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前肠畸形的支气管肺和神经肠形式。诊断与管理的影像学检查

Bronchopulmonary and neurenteric forms of foregut anomalies. Imaging for diagnosis and management.

作者信息

Haddon M J, Bowen A

机构信息

University of Pittsburgh School of Medicine, Pennsylvania.

出版信息

Radiol Clin North Am. 1991 Mar;29(2):241-54.

PMID:1998049
Abstract

Bronchopulmonary foregut malformations encompass a great variety of anomalies that may arise from abnormal differentiation of the respiratory and alimentary tracts, abnormal separation of the two systems, or abnormal development of blood supply, perhaps singly or in combination, during early embryogenesis. The pulmonary and neurenteric forms share the common features of a pulmonary parenchymal opacification and/or intrathoracic mass, with the addition of vertebral anomalies in the instance of the neurenteric malformations. Plain radiographs serve as the starting point for diagnostic evaluation and sometimes are all that is needed; more often, though, the plain film findings suggest which road to follow in further imaging. No single imaging approach can be advocated for all patients. The lesion may be found initially, for example, on prenatal sonography. Ultrasonography also can establish the cystic nature of a mass and may help define vascular supply, although it cannot yet be said to have supplanted angiography's role in evaluating suspected sequestrations. For most intramediastinal or intrapulmonary masses without associated vertebral anomalies, CT will satisfactorily establish the cystic nature and should afford a reasonably confident preoperative diagnosis of bronchogenic cysts or type 1 or 2 cystic adenomatoid malformations. Type 3 cystic adenomatoid malformation, because of its relatively "solid" imaging characteristics, may not be diagnosed confidently by preoperative imaging. The finding of vertebral anomalies associated with a mediastinal mass especially warrants MR imaging to define intraspinal involvement. However, the association of vertebral or rib anomalies with apparent unilateral pulmonary agenesis or hypoplasia arouses suspicion of a bronchopulmonary foregut malformation that communicates with the gastrointestinal tract, and this uncommon situation calls for a barium examination. Radionuclide scintigraphy has an ancillary role in assessing foregut anomalies, but many findings from scintigraphy are relatively nonspecific and anatomic definition is poor. Scintigraphy may yield supportive information in cases of sequestration that have inconclusive findings as determined by plain radiographs and CT.

摘要

支气管肺前肠畸形包括多种异常情况,这些异常可能源于呼吸道和消化道的异常分化、两个系统的异常分离或血液供应的异常发育,可能单独出现,也可能在胚胎早期发育过程中合并出现。肺型和神经肠型具有肺实质混浊和/或胸内肿块的共同特征,神经肠畸形还伴有脊柱异常。胸部X线平片是诊断评估的起点,有时仅靠它就足够了;不过,更常见的情况是,平片检查结果提示进一步成像应采用的方法。并非所有患者都能采用单一的成像方法。例如,病变可能最初在产前超声检查中被发现。超声检查也可以确定肿块的囊性性质,并可能有助于确定血管供应,尽管目前还不能说它已经取代了血管造影在评估疑似肺隔离症中的作用。对于大多数无相关脊柱异常的纵隔内或肺内肿块,CT将能令人满意地确定其囊性性质,并应能在术前对支气管囊肿或1型或2型囊性腺瘤样畸形做出较为可靠的诊断。3型囊性腺瘤样畸形由于其相对“实性”的成像特征,术前成像可能无法可靠地诊断。发现纵隔肿块伴有脊柱异常尤其需要进行磁共振成像以确定脊髓受累情况。然而,脊柱或肋骨异常与明显的单侧肺不发育或发育不全相关联时,会引发对与胃肠道相通的支气管肺前肠畸形的怀疑,这种罕见情况需要进行钡剂检查。放射性核素闪烁扫描在评估前肠异常方面起辅助作用,但闪烁扫描的许多结果相对非特异性,解剖结构显示不佳。对于平片和CT检查结果不确定的肺隔离症病例,闪烁扫描可能会提供支持性信息。

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