1.Clinical Observation on Moyamoya Disease in Childhood.
Se Hee HWANG ; Jae Il SOHN ; Yong Seung HWANG
Journal of the Korean Pediatric Society 1990;33(2):178-188
No abstract available.
Moyamoya Disease*
2.A radiologic findings of periappendiceal abscess : comparison of simple abdomen, B.E., and ultrasonography
Kyung Hee JUNG ; Jae Chun CHANG ; Mi Soo HWANG
Journal of the Korean Radiological Society 1985;21(6):975-984
With simple abdomen, double contrast colon study, and ultrasongraphy, authors retrospectively analyzedradilogic findings of 46 cases which were proved periappendiceal abscess, due to perforation of appendix, byhistology or follow-up ultrasnongraphy from May in 1983 to July in 1985 at Yeung-Nam University Hospital. Theresuls obtained were as follows: 1. Of 46 cases, 24 cases were males and 22 cases females, with the results ofabove statistics, periappendiceal abscess was not influenced by sex. 2. Periappendiceal abscess was mostfrequently demonstrated in forties. 3. Comparison of ultrasonography and B.E. Pseudorenal pattern(Ultrasonography)- well defined defect (B.E.) Cystic pattern(Ultrasonography)- serrated defect (B.E.) 4. Missed 2 cases inultrasonography were detected in B.E., i.e. sensitivity of B.E. is higher than that of ultrasonography. 5.Differences of ultrasonography and B.E.
Abdomen
;
Abscess
;
Appendix
;
Colon
;
Female
;
Follow-Up Studies
;
Humans
;
Male
;
Retrospective Studies
;
Sensitivity and Specificity
;
Ultrasonography
3.A Case of Primary Pulmonary Hypertension Associated with Pregnancy.
In Hu HWANG ; Jae Woong CHOI ; Eui Kyeong HWANG ; Chan Hee MUN ; Hyun Cho MIN ; Chang Sub SONG
Korean Circulation Journal 1997;27(8):881-886
Primary pulmonary hypertension is a rar, incurable, and progressive clinical entity. When associated with pregnancy, the prognosis of primary pulmonary hypertension is worsened with maternal mortality rates of at least 50%. The patient was a 29-year-old mother in her 2nd pregnancy, with previous uncomplicated gestation, 5 years ago. She had been well until the 28th week of present gestation when she was admitted because of increasing dyspnea on exertion. She was a housewife with no remarkable family and past histories. We have experienced a patient with primary pulmonary hypertension in pregnancy. She was treated with an oral calcium-channel blocker and low-molecular-weight heparin and was delivered vaginally with good maternal and fetal outcome. So we report a case of primary pulmonary hypertension associated with pregnancy and review literature.
Adult
;
Dyspnea
;
Heparin, Low-Molecular-Weight
;
Humans
;
Hypertension, Pulmonary*
;
Maternal Mortality
;
Mothers
;
Pregnancy*
;
Prognosis
4.A Clinico-Epidemilological Study of 55 Cases of Chidhood Idiopathic Thrombocytopenic Purpura.
Won Ho KANG ; Myung Hee KOOK ; Yong Sang YOO ; Jae Suk MA ; Tai Ju HWANG
Journal of the Korean Pediatric Society 1987;30(11):1207-1212
No abstract available.
Purpura, Thrombocytopenic, Idiopathic*
5.Two cases of virus associated hemophagocytic syndrome.
Jae Hee HAN ; Hyun Chul LEE ; Hwang Min KIM ; Jong Soo KIM ; Kyung Won LEE
Journal of the Korean Pediatric Society 1993;36(10):1458-1465
Virus associated hemophagocytic syndrome, class ll histiocytoses, characterized by high fever, severe constitutional symptoms, abnormal liver function and coagulation, perigheral blood pancytopenia and histiocytic hyperplasis with prominent hemophagocytosis in bone marrow and lymph nodes has been reported and associated with active viral infection. It is non-malignant and reversible. It must be differentiated from histiocytic medullary reticulosis because of the inappopriateness of immunosuppressive of cytotozic therapy which is the therapeutic method for HMR, but is contraindicated in the treatment of VAHS. This paper describes two patients whose clinicopathology was compatible with the diagnosis of virus associated hemophagocytic syndrome.
Bone Marrow
;
Diagnosis
;
Fever
;
Histiocytosis
;
Humans
;
Liver
;
Lymph Nodes
;
Lymphohistiocytosis, Hemophagocytic*
;
Pancytopenia
6.Simultaneous Bilateral Cementless Total Hip Arthroplasty: a Minimum 17-year Follow-up Study - Comparison Study with Unilateral Cementless Total Hip Arthroplasty -.
Sung Kwan HWANG ; Jang Hee PARK ; Won Sik YOON ; Jae Hack CHA
Hip & Pelvis 2013;25(1):21-29
PURPOSE: Long-term follow-up results of concurrent bilateral or unilateral cementless hip arthroplasty were compared. MATERIALS AND METHODS: Forty eight and 49 patients with concurrent bilateral and unilateral hip artrhoplasties who had more than a 17-year follow-up time were selected. At final follow-up, mean ages were 69.1 and 66.7 years old in the bilateral and unilateral groups, respectively. Mean follow-up times were 21.5 and 22.4 years in the bilateral and unilateral groups, respectively. Clinical results were attained using Harris hip score and standardized anteroposterior and lateral view X-rays. RESULTS: The bilateral group had mean Harris scores of 44.3(standard deviation 3.78) preoperatively, and 81.2 (10.75) at final follow-up. For the unilateral group, the mean scores were 46.5(3.27) preoperatively, and 80.1 (12.05) at final follow-up. At final follow-up, an acetabular cup was securely located in 78.9% and 82.8% of the bilateral and unilateral groups, respectively, and all cases showed firm fixation of the femoral stem in both groups. Osteolysis around the cup and stem were found in 26.3% and 31.4% of the bilateral group and 16.6% and 17.1% of the unilateral group, respectively. Polyethylene wear rate was 0.17 mm/yr and 0.16 mm/yr in the unilateral and bilateral groups, respectively. Using the Kaplan-Meier method, 17-year survival rates for cup and stem were 78% and 89% in the bilateral group, respectively, and 78% and 86% in the unilateral group, respectively. CONCLUSION: In 17-year long-term follow-up, concurrent bilateral hip arthroplasty was insignificantly different clinically and radiologically from the result of unilateral hip arthroplasty.
Arthroplasty
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Follow-Up Studies
;
Hip
;
Humans
;
Osteolysis
;
Polyethylene
;
Survival Rate
7.Three cases of purpura fulminans.
Sun Hee SUH ; Hwang Min KIM ; Jae Seung YANG ; Baek Keun LIM
Journal of the Korean Pediatric Society 1993;36(5):725-732
Purpura fulminans is one of rare consumptive coagulopathy in children. The most common predisposing conditions of purpura fulminans are infectious disease like streptococcal infection and chickenpox. This disease is characterized by ecchymotic lesions that are usually distributed symmetrically on the lower extremities and buttocks. These ecchymotic lesions undergo necrosis, unless there is effective treatment. We experienced 3 cases of purpura fulminans which improved almost completely after early heparin administration. In the case 1, a 12 month old girl, purpura fulminans developed during sepsis and gastroenteritis. In the case 2, a 4 month old boy, purpura fulminans developed during acute sepsis. We reported 3 cases with a brief review of related literature.
Buttocks
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Chickenpox
;
Child
;
Communicable Diseases
;
Dacarbazine
;
Female
;
Gastroenteritis
;
Heparin
;
Humans
;
Infant
;
Lower Extremity
;
Male
;
Necrosis
;
Purpura Fulminans*
;
Purpura*
;
Sepsis
;
Streptococcal Infections
8.A case of primary carcinoma of the uterine tube.
Jae Hee HAN ; Jeong Beom HWANG ; Wan Cheol HONG ; Nong Su PARK
Korean Journal of Obstetrics and Gynecology 1993;36(7):3208-3213
No abstract available.
Fallopian Tubes*
;
Female
9.A Case of Sotos Syndrome.
In Seok KIM ; Joon Hee KIM ; Young Youn CHOI ; Jae Sook MA ; Tai Joo HWANG
Journal of the Korean Pediatric Society 1995;38(5):725-729
No abstract available.
Sotos Syndrome*
10.A case of anencephaly combined with twin pregnancy.
Sang No YU ; Kug Hee LEE ; Young Kwon PARK ; Jae Yul KANG ; Hwan KIM ; In TaCK HWANG
Korean Journal of Obstetrics and Gynecology 1993;36(7):3149-3154
No abstract available.
Anencephaly*
;
Humans
;
Pregnancy, Twin*
;
Twins*