1.A Study on the Quantitiation of the Autologous Rosette Forming Lymphocytes in the Human Peripheral Blood.
Jeung Hoon LEE ; Won Suk KIM ; Hee Chyl EUN
Korean Journal of Dermatology 1982;20(1):23-27
The formation of spontaneous rosettes between human lymphocytes and sheep erythro ytes under suitable conditions is a constant feature of T-lymphocytes. Recently. It has been demonstrated in the mouse, rat, guinea pig and in man that a certain proportion of peripheral blood lymphocytes has the property to bind autolognus erythrocytes in vitro. These lymphocytes are called auiologous rosette forming cells(ARFC). Although there are several reports on human ARFC. the results are not in accordance. The present study was undertaken to demonstrate the autologous rosette forming property of human peripheral blood lymphocytes, and to enumerate the percentage of ARFC in different sex and age guoups. Fifty healthy persons entered this study between Martch and September. 1980. at the Department of Dermatolgy, Seoul National Universty Hospital. The method of quantitation of AREC was s sight modification of that of Lambermont et al(1977). The results were as follows.
Male
;
Humans
;
Mice
;
Animals
2.Pigmented Contact Dermatitis.
Hee Chul EUN ; Kea Jeung KIM ; Yoo Shin LEE
Korean Journal of Dermatology 1983;21(5):611-615
Pigmented contact dermatitis, firstly reported by Dr. Osmudsen in 1970, is a disease result from recurrent contact dermatitis due to hypersensitivity to cosmetic companents, which produces secondary bizarre dark brown hyperpigmentation. Histological examination of this condition reveals liquefaction degeneration of the basal cells of the epidermis and melanophages in the upper dermis. However, this entity has not been reported in the Korean literature until now. We report three cases of pigmented contact dermatitis which were diagnosed by the histological examinations and the patch tests.
Dermatitis, Contact*
;
Dermis
;
Epidermis
;
Hyperpigmentation
;
Hypersensitivity
;
Patch Tests
3.A case of diffuse spinal cord atrophy proven by MRI complicated by acute transverse myelitis.
Ji Eun CHOI ; Hang Bo JEUNG ; Back Hee LEE ; Se Hee WHANG ; In One KIM
Journal of the Korean Child Neurology Society 1993;1(2):166-169
No abstract available.
Atrophy*
;
Magnetic Resonance Imaging*
;
Myelitis, Transverse*
;
Spinal Cord*
4.A study of garlic sensitivity in patients with hand eczema.
Bong Koo LEE ; Kea Jeung KIM ; Hyung Jai KANG ; Hee Chul EUN ; Jeong Aee KIM
Korean Journal of Dermatology 1992;30(2):197-201
The importance of garlic as a cause of hand eczema has been a matter of debate. Diallyldisulfide is considered as the main allergen in garlic. Twentv two antigens of the modified European standard series and diallyldisulfide of 5%, 2%, 1%, 0.5%, 0.1% in petrolatum were patch tested in 44 patients with hand eczema. Diallylclisi.!lfide was also tested in 13 women as a control. The results were summerized as follows. l. In patch testing with the European standard series, nickel sulfate (22.7%), cobalt chloride (18.2%), fragrance mix (13.6%), balsam of Peru (9.1%) and termerosal (6.8%) were the cornmon allergens which showed positive reactions. The overal positive rate was 59.1 % (26/44). 2.5% diallyldisulfide showed an irritant reaction in 6 (46.2%) out of 13 controls and in 16 (36.4% ) out of 44 patients. 2% diallyldisulfide showed an irritant reaction in 2/13 (15.4 %) in the control group and 6/44 (13.6%) in the patient group. All 13 controls and 44 patients were negative iin tests with diallyldisulfide of 1%, 0.5%, 0.1%. Our results indicate that patch testing with diallyldisulfide of 1% petrolatum is reommended in order to avoid an irritant reaction when contact allergy to garlic is suspetel. 3. Garlic is suspected as an irritant in provoking hand eczema. True contact allergy to garlic in hand eczema seems to be rare.
Allergens
;
Cobalt
;
Eczema*
;
Female
;
Garlic*
;
Hand*
;
Humans
;
Hypersensitivity
;
Nickel
;
Patch Tests
;
Peru
;
Petrolatum
5.Various Pulmonary Manifestations of the Cryptococcal Pneumoniae in the three Immunocompetent Patients.
Jin Chan PARK ; Hyung Tae KIM ; Hun JEUNG ; Ji Han PARK ; Jae Hyuck CHOI ; Hyeon Tae KIM ; Jae Min PARK ; Yong Hee LEE ; Jeung Sook KIM
Tuberculosis and Respiratory Diseases 2001;50(3):359-366
More than half of the cryptococcal infections occur in acquired immune deficiency (AIDS) patients, and more than half of the non-AIDS patients with cryptococcosis are immunocompromised. Most immunocompromised patients have meningoencephalitis at the time of diagnosis. Without the appropriate therapy, this from of the infection is invariably fatal. Death can occur any time from 2 weeks to several years after the onset of symptoms. Pulmonary crytococcosis in immunocompromised patients is usually asymptomatic, but coughing, chest pain, fever, or hemoptysis may occur in immunocompetent patients. Pulmonary cryptococcosis symptoms in immunocompetent patients tend to improve without treatment. Here, we describe the various pulmonary manifestations of cryptococcal pneumoniae in three immunocmpetent patients.
Chest Pain
;
Cough
;
Cryptococcosis
;
Diagnosis
;
Fever
;
Hemoptysis
;
Humans
;
Immunocompromised Host
;
Meningoencephalitis
;
Pneumonia*
6.Achondrogenesis Type 2: An autopsy case.
Joon Mee KIM ; Young Chae CHU ; Soo Kee MIN ; Hee Jeung CHA ; Je Geun CHI
Korean Journal of Pathology 1997;31(5):482-488
Achondrogenesis type 2 is a lethal form of congenital skeletal dysplasia characterized by severe short-limbed dwarfism, decreased vertebral ossification and normal ossification of the skull. We report an autopsy case of achondrogenesis type 2 in a female fetus terminated at 29 weeks of gestation. External morphology revealed a relatively large head, short upper and lower extremities, short neck, and distended abdomen. The x-ray finding showed normal calvarial ossification, hypoplastic ilium and unossified ischium, and metaphyseal flares of the femur and tibia. Histologically, chondrocytes were large and irregular with increased vascularity.
Abdomen
;
Autopsy*
;
Chondrocytes
;
Dwarfism
;
Female
;
Femur
;
Fetus
;
Head
;
Humans
;
Ilium
;
Ischium
;
Lower Extremity
;
Neck
;
Pregnancy
;
Skull
;
Tibia
7.Clinical and pathologic study of dysfunctional uterine bleeding.
Boo Soo HA ; Jong Gi JEUNG ; So Heuy KANG ; Chul KIM ; Chung Hee CHI
Korean Journal of Obstetrics and Gynecology 1993;36(6):847-853
No abstract available.
Female
;
Metrorrhagia*
8.Two Cases of Cerebral Gigantism (Sotos Syndrome).
Hee Jeung AHN ; Young Tae KIM ; In Hoon SEOL ; Jeh Hoon SHIN
Journal of the Korean Pediatric Society 1990;33(8):1153-1156
No abstract available.
Sotos Syndrome*
9.Clear Cell Meningioma.
Hee Jeung CHA ; Soo Kee MIN ; Joon Mee KIM ; Young Chae CHU
Korean Journal of Pathology 1997;31(8):782-787
Clear cell meningioma is a recently recognized morphologically unique entity. It shows no sex predilection, affects primarily the lumbar region, and the cerebellopontine angle. Despite its benign appearance, it may be aggressive, particularly in intracranial cases. All lesions are moderately cellular, with the exception of stromal hyalinization. The tumor consists largely of a sheet- like or somewhat lobular pattern of polygonal cells, the cytoplasm of which is clear. No close association is noted between the recurrence or the clinical outcome and factors such as mitotic activity, the PCNA index, and the DNA ploidy status. But the MIB-1 proliferation index is appreciably higher in recurrent tumors. We experienced a case of clear-cell meningioma showing a characteristic histologic finding. A 39-year-old man was admitted due to the recent onset of right-sided, facial-nerve palsy, left hemiparesis and general weakness. A CT scan of the head showed a well defined mass in the petroclival area. After surgical resection, the patient was in good condition, but 1 year later symptoms recurred. A CT scan of the head showed a huge, recurrent petroclival tumor with adhesion to the surrounding brain parenchyme.
Adult
;
Brain
;
Cerebellopontine Angle
;
Cytoplasm
;
DNA
;
Head
;
Humans
;
Hyalin
;
Lumbosacral Region
;
Meningioma*
;
Paralysis
;
Paresis
;
Ploidies
;
Proliferating Cell Nuclear Antigen
;
Recurrence
;
Tomography, X-Ray Computed
10.Angiodysplasia Arising in the Bowels: Two cases report.
Soo Kee MIN ; Hee Jeung CHA ; Joon Mee KIM ; Young Chae CHU
Korean Journal of Pathology 1997;31(12):1308-1313
Gastrointestinal angiodysplasia is a distinct disease entity which causes frequent gastrointestinal bleeding. It predominantly arises at the stomach and duodenum in the upper gastrointestinal tract and cecum and ascending colon in the lower gastrointestinal tract. The general histological finding of the angiodysplasia is a submucosal vascular ectasia and tortuosity. We have experienced two cases of the intestinal angiodysplasia. The first case occurred on a jejunum in a 22-year-old woman who had anemia. The second case occurred on a sigmoid colon in a 59-year-old man who had constipation. In addition to the general histologic finding of the angiodysplasia, the microscopic findings of the first case revealed some capillary hemangioma-like areas; and in the second case, there was a marked ischemic change and the thickening of the wall.
Anemia
;
Angiodysplasia*
;
Capillaries
;
Cecum
;
Colon, Ascending
;
Colon, Sigmoid
;
Constipation
;
Dilatation, Pathologic
;
Duodenum
;
Female
;
Gastrointestinal Tract
;
Hemorrhage
;
Humans
;
Jejunum
;
Lower Gastrointestinal Tract
;
Middle Aged
;
Stomach
;
Upper Gastrointestinal Tract
;
Young Adult