1.Intralesional Recombinant Alpha-2a Interferon for the Treatment of Patients With Verruca.
Seung Won AHN ; Seong Joon SEO ; Chang Kwun HONG
Annals of Dermatology 2000;12(3):155-159
BACKGROUND: Interferon alpha-2a has already been shown to be effective in clinical use of virus-originated diseases such as hairy cell leukemia, condyloma acuminatum, and AIDS-related Kaposi's sarcoma. The use of recombinant alpha-interferon may allow common warts to be treated relatively atraumatically and with less incidence of recurrence. OBJECTIVE: We tried to determine the safety and effectiveness of intralesional injections of recombinant alpha-2a interferon in the treatment of patients with common warts. METHODS: A single wart on each patient was weekly injected with 0.75 to 1.5×10(5) IU/25mm2 of interferon for 8 weeks, and the response to treatment was followed up-to 6 months. RESULTS: Clearing of the treated wart at the end of treatment occurred in 5(71%) out of 7 patients and the rest showed no improvement. With evaluation for relapses up-to 6 months after treatment, warts relapsed in 2(40%) out of 5 patients. Therefore, 3(43%) out of 7 patients were completely free of warts 6 months after treatment. CONCLUSION: Intralesional recombinant interferon alpha-2a has a limited therapeutic effect, but may be considered as a therapeutic modality of recalcitrant verruca or when it can be anticipated that destructive techniques or blistering agents will not be tolerated.
Blister
;
Humans
;
Incidence
;
Injections, Intralesional
;
Interferon-alpha
;
Interferons*
;
Leukemia, Hairy Cell
;
Recurrence
;
Sarcoma, Kaposi
;
Warts*
2.Appendiceal Mucocele with Lower Gastrointestinal Bleeding.
Jong Soo KIM ; Joon Seong LEE ; Seong Won CHO ; Chan Sup SHIM ; Jae Joon KIM ; Hee YOO ; Dong Hwa LEE
Korean Journal of Gastrointestinal Endoscopy 1987;7(1):59-63
The appendiceal mucocele is very rare disease of 0.2% incidence. About 24% of patients are asymptomatic and symptomatic patients present with pain in the right lower quadrant of abdomen in 64%, plapable maas in the right lower quadrant of abdomen in 50%, and rarely, melena, hematochezia, anemia, diarrhea, malaise, and abdominal distension. The gastrointestinal bleeding may be presented in the patient with intussusception, but the massive bleeding is generally absent. We report a case of appendiceal mucocele accompanying with gastrointestinal bleeding and review of literature.
Abdomen
;
Anemia
;
Diarrhea
;
Gastrointestinal Hemorrhage
;
Hemorrhage*
;
Humans
;
Incidence
;
Intussusception
;
Melena
;
Mucocele*
;
Rare Diseases
3.Concurrent Malignant Lymphoma of the Colon and Small Bowel as the Primary Origin.
Joon Seong LEE ; Seong Won CHO ; Chan Sup SHIM ; Jae Joon KIM ; Hee YOO ; Dong Hwa LEE
Korean Journal of Gastrointestinal Endoscopy 1987;7(1):53-57
Primary gastrointestinal lymphoma primarily confined to gastrointestinal tract is relatively rare diaease. Although the lymphoma primarily involved colorectum or small bowel was commonly reported than primary gastric lymphoma in Korea, the concurrent primary lymphoma of colon and small bowel is very rare in reported cases. We report a case of combined primary malignant lymphoma of the jejunum and cecum, who was admitted due to melena and anemia. She had right hemicolectomy and end-to-side ileotransverse colostomy at 2 months ago, due to primary colon lymphoma. The laparotomy was performed and identified hard, 2 x 3 cm sized masses on distal 25 cm, 80 cm and 150 cm from the Treitz ligament. The histology of these small ma showed histiocytic lymphoma as same as cecal specimen. In general, the small bowel lymphoma shaws poor prognosis than gastric or colorectal lymphoma due to diffieulty in diagnosis and late symptoms, but this problem could be resolved through the knowledge about primary gastrointestinal lymphoma and the development of diagnostic methods.
Anemia
;
Cecum
;
Colon*
;
Colostomy
;
Diagnosis
;
Gastrointestinal Tract
;
Jejunum
;
Korea
;
Laparotomy
;
Ligaments
;
Lymphoma*
;
Lymphoma, Large B-Cell, Diffuse
;
Melena
;
Prognosis
4.Recurrent Transitional Cell Carcinoma in the Anastomotic site of Ileal Conduit and Ureter: A Report of Two Cases.
Joon Won KANG ; Chang Kyu SEONG ; Seung Hyup KIM
Journal of the Korean Radiological Society 2001;44(1):103-106
The authors report two cases of recurrent transitional cell carcinoma at the anastomotic site of the ileal conduit and ureter after total cystectomy. In one patient, a recurrent tumor was also found in the distal ureter which had not been removed during previous nephrectomy. At follow up, the patients presented with gross hematuria or hydronephrosis, and the presence of mass lesions was demonstrated by intravenous urography,antegrade pyelography, and/or loopography. Transitional cell carcinoma was diagnosed by surgery and pathologic examination.
Carcinoma, Transitional Cell*
;
Cystectomy
;
Follow-Up Studies
;
Hematuria
;
Humans
;
Hydronephrosis
;
Nephrectomy
;
Ureter*
;
Urinary Bladder Neoplasms
;
Urinary Diversion*
;
Urography
5.Keratoacanthoma in Co-existence with Nevus Sebaceus.
Seung Won AHN ; Tae Jong CHUN ; Seong Joon SEO ; Chang Kwun HONG
Annals of Dermatology 2000;12(2):138-140
Nevus sebaceus of Jadassohn has been referred to as a organoid nevus that classically evolves through three stages and may be associated with a range of skin tumors, and of these, syringocystadenoma papilliferum and basal cell carcinoma have been commonly reported to occur. The occurrence of keratoacanthoma is a very rare event in nevus sebaceus. Herein we report on a 23-year-old man with nevus sebaceus of the cheek. He represents a keratoacanthoma arising within nevus sebaceus.
Carcinoma, Basal Cell
;
Cheek
;
Humans
;
Keratoacanthoma*
;
Nevus*
;
Nevus, Sebaceous of Jadassohn
;
Organoids
;
Skin
;
Young Adult
6.The Significance of Teardrop Changes in Developmental Dislocation of the Hip.
Seok Hyun LEE ; Won Young SHON ; Hyeon Il JEOUNG ; Joon Gyu MOON ; Ki Seong KIM
The Journal of the Korean Orthopaedic Association 1998;33(2):319-325
Prediction of acetabular development after reduction in treatment of developmental dysplasia of thc hip (DDH) is earlier, the hetter results because it would help ensure optimal timing of additional procedure if necessary. In this respect, authors reviewed retrospectively the radiographs of the hips of 35 children with DDH who had unilateral involvement and treated hy senior author (S.H.Lee) from the heginning with single successful attempt of reduction. The radiographs which were made at the time of initial diagnosis, one, two year nfter reduction und final follow up were assessed of teardrop figures. The results of treatment were classified as satisfactory group(CE > 10degrees ) and unsatisfactory group(CE < 10degrees) judged hy center-edge angle(CE degrees) at final follow-ups. 1. The teardrop figures were classifiable into 4 distinct groups as i)absent. ii)V-shaped, iii)Ushaped, iv) inverted D-shaped. 2. The teardrop figures in normal sides of hip were all U-shaped. 3. In dislocated but with satisfactory result group(24 cases), absent at 2 cases(8%), U-shaped teardrop was seen at 13 cases(54%), V-shaped in 9 cases(38%), and inverted 2-shaped in 0 case at I year after reduction. 4. In dislocated but with unsatisfactory result group( 11 cases), they were mostly of V-shaped(7 cases, 64%). The rest were of ahsent in 4 cases(36%) . hut none of U-shaped and inverted 2-shaped. In conclusions, teardrop figures appeared as significant predictor of future development of hip joint. Teardrop figure which stay as V-shaped at one year after reduction seems suggestive of insufficient reduction of DDH, therehy calls for early additional procedure.
Acetabulum
;
Child
;
Diagnosis
;
Dislocations*
;
Dronabinol
;
Follow-Up Studies
;
Hip Joint
;
Hip*
;
Humans
;
Retrospective Studies
7.Gestational Diabetes Mellitus and Long-Term Prognosis of the Offsprings
Journal of Korean Diabetes 2020;21(2):81-87
The hyperglycemia and adverse pregnancy outcomes (HAPO) study demonstrated a linear increase in the risk of adverse pregnancy outcomes with increasing maternal glycemia that can be less severe than overt diabetes and is often untreated. Recently, HAPO follow-up studies were published on longterm consequences on children of gestational diabetes mellitus (GDM) gravidas. Two articles examined the association of untreated maternal glycemia with markers of glucose metabolism in a total of 4,160 ethnically diverse children 10~14 years of age. Children of mothers with GDM had higher prevalence of impaired glucose tolerance (IGT). Moreover, there were strong positive associations between maternal continuous and categorical glycemia status and child’s 75-g glucose tolerance test, A1C, IGT, and impaired fasting glucose. Another two articles evaluated the risk of childhood adiposity of 4,832 children born from mothers with GDM. GDM was associated with childhood adiposity as evaluated by multiple methods. Additionally, maternal glucose level across a continuum was associated with childhood obesity, percentage body fat, and sum of skinfolds > 85th percentile after adjustment for maternal body mass index. These findings could have implications for glucose targets in mothers with GDM and indicate that even mild hyperglycemia can affect adversely glucose metabolism and obesity in the children of mothers with GDM.
8.Clinical Manifestations of Leber's Hereditary Optic Neuropathy with 11778 mtDNA Mutation.
Seong Joon KIM ; Jeong Min HWANG ; Hye Won PARK
Journal of the Korean Ophthalmological Society 1996;37(8):1389-1396
Leber's hereditary optic neuropathy is caused by a single nucleotide change in the mitochondrial deoxynucleic acid(mtDNA) and accounts for 30% of bilateral optic atrophy of unknown etiology. The authors found 11778 mtDNA mutation in 12 patients and evaluated the clinical manifegtations. We confirmed various phenotypes exist in Leber's hereditary optic neuropathy in Korea.
DNA, Mitochondrial*
;
Humans
;
Korea
;
Optic Atrophy
;
Optic Atrophy, Hereditary, Leber*
;
Phenotype
9.Erratum: Author's name correction.
Hyun Mi KIM ; Jin Young BAE ; Yoo Jin CHO ; Mi Ju KIM ; Hyun Hwa CHA ; Won Joon SEONG
Obstetrics & Gynecology Science 2014;57(2):180-180
The Editorial Office of Obstet Gynecol Sci would like to correct the author's name. The Editorial Office apologizes for any inconvenience that it may have caused.
10.Studies on Alkaline Phosphatase Isoenzyme in the Serum and Organs of the Rat.
Won Joon KIM ; Hye Seong CHO ; Sa Suk HONG
Yonsei Medical Journal 1984;25(2):142-148
Isoenzymes of alkaline phosphatase from purified extracts of liver, intestine, pancreas and bone of rats were determined by their isoelectric points and compared with those from serum. 1) The extracts obtained from homogenized tissues were centrifuged at 65,000xg and filtered through an Ultrogel AcA 34 column. Among the three major peaks obtained by gel filtration, the second peak fractions were further separated by isoelectric focusing. Isoenzymes of alkaline phosphatase were found only in the second peak. 2) Isoenzymes of alkaline phosphatase were distinguishable with pH 3.5-10 ampholytes. When pH 3-6 ampholytes were used, isoenzymes were more clearly separated, e.g., 4in serum, 5 in intestine and 2 each in the liver, pancreas, and bone. 3) Comparing the bands of the isoenzymes of alkaline phosphatase to those of serum, only the band with 5.04 pI was the same between serum and intestine. These results indicate that several forms of alkaline phosphatase, even though all are from the rat, may exist; and some of the isoenzymes of alkaline phosphatase found in the serum originated from the intestine.
Alkaline Phosphatase/analysis*
;
Alkaline Phosphatase/blood
;
Animal
;
Isoenzymes/analysis*
;
Isoenzymes/blood
;
Rats