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A Case of Coexisting Behcet`s Disease and Ankylosing Spondylitis (pp.70-72)
Hwan Herr,Eun Hee Cho,Jeong Uk Kim,Hyun Kyu Chang 대한내과학회 2000 The Korean Journal of Internal Medicine Vol.15 No.1
Behcet`s disease (BD) is a chronic inflammatory condition involving several organs, such as skin, mucous membrane, eye, joint, intestine, lung and central nervous system. Ankylosing spondylitis (AS) is a prototype of seronegative spondyloarthropathy, and a
허환(Hwan Herr),김영태(Young Tae Kim),김재홍(Jae Hong Kim),김중환(Joong Hwan Kim) 대한피부과학회 1986 대한피부과학회지 Vol.24 No.4
Fifty six year old woman with liver cirrhosis and 31 year old man in good health had similar skin lesions which were well-defined, round to oval, isolated or confluent, scaly brown patches on her lower back, and his trunk and thighs, respectively, without any symptom. The biopsy specimens taken from the lesions showed slight hyperkeratosis with occasional follicular pluggings, presence of a granular layer, and epidermal flattening in case 1; increased melanin pigment in the basal layer in case 2. In both cases, the upper dermis revealed minirnal perivascular lymphohistiocytic inf iltration. We, therefore, present two cases of pityriasis rotunda and review the literature.
단순 포진 바이러스에 기인된 것으로 사료되는 재발성 다형 홍반
허환(Hwan Herr),이창우(Chang Woo Lee) 대한피부과학회 1987 대한피부과학회지 Vol.25 No.6
We describe four patients with herpes-associated erythema multiforme, who had clinical and histopathological features consistent with the so-called erythema multiforme minor. The appearance of lesions of herpes simplex were followed with intervals between 6 and 10 days by the recurrent developments of erythema multiforme several times in a year in each patient. Sinee herpes simplex virus infection is considered one of the major factors provocating erythema multiforme one may have to pay more attention to patient's history to define the nature of erythema multiforme.
허환(Hwan Herr),김영태(Young Tae Kim),김중환(Joong Hwan Kim) 대한피부과학회 1987 대한피부과학회지 Vol.25 No.1
The patient was a sixty-year-old obese woman with the long history of hypertension, amenorrhea and occasional psychic disturbances. She had eigbt, thumb to adult-fist sized, slightly movable, relatively soft, and painful subcutaneous nodules with tenderness and paresthcsia, of which overlying skin appeared to be normal except senile changes, on the abdomen and both upper extremities for 10 years. There was no evidence of inheritance in her family. Laboratory data revealed no abnormalities in lipid metabolism or in a variety of endocrinological functions. Microscopically, an excised mass from the forearm showed thin connective tissue capsule encircling numerous lobules cornposed entirely of the mature fat. cells vith minimal focal capillary proliferatios.
단순 남성 임질에 대한 Norfloxacin의 치료 효과
김중환(Joong Hwan Kim),윤정용(Jeong Yong Yoon),허환(Hwan Herr),김영태(Young Tae Kim) 대한피부과학회 1987 대한피부과학회지 Vol.25 No.5
From November 18 to December 31, 1986, seventy-five male patients with unconplicated gonococcal urethritis at the Venereal Disease Clinic of Choong-ku Public Health Center in Seoul were allocated randomly into one of two treatment regimens, and seventy patients were followed. All thirty-five patients including PPNG infections, treated with single oral dose of norfloxacin 600mg, were recovered(100%). One of thirty-five patients treated with a single oral dose of norfloxacin 800mg, failed. This failed case was one of eighteen nonPPNG infections (failure rate of 5.6%). Susceptibility test with disks containing norfloxacin 10ug showed the inhibition zone greater than 30mm. It is suggested that a single oral dose of 600mg or 800mg norfloxacin has good effect in the treatment of gonococcal urethritis with minimal side effects. Because of high prevalence of PPNG, it can be recommended as the first line treatment for gonorrhoea in Korea.
Kim, Chung Hwan,Koh, Jai Kyoung,Herr, Hwan,Kim, Jeong Uk,Chung, Haing Sub 대한피부과학회 2000 Annals of Dermatology Vol.12 No.3
Rud's syndrome(RS), basically composed of ichthyosis, mental deficiency and hypogonadism, is a rare hereditary disease. Some varying dermatologic, neurologic, endocrinologic, ophthalmologic and musculoskeletal abnormalities have coincided with RS. No case of RS has been documented from Asian countries except one from Japan. We describe a 16-year-old girl who presented with lamellar ichthyosis, mental retardation, hypogonadism, short stature, alopecia, sparse eyebrows, strabismus, cataracts, and congenital dislocation of the hip. To our knowledge, RS coexisting congenital dislocation of the hip herein is the first case in English literature.
허환,김재홍 한양대학교 의과대학 1999 한양의대 학술지 Vol.19 No.2
Nodular formation may be a rare feature in association with repeated bee-stings at the same sites. Histologically, such nodules are sometimes shown to be granuloma and pseudolymphoma reactions. We present the male patient with a nodule over the knee. He had the knee stung by bees two times at an interval of about 1 month for the treatment of arthralgia at the knee. Three months after the last bee-sting therapy, itchy, mildly tender, and yellow-ivory colored nodule, 2cm in diameter, developed at the site of bee-stings. A possible histogenesis may be due to antigen persistence. The biopsy specimen demonstrated eosinophilic granuloma mixed with lymphohistiocytic infiltration. The patient was treated with intralesional injections of triamcinolone suspension.