Hasan Syed M, Ahmed Nida N, Ahmed Zunirah, Seibert Allan
University of Alabama at Birmingham, Montgomery, AL, USA.
J Investig Med High Impact Case Rep. 2018 Mar 7;6:2324709618760079. doi: 10.1177/2324709618760079. eCollection 2018 Jan-Dec.
Amyloidosis is a rare disorder with a wide spectrum of presentations and anomalies. It is subdivided into 2 broad categories based on protein deposition; primary and secondary amyloidosis. It can present as a single-organ involvement or as a diffuse infiltrative multi-organ process. Isolated hepatic amyloidosis presentation is a rare phenomenon that develops due to insoluble amyloid deposition in liver. Its clinical presentation is usually vague and ranges from mild hepatomegaly with elevated liver enzymes to acute liver failure and hepatic rupture. Currently, there are scarce data available regarding treatment options for biopsy-proven hepatic amyloidosis. In this review article, we present an interesting case of hepatic amyloidosis and its poor outcome to new molecular targeted chemotherapy. Furthermore, we aim to review current and future diagnostic tools for early detection and advancements in targeted chemotherapeutics options available for hepatic amyloidosis.
淀粉样变性是一种罕见的疾病,具有广泛的临床表现和异常情况。根据蛋白质沉积情况,它可分为两大类:原发性和继发性淀粉样变性。它可表现为单器官受累或弥漫性浸润性多器官病变。孤立性肝淀粉样变性表现是一种罕见现象,是由于肝脏中不溶性淀粉样蛋白沉积所致。其临床表现通常不明确,范围从伴有肝酶升高的轻度肝肿大到急性肝衰竭和肝破裂。目前,关于经活检证实的肝淀粉样变性的治疗选择,可用数据很少。在这篇综述文章中,我们介绍了一例肝淀粉样变性的有趣病例及其对新型分子靶向化疗的不良预后。此外,我们旨在综述当前和未来用于早期检测的诊断工具,以及肝淀粉样变性可用的靶向化疗选择的进展。