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Cardiac, lung, and brain thrombosis in a child with obstructive sleep apnea.

机译:阻塞性睡眠呼吸暂停患儿的心脏,肺和脑血栓形成。

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A 3-year-old boy with failure to thrive and severe adenotonsillar hypertrophy with a clinical presentation of prolonged obstructive sleep apnea (OSA), was referred to the emergency room due to severe respiratory distress and anasarca. Echocardiography revealed right heart failure, a cystic lesion in the right ventricle and severe pulmonary hypertension. D-dimer was elevated but spiral computerized tomography (CT) and lung scan did not show any perfusion defects. Excision of the cardiac lesion during open-heart surgery, lung biopsy, and adenotonsillectomy were performed. Pathological examination showed an intracadiac organized thrombus and eccentric intimal fibrosis of the pulmonary arteries-which is a pathognomonic of pulmonary arterial microemboli. Brain CT revealed vein thrombosis of the left sigmoid sinus. Blood tests for inherited thrombophilia were normal. Today, 5 years after adenotonsillectomy, the child is normally developed, completely asymptomatic, free of any medications, and has a normal echocardiography. This case report may indicate that prolonged OSA can be a procoagulant state which can cause severe cardiovascular morbidity in children.
机译:一名3岁男孩因重度呼吸窘迫和阿那卡斯病而无法ive壮成长并伴有严重的阻塞性睡眠呼吸暂停(OSA)临床表现严重的腺扁桃体肥大,被转诊至急诊室。超声心动图显示右心衰竭,右心室有囊性病变和严重的肺动脉高压。 D-二聚体升高,但螺旋计算机断层扫描(CT)和肺部扫描未显示任何灌注缺陷。进行心脏直视手术,肺活检和腺扁桃体切除术期间的心脏病变切除。病理检查显示,颅内组织性血栓和肺动脉内膜纤维化偏心,这是肺动脉微栓塞的病理特征。脑CT显示左乙状窦静脉血栓形成。遗传性血友病的血液检查是正常的。今天,腺扁桃体切除术后5年,该儿童正常发育,完全无症状,没有任何药物,并且超声心动图正常。该病例报告可能表明长时间的OSA可能是促凝状态,可能导致儿童严重的心血管疾病。

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