2.Congenital Anomalies of the Hand
Won Sik CHOY ; Moon Sang CHUNG ; Woo Chun LEE
The Journal of the Korean Orthopaedic Association 1982;17(5):933-936
Congenital anomalies of the hand were reviewed, which were treated at Seoul National University Hospital from 1973 to 1982. The Conclusions are as follows. 1. Polydactyly is the most common congenital anomaly of the hand in this series. The next common congenital hand anomalies are trigger digit, syndactyly in that order. 2. Better results had been obtained with early reconstructive surgery within one year after birth. 3. Authors propose a new classification of polydactyly. In Joint type (type 1), the extradigit has its own epiphysis in its origin,and in Epiphyseal plate type (type 2) the extradigit do not have its own epiphyseal plate and seems to be derived from the physis of the more developed adjacent digit. We observed 22 cases of joint type and 10 cases of epiphyseal plate type. 4. 6 cases of macrodactyly had been observed. The complicated reconstructive surgery such as Tsuge and Barsky operation resulted in digital necrosis. So more simple and effective operation such as symphalangization would be attempted.
Classification
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Epiphyses
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Growth Plate
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Hand
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Joints
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Necrosis
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Parturition
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Polydactyly
;
Seoul
;
Syndactyly
;
Trigger Finger Disorder
3.Endoscopic Examination in Patients following Gastrectomy.
Yong Taek CHUN ; In Sik CHUNG ; Ahn Kie LEE ; Kyu Won CHUNG ; Hee Sik SUN ; Boo Sung KIM ; Whan Kook CHUNG
Korean Journal of Gastrointestinal Endoscopy 1984;4(1):13-19
It had heen emphasized the necessity for upper gastrointestinal endoscopic examinations in patients. Who has had gastrectomy and presents persisting gastrointestinal symptoms. This study was conducted to evaluate endoscopic findings and clinical symptoms in patients following gastrectomy. (continue...)
Gastrectomy*
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Humans
4.A case of bronchopulmonary dysplasia.
Sun A CHUN ; Byung Jun CHOI ; Bo Kyung CHO ; Chung Sik CHUN ; Sung Hoon CHO
Journal of the Korean Pediatric Society 1989;32(11):1553-1559
No abstract available.
Bronchopulmonary Dysplasia*
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Humans
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Infant, Newborn
5.A Case of Rare Craniofacial Clefts: Tessier No .7 Cleft.
Hyun Jung LEE ; Nak Gyun CHUNG ; So Young KIM ; In Kyung SUNG ; Chung Sik CHUN
Journal of the Korean Society of Neonatology 1998;5(1):95-99
Craniofacial clefts are rare among facial anomalies with an incidence of 1.5 to 5 per 100,000 births, and 1 per 100 cases of cleft lip and palate. The Tessier No. 7 clefts are unusual lesions that result from failure of the embryonic mandibular and maxillary processes to properly fuse and form the corners of the mouth. We experienced a case of Tessier No. 7 craniofacial cleft in a 1 day-old female patient who presented with a macrostomia and auricular malformation. The diagnosis was established by clinical and radiographic findings. A brief review of literature was made.
Cleft Lip
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Diagnosis
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Female
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Humans
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Incidence
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Macrostomia
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Mouth
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Palate
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Parturition
6.Clinical Experience of the Neurofibromatosis: Report of Three Cases.
Yi Shiung TSANG ; Hyo Sook CHUNG ; Chun Sik CHOI ; Mun Bae JU
Journal of Korean Neurosurgical Society 1989;18(7-12):1088-1092
The usual form of neurofibromatosis is characterized by cafe-au-Iait skin pigmentation and pedunculated fibrous skin tumors but in the severe form, malformations and tumors of the central nervous system may be associated with von Recklinghausen's disease. Schwannoma of the spinal sensory roots, of the vestibular part of 8th cranial nerve, and of the sensory root of the 5th cranial nerve are particularly common. Outside the central nervous system, other neuroectodermal tumors may develop including renal, pancreas, and suprarenal tumors. Recently, neurofibromatosis is subdivided into type 1 and 2, according to the site of involvement. Type 1 is classic von Recklinghausen's disease, and type 2 represents bilateral acoustic neurinomas. The authors experienced 2 cases neurofibromatosis type 1 and 1 case of neurofibromatosis type 2 in which neurofibromas involve both cerebello-pontine angles, multiple levels of spinal cord and cauda equina.
Cauda Equina
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Central Nervous System
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Cranial Nerves
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Neurilemmoma
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Neuroectodermal Tumors
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Neurofibroma
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Neurofibromatoses*
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Neurofibromatosis 1
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Neurofibromatosis 2
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Pancreas
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Skin
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Skin Pigmentation
;
Spinal Cord
7.A Case of the Foutrh Branchial Cleft Cyst Causing Respiratory Difficulty in Neonatal Period.
In Kyung SUNG ; Chung Sik CHUN ; So Young KIM ; Ju Ok LEE ; Sang Yong KIM
Korean Journal of Perinatology 1998;9(2):180-184
It is commonly believed that the branchial anomalies are persistent remnants of the embryologic branchial apparatus. These anomalies are originated from branchial cleft and most commonly involved in second branchial deft. Clinically they present palpable mass, discharge from fistula, recurrent infection due to obstruction of Gstula tract. As respiratory symptoms, they may present hoarseness, preceeded by or associated with upper respiratory infection. However, it has not been reported that they caused airway obstruction in newborn infants. Wc experienced a case of the fourth branchial deft cyst in a 2 day old infant who showed respiratory difficulty due to airway obstruction.
Airway Obstruction
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Branchial Region*
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Branchioma*
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Fistula
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Hoarseness
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Humans
;
Infant
;
Infant, Newborn
8.A Case of Dandy-Walker Syndrome Associated with Multiple Congenital Anomalies.
Gye Weon SHIN ; Chul Ho LEE ; Bo Kyung CHO ; Chung Sik CHUN ; Sung Hun CHO
Journal of the Korean Pediatric Society 1990;33(6):848-853
No abstract available.
Dandy-Walker Syndrome*
9.The Effect of Erythromycin on Gastric Antrum and Low Esophageal Sphincter in the Newborn Rabbit.
Sung Dong CHOI ; Chung Sik CHUN
Journal of the Korean Pediatric Society 2000;43(1):34-42
PURPOSE: We studied smooth muscle strips from rabbit gastric antrum and low esophageal sphincter (LES) to explore the difference between newborn and adult rabbit on erythromycin (EM)- induced contractions. Another aim of this study was to determine the mechanism of LES contractile activities induced by erythromycin (EM). METHODS: Muscle strips prepared from newborn and adult rabbits were stimulated with agonists such as KCl, motilin and EM, and the isometric tensions were measured. To study the underlying mechanism of EM-stimulated contraction of LES, the receptor antagonsts, including tetrodotoxin, hexamethonium, atropine, propranolol and phentholamine, were used. A high concentration of motilin (1 micrometer) was employed to provoke tachyphylaxis. RESULTS: Antral smooth muscle and LES from newborn rabbits developed less active force than those from adult rabbits when stimulated with KCl, motilin and erythromycin, however, the effective concentrations (EC50s) were similar in both age groups. Antral smooth muscle strips showed both tonic and phasic contractions but LES muscle strips showed only tonic contractions. These findings were observed in both newborn and adult rabbits. The contraction force of antral smooth muscle strips in response to agonists was greater than that of LES. The contractile response of LES to repeated motilin or EM administration was markedly decreased. EM- induced contractions of LES were markedly decreased by motilin tachyphylaxis but were unaffected by tetrodotoxin, hexamethonium, atropine or propranolol plus phentolamine. CONCLUSOIN: The data suggest that the contractilities of antrum and LES smooth muscle from newborn rabbit are less than those from adult ones, however, the effective concentratons of EM (EC50) are not different between the two age groups. The results also suggest that erythromycin induces the contraction of rabbit LES via motilin receptor in vitro.
Adult
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Atropine
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Erythromycin*
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Gastrointestinal Motility
;
Hexamethonium
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Humans
;
Infant, Newborn*
;
Motilin
;
Muscle, Smooth
;
Phentolamine
;
Propranolol
;
Pyloric Antrum*
;
Rabbits
;
Tachyphylaxis
;
Tetrodotoxin
10.A clinical analysis on neonates who received operation during first month of life.
Ji Whan HAN ; Soo Jung LEE ; Chung Sik CHUN ; Sung Hoon CHO
Korean Journal of Perinatology 1991;2(2):28-34
No abstract available.
Humans
;
Infant, Newborn*