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疑似杆状体肌病导致的极低肌张力和呼吸衰竭在一名早产儿中的病例

Profound Hypotonia and Respiratory Failure due to Suspected Nemaline Myopathy in a Preterm Infant.

作者信息

Akuamoah-Boateng Gloria, Stetson Raymond C, Kaemingk Bethany D, Bieber David A, Brumbaugh Jane E

机构信息

Department of Pediatric and Adolescent Medicine, Mayo Clinic, Rochester, Minnesota.

Division of Neonatal Medicine, Department of Pediatric and Adolescent Medicine, Mayo Clinic, Rochester, Minnesota.

出版信息

AJP Rep. 2021 Apr;11(2):e91-e94. doi: 10.1055/s-0041-1728782. Epub 2021 Jun 23.

Abstract

Congenital myopathies, such as nemaline myopathy, may present with hypotonia and respiratory failure in the neonatal period. Respiratory function can be further compromised in affected infants by the development of chylous effusions. We present the case of a preterm male infant born at 32 weeks' gestation, who was profoundly hypotonic and required intubation at birth. His clinical course progressed from acute to chronic respiratory failure with mechanical ventilation dependence. He developed bilateral chylous pleural effusions during the newborn period. Whole exome sequencing identified an gene mutation leading to the presumed diagnosis of nemaline myopathy. This case highlights the need to include congenital myopathies in the differential for a preterm newborn with hypotonia and respiratory failure.

摘要

先天性肌病,如杆状体肌病,在新生儿期可能表现为肌张力减退和呼吸衰竭。患有乳糜性积液的患病婴儿的呼吸功能可能会进一步受损。我们报告了一例孕32周出生的早产男婴,他出生时肌张力严重减退,出生时需要插管。他的临床病程从急性呼吸衰竭发展为慢性呼吸衰竭,并依赖机械通气。他在新生儿期出现双侧乳糜性胸腔积液。全外显子组测序确定了一个基因突变,从而推定诊断为杆状体肌病。该病例强调,对于患有肌张力减退和呼吸衰竭的早产新生儿,鉴别诊断时需要考虑先天性肌病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7667/8221836/dd96ffe90282/10-1055-s-0041-1728782-i200135-1.jpg

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