Literature DB >> 15185110

Congenital cystic adenomatoid malformation of the lung: indications and timing of surgery.

J K Khosa1, S L Leong, P A Borzi.   

Abstract

We review a single surgeon and surgical centre's experience with congenital cystic adenomatoid malformation of the lung (CCAML) in relation to clinical spectrum, operative experience, and postoperative course. A retrospective hospital record review was done on surgically treated cases of CCAML over a 10-year period, focusing on number with antenatal diagnosis, spectrum of postnatal presentation, type of surgery performed, and outcome. Forty-seven patients from birth to 14 years of age underwent surgery for CCAML. Antenatal diagnosis (ante) was made in 30 cases. Of these, 10 became symptomatic before surgery. Six of the 17 postnatally-diagnosed (pnd) cases were an asymptomatic incidental finding. Overall, 16 were symptomatic in the 1st year of life, and five were symptomatic beyond 1 year of age. Symptoms varied from respiratory distress (seven ante, six pnd) to chronic cough (three, and recurrent chest infection (three ante, two pnd). All preoperative diagnoses were confirmed with chest CT. Most patients (25) were operated on before 3 months of age. Eleven were operated on in the first 2 weeks of life as emergency surgery for respiratory distress. The most common lobe involved was the right upper lobe (16), and lobectomy was performed in 42 cases, segmentectomy in four, and pneumonectomy in one. Seventeen cases were extubated immediately postoperatively; 29 required postoperative ventilation overnight, and nine needed more prolonged ventilation. Early postoperative complications included pneumothorax (two), pleural effusion (one), and chylous effusion (one). Late complications included recurrence in three cases (all segmentectomy), who then subsequently underwent lobectomy. There was one death from respiratory failure. Because there is an increasing trend in the detection of asymptomatic antenatally-diagnosed CCAML, consideration of early surgical excision to prevent complications is suggested by our series. CT scanning is mandatory for postnatal evaluation because chest x-ray could be normal. Safe elective excision after 3 months is supported by our low morbidity and less need for postoperative ventilation. Lobectomy is the procedure of choice to prevent recurrence.

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Year:  2004        PMID: 15185110     DOI: 10.1007/s00383-004-1225-4

Source DB:  PubMed          Journal:  Pediatr Surg Int        ISSN: 0179-0358            Impact factor:   1.827


  18 in total

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Review 3.  Embryonal rhabdomyosarcoma of the lung arising in cystic adenomatoid malformation: case report and review of the literature.

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7.  Experience with thoracoscopic lobectomy in infants and children.

Authors:  Steven S Rothenberg
Journal:  J Pediatr Surg       Date:  2003-01       Impact factor: 2.545

8.  Surgical management of lung bud anomalies: lobar emphysema, bronchogenic cyst, cystic adenomatoid malformation, and intralobar pulmonary sequestration.

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  14 in total

1.  Prospective study of antenatally diagnosed congenital cystic adenomatoid malformations.

Authors:  P Raychaudhuri; A Pasupati; A James; B Whitehead; R Kumar
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2.  Lung resections in children for congenital and acquired lesions.

Authors:  Subhasis Roy Choudhury; Rajiv Chadha; Atul Mishra; Virendra Kumar; Varinder Singh; Nand Kishore Dubey
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Review 3.  Optimal age for elective surgery of asymptomatic congenital pulmonary airway malformation: a meta-analysis.

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4.  Thoracoscopy in the management of congenital lung diseases in infancy.

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Review 5.  Thoracoscopic Lobectomy for Congenital Lung Lesions.

Authors:  Jarrett Moyer; Hanmin Lee; Lan Vu
Journal:  Clin Perinatol       Date:  2017-09-28       Impact factor: 3.430

6.  Outcome and treatment in an antenatally diagnosed congenital cystic adenomatoid malformation of the lung.

Authors:  Kouji Nagata; Kouji Masumoto; Risa Tesiba; Genshirou Esumi; Kiyomi Tsukimori; Wake Norio; Tomoaki Taguchi
Journal:  Pediatr Surg Int       Date:  2009-09       Impact factor: 1.827

7.  Presentation and management of pulmonary sequestration with total visceral inflow and outflow.

Authors:  Christopher L Sudduth; Sarah J Hill; Mehul V Raval
Journal:  Pediatr Surg Int       Date:  2016-03-11       Impact factor: 1.827

Review 8.  Treatment of congenital pulmonary airway malformations: a systematic review from the APSA outcomes and evidence based practice committee.

Authors:  Cynthia D Downard; Casey M Calkins; Regan F Williams; Elizabeth J Renaud; Tim Jancelewicz; Julia Grabowski; Roshni Dasgupta; Milissa McKee; Robert Baird; Mary T Austin; Meghan A Arnold; Adam B Goldin; Julia Shelton; Saleem Islam
Journal:  Pediatr Surg Int       Date:  2017-06-06       Impact factor: 1.827

9.  Congenital bronchopulmonary malformations: a single-center experience and a review of literature.

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Journal:  Ann Thorac Med       Date:  2008-10       Impact factor: 2.219

10.  Long-term outcome of asymptomatic patients with congenital cystic adenomatoid malformation.

Authors:  A Wong; D Vieten; S Singh; J G Harvey; Andrew J A Holland
Journal:  Pediatr Surg Int       Date:  2009-04-30       Impact factor: 1.827

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