Bennett Christopher L, Aziz Hamza, Sparks Elizabeth, Shah Trushil, Yoder Mark, MacCarrick Gretchen, Dietz Harry C
University of North Carolina School of Medicine, Chapel Hill, North Carolina.
The Howard Hughes Medical Institute, Baltimore, Maryland.
Am J Med Genet A. 2016 Mar;170(3):725-7. doi: 10.1002/ajmg.a.37487. Epub 2015 Nov 27.
We describe four unrelated individuals with Loeys-Dietz syndrome (LDS) who presented with massive hemoptysis of unknown etiology. LDS is an autosomal dominant connective-tissue disorder characterized by altered cardiovascular, craniofacial, and skeletal development that is attributed to mutations in the TGFBR1, TGFBR2, SMAD3, or TGFB2 genes. Massive hemoptysis (MH) is a rare and often fatal pulmonary medical emergency. This is the first report of MH in individuals with LDS and establishes it as part of the LDS spectrum. It compels providers to educate their LDS patients on MH, although much investigation needs to be done to determine etiology and appropriate treatment for this newly described LDS feature.
我们描述了四名患有洛伊氏综合征(LDS)的非亲缘个体,他们出现了病因不明的大量咯血。LDS是一种常染色体显性遗传性结缔组织疾病,其特征为心血管、颅面和骨骼发育异常,这归因于TGFBR1、TGFBR2、SMAD3或TGFB2基因的突变。大量咯血(MH)是一种罕见且常致命的肺部医疗急症。这是关于LDS个体出现MH的首例报告,并将其确立为LDS谱系的一部分。这促使医疗人员对其LDS患者进行关于MH的教育,尽管要确定这种新描述的LDS特征的病因和适当治疗方法还需要进行大量研究。