- Pityriasis Rotunda with Familial Occurrence
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Yang JK, Lee DW, Cho BK
- KMID: 2360362
- Ann Dermatol.
- 1997 Jul;9(3):194-196.
- doi: 10.5021/ad.1997.9.3.194
Pityriasis rotunda is an uncommon chronic dermatosis characterized by multiple, round or oval, hyperpigmented or hypopigmented patches that have a fine scale on the trunk and extremities. Most of the... -
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- A Case of Multiple Trichilemmal Cysts
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Chung HS, Lee NH, Choi EH, Lee WS, Ahn SK
- KMID: 2360370
- Ann Dermatol.
- 1997 Jul;9(3):228-230.
- doi: 10.5021/ad.1997.9.3.228
A case of multiple trichilemmal cysts (TC) is presented. TC is known to be a kind of keratinous cyst with lining cells showing trichilemmal keratiniration. A 63-year-old female patient presented... -
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- A Case of Primary Erythermalgia
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Lee BS, Oh CW, Yoon TJ
- KMID: 2360369
- Ann Dermatol.
- 1997 Jul;9(3):224-227.
- doi: 10.5021/ad.1997.9.3.224
An 18-year-old man had suffered from intense burning with redness and an increased temperature of both the lower legs, forearms and hands since the age of 5. Symptoms were exacerbated... -
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- A Case of Giant Basal Cell Carcinoma
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Lee JH, Park HJ, Kim YC, Cinn YW
- KMID: 2360372
- Ann Dermatol.
- 1997 Jul;9(3):236-238.
- doi: 10.5021/ad.1997.9.3.236
Giant basal cell carcinoma(BCC) is a clinical expression of a large-sized BCC, which can cause extensive local invasion and disfigurement and have a particular capacity for metastasis. In the development... -
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- Congenital CMV Infection with Blueberry-muffin Skin Lesions Showing Dermal Erythropoiesis
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Kim SJ, Lim MH, Lee SC, Won YH, Chun IK, Choi YR, Park CS
- KMID: 2360367
- Ann Dermatol.
- 1997 Jul;9(3):215-218.
- doi: 10.5021/ad.1997.9.3.215
Blueberry muffin rashes occur in various diseases including TORCH syndrome, transfusion reactions, leukemia, hereditary spherocytosis and neonatal sepsis. We report a case of congenital CMV(cytomegalovirus) infection showing blueberry muffin skin... -
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- Contact Urticaria due to Dinitrochlorobenzene
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Kim JK, Yoon TJ, Oh CW, Kim TH
- KMID: 2360361
- Ann Dermatol.
- 1997 Jul;9(3):191-193.
- doi: 10.5021/ad.1997.9.3.191
A 33-year-old man with alopecia totalis presented with facial erythema and flares, conjunctival injection, and dyspnea developed within several minutes following the ninth application of dinitrochlorobenzene (DNCB). A scratch skin... -
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- Total Micrografting Hair Transplantation Using a New Hair Implanter
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Kim IH, Kye YC
- KMID: 2360358
- Ann Dermatol.
- 1997 Jul;9(3):177-181.
- doi: 10.5021/ad.1997.9.3.177
BACKGROUND: Hair transplantation is a continuously evolving era towards a more natural style and micrografting in greater quantities is becoming an unmistakable trend. OBJECTIVE: A rapid, simple method to make a... -
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- Three Cases of Chronic Actinic Dermatitis Treated with Systemic PUVA Therapy
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Kim JK, Chen L, Kim TH
- KMID: 2360363
- Ann Dermatol.
- 1997 Jul;9(3):197-200.
- doi: 10.5021/ad.1997.9.3.197
Chronic actinic dermatitis is an uncommon disabling ecxematous photosensitive eruption. The skin lesion is characterized by persistent eczematous eruptions on sun exposed skin with possible extension into nonexposed areas. The... -
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- Two Cases of Cutaneous Protothecosis : Unique Histopathological Findings with Crystal Violet Staining and the Therapeutic Effect of Itraconazole
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Kim JA, Moon SE, Song KY
- KMID: 2360364
- Ann Dermatol.
- 1997 Jul;9(3):201-207.
- doi: 10.5021/ad.1997.9.3.201
Cutaneous protothecosis sometimes poses diagnostic and therapeutic problems. Isolation of the causative organism may not be successful and spores may be mistaken for other skin diseases unless the characteristic sporangia... -
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- Congenital Anonychia of the Toes with Absence of Underlying Phalangeal Bones
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Kim SJ, Lim MH, Lee SC, Won YH, Chun IK
- KMID: 2360360
- Ann Dermatol.
- 1997 Jul;9(3):188-190.
- doi: 10.5021/ad.1997.9.3.188
Congenital absence of nails usually occur as a rare isolated anomaly or combined with other ectodermal defects. This anomaly is regarded as an inherited disorder either dominantly or recessively but... -
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- A Sporadic Case of Ichthyosis Bullosa of Siemens
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Choi GS, Song JS, Lee ES, Kang WH, Lee S
- KMID: 2360366
- Ann Dermatol.
- 1997 Jul;9(3):211-214.
- doi: 10.5021/ad.1997.9.3.211
Few cases of ichthyosis bullosa of Siemens(IBS) have been reported since 1939, as a distinct entity from bullous congenital ichthyosiform erythroderma(BCIE). IBS can be differentiated from BCIE by the absence... -
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- A Case of Multiple Basal Cell Epithelioma in the Nevus Sebaceus of Jadassohn
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Ha SJ, Paik JH, Lee JY, Seo EJ, Kim JW
- KMID: 2360365
- Ann Dermatol.
- 1997 Jul;9(3):208-210.
- doi: 10.5021/ad.1997.9.3.208
Nevus sebaceus of Jadassohn is a hamartoma of the skin with the potential to develop benign and malignant neoplasms. This case was characterixed by multiple basal cell epitheliomas, clinically one reddish... -
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- A Case of Estrogen Dermatitis
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Chung HS, Shin HK, Lee KH
- KMID: 2360371
- Ann Dermatol.
- 1997 Jul;9(3):231-235.
- doi: 10.5021/ad.1997.9.3.231
Sensitivity to estrogen has been described previously. The clinical picture is varied with pruritus, either generalized or localued or as urticaria. The hallmark of estrogen dermatitis is the cyclic premenstrual... -
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- A Case of Multiple Lentigines Syndrome
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Shin DY, Koo DW, Roh JY
- KMID: 2360368
- Ann Dermatol.
- 1997 Jul;9(3):219-223.
- doi: 10.5021/ad.1997.9.3.219
The multiple lentigines syndrome or LEOPARD syndrome is an autosomal dominantly inherited disorder with a variety of abnormalities and a familial occurrence. This syndrome is characterized by the presence of... -
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- Molecular Analysis of Oculocutaneous Albinism Patients in Korea
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Hwang JH, Youn SW, Ahn JS, Kim KH, Park KC
- KMID: 2360359
- Ann Dermatol.
- 1997 Jul;9(3):182-187.
- doi: 10.5021/ad.1997.9.3.182
BACKGROUND: Oculocutaneous albinism (OCA) is a genetic disorder of the melanin pigment system in which melanin synthesis is reduced or absent in the skin, hair, and eyes. OCA is classified... -
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