Súlyos szívelégtelenség hátterében álló transthyretin-amyloidosis elkésett diagnózisa

V. Nagy, Gergely Rácz, Bence Radics, Lidia Hategan, Hedvig Takács, Árpád Kormányos, László Rudas, B. Iványi, Róbert Sepp
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Abstract

Several heart muscle diseases can cause heart failure, the etiological diagnosis of which may serve the basis of targeted, tailored, effective personalized therapy. Such a heart muscle disease is transthyretin amyloidosis (ATTR) which is an infiltrative disorder affecting most frequently the heart and peripheral nerves, due to the accumulation of transthyretin protein. Deposition of mutant transthyretin, due to mutations in the TTR gene encoding for transthyretin, occurs in the familial form of the disease (hATTR), while in senile amyloidosis, wild-type transthyretin accumulates (wtATTR). We report on a 79-years-old male patient who presented 9 years before because of novel onset atrial fibrillation. Echocardiography at that time showed severe concentric left ventricular hypertrophy which progressed through the years. Laboratory values displayed increased liver enzymes and troponin T levels. He was hospitalized several times because of left- and later right-sided heart failure, with increasing tendency towards hypotension. At last admission he was admitted to us after suffering syncope at home necessitating cardiopulmonary resuscitation. Transthoracic echocardiography showed severe, concentric biventricular hypertrophy (LV wall thickness 22 mm, RV wall thickness 12 mm), with depressed LV and RV function, apical sparing, and low cardiac output. Taking low voltage, seen on ECG, and other anamnestic data into consideration, the suspicion of ATTR amyloidosis was raised. The patient died after a short observational period due to intractable heart failure. Autopsy and histology revealed systemic amyloidosis, affecting predominantly the heart which was interpreted as wtATTR according to immunohistochemistry, negative TTR gene sequencing and the lack of monoclonal gammopathy. Our case illustrates the importance of the diagnostic delay which is very frequently encountered in TTR amyloidosis. Features of ATTR which includes the multidisciplinary nature of assessment, specialized diagnostic modalities and unique therapy call for the need of specialized diagnostic centers.
几种心肌疾病可导致心力衰竭,其病因诊断可能为有针对性,量身定制,有效的个性化治疗提供基础。这种心肌疾病就是甲状腺转蛋白淀粉样变性(ATTR),它是一种浸润性疾病,最常影响心脏和周围神经,是由甲状腺转蛋白积累引起的。由于编码转甲状腺素的TTR基因突变,突变型转甲状腺素的沉积发生在家族型疾病(hATTR)中,而在老年性淀粉样变性中,野生型转甲状腺素积累(wtATTR)。我们报告了一位79岁的男性患者,他在9年前因新发房颤而出现。当时的超声心动图显示严重的同心性左心室肥厚,并持续多年。实验室值显示肝酶和肌钙蛋白T水平升高。他曾多次因左、右心衰住院,并有低血压的趋势。最后入院时,他在家里晕厥,需要心肺复苏术。经胸超声心动图显示严重的同心双室肥厚(左室壁厚22 mm,右室壁厚12 mm),左室和右室功能下降,心尖保留,心输出量低。结合心电图低电压及其他记忆资料,提出ATTR淀粉样变的怀疑。由于顽固性心力衰竭,患者在短暂观察期后死亡。尸检和组织学显示系统性淀粉样变,主要影响心脏,根据免疫组织化学,TTR基因测序阴性和缺乏单克隆γ病,解释为wattr。我们的病例说明了诊断延迟的重要性,这在TTR淀粉样变中非常常见。ATTR的特点包括评估的多学科性质、专门的诊断方式和独特的治疗方法,需要专门的诊断中心。
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