May 2024 Medical Image of the Month: Hereditary Hemorrhagic Telangiectasia in a Patient on Veno-Arterial Extra-Corporeal Membrane Oxygenation

Theodore Loftsgard, Kari Wilson, John Bohman
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Abstract

No abstract available. Manuscript truncated after 150 words. A 54-year-old man with a complex cardiac history, including Tetralogy of Fallot requiring Blalock-Taussig shunt in infancy, infundibular patch repair at age 7, and bioprosthetic tricuspid valve replacement at age 52, had ongoing frequent hospitalizations with decompensated right ventricular heart failure secondary to native pulmonary valve mixed stenosis plus regurgitation and left pulmonary artery stenosis. His case was further complicated by his history of hereditary hemorrhagic telangiectasia (HHT) with recurrent epistaxis and recent GI bleeds with multiple angiodysplastic lesions throughout the stomach, duodenum, and descending colon which were previously treated with argon plasma coagulation. The patient was admitted to our hospital in NYHA class IV heart failure receiving a continuous dopamine infusion and aggressive diuresis. Upon admission, a right heart catheterization demonstrated severe pulmonary valve regurgitation, left pulmonary artery stenosis, and systemic hypoxemia suggestive of an intrapulmonary shunt. Admission transthoracic echocardiogram demonstrated normal left ventricular ejection fraction of 55-60%, a …
2024 年 5 月 "本月医学影像":静脉-动脉体外膜氧合患者的遗传性出血性远端血管扩张症
无摘要。稿件在150字后截断。一名 54 岁的男子有复杂的心脏病史,包括法洛氏四联症,婴儿期需要进行 Blalock-Taussig 分流术,7 岁时进行了肺底补片修补术,52 岁时进行了生物人工三尖瓣置换术。遗传性出血性毛细血管扩张症(HHT)导致反复鼻衄,近期消化道出血,胃、十二指肠和降结肠多处血管增生性病变,曾用氩等离子体凝固治疗,这些病史使他的病情更加复杂。患者因 NYHA IV 级心力衰竭入院,接受持续多巴胺输注和积极的利尿治疗。入院时,右心导管检查显示患者存在严重的肺动脉瓣反流、左肺动脉狭窄和全身低氧血症,提示存在肺内分流。入院时经胸超声心动图显示,左心室射血分数正常,为55%-60%,左肺动脉狭窄,全身低氧血症,提示肺内分流。
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