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박규주 ( Kyu Joo Park ) 대한소화기기능성질환·운동학회 2004 Journal of Neurogastroenterology and Motility (JNM Vol.10 No.2
이상에서 알 수 있듯이 ICC는 위장관의 pacemaker 역할을 하는 중요한 세포로서, 최근 들어 신경전달에도 관여하는 바가 알려졌다. 이런 맥락에서 보면 ICC는 위장관 운동에 있어서 가장 핵심이 되는 세포라 할 수 있다. 최근 들어 ICC의 활성화 기전 및 서파의 propagation 기전 등의 연구에 있어서 획기적인 발전이 이루어졌다. 그러나 ICC의 수적 및 기능적 변화와 소화관 운동질환과의 연관성에 대한 연구는 아직도 초기 단계에 머물고 있는
한국인 가족성 용종증 환자의 가계도 분석 - 한국 용종증 등록소 -
박규주 ( Kyu Joo Park ),박재갑 ( Jae Gahb Park ),최규완 ( Kyoo Wan Choi ),원치규 ( Chi Kyooh Won ),김광연 ( Kwang Yun Kim ),김세민 ( Sea Min Kim ),김영진 ( Young Jin Kim ),김용일 ( Yong Il Kim ),김응국 ( Eung Kook Kim ),김종훈 ( J 대한소화기학회 1992 대한소화기학회지 Vol.24 No.5
Familial adenomatous polyposis (FAP) is a disease characterzed by the development of 100 to several thousand colorectal adenomas, of which one or more will degenerate into carcinoma unless prophylactic colectomy is performed. It is characterized by autosomal dominant mode of inheritance, but sporadic cases without family history of the disease has been reported in up to one-third of patients. (continue...)
박영수 ( Young Soo Park ),안소정 ( So Jung An ),이경희 ( Kyung Hee Lee ),전성욱 ( Sung Wook Chun ),박찬욱 ( Chan Wook Park ),박중신 ( Joong Shin Park ),박규주 ( Kyu Joo Park ),전종관 ( Jong Kwan Jun ),신희철 ( Hee Chul Syn ) 대한산부인과학회 2007 Obstetrics & Gynecology Science Vol.50 No.12
Small bowel obstruction in pregnancy is a rare critical condition with high morbidity and mortality. The diagnosis of small bowel obstruction in pregnancy is often delayed because the symptoms such as nausea, vomiting, and abdominal pain mimic typical pregnancy-associated complaints. So, a high level of suspicion especially in patients with a history of previous abdominal surgery is essential for early diagnosis. Once the diagnosis is made, surgery should be performed immediately. We present the first case of small bowel obstruction during pregnancy in Korea with a brief review of the literature.
홍경섭 ( Kyoung Sup Hong ),박규주 ( Kyu Joo Park ),박성혜 ( Sung Hye Park ),김상균 ( Sang Gyun Kim ),정현채 ( Hyun Chae Jung ),송인성 ( In Sung Song ),김주성 ( Joo Sung Kim ) 대한장연구학회 2008 Intestinal Research Vol.6 No.2
Chronic colonic pseudo-obstruction is a rare disease that results in colorectal dilatation without any obstructing lesions. Colonic dilatation does not usually cause colonic wall thickening and colonic visceral myopathy with muscular hypertrophy has not been reported in Korea. A 31-year-old female patient was transferred for treatment of refractory constipation accompanied by megacolon. She had suffered from recurrent attacks of severe abdominal pain with the sensation of a mass in the left lower quadrant. An abdominal CT revealed a large luminal dilatation of the sigmoid colon where massive stool was impacted. There was no obstructing lesion or luminal dilatation of the rectum. To relieve her refractory symptoms, a total colectomy with an ileorectal anastomosis was performed. Pathologic examination of the sigmoid colon revealed that the muscle layers were dysplastic and hypertrophied, and the innervations into the muscle fibers were markedly decreased. She was discharged without any intra-abdominal symptoms. (Intest Res 2008;6:145-149)
성인에서 발생한 대장의 Aganglionosis 1 예
박수철(Su Cheol Park),김병관(Byeong Gwan Kim),김 원(won Kim),우열근(Yeol Keun Woo),이종열(Jong Yeul Lee),이상협(Sang Hyub Lee),예병덕(Byong Duk Ye),김주성(Joo Sung Kim),박규주(Kyu Joo Park),김우호(Woo Ho Kim),정현채(Hyun Chae Jung 대한소화기학회 2001 대한소화기학회지 Vol.37 No.6
Aganglionosis is a rare form of neuronal intestinal malformation, which includes hypoganglionosis, neuronal intestinal dysplasia A (NID type A), B (NID type B) or combined type. Classic aganglionosis, or Hirschsprung’s disease is a neurogenic form of neonatal bowel obstruction characterized by a congenital absence of ganglionic cells in the submucosal and myenteric plexus, and presents in childhood with symptoms of constipation, colonic obstruction or sepsis due to enterocolitis. However, aganglionosis can be diagnosed first in adult due to short segment Hirschsprung`s disease with mild symptom and maybe also due to acquired process. We experienced a case of adult type aganglionosis assumed to be acquired type without malignancy or other neurological involvement. (Korean J Gastroenterol 2001;37:470-474)