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混合性结缔组织病累及双侧膈肌的非典型表现。

Atypical Presentation of Mixed Connective Tissue Disorder Involving Bilateral Diaphragm.

作者信息

Saragadam Sailaja Devi, Mukkera Srikanth

机构信息

Department of Internal Medicine, Texas Tech University Health Sciences Center at Permian Basin, Odessa, USA.

Department of Internal Medicine, Texas Tech University Health Science Center at Permian Basin, Odessa, USA.

出版信息

Cureus. 2022 Feb 12;14(2):e22154. doi: 10.7759/cureus.22154. eCollection 2022 Feb.

Abstract

Pulmonary manifestations can be present in 20-80% of patients having mixed connective tissue disorder (MCTD) and are usually subacute. MCTD when associated with polymyositis can rarely involve the diaphragm, causing respiratory failure. We present herein the case of a 49-year-old female having MCTD with a component of polymyositis who presented with bilateral diaphragmatic paralysis followed by heart failure requiring respiratory support with non-invasive mechanical ventilation. We are aware of only one prior instance of MCTD associated with unilateral diaphragmatic weakness causing mild respiratory dysfunction. To the best of our knowledge, this is the second reported case of diaphragmatic involvement in the MCTD population, with bilateral diaphragmatic paralysis causing severe respiratory failure. This is also the first reported case of such an unusual initial presentation in this patient group. Pulmonary involvement has a poor prognosis. Early diagnosis with the initiation of therapy can improve mortality outcomes in this patient population.

摘要

肺部表现可见于20%-80%的混合性结缔组织病(MCTD)患者,通常呈亚急性。MCTD与多发性肌炎相关时,很少累及膈肌,导致呼吸衰竭。本文介绍了一例49岁女性患者,患有合并多发性肌炎成分的MCTD,该患者出现双侧膈肌麻痹,随后发生心力衰竭,需要无创机械通气进行呼吸支持。我们仅知晓此前有1例MCTD与单侧膈肌无力相关,导致轻度呼吸功能障碍。据我们所知,这是第二例报道的MCTD患者出现膈肌受累且双侧膈肌麻痹导致严重呼吸衰竭的病例。这也是该患者群体中首例报道的如此不寻常的初始表现。肺部受累预后较差。早期诊断并开始治疗可改善该患者群体的死亡率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16c0/8919897/cb0fe5cb64f5/cureus-0014-00000022154-i01.jpg

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