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1.
Korean Journal of Dermatology ; : 187-192, 1973.
Article in Korean | WPRIM | ID: wpr-168330

ABSTRACT

Letterer-Siwe disease occurred in a 3 year 7 month old male child showing severe emaciation, hepatosplenomegaly, otitis media, hemorrhagic and impetiginous crusted patches on the body, and seborrheic dermatitis like skin rashes in the scalp. Also showed are severe anemia, thrombocytopenia, bronchopneumonia and multiple bony defects in skull. The child expired in a month after admission.


Subject(s)
Child , Humans , Infant , Male , Anemia , Bronchopneumonia , Dermatitis, Seborrheic , Emaciation , Exanthema , Histiocytosis, Langerhans-Cell , Otitis Media , Scalp , Skull , Thrombocytopenia
2.
Korean Journal of Dermatology ; : 85-88, 1973.
Article in Korean | WPRIM | ID: wpr-100765

ABSTRACT

Angiosarcoma is rare disease not only in Korea but throughout the world; it is all the more so on the skin. We made an observation on a case of angiosarcoma on the scalp of a 57 year-old man. Noteworthy in this case are: (1) the patient was suffered from a head trauma 6 years prior to onset of the disease, (2) the progress of the disease showed an extreme rapidity accompanied by severe headache intolerable by any medication, (3) no effect was resulted from X-ray irradiation, and (4) the patient survived for 7 months with the disease.


Subject(s)
Humans , Middle Aged , Craniocerebral Trauma , Headache , Hemangiosarcoma , Korea , Rare Diseases , Scalp , Skin
3.
Korean Journal of Dermatology ; : 27-32, 1973.
Article in Korean | WPRIM | ID: wpr-34468

ABSTRACT

The clinical studies were made on 40 cases of malignant cutaneous tumors who visited to Department of Dermatology, Kyungpook National University Hospital during last 6 years from 1967 to 1972. 1) Among 40 cases, 23 were squamous cell carcinomas, 10 basal cell carcinonias, two mycosis fungoides, one Hodgkins disease, one malignant melanoma, one angiosarcoma, one fibrosarcoma, and one metastatic adenocarclonoma. 2) The patient with malignant tumors were increasing by the year, being 0.06% of total out patients in 1967 but increased to 0.64% by 1971. 3) Squamous cell carcinomas were seen above the age 30 but basal cell carcinomas were seen above the age 40. Mycosis fungoides and malignant melanoma were seen in 20th of age, while Hodgkins disease, angiosarcoma, fibrosarcoma, and metastatic adenocarcinoma were seen in 50th of age. 4) The ratio of squamous cell carcinoma to basal cell carcinoma was 2.3:1, contrary to higher incidence of basal cell carcinoma than squamous cell carcinoma among caucasians. 5) Among 23 cases of squamous cell carcinoma, 7 cases were derived from Bowens disease, 4 cases were from chronic burn scar, two from senile keratosis, one from tropic ulcer, and remaining 9 were not able to elucidate its cause. 6) The predilection sites of squamous cell carcinoma were four extremities particulary on lower extremities, while basal cell carcinomas were on the face predominantly. 7) Among 10 cases of basal cell carcinomas, 8 cases were ulcerative form and the rest of two were nodular form. 6 cases showed dark pigmentation in the lesions sugge stive of pigmented basal cell carcinoma but only 3 of them were proved to be true pigmented form histologically. 6 cases showed solid type of basal cell carcinoma and 2 showed pigmented type among 8 cases of ulcerative form. Those two cases of nodular form, one showed pigmented type and the other adenocystic type histologically.


Subject(s)
Humans , Adenocarcinoma , Bowen's Disease , Burns , Carcinoma, Basal Cell , Carcinoma, Squamous Cell , Cicatrix , Dermatology , Extremities , Fibrosarcoma , Hemangiosarcoma , Hodgkin Disease , Incidence , Keratosis , Lower Extremity , Melanoma , Mycosis Fungoides , Outpatients , Pigmentation , Ulcer
4.
Korean Journal of Dermatology ; : 91-95, 1971.
Article in Korean | WPRIM | ID: wpr-134647

ABSTRACT

Two cases of Klippel-Trenaunay-Weber Syndrome were presented and its literatures were reviewed. The patients were 25 year old male farmer and 38 year old housewife. Both had hypertrophy, port-wine nevus, and varicosities in case 1, on left lower extremity since birth. The length and cirumference of the affected leg were longer than the other side, and X-ray showed osteohypertrophy of tibia of the involved leg,


Subject(s)
Adult , Humans , Male , Hypertrophy , Klippel-Trenaunay-Weber Syndrome , Leg , Lower Extremity , Nevus , Parturition , Tibia
5.
Korean Journal of Dermatology ; : 91-95, 1971.
Article in Korean | WPRIM | ID: wpr-134646

ABSTRACT

Two cases of Klippel-Trenaunay-Weber Syndrome were presented and its literatures were reviewed. The patients were 25 year old male farmer and 38 year old housewife. Both had hypertrophy, port-wine nevus, and varicosities in case 1, on left lower extremity since birth. The length and cirumference of the affected leg were longer than the other side, and X-ray showed osteohypertrophy of tibia of the involved leg,


Subject(s)
Adult , Humans , Male , Hypertrophy , Klippel-Trenaunay-Weber Syndrome , Leg , Lower Extremity , Nevus , Parturition , Tibia
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