Lymphangioleiomyomatosis: A Review.

Mohammed Amine Bouanzoul, Yale Rosen
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引用次数: 0

Abstract

Context.—: Lymphangioleiomyomatosis is a rare multisystem disorder belonging to the family of neoplasms exhibiting perivascular epithelioid differentiation. It primarily affects women of childbearing age. The disease is characterized by a proliferation of smooth muscle-like cells (lymphangioleiomyomatosis cells) within all lung compartments, leading to cystic parenchymal destruction and, in some cases, respiratory failure. These cells carry mutations in one or both tuberous sclerosis (TSC) genes and coexpress smooth muscle and melanocytic markers. Female hormones, particularly estrogens, influence the course of the disease. Symptoms of lymphangioleiomyomatosis vary significantly among patients, ranging from exertional dyspnea and coughing to chest pain and recurrent pneumothorax.

Objective.—: To present the latest advancements in the understanding of disease pathogenesis and diagnosis, illustrate the pathologic and radiologic findings, provide a reference for pathologists and other health care professionals, briefly discuss recent evidence-based therapeutic approaches, and emphasize the importance of adopting a multidisciplinary approach to diagnosis and optimization of patient care.

Data sources.—: A comprehensive review of pertinent medical literature published in the last 30 years, focusing on publications written in the English language, was performed.

Conclusions.—: Despite the recent significant advancements in the understanding and management of lymphangioleiomyomatosis, there are still significant gaps in our knowledge of its pathophysiology and the role of the immune system in the genesis and progression of the disease. The current changes in diagnostic algorithms favor the adoption of minimally invasive procedures as the standard of care. As a result, the clinical laboratory will play a larger role in the diagnosis of lymphangioleiomyomatosis, and surgical pathologists will likely be less involved in the diagnosis of pulmonary lymphangioleiomyomatosis than they currently are.

淋巴管瘤病:综述。
内涵:淋巴管瘤病是一种罕见的多系统疾病,属于血管周围上皮样分化的肿瘤家族。它主要影响育龄妇女。该病的特点是平滑肌样细胞(淋巴管瘤细胞)在肺部各处增生,导致肺实质囊性破坏,在某些情况下还会导致呼吸衰竭。这些细胞携带一个或两个结节性硬化症(TSC)基因突变,共同表达平滑肌和黑色素细胞标记。女性荷尔蒙,尤其是雌激素会影响疾病的进程。淋巴管瘤病的症状因人而异,从劳累性呼吸困难和咳嗽到胸痛和复发性气胸不等:介绍在了解疾病发病机制和诊断方面的最新进展,说明病理学和放射学检查结果,为病理学家和其他医护人员提供参考,简要讨论最新的循证治疗方法,并强调采用多学科方法进行诊断和优化患者护理的重要性:数据来源:对过去 30 年出版的相关医学文献进行了全面回顾,重点是以英语撰写的出版物:尽管近年来对淋巴管瘤病的认识和治疗取得了重大进展,但我们对其病理生理学以及免疫系统在疾病发生和发展过程中的作用的认识仍有很大差距。目前诊断算法的变化有利于采用微创手术作为治疗标准。因此,临床实验室将在淋巴管瘤病的诊断中发挥更大的作用,而外科病理学家在肺淋巴管瘤病的诊断中的参与度可能会比现在低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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