1.Research on some factors related to congenital malformation
Journal of Medical and Pharmaceutical Information 2004;0(7):31-33
Background: In 2005, a report showed that the mortality of fetal malformations accounts for 12.9% causes of death in newborns. It is importance for obstetricians and society as a whole to detect prenatal fetal malformations. Objective: To define various factors that might influence malformations in newborns. Subjects and method: A comparison study performed on 926 pregnant women with fetal malformations and 1852 pregnant women without fetal malformations amongst 20,345 pregnant women screened by prenatal ultrasound at the Central Hospital of Obstetrics and Gynecology, from July 2003 to July 2006. Results and conclusions: In comparing to 1826 pregnant women without fetal malformations, the fetal malformations were more frequently in young or older mothers (19 years old or less and 40 years old or over), farmers, the mother had been suffering from fever in the first three months of pregnancy; parents exposed to chemicals and pesticides. Mother\u2019s that previously had children with congenital malformation affected significantly the fetal malformation.
Fetal malformation
;
congenital malformation
;
pregnancy
2.Surgical treatment of congenital cystic adenomatoid malformation.
Zhung Hi LEE ; Hyung Ho CHOI ; Jin Soo IM
The Korean Journal of Thoracic and Cardiovascular Surgery 1993;26(4):320-324
No abstract available.
Cystic Adenomatoid Malformation of Lung, Congenital*
3.A ten-year review of congenital pulmonary airway malformation cases in a pediatric tertiary hospital
Kimberly Jane M. Monroy ; Beatriz Praxedes Apolla I. Mandalas-Paz
The Philippine Children’s Medical Center Journal 2024;20(1):73-83
Objective:
A retrospective study of the demographic, clinical and diagnostic profile,
intervention and outcomes of children with Congenital Pulmonary Airway Malformation (CPAM)
in Philippine Children’s Medical Center (PCMC) from January 2011 to December 2021 was
presented.
Methodology:
Medical charts of identified patients were reviewed. Data obtained
included demographic profile, clinical history, diagnostic procedures, intervention, and outcomes.
The findings were analyzed and correlated with the synthesized findings from relevant studies
about CPAM.
Results:
Twenty-three cases (n=23) were included in the study. Most of the patients were
diagnosed at 1 to 11 months of age, accounting for 43.48% while there is a minimal disparity in
terms of gender distribution. Seventy-five percent of neonates presented with respiratory distress
while recurrent pneumonia occurred more frequently beyond the neonatal period. Four patients at
17.39% had incidental findings of CPAM on prenatal ultrasound. All cases were confirmed using a
Chest CT scan and only six patients at 26.09% had Chest X-ray results consistent with CPAM.
Eight cases were confirmed using biopsy wherein results were mainly Type I seen in 87.5% of
cases. Lobectomy is the procedure of choice with 92.86% success rate. Overall, patients who
underwent surgical intervention had a low complication rate at 6.25%.
Conclusion
CPAM is most common in patients aged 1 to 11 months and has no gender
predilection. Neonates often present with respiratory distress while recurrent pneumonia is the most
common clinical manifestation beyond neonatal period. CPAM can be detected using ultrasound
prenatally and CT scan can confirm CPAM postnatally. Surgical intervention particularly
lobectomy is the preferred option over conservative management which showed a favorable
outcome. CPAM has an overall good prognosis. Findings of this research may guide clinicians in
the diagnosis and management of CPAM in the Philippines.
Cystic Adenomatoid Malformation of Lung, Congenital
4.Antenatal ultrasonographic diagnosis of congenital cystic adenomatoid malformation of lung: report of a case.
Jin Sook HUH ; Young Ho JUNG ; Yong Pil KIM ; Eui Sun RO ; Soon Uk KWON ; Choong Ki PARK ; Min Chul LEE
Korean Journal of Obstetrics and Gynecology 1992;35(9):1401-1406
No abstract available.
Cystic Adenomatoid Malformation of Lung, Congenital*
;
Diagnosis*
5.Clinical features of congenital cystic adenomatoid malformation of the lung.
Seok Won PARK ; Soo Young LEE ; Byung Joo JEUNG ; Kyu Earn KIM ; Ki Young LEE
Pediatric Allergy and Respiratory Disease 1993;3(2):94-102
No abstract available.
Cystic Adenomatoid Malformation of Lung, Congenital*
;
Lung*
6.Congenital cystic adenomatoid malformation of the lung.
Myung In KIM ; Eung Joong KIM ; Seung Pyung LIM ; Young LEE
The Korean Journal of Thoracic and Cardiovascular Surgery 1991;24(8):819-823
No abstract available.
Cystic Adenomatoid Malformation of Lung, Congenital*
;
Lung*
7.A case of congenital cystic adenomatoid malformation in adult patient.
Jae Seck SEO ; Yong Chul LEE ; Yang Keun RHEE
Korean Journal of Medicine 1993;45(1):104-108
No abstract available.
Adult*
;
Cystic Adenomatoid Malformation of Lung, Congenital*
;
Humans
9.A Case of Congenital Cystic Adenomatoid Malformation (Type1) of the Lung.
Dong Sik KIM ; Hwang Min KIM ; Jae Seung YANG ; Baek Keun KIM ; Jong Soo KIM ; Dong Hwan SHIN
Journal of the Korean Pediatric Society 1990;33(6):830-834
No abstract available.
Cystic Adenomatoid Malformation of Lung, Congenital*
;
Lung*
10.Perioperative anesthetic care of children with Congenital Cystic Adenomatous Malformation: A report of 3 cases.
Ralph Philip M. Anislag ; Grace G. Catalan
Acta Medica Philippina 2022;56(18):28-34
Congenital cystic adenomatoid malformation (CCAM) is a rare developmental entity. Symptomatic patients must undergo thoracic surgery for lobectomy. Perioperative anesthetic management is challenging because it involves
thoracotomy in a young patient that may lead to hemodynamic compromise and inadequate ventilation. We present 3 cases of pediatric patients (6 months - 2 years old) with CCAM who underwent lobectomy.
Cystic Adenomatoid Malformation of Lung, Congenital ; Airway Extubation