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先天性胸壁畸形的解剖学、组织学和遗传学特征。

Anatomical, histologic, and genetic characteristics of congenital chest wall deformities.

作者信息

Fokin Alexander A, Steuerwald Nury M, Ahrens William A, Allen Karen E

机构信息

Heineman Medical Research Laboratories, Carolinas Medical Center, Charlotte, NC 28203, USA.

出版信息

Semin Thorac Cardiovasc Surg. 2009 Spring;21(1):44-57. doi: 10.1053/j.semtcvs.2009.03.001.

Abstract

There is a large and diverse group of congenital abnormalities of the thorax that manifest as deformities and/or defects of the anterior chest wall and, depending on the severity and concomitant anomalies, may have cardiopulmonary implications. Pectus excavatum, the most common anterior chest deformity, is characterized by sternal depression with corresponding leftward displacement and rotation of the heart. Pectus carinatum, the second most common, exhibits a variety of chest wall protrusions and very diverse clinical manifestations. The cause of these conditions is thought to be abnormal elongation of the costal cartilages. Collagen, as a major structural component of rib cartilage, is implicated by genetic and histologic analysis. Poland syndrome is a unique unilateral chest/hand deficiency that may include rib defects, pectoral muscle deficit, and syndactyly. Cleft sternum is a rare congenital defect resulting from nonfusion of the sternal halves, which leaves the heart unprotected and requires early surgical intervention.

摘要

有一大类多样的先天性胸廓异常,表现为前胸壁的畸形和/或缺陷,根据严重程度和伴随的异常情况,可能会对心肺产生影响。漏斗胸是最常见的前胸畸形,其特征是胸骨凹陷,心脏相应地向左移位和旋转。鸡胸是第二常见的畸形,表现为多种胸壁突出,临床表现也非常多样。这些情况的病因被认为是肋软骨异常延长。作为肋软骨的主要结构成分,胶原蛋白在基因和组织学分析中受到牵连。波兰综合征是一种独特的单侧胸部/手部缺损,可能包括肋骨缺陷、胸肌缺损和并指畸形。胸骨裂是一种罕见的先天性缺陷,由胸骨两半未融合引起,使心脏得不到保护,需要早期手术干预。

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