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이두연,윤여준,조범구,홍승록,이옥순,최인준,Lee, D.Y.,Yoon, Y.J.,Cho, B.K.,Hong, S.N.,Rkee, O.S.,Choi, I.J. 대한흉부심장혈관외과학회 1976 Journal of Chest Surgery (J Chest Surg) Vol.9 No.1
Pulmonary hamartoma is often incidental, asymptomatic finding on routine chest roentgenogram. It has been considered a congenital malformation. Since the original description by Albrecht in 1908, it has been classified into two types, a small, fibrocartilaginous mass in adults, and a cystic lobar mass in infants. We experienced two cases of pulmonary hamartoma which proved to be the adult form of hamartoma. One was located in left upper lobe of a 58 year old male patient, the other was located in the perihilar region of the right middle lobe of a 38 year old male patient. The former case was treated by wedge resection: the latter by right middle lobectomy and the postoperative courses of both cases were very good and without complication.
민진식,조장환,조광식,강진경,정유희,박찬일,최인준 ( J S Min,C H Cho,K S Cho,J K Kang,U H Chung,C I Park,I J Choi ) 대한소화기학회 1980 대한소화기학회지 Vol.12 No.1
Rarely the stomach may be invaded by pyogenic bacteria which produces phlegmonous gastritis. It is a bacterial infection of the gastric wall, most of ten caused by streptococci, .a.lthough staphylococci, pneumococci, Escherichia coli, or gas forming bacteria could he responsible. Phlegmonous gastritis generally occurs in middle aged male alcoholics with hypochlororhydria, and the lesion may be secondary to a bacteremia, or may arise in previ- ously ulcerated gastric lesions. It has usual clinical course of acute upper abdominal inflam- mation, with signs and laboratory evidences of peritonitis. Preoperative diagnosis is rare but can be made gastroscopically and radiologically if gas is present in the abscess. The majority of published cases has been diagnosed at autopsy and on occation at laparotomy. A case of diffuse phlegmonous gastritis diagnosed at laparotomy is reported here, briefly reviewing tl:e clinicopathologic features and treatment.
安在榮,金正基,張世勳,李敦錫,최인준 中央醫學社 1967 中央醫學 Vol.12 No.4
Since Hagstrorn's first case report of placental polyp in 1940, only 14 cases have been reported in the English literature. Recently, we have experienced a patient with a placental polyp that had induced severe vaginal bleeding 4 months after the abortion. The patient is a 34 years old G5, P3, AB2. Korean female who underwent a D & C for the control of haginal-bleeding with no effect. The total hysterectomy was performed and the cause of bleeding was found to be due to the presence of a placental polyp of 7.0 x 5.5 X 3. 5 cm in size. Although the placental polyp is a rare clinical entity, it is suggested that this entity should be considered as a cause of late puerperal and post abortal hemonhoge.
한운섭,이용배,최인준,김동식 최신의학사 1974 最新醫學 Vol.17 No.11
A case of functioning arrhenoblatoma arisingg from the ovary in 19-year-old women was reported. She had amenorrhea, hirsutism on both extremities, male voice, acne, obesity and abdominal pain with palpable mass. The mass, 3300gm, showed almost cystic and hemorrhagic areas with focal solid' slightly yellowish gray tissue on cut sections. The microscopic findings of the tumor presented the most undifferentiated variety (type III) of the arrhenoblastoma which contained also a number of Leydig cells. The tumor cells were poor in cytoplasmic organelles among which the mitochondrias, a few RER and free ribosomes.. were demonstrated on electron microscopic examinations. Large fat globules.were also found. The interdigitation of. cytoplasm, each ether, with desmosomes was noted.