We present two cases of linear lichen simplex chronicus. One is a 44-year-old male patient who had a linear licbenified patch on the left upper extremity, and the other is a 45-year-old female patient who had linear pruriginous nodules on the right lower extremity. The one is coincidental with localized lichen simplex chronicus, the other is coincidental with prurigo nodularis histopathologically.
Adult ; Female ; Humans ; Lichens* ; Lower Extremity ; Male ; Middle Aged ; Neurodermatitis* ; Prurigo ; Upper Extremity

Human sparganosis is not uncommon and over 60 cases are reported in Korea but the case infested with multiple spargana is rare. The case we are reporting here is a 33 year-old Korean male having had an abscess and several bean-sized nodules on the left thigh. The patient had the history of eating frogs as a tonic food 3 years ago. Five spargana were removed from the lesions by surgical excision. Two of them were alive and other three were degenerated or calcified.
Abscess ; Adult ; Eating ; Humans ; Korea ; Male ; Scabies* ; Sparganosis ; Thigh

A 22-year-old male has had multiple, grouped, asymptomatic, yellowish flat papules, nodules, and plaques on the knees, elbows, butteeks, hands, and feet. Yellowish nodules first appeared on the heels after birth, and gradually increased in size and number and spread to the knees, elbows, buttocks, and hands. Physical examination revealed normaI except for the skin lesions. Gross finding of the serum was clear and paper electrophoresis revealed marked increase in betalipo-protein and mild increase in prebetalipoprotein, suggesting type II hyperlipoproteinemia Serum cholesterol was 510 mg%, and serum triglyceride was 190mg%. Histopathology showed many aggregates of foam cells on H-E stain and many lipid droplets in the dermis on oil red O stain.
Buttocks ; Cholesterol ; Dermis ; Elbow ; Electrophoresis, Paper ; Foam Cells ; Foot ; Hand ; Heel ; Humans ; Hyperlipoproteinemia Type II* ; Knee ; Male ; Parturition ; Physical Examination ; Skin ; Triglycerides ; Xanthomatosis* ; Young Adult

Dyschromatosis universalis hereditaria is a rare pigmentary disorder characterized by widespread mothed hyperpigmentation and hypopigmentation. We report a 40-year-old male patient with numerous hyperpigmenter, and hypopigmented macules all over the body except on the palms and soles. The family history revealed similar pigmentary changes in 5 other members through 4 generations, and we could guess the hereditary pattern of the disease of this family to be autosomal dominant inheritance.
Adult ; Family Characteristics ; Humans ; Hyperpigmentation ; Hypopigmentation ; Male ; Moths ; Wills

Cerebriform intradermal melanocytic nevus is a cause of cutis veticis gyrata, a morphologic term which describes the hypertrophy and folding of the skin, typically occurring on the scslp, to present a gyrate or cerebriform appearance. We report a 37-year-old woman with a 17 x 22cm soft, convoluted mass over most of the occipital, parietal, and temporal scalp. At birth, she had a small brownish macide on the occipital scalp that enlarged to form this extensive lesion. Histologically, nests of nevus cells were shown in the upper and the mid dermis.
Adult ; Dermis ; Female ; Fibroadenoma ; Humans ; Hypertrophy ; Nevus ; Nevus, Pigmented* ; Parturition ; Rabeprazole ; Scalp ; Skin

A 51-year-old female developed a distinctive perioral rash, conisting of discrete or confluent erythematous papules for one and a half years. Histopathologic examiriation revealed upper dermal granulomas admixed with lymphoytes. Pieces of hair shaft were staincd peri-dish by AFB in the center of granuloma, which might play a role in the formation of the granuloma She also had used corticosteroid ointment intermittently duririg this time. There were no associated systemic abnormalities. The lesions resolved after two month treatment with oral corticosteroid and tetrac cline.
Dermatitis, Perioral* ; Exanthema ; Female ; Granuloma ; Hair ; Humans ; Middle Aged

Although acquired ichthyosis has been associated with a number of systemic illnesses, an association with sarcoidosis has rarely been reported. We report a patient with aquired ichthyosis of the lower and upper extrimities whose diagnosis of cutaneous sarcoidosis was confirmed by histologic examination. Systemic involvement in the patient revealed occular, pulmonary and nerve disease. A diagnosis of sarcoidosis must be considered when a patient presents with acquired ichthyosis.
Diagnosis ; Humans ; Ichthyosis ; Sarcoidosis*

Leicmyomas represent benign painful tumor principally derived from cutaneous smooth muscle. The majority of these lesions arised from arrector pili muscles, the media of blood vessels, or smooth muscle of scrotum, labia majora, and nipples. Cutaneous leiomyomas may be solitary or rnultiple and generally present as pink, red or dusky brown firm derrnal nodules of varying sizes. We present a case of multiple leiomyoma cutis in a 44-year-old male. The skin lesions were characterized clinically by numerous, miliary to bean sized, reddish brow papules and nodules on the both shoulders, right arm, right side of the neck, upper chest, and upper back, which were pinful by pressure. The histopathologic examination revealed interlacing bundles of the smooth muscle fibers in the dermis, slight atrophy of epidermis, and a grenz zone of normal corium hetween the epidermis and the tumor.
Adult ; Arm ; Atrophy ; Blood Vessels ; Dermis ; Epidermis ; Humans ; Leiomyoma* ; Male ; Muscle, Smooth ; Muscles ; Neck ; Nipples ; Scrotum ; Shoulder ; Skin ; Thorax

Cystic hygroma, or cystic lymphangioma, is a true, benign, congenital rnulticystic tumor arising from sequestrations of embryonic ly mphatic iissue. Most often it occurs. At birth or early in life, and it is found most commonly in the neck, and its distribution coincides with that of the prirnitive lymph sacs. We report herein a case of huge cystic hygroma on the face and neck in a 2 month-old male infant. The swelling was softly cystic, and was partially compressible, and it was brilliantly translucent. The cystic mass contained a serous fluid. Biopsy findings showed simple endothelium-lined lymphatic vessel and loose, lace-like fibrous tissue stroma, and dilated muscle space filled with serous fluid.
Biopsy ; Humans ; Infant ; Lymphangioma, Cystic* ; Lymphatic Vessels ; Male ; Neck ; Parturition

A case of plane xanthoma arising in type IV hyperlipoproteinemia in a 53-year old woman is reported. The patient had well-defined yellowish to orange colored slightly elevated plaques on both upper eyelids, cheeks, neck, and upper chest. The laboratory findings showed increased serum triglyceride on lipid profile, and widening of pre-beta band on electrophoresis lipoprotein. She had a fatty liver, mild hepatomegaly, but other systemic diseases such as multiple myeloma, leukemia and lymphoma were not found.
Cheek ; Citrus sinensis ; Electrophoresis ; Eyelids ; Fatty Liver ; Female ; Hepatomegaly ; Humans ; Hyperlipoproteinemia Type IV* ; Leukemia ; Lipoproteins ; Lymphoma ; Multiple Myeloma ; Neck ; Thorax ; Triglycerides ; Xanthomatosis*