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A Case of Idiopathic Hypereosinophilic Syndrome Causing Mitral Valve Papillary Muscle Rupture

机译:二尖瓣乳头肌破裂致特发性嗜酸粒细胞增多综合征一例

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Idiopathic Hypereosinophilic Syndrome (IHES) is a rare disease that can be difficult to diagnose as the differential is broad. This disease can cause significant morbidity and mortality if left untreated. Our patient is a 17-year-old adolescent female who presented with nonspecific symptoms of abdominal pain and malaise. She was incidentally found to have hypereosinophilia of 16,000 on complete blood count and nonspecific colitis and pulmonary edema on computed tomography. She went into cardiogenic shock due to papillary rupture of her mitral valve requiring extreme life support measures including intubation and extracorporal membrane oxygenation (ECMO) as well as mitral valve replacement. Pathology of the valve showed eosinophilic infiltration as the underlying etiology. The patient was diagnosed with IHES after the exclusion of infectious, rheumatologic, and oncologic causes. She was treated with steroids with improvement of her symptoms and scheduled for close follow-up. In general patients with IHES that have cardiac involvement have poorer prognoses.
机译:特发性嗜酸性粒细胞增多症(IHES)是一种罕见疾病,由于差异很大,因此很难诊断。如果不及时治疗,这种疾病可导致明显的发病率和死亡率。我们的患者是一名17岁的青春期女性,表现出腹痛和不适的非特异性症状。偶然发现她的全血细胞计数为16,000的嗜酸性粒细胞增多,计算机断层扫描显示为非特异性结肠炎和肺水肿。由于二尖瓣乳头破裂,她陷入了心源性休克,需要极端的生命支持措施,包括插管和体外膜氧合(ECMO)以及二尖瓣置换。瓣膜病理表现为嗜酸性浸润为潜在病因。在排除感染,风湿病和肿瘤病因后,该患者被诊断出患有IHES。她接受了激素治疗,症状得到改善,并计划进行密切随访。通常,心脏受累的IHES患者的预后较差。

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