1.A Case of Wells' Syndrome Associated with Pancreatic Carcinoma.
Jin Hyoung KIM ; So Yun CHO ; Jeong Hee HAHM
Korean Journal of Dermatology 1999;37(6):785-789
Wells' syndrome or eosinophilic cellulitis is an uncommon cutaneous disorder characterized by recurrent erythematous and edematous plaques that often resemble acute cellulitis. The characteristic microscopic findings are diffuse dermal eosinophilia with marked edema, and flame figures consisting of amorphous or granular eosinophilic material around collagen bundles of the dermis. Etiology and pathogenesis are unknown, but the disease has been found to be associated with infections, arthropod bites, drug administration, surgery and hematologic disorders. We report the case of a 55-year-old man with pancreatic carcinoma who was presented with an asymptomatic erythematous to brownish subcutaneous nodule on the left buttock of several days' duration. A biopsy specimen taken from the erythematous to brownish nodule showed many flame figures and diffuse infiltration of eosinophils in the dermis and subcutaneous fat tissue. The rapid resolution of the skin lesion with chemotherapy of the pancreatic carcinoma supports a relationship between the two conditions.
Arthropods
;
Biopsy
;
Buttocks
;
Cellulitis
;
Collagen
;
Dermis
;
Drug Therapy
;
Edema
;
Eosinophilia
;
Eosinophils
;
Humans
;
Middle Aged
;
Skin
;
Subcutaneous Fat
2.A Case of Solitary Congenital Calcified Nodule of the Ear.
Yun Jin KIM ; So Yun CHO ; Yeon Soon LIM ; Hae Young CHOI ; Ki Bum MYUNG
Korean Journal of Dermatology 1999;37(1):74-77
We report a case of solitary congenital calcified nodule of the ear in a 1-year-old female. The lesion was a 2 X 2mm-sized, elevated, slightly erythematous and whitish-centered nodule located since birth on the superior helical rim of her left ear. Histopathological findings fram the totally excised lesion showed calcium deposits as amorphous, basophilic masses in the upper dermis and focal discharge of calcium by means of transepidermal elimination. Surrounding the calcium deposits, lymphohistiocytic infiltrations were present.
Basophils
;
Calcium
;
Dermis
;
Ear*
;
Female
;
Humans
;
Parturition
3.A Case of Allergic Contact Dermatitis due to Lanolin.
Na La SHIN ; Yun Jin KIM ; Hyun Joo KIM ; Young Sook KIM ; So Yun CHO ; Jeong Hee HAHM
Korean Journal of Dermatology 1999;37(5):620-623
Lanolin is a complex material consisting of a mixture of numerous esters and polyesters of high-moleculer-weight alcohols and fatty acids, Lanolin allergy is important because lanolin is widely used as an emulsifier in topical medicaments and in numerous cosmetic preparations. We report a case of allergic contact dermatitis in a 27-year-old female. An erythematous pruritic rash develgood around the eyelid developed after applying a new eye cream and was aggravated after applying Cambison ophthalmic ointment. Patch testing showed positive reactions to Cambison ophthalmic ointment, 30% wool alcohol, Amerchol L101 and Nivea cream. A use test with 100% Cambison ophthalmic ointment base was positive
Adult
;
Alcohols
;
Dermatitis, Allergic Contact*
;
Esters
;
Exanthema
;
Eyelids
;
Fatty Acids
;
Female
;
Humans
;
Hypersensitivity
;
Lanolin*
;
Patch Tests
;
Polyesters
;
Wool
4.A Case of Proliferating Trichilemmal Tumor Developing in the Public Area of a Patient Underdoing Hemodialysis.
Youn Jin KIM ; Ji Hyun KIM ; So Yun CHO ; Kyu Kwang WHANG ; Jeong Hee HAHM
Korean Journal of Dermatology 2000;38(5):676-678
No Abstract Available.
Humans
;
Renal Dialysis*
5.A Case of Tufted Angioma Showing a Good Response to Interferon-alpha.
Yun Jin KIM ; Ji Hyun KIM ; So yun CHO ; Mi Ae LEE ; Hyung Chul KANG ; Jeong Hee HAHM
Korean Journal of Dermatology 1999;37(3):376-380
A 13-month-old boy had irregularly shaped, erythematous to dusky red, slightly raised patches and plaques on the left antecubital fossa and arm for 7 months. The lesions were firm and tender. Histopathologically the lesion consisted of small, circumscribed, angiomatous tufts and lobules with a cannonball appearance scattered throughout dermis, a characteristic feature of tufted angioma. For 15 weeks, interferon-a intralesional injections have been performed and the lesions showed an improvement.
Arm
;
Dermis
;
Hemangioma*
;
Humans
;
Infant
;
Injections, Intralesional
;
Interferon-alpha*
;
Male
6.A Retrospective Study with Immunohistochemical Analysis of Axillary Nodal Micrometastasis in Breast Cancer .
Hyun Seog SO ; Suck Hwan KOH ; Yun Hwa KIM
Journal of Korean Breast Cancer Society 1999;2(2):240-250
PURPOSE: It is well established that the presence of axillary nodal metastases is the most important prognostic factor in primary operable breast cancer. However, it has also been shown that 15-30% of patients without lymph node metastases as assessed by light microscopy have recurrence within 10 years. In this study, our aim was first to investigate the diagnostic value of immunohistochemical staining in detecting micrometastases and secondly to correlate their presence with prognosis (recurrence and survival) MATERIALS AND METHODS: We retrospectively analyzed 492 axillary nodes from 49 consecutive node-negative invasive breast cancers treated at Kyung-Hee University Hospital from 1991 to 1995 with average follow-up of 60.2 (21-100) months. An additional section of original paraffin blocks was cut and stained by immunohistochemical chemical technique using monoclonal antibodies (AE 1/3 and No.7) to cytokeratin. RESULTS: Micrometastases with individual cell and cell clusters were readily detected by this technique in 27% of the cases. These were no predictors of micrometastses among the clinicopathological data of patient. The presence of micometastases wes not associated with disease-free and overall survival but loco-regional recurrence rate. CONCLUSIONS: A combination of immunohistochemistry and serial sectioning of axillary lymph node would help evaluate the significance of occult axillary metastases. Patients with node-negative disease may relapse after many years and prolonged follow-up is required to establish the role of mirometastases. Such an approach, together with a search for bone marrow micrometastases and epidemiologic, clinical, pathologic and/or biochemical prognostic factors, may serve to identify high risk patients in the presumed node-negative group. It would provide a rational basis for the selective use of adjuvant therapy.
Antibodies, Monoclonal
;
Bone Marrow
;
Breast Neoplasms*
;
Breast*
;
Follow-Up Studies
;
Humans
;
Immunohistochemistry
;
Keratins
;
Lymph Nodes
;
Microscopy
;
Neoplasm Metastasis
;
Neoplasm Micrometastasis*
;
Paraffin
;
Prognosis
;
Recurrence
;
Retrospective Studies*
7.Factors Predictive of Response to Interferon Therapy in Chronic HCV Infection.
Yun Soo KIM ; So Young KWAN ; Dong Jin SUH ; Chang Hong LEE
The Korean Journal of Hepatology 1996;2(2):176-185
BACKGROUND/AIMS: Although interferon-a(IFNa) is currently the most effective antiviral agent for treating patients with chronic hepatitis C, its efficacy is not always reliable. Factors suggested to infruence outcome of IFN-a therapy for chronic hepatitis C are histological activity, level of viremia and HCV genotype, etc. The aim of this study was to determine the relationship between several pretreatment factors and response to IFN-a therapy in patients with chronic HCV infection. METHODS: Fifty-four patients with chronic HCV infection(47 with chronic hepatitis and 7 with liver cirrhosis) who received IFN-a(2a or 2b) therapy(3 6 MU, three times a week, for 3 12 months) were included. Level of serum HCV RNA(50 patients), HCV genotype(27 patients) and IgM anti- HCV(21 patients) during pretreatment period were assayed. RESULTS: Overall, 19(35%) subjects achieved sustained response(SR), 12(22%) had transient response(TR) and 23(43%) did not respond (nonresponse;NR). Mean age of patients with SR, TR and NR was 46+ 10, 51+ 7.5 and 54+ 9.7 years, respectively(p<0.05 between SR and NR). Among 30 patients with biopsy-proven chronic hepatitis, 13(43%) achieved SR;but only one(14%) in 7 patients with liver cirrhosis. Mean serum HCV RNA level(X10' copies/ml) was higher in nonresponders(7,7+ 13.0) compared with SR(2.3+ 2. 7) or TR(3.1+ 4.9), although statistically insignificant HCV genotyping in 27 patients revealed type la in 5(18.5%), 1b in 14(52%), 2a in 5(18.5%), 2b in 1(3.7%) and 4 in 2(7%), respectively. In non-1b patients, SR rate was significantly higher than 1b patients(69.2% vs. 21.4%, p=0.03). Although IgM anti-HCV was positive in 12(57%) among 21 patients studied, the positive rate and the titer of IgM anti-HCV was not significantly different in three groups. CONCLUSION: Our results suggest that in patients with chronic hepatitis C, infection with genotype 1b, old age, high serum HCV RNA level and the presence of cirrhosis would predict poor response to IFN therapy.
Fibrosis
;
Genotype
;
Hepatitis C, Chronic
;
Hepatitis, Chronic
;
Humans
;
Immunoglobulin M
;
Interferons*
;
Liver
;
Liver Cirrhosis
;
RNA
;
Viremia
8.A Case of Churg-Strauss Syndrome.
Ji Hyun KIM ; Min Jung KANG ; So Yun CHO ; Kyu Kwang WHANG ; Jeong Hee HAHM
Korean Journal of Dermatology 2000;38(5):646-649
No Abstract Available.
Churg-Strauss Syndrome*
9.Clinical and Histopathological Study of the Ossifying Fibroma of Long Bone
Yeo Hon YUN ; Soo Bong HAHN ; Nam Hyun KIM ; So Young JIN ; In Joon CHOI
The Journal of the Korean Orthopaedic Association 1990;25(5):1496-1503
Nine typical cases of ossifying fibroma in the tibia or fibula were retrospectively reviewed for clinical and histopathological aspects of this disease. Along with the case analysis, light and polarized microscopic examinations were performed in each case. Differential points with monostotic fibrous dysplasia were as follows; 1) ossifying fibroma begins in the significantly younger age, which is in most cases below 10 years of age, 2) it is confined to diaphysis of tibia or fibula, 3) radiologically, multilocular osteolytic destructive change in eccentric pattern is usually combined with anterior or anterolateral bowing deformity, 4) microscopically, characteristic findings are presence of osteoblastic rimming, peripheral maturation, and zonal phenomenon. In the treatment of ossifying fibroma, definitive surgical treatment should be delayed until skeletal maturity, when segmental resection in wide margin including periosteum might be preferred.
Congenital Abnormalities
;
Diagnosis
;
Diaphyses
;
Fibroma, Ossifying
;
Fibrous Dysplasia, Monostotic
;
Fibula
;
Fluconazole
;
Osteoblasts
;
Periosteum
;
Retrospective Studies
;
Tibia