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Platypnea-Orthodeoxia Syndrome: A Case of Chronic Paroxysmal Hypoxemia

机译:蛋白质蛋白质酸氧体综合征:一种慢性阵测缺氧血症的案例

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摘要

A 75-year-old man with chronic (30-year) unexplained paroxysmal hypoxemia presented with postural hypoxemia and desaturation consistent with a clinical manifestation of platypnea-orthodeoxia syndrome. His history included a lack of significant past pulmonary disease, yet with intermittent need for oxygen supplementation. On admission he was found to have an interatrial shunt through a patent foramen ovale. Device closure by percutaneous catheterization led to sustained resolution of symptoms. Platypnea-orthodeoxia syndrome is a rare but important consideration in the differential diagnosis of hypoxemia, as it represents a potentially curable cause of hypoxemia, with missed diagnosis leading to possible patient morbidity if untreated. Even more importantly, an astute and careful history and physical examination are integral to the diagnosis of this rare but likely under-recognized syndrome.
机译:一个75岁的男子患有慢性(30年)无法解释的阵发性低氧血症,呈现出姿势低氧血症和去饱和,与普氏藻藻综合征的临床表现一致。 他的历史包括缺乏显着的过去的肺病,但随时间歇性需要氧气补充。 在入学时,他被发现通过专利觅食卵形具有间隙分流。 通过经皮导管闭合导致症状的持续分辨率。 蛋白质蛋白质氧化综合征是在缺氧血症的鉴别诊断中罕见但重要的考虑因素,因为它代表了缺氧血症的可能可治愈的原因,错过诊断,如果未经处理,可能导致可能的患者发病率。 更重要的是,精明和谨慎的历史和体格学对这种罕见但可能的识别综合征的诊断是一体的。

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