1.Photographic Analysis of Lip Repair in the Bilateral complete cleft lip and palate.
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1999;26(2):222-228
Characteristic residual deformities are thought to be unavoidable in most bilateral complete cleft lip and palate patients. Newly-adopted designs and modified surgical strategies were applied to 40 consecutive patients of bilateral complete cleft lip and palate and some characteristic deformities could be overcome. The future midline on the lateral lip segment was marked on the white roll of thickest vermilion and the alar base was transposed medially without circumalar incision. The prolabial width was reduced to 4-5 mm in consideration of further widening. To evaluate the outcome of bilateral cleft lip repair, 15 patients with adequate photographic records were assessed separately and overall by a panel of judges. Gross facial attractiveness of the visual analog recording scale correlated well with the cleft impairment scale. Full-bodied vermilion with tubercle was achieved and upper lip tightening and tower lip pouting could be avoided. Adequate philtral width was maintained over a 3-year follow-up. Nasal tip projection and proper alar position could be accomplished without circumalar incision. Cleft impairment scale showed impaired characteristics os short columella, no nostril sill, transverse nostril axis, flat and undimpled philtrum, convex-profiled upper lip and a downward drawn nose. Columellar length and nostril axis were expected to improve with growth and development. Absence of the philtral dimple and convex-profilled upper lip still remain to be solved. A reliable, easy to perform, and inexpensive evaluation protocol was provided for bilateral cleft lip repair and selected surgical procedures and postoperative outcomes could be assessed with photographic records.
Axis, Cervical Vertebra
;
Cleft Lip*
;
Congenital Abnormalities
;
Follow-Up Studies
;
Growth and Development
;
Humans
;
Lip*
;
Nose
;
Palate*
2.Clinocopathological study about malignant potentiality of gall-bladder adenoma.
Yong Sik KIM ; Young Gwan KO ; Sung Wha HONG ; Choong YOON ; Yoon Wha KIM
Journal of the Korean Surgical Society 1993;45(2):240-248
No abstract available.
Adenoma*
3.Antihypertensive and Beta-Blocking Effect of Long-Acting Propranolol.
Jong Wha KIM ; Young Chul KIM ; Hak Choong LEE
Korean Circulation Journal 1983;13(1):225-231
Antihypertensive and beta-adrenoceptor blocking effect of long-acting propranolol were observed in the outpatient department, Department of Internal Medicine, National Medical Center during the period between December, 1981 and May, 1982. The clinical effects of long-acting propranolol were compared with those of conventional propranolol and following results were obtained. 1) Direct cross-over from conventional propranolol 20mg three times a day for several days to long-acting propranolol 160mg once daily was not accompanied by appreciable side effect and there was fairly good antihypertensive effect either in systolic or diastolic pressure. 2) Antihypertensive and bata-adrenoceptor blocking effect of long-acting propranolol 160mg once daily were comparable to those of conventional propranolol 40mg three or four times a day. The compliance of the patients to long-acting propranolol once daily was naturally better than that to conventional propranolol which must be taken three to four times daily. 3) In several cases of trial, the patients who tolerated the long-acting propranolol 160mg per day also well tolerated the regimen of long-acting propranolol 320mg per day, 4) The regimen of long-acting propranolol once daily was recommendable to those patients who were on beta-blocking agents for prolonged period of time for their indications such as hypertension and other chronic cardiovascular diseases, in view of the aspects of good patient compliance, good antihypertensive and beta-blocking effect.
Blood Pressure
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Cardiovascular Diseases
;
Compliance
;
Humans
;
Hypertension
;
Internal Medicine
;
Outpatients
;
Patient Compliance
;
Propranolol*
4.The clinical analysis ofcholedochal cyst.
Keun Eui KIM ; Young Gwan KO ; Sung Wha HONG
Journal of the Korean Surgical Society 1992;42(5):625-635
No abstract available.
5.Sebaceous Gland Tumor Arising in Cystic Teratoma of the Ovary: An unique form of monodermal teratoma.
Dae Joong KIM ; So Young JIN ; Dong Wha LEE
Korean Journal of Pathology 1992;26(1):82-87
Although cystic teratoma is the most common benign tumor of the ovary, the association of sebaceous gland tumor with cystic teratoma is rare. We have recently experienced a case of sebaceous gland tumor, arising in the cystic teratoma of the ovary in a 78-year-old Korean woman. Histologically, the tumor was characterized by an organoid lobular architectures of the sebaceous glands which are exculsively composed of germinative and mature sebaceous cells. Although it is difficult to come to a valid conclusion due to the presence of atypical mitosis and necrosis, this tumor was regarded as benign from the viewpoint of preserved organoid structures, and absence of capsular invasion or metastasis.
Female
;
Humans
6.Pelvic actinomycosis: a case report.
Dae Joong KIM ; So Young JIN ; Dong Wha LEE
Korean Journal of Cytopathology 1991;2(2):172-178
No abstract available.
Actinomycosis*
7.Leiomyosarcoma arising from the inferior vena cava: a case report
Duck Jong HAN ; Suk Koo KIM ; Young Wha JUNG
Journal of the Korean Society for Vascular Surgery 1992;8(1):90-95
No abstract available.
Leiomyosarcoma
;
Vena Cava, Inferior
8.Radiological evaluation congenital gastrointestinal tract anomalies
Young Hee CHO ; Jung Wha JANG ; Ock KIM
Journal of the Korean Radiological Society 1983;19(2):414-425
With the improvements, during recent years, in the control of the infections and nutritional diseases thesubject of congenital malformation becomes of increasing importance. The radiologic signs are crucial for promptdiagnosis of anomalies of alimentary tract and with early identification of resulting complication, surgicaltherapy is usually life-saving. 30 cases of congenital anomalies of alimentary tract in infants were reviewed inrespect of age, sex, incidence and radiological findings. 1. The most common lesion was hypertrophic pyloricstenosis, followed by congenital megacolon and anorectal anomaly, tracheoesophageal fistula, intestinal atresia.2. Male outnumbered female in most congenital anomalies of alimentary tract. 25 cases were under the age of 1month. 3. Common symptoms of upper gastrointestinal tract obstruction are vomiting and abdominal distention. Inthe obstruction of lower gastrointestinal tract, abdominal distention and failure of meconium passage were noted.4. Roentgenologic finding were as follows, a. Chest A-P and lateral view; In tracheoesophageal fistula, sacculardilatation of upper esphagus and displacement of trachea anterolaterally were the most common finding. b. Simpleabdomen: Obstructive pattern of proximal portion of duodenum shows in 11 cases, of distal bowel shows in 16 cases.Duodenal atresia showed “double bubble” sing, hypertrophic pyloric stenosis showed marked gastric distention,paucity of air in small bowel and increased gastric peristalsis were the most common finding. Hirschsprung'sdisease showed absence of rectal gas almostly. The variable length between blind hindgut to anus was seen inanorectal anomalies. c. Esophagogram: Blind sac of upper esophagus was seen at the 4th thoracic spinal level anddisplacement of trachea anteriolaterally. 1 case of tracheoesophageal fistula had an intact esophageal lumen. d.Upper G-I series; In hypertrophic pyloric stenosis, delayed gastric emptying, string or double tract sign were themost common finding and catapiller sign, tit sign, shoulder sing or open umbrella sign were noted. e. Bariumenema; In congenital megacolon, transitional zone and irregular bizzar contraction, “choppywave” were noted.Radiograph made 24 hours after barium enema showed retained barium in the colon. f. Selective retrogradefistulogram, distal loopgram & voiding cystogram: In anorectal anomalies, 3 cases showed rectourethral fistula and2 cases showed rectovaginal fistula and 1 case showed rectovesical fistula. And membranous imperforate anus is in1 case.
Anal Canal
;
Anus, Imperforate
;
Barium
;
Colon
;
Duodenum
;
Enema
;
Esophagus
;
Female
;
Fistula
;
Gastric Emptying
;
Gastrointestinal Tract
;
Hirschsprung Disease
;
Humans
;
Incidence
;
Infant
;
Lower Gastrointestinal Tract
;
Male
;
Meconium
;
Peristalsis
;
Pyloric Stenosis, Hypertrophic
;
Rectovaginal Fistula
;
Shoulder
;
Thorax
;
Trachea
;
Tracheoesophageal Fistula
;
Upper Gastrointestinal Tract
;
Vomiting
9.Ectopic Epididymis in Testicular Appendices: Report of Two Cases.
Hyun Soo KIM ; Gou Young KIM ; Hyung Lae LEE ; Youn Wha KIM ; Sung Jig LIM
Korean Journal of Pathology 2011;45(Suppl 1):S11-S14
We report two cases of ectopic epididymal ducts and efferent ductules in the testicular appendices (TAs) of adult men with normally descended testes. In both cases, a sessile TA was incidentally found at the upper pole of the right testis during the scrotal hydrocelectomy. Microscopically, a few closely arranged tubules were detected within the TA. In the first case, the tubules were lined with a pseudostratified columnar epithelium with numerous, long microvilli, and were surrounded by a smooth muscle coat. In contrast, in the second case, the tubules had a wavy luminal surface, because ciliated columnar cells alternated with groups of cuboidal cells. In both cases, strong CD10 immunoreactivity was observed in the luminal border of the lining epithelium. Surgical pathologists should be aware of the presence of both ectopic epididymal ducts and efferent ductules that can occur in TAs, in order to avoid misinterpretation as transected, functional reproductive structures.
Adult
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Choristoma
;
Epididymis
;
Epithelium
;
Female
;
Humans
;
Male
;
Microvilli
;
Muscle, Smooth
;
Parovarian Cyst
;
Phenobarbital
;
Testis
;
Wolffian Ducts
10.A study on the usefulness of HbA1c for diagnosis in patients withdiabetes mellitus.
Young Sik CHOI ; Young Ho YOON ; Wha Soon CHUNG ; Tae Yeal CHOI ; Choon Won KIM
Korean Journal of Clinical Pathology 1991;11(1):31-39
No abstract available.
Diagnosis*
;
Humans