Literature DB >> 15784369

Treatment of congenital cystic adenomatoid malformation-does resection in the early postnatal period increase surgical risk?

Young Tae Kim1, Jun Sung Kim, June Dong Park, Chang Hyun Kang, Sook Whan Sung, Joo Hyun Kim.   

Abstract

OBJECTIVE: The recent development of fetal ultrasonography has allowed for an increasing number of prenatal diagnoses for congenital cystic adenomatoid malformation (CCAM). However, the appropriate surgical timing of these patients has not been studied as of yet. The aim of this study is to suggest a safe strategy for the treatment of CCAM by identifying the relationship between the timing of surgery and postoperative outcome.
METHODS: Between 1987 and 2003, 40 patients (28 males, 12 females) underwent surgical resection for CCAM. The mean age was 38.6+/-9.1 (2 days-13 years) months. CCAM was diagnosed by prenatal ultrasonography in eight patients. Early operations were performed in four out of the eight. Operation was deferred until 2-12 months of age for the remaining four patients.
RESULTS: Type I CCAM was found in 20 patients, type II in 20 and no patient exhibited type III. Five patients had associated pectus excavatum anomaly. There were no cases of operative mortality. Seventeen minor postoperative complications developed in 16 patients (40.0%): prolonged chest tube drain in 10, wound infection in 4, and 1 case of pneumonia, empyema and pleural space, respectively. The average hospital stay was 11.8 (6-29) days. During the mean follow-up period of 67.5 months, one patient died of accidental aspiration 7 months after operation during the postoperative recovery course of Ravich operation for pectus excavatum. The remaining patients reported doing well with normal physical activity. All five patients who underwent surgery at the age of under 1 month did not exhibit increased postoperative morbidity.
CONCLUSIONS: We concluded that surgery for CCAM could be safely performed in all age groups with satisfactory long-term outcomes. It is suggested that early elective surgical correction can be recommended for a patient whose diagnosis was made in utero.

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Year:  2005        PMID: 15784369     DOI: 10.1016/j.ejcts.2005.01.028

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


  8 in total

Review 1.  Optimal age for elective surgery of asymptomatic congenital pulmonary airway malformation: a meta-analysis.

Authors:  Katrina J Sullivan; Michelle Li; Sarah Haworth; Elizabeth Chernetsova; Carolyn Wayne; Jessica Kapralik; Emily Chan; Ahmed Nasr
Journal:  Pediatr Surg Int       Date:  2017-03-14       Impact factor: 1.827

2.  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

Review 3.  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

4.  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

5.  Managing prenatally diagnosed asymptomatic congenital cystic adenomatoid malformation.

Authors:  Ryo Sueyoshi; Tadaharu Okazaki; Naoto Urushihara; Toshio Fujiwara; Shigeru Tobayama; Koji Fukumoto; Fumiko Horigome; Eri Tei; Geoffrey J Lane; Shiro Hasegawa; Atsuyuki Yamataka
Journal:  Pediatr Surg Int       Date:  2008-10       Impact factor: 1.827

6.  Surgical intervention for congenital pulmonary airway malformation (CPAM) patients with preoperative pneumonia and abscess formation: "open versus thoracoscopic lobectomy".

Authors:  Ryo Sueyoshi; Hiroyuki Koga; Kenji Suzuki; Go Miyano; Manabu Okawada; Takashi Doi; Geoffrey J Lane; Atsuyuki Yamataka
Journal:  Pediatr Surg Int       Date:  2015-12-12       Impact factor: 1.827

7.  Congenital cystic adenomatoid malformation - diagnostic and therapeutic procedure: 8-year experience of one medical centre.

Authors:  Bogumiła Strumiłło; Andrzej Jóźwiak; Anna Pałka; Krzysztof Szaflik; Anna Piaseczna-Piotrowska
Journal:  Kardiochir Torakochirurgia Pol       Date:  2018-03-28

8.  Life-Threatening Congenital Cystic Adenomatoid Malformation in the Premature Neonate.

Authors:  Yooyoung Chong; Youn Ju Rhee; Sung Joon Han; Hyun Jin Cho; Shin Kwang Kang; Min-Woong Kang
Journal:  Korean J Thorac Cardiovasc Surg       Date:  2016-06-05
  8 in total

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