1.The Frequency of Apnea and Loss of Consciousness According to Propofol Dosage in Premedicated Patients with Midazolam.
Jung Won HWANG ; Yong Seok OH ; Sung Hee HAN
Korean Journal of Anesthesiology 1997;33(1):68-72
BACKGROUND: Respiratory depression with high dose of propofol during induction is one of the major complications. We studied the effects of midazolam as premedicant on frequency and duration of apnea and frequency of loss of consciousness in relation to single dose of propofol. METHODS: We selected 194 adult patients who had clear consciousness and no depression of respiration. We allocated patients randomly to control group and midazolam group. In midazolam group, we injected 0.06mg/kg of midazolam intravenously 10min before induction, and in control group, we did nothing. Under mask oxygenation with 100% oxygen, we administered a bolus of propofol (1, 1.5, 2 mg/kg to subgroup 1, 2, 3 respectively) intravenously. The change of respiration and loss of consciousness were observed. RESULTS: The frequency and duration of apnea increased with the dose of propofol in both control and midazolam group. But there were no difference between groups except frequency of apnea with 1.5 mg/kg of propofol. In control group, frequency of loss of consciousness increased with the increasing dose of propofol. But in midazolam group, nearly all the patients was slept without difference by the dose. CONCLUSIONS: Premedication with midazolam reduce the sleeping dose of propofol to induce anesthesia, so the frequency and duration of apnea which is caused by high dose of propofol can be decreased.
Adult
;
Anesthesia
;
Apnea*
;
Consciousness
;
Depression
;
Humans
;
Masks
;
Midazolam*
;
Oxygen
;
Premedication
;
Propofol*
;
Respiration
;
Respiratory Insufficiency
;
Unconsciousness*
2.A Case of Plexiform Neurofibroma of the Right Upper Eyelid and Orbit in Neurofibromatosis.
Dong Seok KIM ; Sang Won KIM ; Han Ik BAE
Korean Journal of Dermatology 1986;24(5):734-738
We have experienced a case of plexiform neurofibrorna of the right upper eyelid and orbit in a 12-year-old girl who had typical skin features of neurofibromatosis and no family history. The non-pulsating proptosis of the right eye and diffuse thickening with hypertrophy of the upper lid, had increased insiduciusly since the birth on. Biopsy taken from eyelirl lesion showed the features of plexiform neurofibroma. Skull X-ray and brain computerized tomogram showed that the right orbit was wider, with the enlarged mass and defects in orbital roof and lesser and greater wings of the sphenoid bone. The surgical excision of the right eyelid lesion was performed.
Biopsy
;
Brain
;
Child
;
Exophthalmos
;
Eyelids*
;
Female
;
Humans
;
Hypertrophy
;
Neurofibroma, Plexiform*
;
Neurofibromatoses*
;
Orbit*
;
Parturition
;
Skin
;
Skull
;
Sphenoid Bone
3.A case of recurrent Malaria : imported infection.
Se Hwan HAN ; Dong Won BYUN ; Won Seok CHU ; Jun Hee WOO ; Sung Tae HONG
Korean Journal of Infectious Diseases 1991;23(2):125-129
No abstract available.
Malaria*
5.A Case of Battered Child Syndrome with Subdural hemorrhage.
Young Jun SONG ; Won Seop KIM ; Heon Seok HAN ; Soo Ahn CHAE
Journal of the Korean Child Neurology Society 1998;5(2):388-392
The diagnosis of a Battered Child Syndrome is made by the pediatrician, surgeon and the radiologist because almost parents deny the diagnosis or refuse to answer the doctor's questions. The imaging modalities play a key role in the investigation and documentation of the battered child syndrome, because of the high frequency of the typical skeletal lesion. Although physical abuse is denied by parents, the recognition of this entity is possible by the primary diagnostic imaging study in the suspected child abuse. The imaging studies are either a bone scan and x-ray series or a complete radiolographic skeletal survey by X-ray series. In an expected intracranial injury, a CT scan of the head is mandatory We experienced a case of Battered Child Syndrome in a 6 month-old male infant who had subdural hemorrhage and fractures of skull and ribs in different stages of healing and repair. The brief review of the literature was made.
Battered Child Syndrome*
;
Child
;
Child Abuse
;
Diagnosis
;
Diagnostic Imaging
;
Head
;
Hematoma, Subdural*
;
Humans
;
Infant
;
Male
;
Parents
;
Ribs
;
Skull
;
Tomography, X-Ray Computed
6.Trichoblastic Fibroma: A Pathologic Analysis of 4 Cases.
Ah Won LEE ; Ji Han JUNG ; Jin Young YOO ; Seok Jin KANG ; Byung Kee KIM
Korean Journal of Pathology 2000;34(8):574-580
Trichoblastic fibroma is a benign trichogenic tumor that has both epithelial and mesenchymal components and exhibits partial follicular induction. We studied 4 cases of trichoblastic fibroma and reviewed their clinical and histologic features. Two tumors were present in the face. The remaining two were in the vulva and perianal area, respectively. The age of the patients ranged from 53 to 68 years, with an average age of 62. All were female. Histologically, the lesions showed a well circumscribed mass, located at dermo-subcutaneous junction in three patients and subcutaneous in one. They demonstrated mesenchymal induction evidenced by hair germ-like structure and perifollicular sheath. There was no connection between the tumor and epidermis. Differentiation toward hair structure led to the formation of the infundibulum through inner root sheath. Trichoblastic fibroma may be confused clinically and/or histologically with basal cell carcinoma. Identification of the mixed epithelial and mesenchymal components, and the absence of epidermal connection and cleft within the stroma are important in differentiating this benign neoplasm from basal cell carcinoma.
Carcinoma, Basal Cell
;
Epidermis
;
Female
;
Fibroma*
;
Hair
;
Humans
;
Vulva
7.Solid pseudopapillary tumor with hepatic metastasis.
Woo Seok NAM ; Yong Sung WON ; Dong Do YOU ; Jin Mo YANG ; Jee Han JUNG
Journal of the Korean Surgical Society 2011;81(Suppl 1):S55-S58
Solid pseudopapillary tumor of the pancreas is a rare tumor that affects young females with low malignant potential and good prognosis with more than 90% survival at 5 years. Metastasis is very rare. We report the case of a 74-year-old female who had pancreatic solid-pseudopapillary tumor and synchronous hepatic metastasis.
Aged
;
Female
;
Humans
;
Neoplasm Metastasis
;
Pancreas
;
Pancreatic Neoplasms
;
Prognosis
8.The etiologies and the clinical manifestations of hypoglycemia in infancy and childhood.
Nam Seon BECK ; Dong Joo SHIN ; Heon Seok HAN ; Sei Won YANG ; Hyung Ro MOON
Journal of the Korean Pediatric Society 1991;34(4):480-486
No abstract available.
Hypoglycemia*
9.Four Cases of Double Primary Cancer.
Myung Sik SUNG ; Sang Young HAN ; Seok Reyol CHOI ; Woo Won SHIN
Korean Journal of Gastrointestinal Endoscopy 1993;13(1):69-74
Double primary cancer is defined as the case of primary malignant tumors in one person, which must be arisen in different sites and have a different histologic appearances in each other. The number of reported cases of multiple primary malignant tumors has increased in recent years, because of more developed diagnostic procedure and long survival of cancer patients, We have experienced 4 cases of double primary malignant tumors which were stomach cancer with colon, bronchus and esophagus cancer, and report these cases with review of literatures.
Bronchi
;
Colon
;
Esophageal Neoplasms
;
Humans
;
Stomach Neoplasms
10.Four Cases of Double Primary Cancer.
Myung Sik SUNG ; Sang Young HAN ; Seok Reyol CHOI ; Woo Won SHIN
Korean Journal of Gastrointestinal Endoscopy 1993;13(1):69-74
Double primary cancer is defined as the case of primary malignant tumors in one person, which must be arisen in different sites and have a different histologic appearances in each other. The number of reported cases of multiple primary malignant tumors has increased in recent years, because of more developed diagnostic procedure and long survival of cancer patients, We have experienced 4 cases of double primary malignant tumors which were stomach cancer with colon, bronchus and esophagus cancer, and report these cases with review of literatures.
Bronchi
;
Colon
;
Esophageal Neoplasms
;
Humans
;
Stomach Neoplasms