http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
조유숙,임윤정,김성호,이재천,임미경,유빈,문희범 ( You Sook Cho,Yeun Jeong Lim,Jae Cheon Lee,Seoung Ho Kim,Mi Kyoung Lim,Bin Yoo,Hee Bom Moon ) 대한천식알레르기학회 1998 천식 및 알레르기 Vol.18 No.3
Backgroand: Oral allergy syndrome(OAS) is composed of it,ching sense and edema in oral cavity, lips, throat, pharynx, and larynx following eating some fresh fruits or vegetables. It has been known that most of patients with OAS are allergic to pollens. Common epitopes were found among pollens, fruits and vegetables. Although OAS is a common farm of food allergy in adults, this is the first epidemiologic study of OAS in Korea. Muterial and metkod: One hundred and fifty one patients who showed positive skin reaction to pollens were telephone-interviewed. Investigation of the prevalence and clinical manifestations of OAS was possible in 81 patients. Result: The prevalence of OAS among these patients was 34.6% (28/81). OAS was found in 24(48%) out of 50 patients sensitized to tree pollens, whereas 4(13%) of 31 grass or weed pol- len-sensitized paients had OAS. Most common causative food was apple and all of 17 apple- OAS patients were sensitized to tree pollens. Peach was the second common food and 14 of 15 peach-OAS patients were sensitized to tree pollens. Besides oral symptoms, rhinitis, asthma, diarrhea, nausea, vomiting or generalized urticaria were accompanied in half of the OAS patients (14/28). Some patients showed OAS to some unique Korean foods such as dropwort, taro and Aster. Conclasion.' OAS was very common in pollen-sensitized patients. Larger epidemiologic studies are needed to find unique Korean foods and their antigensm causing OAS.
비정형 림프구증가증과 만성 Epstein-Barr virus 감염을 동반한 모기 침산 과민반응 1례
박소연 ( So Yeon Park ),조유숙 ( You Sook Cho ),김성호 ( Seung Ho Kim ),이창근 ( Chang Keun Lee ),유빈 ( Bin Yoo ),김상위 ( Sang Wi Kim ),오흥범 ( Heung Bum Oh ),박찬정 ( Chan Jeoung Park ),문희범 ( Hee Bom Moon ) 대한천식알레르기학회 2003 천식 및 알레르기 Vol.23 No.2
Hypersensitivity to mosquito bites is a disorder characterized by necrotic skin reactions and systemic generalized symptoms subsequent to mosquito bites. This disease has been reported mostly in Japanese patients in their first two decades of life. Recent
김선희 ( Seon Hee Kim ),김영학 ( Young Hak Kim ),조유숙 ( You Sook Cho ),김찬 ( Chan Kim ),최승원 ( Seung Won Choi ),유빈 ( Bin Yoo ),이명종 ( Myoung Chong Lee ),문희범 ( Hee Bom Moon ) 대한류마티스학회 1995 대한류마티스학회지 Vol.2 No.2
Sjogren`s syndrome is a heterogenous autoimmune disease characterized by progressive destruction of the exocrine glands and accompanied by a variety of autoimmune phenomena. Sjogren`s syndrome patients can develop symptoms of ocular and oral dryness as well as extraglandular complications including central and peripheral nervous system disease. Sometimes neuropathy precedes the diagnosis of Sjogren`s syndrome. Adie`s syndrome is characterized by tonic pupil and the absence of tendon reflex. Sweating abnormality and chronic peripheral polyneuropathy can also be present. We report a case of primary Sjogren`s syndrome preceded by Adie`s syndrome with peripheral neuropathy. A 26-year-old woman was admitted for photophobia and paresthesia. On examination. her pupils were anisocoric and did not react to light but constricted promptly to pilocarpin. Sensation decreased on her left side of body and deep tendon reflexes were absent. Biopsy of minor salivary gland demonstrated infiltration by lymphocyte consistent with Sjogren`s syndrome, but Schirmer test was negative. So she was diagnosed as Adie`s syndrome with peripheral neuropathy. Five month later she complained of dry eye and dizziness. Rose bengal staining was positive. Sjogren`s syndrome was diagnosed and she was discharged with local therapy for the sicca symptoms.
박주상 ( Ju Sang Park ),김성호 ( Seong Ho Kim ),김찬 ( Chan Kim ),조유숙 ( You Sook Cho ),유빈 ( Bin Yoo ),지현숙 ( Hyun Sook Chi ),문희범 ( Hee Bom Moon ) 대한류마티스학회 1998 대한류마티스학회지 Vol.5 No.1
A 42-year-old man presented with severe pancytopenia and uncontrolled epistaxis. The diagnosis of SLE was made and the pancytopenia was found to be due to myelofibrosis. The pulse therapy with methylprednisolone and maintenance therapy with prednisolone reversed both pancytopenia and myelofibrosis. Although myelofibrosis has been described in SLE, this coexistence must be very rare since there has been only 19 cases showing this combination. We report a case of SLE with myelofibrosis which was reversed by the treatment with glucocorticoid.
김성호 ( Seong Ho Kim ),임희영 ( Hee Young Lim ),조유숙 ( You Sook Cho ),김찬 ( Chan Kim ),유빈 ( Bin Yoo ),고윤석 ( Yoon Seok Ko ),김우성 ( Woo Seong Kim ),문희범 ( Hee Bom Moon ) 대한류마티스학회 1998 대한류마티스학회지 Vol.5 No.1
Relapsing polychondritis, a rare multisystem disease, is characterized by widespread potentially destructive inflammatory lesions, involving cartilaginous structures throughout the body. Auricular chondritis is the most frequent presenting sign of this disease, with arthritis being the second. Other clinical menifestations include nasal chondritis, scleritis, damage to tracheobroncheal cartilage, and cardiovascular and renal involvement. We experienced three cases of relapsing polychondritis. One case is 66 year old male with bilateral auricular chondritis with histologic confirmation, episcleritis, polyarthritis, periarterial vasculitis, and sensorineural hearing loss. Another case is 42 year old male with respiratory, nasal, auricular chondritis and psoriasis with arthritis. The third case is 46 year old female with three year history of relapsing polychondritis, presenting bilateral auricular and nasal chondritis and severe respiratory tract involvement with histologic confirmation. We also reviewed the other case reports of relapsing polychondritis in Korea. The major presenting manifestations of relapsing polychondritis in Korea were respiratory tract symptoms of dyspnea, cough, and sputum. That is, auricular chondritis was less frequent than laryngotracheal-bronchial involvement.
TGF-β1과 IL-1β에 의한 류마티스 관절염 활막세포 자사(apoptosis)의 억제
김성호 ( Seong Ho Kim ),변원철 ( Won Chul Byun ),임미경 ( Mi Kyoung Lim ),조유숙 ( You Sook Cho ),김찬 ( Chan Kim ),김미정 ( Mi Jung Kim ),유빈 ( Bin Yoo ),문희범 ( Hee Bom Moon ) 대한류마티스학회 1999 대한류마티스학회지 Vol.6 No.2
Objective: To investigate the proliferative and anti-apoptotic effects of TGF-β1 and IL-1β on rheumatoid synovial cells. Methods: Synovial cells obtained from surgical procedure of the rheumatoid joint were cultured with TGF-β1 and IL-1. The proliferative response of synovial cells was examined by non-radioactive cell proliferation assay. Fas-mediated apoptosis of synovial cells was measured by flowcytometry after addition of anti-Fas antibody. Results: TGF-β1 and IL-1β proliferated synovial cells in a dose-dependent manner. They also made synovial cells resistant to anti-Fas antibody induced apoptosis. Conclusion: TGF-β1 and IL-1β promotes synovial cell proliferation possibly through interference with Fas-mediated apoptosis, suggesting their role in synovial hyperplasia in rheumatoid arthritis.
이은영 ( Eun Young Lee ),안만수 ( Man Su Ahn ),신정현 ( Jung Hyun Shin ),이창근 ( Chang Keun Lee ),조유숙 ( You Sook Cho ),유빈 ( Bin Yoo ),문희범 ( Hee Bom Moon ) 대한류마티스학회 2001 대한류마티스학회지 Vol.8 No.2
A link between sensorineural hearing loss and autoimmune disease is postulated. The pathogenesis of sudden sensorineural hearing loss (SNHL) in patients with systemic lupus erythematosus (SLE) is not clear. However, several reports have suggested vasculitis secondary to SLE as underlying mechanism or association of antiphospholipid antibody (aPL). Although there were some cases of sensorineural hearing loss associated with systemic lupus erythematosus or lupus-like syndrome treated with plasmapheresis or immunosuppressive agents, there has been no case of SNHL in patients with SLE reported in Korea. We describe an 18-year-old female with systemic lupus erythematosus who presented with sudden sensorineural hearing loss. She was treated with high-dose corticosteroids with favorable clinical outcome.
김진용 ( Jin Yong Kim ),엄상용 ( Sang Yong Om ),윤선영 ( Sun Young Yoon ),김태범 ( Tae Bum Kim ),조유숙 ( You Sook Cho ),문희범 ( Hee Bom Moon ),권혁수 ( Hyouk Soo Kwon ) 대한천식알레르기학회 2013 Allergy Asthma & Respiratory Disease Vol.1 No.3
This case report describes a life-threatening anaphylaxis to fentanyl during radiofrequency ablation (RFA). A 50-year-old woman with hepatocellular carcinoma was admitted for RFA. She denied any history of adverse drug reactions or past adverse anesthetic reaction. Physical examination, vital signs, any laboratory findings were all within normal limits. Ten minutes after intravenous administration of 50 mcg of fentanyl before starting RFA, she developed generalized erythema and sudden onset of bronchospasm followed by respiratory arrest. Cardiopulmonary resuscitation (CPR) commenced with 100% oxygen and intravenous administration of epinephrine 1 mg. After 5 minutes of CPR, she had the return of spontaneous circulation. Chest X-ray revealed pulmonary edema which resolved over two days. She recovered completely and was discharged home. After six weeks, intradermal tests performed with fentanyl, remifentanyl, midazolam, and profopol. Among those, only fentanyl induced positive skin response. Fentanyl induced anaphylaxis was diagnosed for this case, and fentanyl was avoided in the subsequent general anesthesia for liver transplantation. This case suggested that fentanyl could induce anaphylaxis combined with uncommon comorbidities like pulmonary edema. (Allergy Asthma Respir Dis 2013;1:284-287)
고주파열치료 중 펜타닐에 의해 발생한 아나필락시스 1예
김진용 ( Jin Yong Kim ),엄상용 ( Sang Yong Om ),윤선영 ( Sun Young Yoon ),김태범 ( Tae Bum Kim ),조유숙 ( You Sook Cho ),문희범 ( Hee Bom Moon ),권혁수 ( Hyouk Soo Kwon ) 대한소아알레르기호흡기학회(구 대한소아알레르기 및 호흡기학회) 1991 소아알레르기 및 호흡기학회지 Vol.1 No.3
This case report describes a life-threatening anaphylaxis to fentanyl during radiofrequency ablation (RFA). A 50-year-old woman with hepatocellular carcinoma was admitted for RFA. She denied any history of adverse drug reactions or past adverse anesthetic reaction. Physical examination, vital signs, any laboratory findings were all within normal limits. Ten minutes after intravenous administration of 50 mcg of fentanyl before starting RFA, she developed generalized erythema and sudden onset of bronchospasm followed by respiratory arrest. Cardiopulmonary resuscitation (CPR) commenced with 100% oxygen and intravenous administration of epinephrine 1 mg. After 5 minutes of CPR, she had the return of spontaneous circulation. Chest X-ray revealed pulmonary edema which resolved over two days. She recovered completely and was discharged home. After six weeks, intradermal tests performed with fentanyl, remifentanyl, midazolam, and profopol. Among those, only fentanyl induced positive skin response. Fentanyl induced anaphylaxis was diagnosed for this case, and fentanyl was avoided in the subsequent general anesthesia for liver transplantation. This case suggested that fentanyl could induce anaphylaxis combined with uncommon comorbidities like pulmonary edema. (Allergy Asthma Respir Dis 2013;1:284-287)