1.Two Cases of Lichen Planus Pigmentosus Presenting with a Linear Pattern.
Sungho HONG ; Jeong Hyun SHIN ; Hee Young KANG
Journal of Korean Medical Science 2004;19(1):152-154
We report two cases of lichen planus pigmentosus (LPP) that developed in a unilateral linear pattern. The patients presented with unilateral linear brown macules on the extremities. Skin biopsy showed orthokeratosis, basal hydropic degeneration with scarce lymphohistiocytic infiltrates, and numerous melanophages in both patients. These patients, to the best of our knowledge, are the first cases of LPP presenting with a linear pattern. LPP should be considered in the differential diagnosis of linear hyperpigmented skin lesions.
Adolescent
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Adult
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Biopsy
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Female
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Human
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Hyperpigmentation/diagnosis/pathology
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Lichen Planus/*diagnosis/pathology
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Skin/pathology
2.Hereditary Sclerosing Poikiloderma.
Hyo Jin LEE ; Dong Hoon SHIN ; Jong Soo CHOI ; Ki Hong KIM
Journal of Korean Medical Science 2012;27(2):225-227
Hereditary sclerosing poikiloderma (HSP) is a very rare disease. The clinical features are principally widespread poikiloderma and linear hyperkeratotic and sclerotic bands. We report an 18-yr-old male who presented reticular hyperpigmented lesions on the trunk and extremities since 2-yr-old. Also, linear sclerosing bands appeared on both antecubital and popliteal fossae after yr. Histopathologic finding showed dense sclerotic collagen fibers with telangiectasia in the upper dermis and fragmentations of damaged elastic fibers in the elastic stain, consistent with HSP. We report the first Korean case of HSP.
Abnormalities, Multiple
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Adolescent
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Elastic Tissue/pathology
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Fingers/abnormalities
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Humans
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Hyperpigmentation/pathology
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Male
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Micrognathism/pathology
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Rothmund-Thomson Syndrome/*diagnosis/pathology
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Sclerosis/pathology
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Skin Diseases/diagnosis/pathology
3.Laugier-Hunziker syndrome: a report of three cases and literature review.
Wen-Mei WANG ; Xiang WANG ; Ning DUAN ; Hong-Liu JIANG ; Xiao-Feng HUANG
International Journal of Oral Science 2012;4(4):226-230
Laugier-Hunziker syndrome (LHS) is an acquired pigmentary condition affecting lips, oral mucosa and acral area, frequently associated with longitudinal melanonychia. There is neither malignant predisposition nor underlying systemic abnormality associated with LHS. Herein, we present three uncommon cases of LHS with possibly new feature of nail pigmentation, which were diagnosed during the past 2 years. We also review the clinical and histological findings, differential diagnosis, and treatment of the syndrome in published literature.
Adult
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Female
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Gingival Diseases
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diagnosis
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Humans
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Hyperpigmentation
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diagnosis
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Lip Diseases
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diagnosis
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Male
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Melanins
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analysis
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Middle Aged
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Mouth Diseases
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diagnosis
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Mouth Mucosa
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pathology
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Nail Diseases
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diagnosis
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Syndrome
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Tongue Diseases
;
diagnosis