Literature DB >> 15621470

Congenital lung malformations--antenatal and postnatal evaluation and management.

Ganesh Shanmugam1, Kenneth MacArthur, James C Pollock.   

Abstract

We reviewed our institutional experience with pulmonary resection for congenital bronchopulmonary malformations and analysed the management and outcome of pregnancies with a prenatal diagnosis of congenital lung malformations. Between January 1993 and December 2003, 31 patients underwent evaluation and pulmonary resection for bronchopulmonary malformations. Common clinical presentations were respiratory distress (9), respiratory infections/pneumonias (22), and dyspnoea (9). Diagnostic modalities included chest radiography, CT scan (22), MRI scan (7), arteriography (1), and bronchoscopy (5). There were 13 congenital cystic adenomatoid malformations (CCAM), six pulmonary sequestrations, three bronchogenic cysts, and nine congenital lobar emphysemas (CLE). Fifteen patients who underwent resection were diagnosed by antenatal ultrasound. No foetus had hydrops or associated malformations. No pregnancy was terminated. There was no foetal demise. Regression of the sonographic appearance was observed in six cases. Amniotic puncture was required for hydramnios in three cases. Eight emergency resections were performed (CCAM 4; CLE 3; Bronchogenic cyst 1). Surgical procedures included 24 lobectomies, one right middle lobectomy with a wedge resection of the right lower lobe, one completion right lower lobectomy, four sequestrectomies, one mediastinal mass excision and one wedge resection for a bronchogenic cyst. There were no deaths. Postoperative complications included: persistent air leak (n=2; one requiring completion lobectomy) and pneumothorax (1). Persistent mild symptoms were present in five patients, at long-term follow-up. Congenital cystic adenomatoid malformation and congenital lobar emphysema were the commonest congenital anomalies. Congenital lung malformations are increasingly diagnosed antenatally, sometimes necessitating emergent surgical resection. The natural history is variable. All infants with a prenatal diagnosis require postnatal evaluation. Patients should be evaluated for associated disorders. The presence of mass effects is an indication for therapeutic decompression. The risk of pulmonary compression, infection and malignant degeneration makes resection imperative, even in asymptomatic patients. Lobectomy is the procedure of choice, is well tolerated, and leads to excellent outcomes.

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Year:  2005        PMID: 15621470     DOI: 10.1016/j.ejcts.2004.10.015

Source DB:  PubMed          Journal:  Eur J Cardiothorac Surg        ISSN: 1010-7940            Impact factor:   4.191


  23 in total

1.  Ball valve obstruction of a bronchus causing lobar emphysema in a neonate.

Authors:  E Clubley; R J England; C Cullinane; D C Crabbe
Journal:  Pediatr Surg Int       Date:  2007-01-06       Impact factor: 1.827

2.  Congenital lobar emphysema: appearance on fetal MRI.

Authors:  Yu-Peng Liu; Shin-Lin Shih
Journal:  Pediatr Radiol       Date:  2008-08-26

Review 3.  [Fetal magnetic resonance imaging. Diagnostics in cases of congenital cystadenomatoid malformation of the lung (CCAM)].

Authors:  K A Büsing; A K Kilian; T Schaible; K W Neff
Journal:  Radiologe       Date:  2006-02       Impact factor: 0.635

Review 4.  Symptom development in originally asymptomatic CPAM diagnosed prenatally: a systematic review.

Authors:  Navot Kantor; Carolyn Wayne; Ahmed Nasr
Journal:  Pediatr Surg Int       Date:  2018-04-09       Impact factor: 1.827

5.  The surgical management and outcome of congenital mediastinal malformations.

Authors:  Quentin Ballouhey; Philippe Galinier; Olivier Abbo; Guillaume Andrieu; Christiane Baunin; Agnès Sartor; Jean Luc Rittié; Bertrand Léobon
Journal:  Interact Cardiovasc Thorac Surg       Date:  2012-03-05

6.  A bronchogenic cyst of the larynx: A case report.

Authors:  Dan Lu; Rong Yu; Hui Yang; Jun Liu
Journal:  Exp Ther Med       Date:  2017-09-29       Impact factor: 2.447

7.  Children with congenital cystic adenomatoid malformation of the lung CT diagnosis.

Authors:  Zeng-Jun Zhang; Ming-Xia Huang
Journal:  Int J Clin Exp Med       Date:  2015-03-15

8.  Antenatally diagnosed congenital cystic adenomatoid malformations (CCAM): Research Review.

Authors:  Fosca Antonia Francesca Di Prima; Adriano Bellia; Genny Inclimona; Francesco Grasso; Maria Teresa; Meli Nazario Cassaro
Journal:  J Prenat Med       Date:  2012-04

9.  Management of fetal bronchogenic lung cysts: a case report and short review of literature.

Authors:  Ulkü Ozmen Bayar; Varîm Numanoğlu; Sibel Bektaş; Hakan Sade; Duygu Tatlî
Journal:  Case Rep Med       Date:  2010-03-21

10.  Congenital pulmonary airway malformation (CPAM) with initial presentation in an adult: a rare presentation of a rare disease.

Authors:  Mohannad Abu Omar; Emily Tylski; Mouhanna Abu Ghanimeh; Ashraf Gohar
Journal:  BMJ Case Rep       Date:  2016-09-26
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