• Search
  • Advanced Search

Search

  • HOME
  • Search
Original Article
A Case of Pneumocystis Carinii Pneumonia Associated with Cytomegalovirus Lung Infection.
K S Lee, Y O Lee, H J Park, M J Shin
Clin Exp Pediatr. 1987;30(11):1274-1281.   Published online November 30, 1987
Pneumocystis carinii pneumonia has been highly prevalent in prematurity, malnourished infants and immunosuppressed patients. Since 1981, it has been by far the commonest opportunistic infection in AIDS. We experienced a case of Pneumocystis carinii pneumonia associated with cytomegalovirus lung infection in a 3 months old malnourished female orphan. She had been suffered from chronic diarrhea, losing body weight 2 kg in a month prior...
Case Report
Intermittent Hydronephrosis.
Hong Kun Kim, Woo Gill Lee, Soo Jee Moon
Clin Exp Pediatr. 1987;30(7):805-811.   Published online July 31, 1987
Episodic flank or abdominal pain with or without nausea and vomiting is most common manifesta- tion of intermittent hydronephrosis. Between episodes of pain, the patient may be asymptomaitc and intravenous urogram usually will be normal. This condition is diagnosed by intravenous urogram or ultrasonogram taken either during episodes of pain or after hydronephrosis precipitated by use of duretics or ingestion of alcoholic beverage, particulary...
Four Cases of Congenital Choledochal Cyst.
Hyun Eog Yang, Yoon Hee Lee, Kyung Tai Whang
Clin Exp Pediatr. 1986;29(11):1269-1274.   Published online November 30, 1986
This paper presents experience with 4 cases of choledochal cyst who were treated at the Dept, of Pediatrics, Catholic Medical College, from December, 1983 to February, 1985. All patients were less than 24 months of age when diagnosed, and the yongest was a 5 days of age, all of whom were female. The common presenting- symptoms in this cases were...
A Case of Potter Syndrome Type I.
Jong Cheol Ryu, Jae Kwang Hong, Jun Taek Park, Jung Sik Min, Chang Jee Choi, Je Geun Chi
Clin Exp Pediatr. 1986;29(10):1152-1156.   Published online October 31, 1986
We have experienced a case of Potter syndrome type I in a newborn infant who presented with severe respiratory distress soon after birth. The diagnosis was made with autopsy findings consisted of bilateral polycystic renal dysplasia, bilateral hypoplastic lung , facies renalis, fibrocystic change of liver, patent ductus arteriosus, patent foramen ovale, ureter and urinary bladder hypoplasia and calcaneovarus. Brief...
Original Article
Clinical Studies on the Biliary Cyst in Childhood.
Young Yull Koh
Clin Exp Pediatr. 1985;28(6):570-580.   Published online June 30, 1985
Cystic abnormalities may occur throughout the biliary ductal system from the finest intralobular hepatic ducts to the intraduodenal portion of the common bile duct. Clinical studies were performed on 18 cases of the biliary cyst who have been admitted to the Pediatric and Pediatric Surgical Dept. 1 of SNUH from January 1979 to December 1984. Results were obtained as follows：...
Case Report
A case of Infantile Polycystic kidney.
Ae Sook Kim, Soon Bock Park, Young Gun Kim, Kwan Hwooy Cho, Jong Soo Kim
Clin Exp Pediatr. 1985;28(2):191-196.   Published online February 28, 1985
Infantile polycystic kidney is uncommon disease and rare in children and is used to refer to a group of heritable conditions that occur predominantly in childhood and is transmitted by autosomal recessive inheritance. By developmental abnormality, multiple cysts are produced from enlargement or giantism of the collecting tubules in association with cellular hyperplasia. Kidneys are grossly enlarged and have a diffusely...
Original Article
Clinical Studies of Urinary Tract Infection in Infancy and Childhood.
Tae Jin Park, Kwang Hyun Kim, Eui Soo Park, Woo Gill Lee
Clin Exp Pediatr. 1984;27(4):366-377.   Published online April 30, 1984
Urinary tract infection (UTI) represents the most common genitourinary disease in children and are the second most common infection in children. Besides, they are potentially dangerous not only because may present as life-threatening episodes with serious prognosis, but also because may be the forerunners of severe renal disease of adulthood. So the importance at early diagnosis and investigation of apparently...
Case Report
Two Autopsy Cases of Pneumocystis Carinii Pneumonia.
Dae Deok Ahn, Tae Suck Jung, Jung Kwon Lee, Yoon Ja Kim
Clin Exp Pediatr. 1984;27(3):271-276.   Published online March 31, 1984
Pneumocystis infection is highly prevalent in humans and lower animals throughout the world. The disease has almost alway been sporadic, rarely epidemic, and has occurred in all age groups. We experienced two cases of pneumocystis carinii pneumonia. They were brought to our hospital from orphanage at the age of 50 day and 86 day old. The initial X-ray findings were...
A Case of Congenital Porencephalic Cyst.
Hong Gyu Park, Man Jin Chung, Jong Doo Kim, Myung Hi Shin, Ji Sub Oh
Clin Exp Pediatr. 1984;27(2):202-206.   Published online February 28, 1984
We experienced a congenital porencephalic cyst with hydrocephalus in a 12 days old female premature infant who was suffered from meningitis. Brain CAT confirmed the diagnosis of porencephaly. Therapy consisted of systemic antibiotics and ventriculo-peritoneal shunt with good effect. She has been in good condition without convulsion or other neurologic sequelae thereafter. A brief review of the related literature was...
A Case of Acardius Twin.
Kyung Hyo Kim, Jung Soo Park, Mina Lee, Hye Kyung Lee, Sung Sik Shin, Je G Chi
Clin Exp Pediatr. 1984;27(1):84-88.   Published online January 31, 1984
A case of acardiac twins to a 30 year-old primiparous mother is presented. This case was diagnosed to have this anomaly by ultrasonography at 28 weeks and 33 weeks of gestation. The acardiac monster was delivered as the second twin without any signs of Life. It weighed 2,175 gms and was connected to the placenta by an umbilical cord having...
A Case of Congenital Cystic Adenomatoid Malformation of Lung Associated with Fetal Ascites.
In Soon Lee, Un Hee Choi, Woon Sik Kim, Heum Rea Park
Clin Exp Pediatr. 1983;26(7):722-725.   Published online July 31, 1983
Cystic adenomatoid malformation is a specific form of cystic lung disease characterized by a cuboidal and columnar epithelium. Reported cases had anasarca or polyhydramnios. We have experienced a case of cystic adenomatoid malformation of lung associated with. fetal ascites and reviewed the pertinent literatures briefly.
Original Article
Study of Urinary Lactic Dehydrogenase and Isoenzyme Patterns in Patients with Urinary Tract Infection.
Eui Soo Park, Jeh Hoon Shin, Woo Gill Lee
Clin Exp Pediatr. 1983;26(5):463-469.   Published online May 31, 1983
The site of the infection is an important factor in the evaluation of the course and prognosis of patients with urinary tract infection (UTI) since patients with bacteriuria of renal origin are probably at risk of developing the renal parenchymal reduction seen in some of these patients. So direct and indirect methods have been developed to accomplish precise location of the...
Case Report
A Case of Pancreatic Pseudocyst.
Tai Gyu Whang, Hyun Gi Jung, In Sun Park, Chul Ho Kim, Soon Yong Lee, Sang Hyo Kim
Clin Exp Pediatr. 1983;26(2):165-169.   Published online February 28, 1983
We observed a case of pancreatic pseudocyst who was an 10 year-old girl with the chief complaints of intermittent abdominal pain and an abdominal mass in left upper quadrant. The cause of pancreatic pseudocyst was idiopathic, and the diagnosis was made by explor- ative laparatomy and biopsy. A brief review of literatures was made.
A Case of Pineal Epidermoid Cyst with Ependymoma in the Third Ventricle.
Chull Kwon Chung, Chang Moo Lee, Myung Hi Shin, Ji Sub Oh, Leland Albright
Clin Exp Pediatr. 1983;26(1):86-90.   Published online January 31, 1983
A 10 years old boy was presented with chief complaints of polypnagia, headache, intermittent vomiting and diplopia. Brain CAT revealed pineal tumor and surgical remove of the tumor mass was successfully done, which was proved to be epidermoid cyst. One month after operation the previous symptoms were recurred and his condition was getting worse progressively. Another brain CAT revealed enlarged...
A Case Of Choledochal Cyst In A Neonate.
Jong Man Lee, In Kyung Sung, Jong Seung Kim, Chang Kyu Oh
Clin Exp Pediatr. 1982;25(10):1068-1072.   Published online October 31, 1982
Congenital choledochal cyst is a rare disease, especially in fetal life and early infancy age. Our case was a 66 days old female baby who had the symptoms of jaundice, clay-colored stool, intermittent vomiting since birth and abdominal distension. Final diagnosis was choledochal cyst with neonatal hepatitis. An early accurate preoperative diagnosis has been associated with a marked decrease in the mortality. Roux-en-Y choledochocystojejunostomy was done. We...
Original Article
Perforated Choledochal Cyst with Bile Peritonitis in an Infant.
Sang Geel Lee, Yen Hee Kang, Ki Chang Han, Su Sang Shon
Clin Exp Pediatr. 1982;25(8):854-858.   Published online August 31, 1982
A case report of a perforated choledochal cyst with bile peritonitis occurring in a 13-month old girl is presented. The perfortion was identified on the right lateral aspect of the common bile duct. And T-tube drainage was instituted. Episodes of ascending cholangitis followed pooling of the stagnant bile in the biliary system. Reoperation was recommended but in vain.
Case Report
Pancreatic Pseudocysts and Ascites as Complications of Chronic Pancreatitis.
Nam Su Kim, Hee Ju Kim, Kyoo Duck Lee, Yong Choi, Hyung Ro Moon
Clin Exp Pediatr. 1982;25(2):183-189.   Published online February 28, 1982
A case of pancreatic pseudocysts and bloody pancreatic ascites as complications of chronic pancreatitis in eleven-year-old girl was reported. She was admitted to the pediatric ward with chief complaints of abdominal distension and bloody ascites. About nine months prior to admission, when she was stuck by a bicycle, she had sustained a blow on her abdomen. She has been apparently...
A Case of the Pancreatic Pseudocyst.
Han Soo Choi, Sang Hak Park, Ki Sup Chung, Duk Jin Yun, Euh Ho Whang
Clin Exp Pediatr. 1981;24(12):1209-1212.   Published online December 15, 1981
One case of pancreatic pseudocyst occuring in a 6 year old boy was presented. The pancreatic pseudocyst was caused by blunt abdominal trauma, and the diagnosis was confirmed by U.G.L series and exploratory laparotomy. The patient was cured with the surgical method of internal drinage, and there was no complications after surgery. We have presented this rare case and reviewed...
A Case of tuberous Sclerosis with Polycystic Kidney.
Won Ik Lee, Il Sin Moon, Poong Man Lee, Jae Chung Lee
Clin Exp Pediatr. 1981;24(11):1100-1105.   Published online November 15, 1981
Tuberous sclerosis is an inherited neurocutaneous disorder characterized by seizures, mental ratardation, cutaneous lesions and visceral hamartomas. The usual renal lesion in tuberous sclerosis is the angiomyolipoma which is a hamartomas, but polycystic kidney is relatively rare. We confirmed tuburous sclerosis on the base of the radiological and clinical characterics in 8 years old girl of mental deficiency with four...
Original Article
Intracranial Cysticercosis: A Report of 6 Cases.
Sang Hak Park, Chang Jun Coe, Duk Jin Yun, Sang Sup Chung, Kyu Chang Lee, Jung Ho Suh
Clin Exp Pediatr. 1981;24(8):766-771.   Published online August 15, 1981
Cysticercosis infestation is a cosmopolitan disease. Recently we experienced six cases of intracranial cysticercosis in childhood, three of them were male and their age distributed from 2 to 15 years. Their main clinical manifestations were symptoms of increased intracranial pressure signs and other neurological sings as well, In diagnostic procedures, brain C-T scan was performed in all cases and Conray...
Case Report
A Case of Congenital Choledochal Cyst.
Joon Ho Kim, Jung Ju Kim, Ko Chang Kim, Byung Yun Cheong, Won Jae Park
Clin Exp Pediatr. 1981;24(6):584-588.   Published online June 15, 1981
We experienced a case of congenital choledochal cyst in a 6 months old korean female infant with complaints of abdominal distension, jaundice, loose stool and a large mass of the abdomenin the right upper quadrant since about 3 months prior to admission. The diagnosis was confirmed by clinical symptoms and signs, physical examination, radiological findings and surgical findings. She was...
Original Article
A Clinical Study of 15 Cases of Pneumocystis Carinii Pneumonia.
Jae Oh Kim, Sung Sook Cho, Jung Woo Suk, Don Hee Ahn, Keun Chan Sohn, Tai Hyuk Yim
Clin Exp Pediatr. 1981;24(2):136-144.   Published online February 15, 1981
Pneumocystis carinii pneumonia is unique infection with unyielding penchant for the debilitated and immunodeficient host. Since several reports of pneumocystis carinii pneumonia in late half of 1950 period, no additional report was found in literature in Korea. We Tecently experienced 15 cases of pneumocystis carinii pneumonia in infants of an institution for foreign adoption, who, were admitted to our*hospital with...
  • PubMed Central
  • PubMed
  • Scopus
  • Directory of Open Access Journals (DOAJ)