Medical Student, La Salle University, Mexico City, Mexico.
Cardiovascular Critical Care Unit, National Institute of Cardiology Ignacio Chavez, Mexico City, Mexico.
Am J Case Rep. 2022 Jul 4;23:e936545. doi: 10.12659/AJCR.936545.
BACKGROUND In cardiac amyloidosis (CA), misfolded proteins deposit in the extracellular space of cardiac tissue. These deposits classically cause restrictive cardiomyopathy with diastolic dysfunction. Although there are at least 30 proteins known to cause amyloid aggregates, 2 main types make up most diagnosed cases: light chain amyloidosis (AL) and transthyretin amyloidosis (ATTR). Since CA is considered a rare condition, it is often underdiagnosed or recognized in the advanced stages. Once amyloid deposits involve the heart tissue, they are associated with a worse outcome and higher mortality rates, especially in patients presenting symptoms of heart failure. CASE REPORT We report a case of a 22-year-old man presenting with acute severe mitral regurgitation, secondary to posterior mitral leaflet chordae tendineae rupture (CTR). Surgical mitral valve replacement with a mechanical prosthesis was performed, and cardiac tissue biopsy samples were obtained. After surgery, the patient improved significantly but suddenly presented with hemodynamic deterioration, until he died due to severe hemodynamic compromise and multiorgan failure. Although the etiology of the CTR was not established before surgical intervention, the histopathological analysis suggested CA. CONCLUSIONS CA diagnosis can be complex, especially in a 22-year-old-man with atypical clinical and imaging manifestations. In this patient, other differential diagnoses were considered, since CA presenting in a young patient is a rare phenomenon and acute mitral regurgitation secondary to CTR presents more frequently in other heart conditions. Furthermore, rapid postoperative deterioration resulted in the patient's death before biopsy samples were available because suspicion of amyloidosis had not been raised until that point.
在心脏淀粉样变性(CA)中,错误折叠的蛋白质在心脏组织的细胞外空间沉积。这些沉积物经典地导致舒张功能障碍的限制性心肌病。尽管至少有 30 种已知的蛋白质可引起淀粉样聚合体,但 2 种主要类型构成了大多数诊断病例:轻链淀粉样变性(AL)和转甲状腺素蛋白淀粉样变性(ATTR)。由于 CA 被认为是一种罕见疾病,因此常常被漏诊或在晚期才被发现。一旦淀粉样沉积物累及心脏组织,它们与更差的预后和更高的死亡率相关,尤其是在出现心力衰竭症状的患者中。
我们报告了 1 例 22 岁男性,表现为急性重度二尖瓣反流,继发于后二尖瓣瓣叶腱索断裂(CTR)。进行了二尖瓣置换手术,采用机械假体,并获得了心脏组织活检样本。手术后,患者明显改善,但突然出现血流动力学恶化,最终因严重血流动力学障碍和多器官衰竭而死亡。尽管 CTR 的病因在手术干预前尚未确定,但组织病理学分析提示 CA。
CA 的诊断可能很复杂,尤其是对于具有非典型临床和影像学表现的 22 岁男性。在该患者中,还考虑了其他鉴别诊断,因为在年轻患者中出现 CA 是一种罕见现象,而继发于 CTR 的急性二尖瓣反流在其他心脏疾病中更为常见。此外,由于直到那时才怀疑淀粉样变性,因此快速的术后恶化导致患者在获得活检样本之前死亡。