Minalyan Artem, Gabrielyan Lilit, Khanal Shristi, Basyal Bikash, Derk Chris
Internal Medicine, Abington Hospital-Jefferson Health, Abington, USA.
Pharmacy, School of Pharmacy, University of Southern California, Los Angeles, USA.
Cureus. 2021 Jan 20;13(1):e12797. doi: 10.7759/cureus.12797.
Systemic sclerosis (SSc) is an autoimmune disorder characterized by the involvement of skin and internal organs. With the introduction of angiotensin-converting enzyme inhibitors (ACEIs), scleroderma renal crisis (SRC) is no longer considered a leading cause of death in affected patients. In fact, pulmonary manifestations [interstitial lung disease (ILD) and pulmonary arterial hypertension (PAH)] are currently the major cause of death in patients with SSc. Historically, many centers have been reluctant to offer lung transplantation to patients with SSc due to multiple extrapulmonary manifestations and the assumption of poor post-transplant survival. The purpose of this review is to highlight the recent advances in the evaluation and management of patients with pulmonary manifestations of SSc. We also engage in a systematic literature review to assess all the available data on the survival of patients with SSc after lung transplantation.
系统性硬化症(SSc)是一种自身免疫性疾病,其特征是皮肤和内脏器官受累。随着血管紧张素转换酶抑制剂(ACEIs)的引入,硬皮病肾危象(SRC)不再被认为是受影响患者的主要死因。事实上,肺部表现[间质性肺疾病(ILD)和肺动脉高压(PAH)]目前是SSc患者的主要死因。从历史上看,由于多种肺外表现以及假设移植后生存率低,许多中心一直不愿意为SSc患者提供肺移植。本综述的目的是强调SSc肺部表现患者评估和管理方面的最新进展。我们还进行了系统的文献综述,以评估关于SSc患者肺移植后生存率的所有现有数据。