1.One Case of Menetrier's Disease.
In Taek OH ; Sea Hyub KAE ; Young Bae KWON ; Rho Won CHUN ; Jin Han KIM ; Sang Aun JOO
Korean Journal of Gastrointestinal Endoscopy 1989;9(1):33-38
Menetrier's disease is a rare disease characterized by the presence of large rugal folds involving part or all of the stomach. Patients with hypertrophic gastropathy often have distressing abdominal symptoms, weight loss and edema due to gastric protein loss. The 48-year-old male patient was admitted to the Hangang Sacred Heart Hospital with cheif complaints of indigestion and epigastric pain. The diagnosis of Menetriers disease is established by radiologic, endoscopic, and pathologic examination. He was treated with soft diet, antacid, H2- receptor antagonist, and IV albumin. We report a case of Menetriers disease with brief review of literatures.
Diagnosis
;
Diet
;
Dyspepsia
;
Edema
;
Gastritis, Hypertrophic*
;
Heart
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Humans
;
Male
;
Middle Aged
;
Rare Diseases
;
Stomach
;
Weight Loss
2.Three cases of pacemaker-mediated tachycardia.
Kae Won LEE ; Chung Whee CHOUE ; Woo Sik KIM ; Heung Sun KANG ; Kwon Sam KIM ; Jung Sang SONG ; Jong Hoa BAE
Korean Circulation Journal 2000;30(3):334-338
Pacemaker-mediated tachycardia (PMT) is a well-known complication of dual-chamber pacemaker with atrioventricular sensing and pacing (DDD) or atrial synchronous, ventricular demand pacemaker (VDD). PMT usually starts with sensing a retrograde P waves linked to ventricular extrasystole with retrograde ventriculoatrial conduction and forms reentrant or circus movement tachycardia with the pacemaker itself as an antegrade limb and the conducting tissue of the heart as a retrograde limb. Recently, a number of pacemaker manufactures have incorporated in their devices a variety of relatively complex algorithms to prevent PMT. Despite these measures, PMT may still occur because of inappropriate programming or unpredictable variations of ventri-culoatrial conduction. We report two cases of PMT in 78 year-old man and 60 year-old man who received DDD type pacemakers due to sick sinus syndrome, and a case of PMT in 69 year-old man who had suffered complete heart block and received a VDD type pacemaker. In these cases, we investigate symptoms, mechanism of PMT, programed parameters of pacemaker and treatments of PMT.
Aged
;
Dichlorodiphenyldichloroethane
;
Extremities
;
Heart
;
Heart Block
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Humans
;
Middle Aged
;
Sick Sinus Syndrome
;
Tachycardia*
;
Ventricular Premature Complexes
3.A case of fetal skelectal anomaly of Campomelic syndrome.
Suk Kyung KIM ; Hyeon Chul KIM ; Seung Joo SHIN ; Mee Wha LEE ; You Me LEE ; Jin Ho CHO ; Yun Jung CHOI ; Kae Won KWON
Korean Journal of Obstetrics and Gynecology 2000;43(2):311-314
Campomelic syndrome is a very rare skeletal dysplasia with a characteristic pattern of deformity involving the proximal and distal extremities, pelvic and shoulder girdles, thoracic cage and palate. Respiratory compromise often leads to death in early infancy. Etiology has not been determined although evidence suggests genetic heterogeneity. Cytogenetic study revealed high incidence of a 46,XY karyotype in phenotypic females. Recently, we had experienced a case of campomelic dysplasia at amenorrhea 30weeks and termination was done, so we report with a brief review of literature.
Amenorrhea
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Campomelic Dysplasia*
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Congenital Abnormalities
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Cytogenetics
;
Extremities
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Female
;
Genetic Heterogeneity
;
Humans
;
Incidence
;
Karyotype
;
Palate
;
Shoulder
5.Two Cases of Struma Ovarii.
Jin Young CHANG ; Kab In CHUNG ; Kae Hyun NAM ; Kwon Hae LEE ; Dong Won KIM
Korean Journal of Gynecologic Oncology and Colposcopy 1998;9(1):87-92
Struma ovarii is a monodermal teratoma composed totally or in overwhelming proportion of thyroid tissue. It is uncommon and accounts for 1% to 3% of benign teratomas of ovary. Grossly, they are encapsulated neoplasms, several centimeters in diameter and have a red, shiny, and meaty surface. Microscopically, the tumor is composed of mature thyroid tissue consisting of various sizes, lined by a single layer of columnar or flattened epithelium. The clinical behavior is benign, and simple excision is adequate treatment. We had experienced two cases of struma ovarii arising in the left ovaries. So we report above cases with brief review of literatures.
Epithelium
;
Female
;
Ovary
;
Struma Ovarii*
;
Teratoma
;
Thyroid Gland
6.A Rare Case of Intra-Areolar Polythelia.
Ryun LEE ; Hee Young LEE ; Ji Hyun KIM ; Kae Won KWON ; Tae Yeon KIM
Archives of Aesthetic Plastic Surgery 2016;22(2):100-102
Among various types of supernumerary nipples, intra-areolar polythelia (IAP) is an extremely rare congenital malformation. The authors report a case of a young woman with unilateral IAP on her right breast. The patient was 24 years old; she had had it since she was 5 or 6 years old, and it had enlarged 3 to 4 years before presentation to our clinic. Surgical excision was performed under local anesthesia as a prophylaxis against breast cancer and cosmetic problems.
Anesthesia, Local
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Breast
;
Breast Neoplasms
;
Female
;
Humans
;
Nipples
;
Reconstructive Surgical Procedures
7.Multiple Primary Carcinoma Associated with Gynecologic Malignancies.
Cheol Ho LEE ; Beak Keun YOO ; Myeng Chan CHOU ; Keum Won LEE ; Jeong Jae LEE ; Kae Hyun NAM ; Kwon Hae LEE
Korean Journal of Gynecologic Oncology and Colposcopy 1993;4(1):103-108
Sixteen multiple primary carcmomas were found in 674 patients with gynecologic malignancies who were treated in our departiment from 1980 to 1992. Cases with possible metastasis or recurrence were not included in this study, The incidence of rnultiple primary carcinomas in gynecologic rnalignancies was 2.1%, Multiple primary carcinomas were encountered in 2.4% of 674 cervical cancers, 1.4% of 73 ovarian cancers respectively. The most frequent sites of uther cancers were seen in the stomach(5/16) and lung(3/l6).
Humans
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Incidence
;
Neoplasm Metastasis
;
Ovarian Neoplasms
;
Recurrence
8.A Case of an Aortic Embolism and Systemic Embolism in Infective Endocarditis.
Kae Won LEE ; Kwan Poy KO ; Heung Sun KANG ; Chung Whee CHOUE ; Kwon Sam KIM ; Jung Sang SONG ; Jong Hoa BAE
Journal of the Korean Society of Echocardiography 1998;6(1):106-111
In spite of advanced diagnostic teclmology and better antimicrpbial therapy, infective endocarditis is relatively common, life-threatening infection. Heart failure and systemic embolism are the common and serious complications associated with the infective endocarditis. Because embolic event caR result in irreversible organ dysfunction or death, prevention is a desirable goal. Identification of pltients who are in the high risk of embolism and who can be helped by early surgical intervenCion is very important. Echocardiography has been generally accepted as the technique of choice for noninvasive diagnosis of infective endocarditis because of its potential for direct visualization of endocarditis-induced lesions. We experienced a case of an aortic embolism and systemic embolism in infective endocarditis in 21 year old male patient. He adrnitted for abdominal pain and dark colored urine for 30 days. Diagnosis of infective endocarditiis was made by clinical manifestation and echocardiography. Abdominal CT showing a low density areas in the spleen and the right kidney suggestive of a splenic infarction and a renal infarction. Aortography revealed dilatation of the bifurcation site of the aorta into common iliac artery and nonvisualization of left common iliac artery. Aortoiliac bypass surgery and splenectomy were done. After antibiotics and anticoagulation therapy, the patient was discharged relatively good condition.
Abdominal Pain
;
Anti-Bacterial Agents
;
Aorta
;
Aortography
;
Diagnosis
;
Dilatation
;
Echocardiography
;
Embolism*
;
Endocarditis*
;
Heart Failure
;
Humans
;
Iliac Artery
;
Infarction
;
Kidney
;
Male
;
Spleen
;
Splenectomy
;
Splenic Infarction
;
Tomography, X-Ray Computed
;
Young Adult