1.A Case of Left Coronary Osteal Stenosis Combined with Moyamoya Disease.
Yong Beom PARK ; Keon Young KIM ; Yong Han BEAK ; Jung Il CHUNG ; Sang Ho CHO ; Seung Yun CHO
Korean Circulation Journal 1996;26(3):740-747
We report a case of a 36 year old female with coronary artery obstructive disease(Left coronary osteal stenosis), who had been admitted due to severe headache and vomitting. In admission, she was diagnosed as moyamoya disease on cerebral angiogram. She had no history of hypertension, diabetes mellitus, hyperlipidemia, smoking. She had experienced angina for 2 years, and 1 year ago she ws diagnosed as bypass surgery with left main coronary artery angioplasty. In moyamoya disease, several portions of extracranial arteries have been found to be involved, but so far, only one case has been reported the coronary involvement on coronary angiogram in the world. And, there has not been a report about moyamoya disease combined with left main osteal lesion yet. This present case indicates that we need to exam for extracranial vascular system including the heart in moyamoya disease.
Adult
;
Angioplasty
;
Arteries
;
Constriction, Pathologic*
;
Coronary Vessels
;
Diabetes Mellitus
;
Female
;
Headache
;
Heart
;
Humans
;
Hyperlipidemias
;
Hypertension
;
Moyamoya Disease*
;
Smoke
;
Smoking
2.A Case of Leiomyomatosis peritonealis disseminata.
Myeng Chan CHOU ; Beak Keun YOO ; Hyun Cheol SHIN ; Keum Won LEE ; Tae Sung CHO ; Dong Han BAE ; Yong Woo SHIN
Korean Journal of Gynecologic Oncology and Colposcopy 1993;4(1):125-129
Leiomyomatosis peritonealis disseminata is a rare non-neoplastic proliferation of histologically benign smooth muscle that occurs in the alxlominal cavity of during the reproductive years of life, often giving rise to false choical imprwsion of d.isseminated carcinomatosis grossly, In 1952 Wilson & Peale described a condition which they called "multiple peritoneal leiomyomas". Taubert et al(1965) clearly delinated the features of the lesion and named it leiomyomatosis peritonealis disseminata(LPD). We report a case of leiomyomatosis peritonealis disseminata with a brief review of literatures.
Carcinoma
;
Leiomyomatosis*
;
Muscle, Smooth
3.An ovarian tumor of probable wolffian origin: Case report in the youngest patient and review of the literature.
Ae Ra HAN ; Yong Soon KWON ; Keon Young KONG ; Soo Jin BEAK ; Jun Woo AN ; Ga Won CHOI ; Jong Hyeok KIM ; Yong Man KIM ; Young Tak KIM ; Joo Hyun NAM
Korean Journal of Obstetrics and Gynecology 2007;50(8):1156-1160
A female adnexal tumor of probable Wolffian origin (FATPWO) is a rare neoplasm believed to originate from Wolffian remnants because the tumors are located in areas where such remnants are abundant. Because FATPWO is so rare that tumor biological behavior is not well defined, especially in cases of ovarian tumors, the collection and investigation of all relevant data, including this case report, are thus crucial to identify the best possible treatment for this type of tumor. We report a 14-year-old girl presented with a huge ovarian tumor that is reminiscent of dysgerminoma on CT scan. Left salpingo-oophorectomy was perfomed. Because the pathologic report on frozen section was malignant neoplasm, additional surgical staging was performed. A ovarian tumor of probable Wolffian origin was diagnosed by the pathologist, finally. No adjuvant therapy was given and there was no clinical evidence of recurrence during the 19 months of follow-up.
Adolescent
;
Dysgerminoma
;
Female
;
Follow-Up Studies
;
Frozen Sections
;
Humans
;
Recurrence
;
Tomography, X-Ray Computed
4.Pulmonary Hypertension in Preterm Infants With Bronchopulmonary Dysplasia.
Hyo Soon AN ; Eun Jung BAE ; Gi Beom KIM ; Bo Sang KWON ; Jae Suk BEAK ; Ee Kyung KIM ; Han Suk KIM ; Jung Hwan CHOI ; Chung Il NOH ; Yong Soo YUN
Korean Circulation Journal 2010;40(3):131-136
BACKGROUND AND OBJECTIVES: With the increasing survival of preterm infants, pulmonary hypertension (PH) related to bronchopulmonary dysplasia (BPD) has become an important complication. The aim of this study was to investigate the characteristics and outcome of PH in preterm infants with BPD and to identify the risk factors for PH. SUBJECTS AND METHODS: We reviewed the records of 116 preterm infants with BPD cared for at a single tertiary center between 2004 and 2008. RESULTS: Twenty-nine (25%) infants had PH >2 months after birth. PH occurred initially at a median age of 65 days (range, 7-232 days). Severe BPD, a birth weight <800 g, long-term ventilator care and oxygen supplementation, a high ventilator setting, infection, and a patent ductus arteriosus (PDA) were related to PH based on univariate analysis (p<0.05). The infants who had longer oxygen supplementation were significantly more likely to have PH (odds ratio, 18.5; 95% confidence interval, 4.1-84.6; p<0.001). PH was improved in 76% of infants after a median of 85 days (range, 20-765 days). Four infants (14%) died. The death of 3 infants was attributed to PH. CONCLUSION: BPD was frequently complicated by PH. Although PH resolved in the majority of infants, PH in preterm infants with BPD can be fatal. Regular screening for PH and adequate management are required.
Birth Weight
;
Bronchopulmonary Dysplasia
;
Ductus Arteriosus, Patent
;
Humans
;
Hydrogen-Ion Concentration
;
Hypertension, Pulmonary
;
Infant
;
Infant, Newborn
;
Infant, Premature
;
Mass Screening
;
Oxygen
;
Parturition
;
Risk Factors
;
Ventilators, Mechanical