标志着一个多世纪的奥尔棒:急性早幼粒细胞白血病的图解回顾。

Ruah Alyamany, Ayman Saad, Ahmad Alotaibi, Marwan Shaheen, Mansour Alfayez
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摘要

1903年,约翰·奥尔(John Auer)博士首次在一位发烧、凝血功能障碍和脾肿大的病人身上观察到针状棒状物,他最初将其误认为淋巴细胞。后来在髓母细胞中发现,这些“奥尔棒”成为髓系恶性肿瘤的一个决定性特征。其中,早幼粒细胞白血病(acute promyelocytic leukemia, APL)于1957年被确认为一个独特的临床实体,因其严重的凝血功能和高得惊人的早期死亡率,曾一度被认为是最致命的急性白血病。然而,里程碑式的突破,特别是20世纪80年代全反式维甲酸和90年代三氧化二砷的引入,将APL转变为最可治愈的急性白血病,前提是尽早开始治疗。这篇图文并茂的综述强调了自Auer棒首次被发现以来的一个多世纪,提供了一个简洁、直观的APL流行病学、临床表现和诊断策略概述。我们探索现代和实用的治疗方法,强调风险适应治疗,并解决主要并发症,包括分化证,凝血功能障碍和中枢神经系统受累。apl的显著进化——从一种高度致命的疾病到最可治疗的白血病——突显了我们对疾病病理生理学和生物学的理解如何改变治疗策略并改善患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Marking over a century of Auer rods: An illustrated review of acute promyelocytic leukemia.

In 1903, Dr. John Auer first observed needle-like rods in what he initially mistook for lymphocytes from a patient with fever, coagulopathy, and splenomegaly. Later discovered in myeloblasts, these "Auer rods" emerged as a defining feature of myeloid malignancies. Among them, acute promyelocytic leukemia (APL), recognized as a distinct clinical entity in 1957, was once considered the most lethal acute leukemia due to its severe coagulopathy and alarmingly high early mortality rate. However, landmark breakthroughs, particularly the introduction of all-trans retinoic acid in the 1980s and arsenic trioxide in the 1990s, transformed APL into the most curable form of acute leukemia, provided that treatment begins early. This illustrated review highlights over a century since Auer rods were first identified, offering a concise, visually guided overview of APL's epidemiology, clinical presentation, and diagnostic strategies. We explore modern and practical therapeutic approaches, emphasize risk-adapted treatments, and address major complications, including differentiation syndrome, coagulopathy, and central nervous system involvement. The remarkable evolution of APL-from a highly fatal disease to the most treatable leukemia-highlights how our understanding of disease pathophysiology and biology can transform treatment strategies and improve patient outcomes.

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