗磷脂综合征或二尖瓣疾病。两个仍然是隐源的。大多数患者出现腹痛(84%),常感觉在左上象限或上腹。相关症状,白细胞增多或血清乳酸脱氢酶升高均不一致(每次〜25%)。胸部X线检查显示22%的中上dia肌提示。因此,典型的诱发因素和/或临床表现应向临床医生建议SI,然后通过计算机断层扫描(CT)进行早期成像,这在非典型表现中也非常有用。并发症很少,抗凝治疗6.5天(中位数)后患者出院。系统的文献综述揭示了SI潜在条件的广泛清单。在某些情况下,SI可能是最早出现的表现形式。 SI是罕见的事件,但在易感患者或具有任何暗示性临床特征的患者中应考虑SI,尤其是腹痛CT评估可诊断性且预后良好。

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