1.A Case of Immune Thrombocytopenic Purpura with Helicobacter Pylori Infection.
Young Jee KIM ; Sook Jung YUN ; Seong Jin KIM ; Seung Chul LEE ; Younh Ho WON ; Jee Bum LEE
Korean Journal of Dermatology 2015;53(4):328-329
No abstract available.
Helicobacter pylori*
;
Purpura, Thrombocytopenic, Idiopathic*
2.A Case of Immune Thrombocytopenic Purpura with Helicobacter Pylori Infection.
Young Jee KIM ; Sook Jung YUN ; Seong Jin KIM ; Seung Chul LEE ; Younh Ho WON ; Jee Bum LEE
Korean Journal of Dermatology 2015;53(4):328-329
No abstract available.
Helicobacter pylori*
;
Purpura, Thrombocytopenic, Idiopathic*
3.A Case of Superficial Acral Fibromyxoma Showing Erythronychia
Ji Hong LEE ; Young Ho WON ; Seung Chul LEE ; Sook Jung YUN ; Jee Bum LEE
Korean Journal of Dermatology 2019;57(9):563-565
No abstract available.
Fibroma
4.Numb-Chin Syndrome in Malignant Hematologic Diseases.
Seung Han SUK ; Il Nam SUNWOO ; Seung Min KIM ; Sung Ju LEE ; Jee Sook LEE ; Jee Sook HAHN ; Yun Woong KO
Journal of the Korean Neurological Association 1992;10(1):89-92
'Num-chin syndrome', isolated mental neuropathy, is a rare manifestaion of malignant hernatologic diseases, but important sign for early diagnosis and prediction of clinical course and prognosis. Here we report 7 cases of numb-chin syndrome; one in leukemic transformation of malignant lymphoma, one in blastic crisis of chronic myelogenous leukemia and 5 in acute leukemia Two cases of acute leukemia revealed the 'numb-chin sign' in early course of disease before the diagnosis of leukemia and other three in aggravating state of acute leukemia. The therapeutic response and prognosis was poor and 5 cases expired in a few months.
Diagnosis
;
Early Diagnosis
;
Hematologic Diseases*
;
Leukemia
;
Leukemia, Myelogenous, Chronic, BCR-ABL Positive
;
Lymphoma
;
Prognosis
5.A case of multiple lentigines syndrome.
Mi Woo LEE ; Jee Ho CHOI ; Seung Chul LEE ; Kyung Jeh SUNG ; Jai Kyoung KOH
Korean Journal of Dermatology 1993;31(5):780-783
Supernunmerary nipple is a developmental anomaly occuring alon, the course of the embryological milk lines. This entity has receieved little attention in the dermatologic literature and has been confused with a pigmented nevus in some cases. We have experienced two ease of the more unusual form of supern umerary nipple. According to the Kajavas classification, our caes are classified as polithelia pilosa and complete breast with nipple
Breast
;
Classification
;
LEOPARD Syndrome*
;
Milk
;
Nevus, Pigmented
;
Nipples
6.Expression of Involucrin and Filaggrin in Various Skin Disorders: Immunohistochemical Study.
Seung Chul LEE ; Jee Bum LEE ; Jae Jeong SEO ; Jin Young PARK ; Young Ho WON
Korean Journal of Dermatology 1999;37(6):708-714
BACKGROUND: The cornified cell envelope (CE) is a unique structure found in the terminal differentiation of the skin. The precursor proteins of the CE are composed of many candidate structural proteins, among which invalucrin and filaggrin are important ones to participate in the complicated process of forming, the complex structure. OBJECTIVE: The purpose of this study was to evaluate the usefulness of expression of involucrin and filaggrin as markers of terminal differentiation in various skin disorders including tumors. METHODS: Immunohistochemical studies were performed in the formalin-fixed, paraffin-embedded skin samples of non-tumors (41 cases) and tumors (43 cases).
Skin*
7.A Case of Angioma Serpiginosum.
Hyoung Chul YOO ; Jee Bum LEE ; Seung Chul LEE ; Young Ho WON
Annals of Dermatology 2000;12(2):152-154
Angioma serpiginosum is a rare acquired vascular lesion that usually presents in the first two decades of life with a predilection for females. A typical lesion is characterized by deeply red nonpalpable puncta that are grouped closely together in macular or netlike patterns on the lower extremities and buttocks. Histopathologically, thin-walled dilated capillaries are seen in some of the dermal papillae and the superficial reticular dermis without extravasation of red blood cells. We report a case of angioma serpiginosum developed on the left chest and left upper extremity in a 18-year-old man.
Adolescent
;
Buttocks
;
Capillaries
;
Dermis
;
Erythrocytes
;
Female
;
Hemangioma*
;
Humans
;
Lower Extremity
;
Thorax
;
Upper Extremity
8.A case of cloacal degormity.
Young Mi JEE ; Seung Jin LEE ; In Kyung SUNG ; Byung Churl LEE
Journal of the Korean Pediatric Society 1992;35(5):667-670
No abstract available.
9.Pityriasis Rubra Pilaris in Down Syndrome.
Min KIM ; Jee Bum LEE ; Seong Jin KIM ; Seung Chul LEE ; Young Ho WON
Annals of Dermatology 2001;13(4):258-261
A 23-year-old woman with Down syndrome presented erythematous keratotic plaques with whitish scales on the elbows, forearm, knee and leg. Histopathological findings revealed acanthosis with broad and short rete ridges, alternating orthokeratosis and parakeratosis oriented in both vertical and horizontal directions, and dermal superficial perivascular lymphocytic infiltration, compatible with pityriasis rubra pilaris.
Down Syndrome*
;
Elbow
;
Female
;
Forearm
;
Humans
;
Knee
;
Leg
;
Parakeratosis
;
Pityriasis Rubra Pilaris*
;
Pityriasis*
;
Weights and Measures
;
Young Adult
10.Eruptive Vellus Hair Cysts in Association with Hypomelanosis of Ito with Turner's Syndrome.
Sook Jung YUN ; Jee Bum LEE ; Young Ho WON ; Seung Chul LEE
Annals of Dermatology 2000;12(4):283-285
A 24-year Korean woman presented with bizarre pigmentary skin changes. Eruptive vellus hair cysts (EVHC) were observed in conjunction with Hypomelanosis of Ito (HI). Also, the karyotype of 45XO with typical clinical symptoms of Turner's syndrome was detected in this patient, which has been rarely reported in HI as a chromosomal defect. EVHC may manifest as a rare skin manifestation of Hl.
Female
;
Hair*
;
Humans
;
Hypopigmentation*
;
Karyotype
;
Skin
;
Skin Manifestations
;
Turner Syndrome*