Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 4 de 4
Filter
Add filters








Language
Year range
1.
Journal of the Korean Pediatric Society ; : 633-637, 1982.
Article in Korean | WPRIM | ID: wpr-166878

ABSTRACT

Acute hydrops of the gallbladder is described in one patient who had mucocutaneous lymph node syndrome. During the course of her illness, acute addominal pain, vomiting and right upper guadrant tenderness were developed. Diagnosis was readily made with ultrasonography, and the patient was followed with this te-chnique. We managed her conventionally without surgical intervention. The galbladder returned to normal size within about 3 weeks. Related literatures are briefly reviewed.


Subject(s)
Humans , Diagnosis , Edema , Gallbladder , Mucocutaneous Lymph Node Syndrome , Ultrasonography , Vomiting
2.
Journal of the Korean Pediatric Society ; : 508-511, 1982.
Article in Korean | WPRIM | ID: wpr-141047

ABSTRACT

A case of lacunar skull, female newborn infant, associated with skin defect on the lumbosacral region, spina bifida, meingomyelocele and paraplegia is reported. Hydrocephalus developed eventually. Diagnosis was made by X-ray of skull. The roentgenographic apperance shows typhical a soap bubble texture or irregular patches of rarefaction. A brief review of the related literature is given.


Subject(s)
Female , Humans , Infant, Newborn , Diagnosis , Hydrocephalus , Lumbosacral Region , Paraplegia , Skin , Skull , Soaps , Spinal Dysraphism
3.
Journal of the Korean Pediatric Society ; : 508-511, 1982.
Article in Korean | WPRIM | ID: wpr-141046

ABSTRACT

A case of lacunar skull, female newborn infant, associated with skin defect on the lumbosacral region, spina bifida, meingomyelocele and paraplegia is reported. Hydrocephalus developed eventually. Diagnosis was made by X-ray of skull. The roentgenographic apperance shows typhical a soap bubble texture or irregular patches of rarefaction. A brief review of the related literature is given.


Subject(s)
Female , Humans , Infant, Newborn , Diagnosis , Hydrocephalus , Lumbosacral Region , Paraplegia , Skin , Skull , Soaps , Spinal Dysraphism
4.
Journal of the Korean Pediatric Society ; : 578-581, 1980.
Article in Korean | WPRIM | ID: wpr-197091

ABSTRACT

A case of a achondroplasia in a 6 month-old-boy was presented with a brief review of the literature. He was admitted with the chief complaints of frequent respiratory infections, and stunted growth. This baby showed stunted growth, short arms and legs, prominent forehead, flatening of the bridge of the nose, and moderate degree of kyphosis. All laboratory datas were nomal. X-ray showed the thickness of the bones and their irregular epiphyseal ends. The pelvis squared, with flat acetabula and distally decreasing interpedunculate distance of the lumbar vertebrae. 14 month follow up study makes it possible to diagnosis as achodroplsia.


Subject(s)
Acetabulum , Achondroplasia , Arm , Diagnosis , Follow-Up Studies , Forehead , Kyphosis , Leg , Lumbar Vertebrae , Nose , Pelvis , Respiratory Tract Infections
SELECTION OF CITATIONS
SEARCH DETAIL