1.A case of thoracic ectopia cordis.
Yong Kwan KIM ; Won Poong SON ; Young Woo JANG ; Sook CHO ; Byung Moon KANG ; Goo Sang KIM
Korean Journal of Obstetrics and Gynecology 1993;36(7):2839-2842
No abstract available.
Ectopia Cordis*
2.Ectopia cordis totalis: Case in images
Jayce V Estrera ; Delbrynth P Mitchao ; Kathleen Rose Descallar-Mata
Southern Philippines Medical Center Journal of Health Care Services 2019;5(1):1-7
Ectopia cordis (EC) is a rare congenital malformation characterized by a complete or partial extrathoracic presentation of the heart,1 2 with an incidence of only 6 to 8 in a million live births globally.3 4 It occurs due to failure of maturation of the midline mesoderm and improper formation of the chest and abdomen during embryonic development.5 6 Depending on the heart’s ectopic location, EC is classified into four types—i.e., thoracic (65% of cases), thoracoabdominal (20%), abdominal (10%), and cervical (5%).1 2 4 7 Only two cases of EC, one thoracic and one thoracoabdominal, from the Philippines had been reported in literature.8 Cantrell’s pentalogy—findings of bifid sternum, absence of the diaphragm, defect of anterior diaphragmatic pericardium, defect of the anterior abdominal wall, and intracardiac defects—usually accompanies the thoracoabdominal type of EC.
Ectopia Cordis
3.A case of prenatal diagnosed ectopia cordis by ultrasonography.
Yong Suk JUNG ; Kae Hyun NAM ; Kwon Hae LEE ; Tai Ho CHO
Korean Journal of Obstetrics and Gynecology 1992;35(8):1233-1237
No abstract available.
Ectopia Cordis*
;
Ultrasonography*
4.A case of prenatal ultrasonographic diagnosis of thoracic ectopia cordis.
Yung Hyun OH ; Yong Hoon CHO ; Young Don YOON ; Tae Bok SONG ; Bong Suck OH
Korean Journal of Obstetrics and Gynecology 1992;35(7):1065-1070
No abstract available.
Diagnosis*
;
Ectopia Cordis*
5.A case of omphalocele and ectopia cordis with diaphragmatic defect.
Young Joo CHOI ; Kyung Don BAIK ; Hong Sup LEE ; Boo Soo HA ; Sang Kap KIM ; Jung Hee CHI
Korean Journal of Obstetrics and Gynecology 1992;35(7):1082-1087
No abstract available.
Ectopia Cordis*
;
Hernia, Umbilical*
7.A Case of Prenatal Diagnosis of Thoracic Ectopia Cordis.
Seong Joon YOON ; Bong Shik SHIN ; Kyo Weon LEE ; Hye Sup SONG ; Jong Seul HAN ; Sung Do KIM ; Joo Seob KEUM ; Myung Sook KIM ; Tae Yun OH
Korean Journal of Obstetrics and Gynecology 1997;40(10):2317-2321
Ectopia cordis is defined as a congenital malposition of the heart partially or completely outside the thorax and often associated with sternal and congenital heart defects:surgical repair is generally unsuccessful because of the magnitude of the deformity and the associat-ed intracardiac anormalies. Four types of ectopia cordis are described : cervical, thoracic, abdominal and thoracoa- bdominal. Cervical and thoracic type are often fatal within days, because the heart is expo- sed and malformed. Abdominal type carries a better prognosis because cardiac abnormalities are less often found. The prognosis of thoraco-abdominal type mainly depends on the pre- sence of intracardiac abnormalities. We have experienced a case of thoracic ectopia cordis at 25 weeks' gestation by ultra- sonography, so present the case and the review with literature briefly.
Congenital Abnormalities
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Ectopia Cordis*
;
Heart
;
Pregnancy
;
Prenatal Diagnosis*
;
Prognosis
;
Thorax
8.Complete Sternal Cleft.
Je Kyoun SHIN ; Jong Pil JUNG ; Dong Gon YOO ; Sung Jong PARK ; Chin Yong CHUNG ; Gun Ho LEE
The Korean Journal of Thoracic and Cardiovascular Surgery 1999;32(10):966-969
Congenital defects of the sternum are rare development anomalies. They result form the failure of the lateral sternal bars to fuse. This malformation may be associated with other ventral midline fusion defects and ectopia cordis. A complete sternal cleft is the rarest form and less than 10 cases have been reported in the medical literature. Here were report a 3-day-old boy with complete sternal cleft without other malformations, who underwent primary surgical repair. Surgical correction of complete sternal cleft should be performed in neonatal period whether the infant if symptomatic or not because it is usually simple, able to achieve good result and primary repair is usually feasible at this period.
Congenital Abnormalities
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Ectopia Cordis
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Humans
;
Infant
;
Male
;
Sternum
9.Repair of Inferior Sternal Cleft Using Bilateral Sternal Bar Turnover Flaps in a Patient with Pentalogy of Cantrell.
Hui Ling CHIA ; Vincent Kok Leng YEOW
Archives of Plastic Surgery 2014;41(1):77-80
We report a case of sternal reconstruction using bilateral sternal bar turnover flaps in a 4-year-old boy with an inferior sternal cleft, as part of Cantrell's pentad. When the patient was 10 months old, he underwent sternal reconstruction using a resorbable poly-L-lactic-polyglycolic acid plate in the first stage when there was insufficient autogenous tissue to provide a reliable reconstruction. Bilateral sternal bar turnover was performed in the second stage at 4 years of age. This operative technique is described in this report. This novel technique provides a robust, dynamic, and reliable reconstruction for inferior sternal defects.
Child, Preschool
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Ectopia Cordis
;
Humans
;
Male
;
Pentalogy of Cantrell*
10.A Case of Ectopia Cordis.
Sun A KIM ; Chun Soo KIM ; Geun Soo PARK ; Myung Sung KIM ; Sang Lak LEE ; Joon Sik KIM ; Tae Chan KWON
Journal of the Korean Pediatric Society 1997;40(3):413-416
Ectopia cordis is a very rare cardiac anomaly that the heart is partially or totally outside the thorax, and it was classified anatomically as 5 types-cervical, thoracocervical, thoracic (most common type), thoracoabdominal, abdominal types. We experienced a case of ectopia cordis (thoracic type) in a newborn who had the symptom of generalized cyanosis since birth, and expired during operation due to recurrent bradycardia and hypotension. The brief review of literature was made
Bradycardia
;
Cyanosis
;
Ectopia Cordis*
;
Heart
;
Humans
;
Hypotension
;
Infant, Newborn
;
Parturition
;
Thorax