Congenital linear porokeratosis with pseudoainhum

European Journal of Dermatology

Volumn 20, Issue 6, 2010, Pages 817-818

  Wei, Bin ^a   Liu, Mei ^a   Qu, Le ^a   Xiao, Ting ^a   Chen, Hong Duo ^a   He, Chun Di ^a  

^a CHINA MEDICAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; CASE REPORT; CLINICAL FEATURE; CONGENITAL SKIN DISEASE; FEMALE; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; LETTER; LINEAR POROKERATOSIS; PHYSICAL EXAMINATION; POROKERATOSIS; PSEUDOAINHUM; SKIN BIOPSY;

ADULT; AINHUM; ARM; BIOPSY; CONSTRICTION, PATHOLOGIC; DIAGNOSIS, DIFFERENTIAL; FEMALE; HUMANS; POROKERATOSIS;

EID: 78649901017     PISSN: 11671122     EISSN: 19524013     Source Type: Journal    
DOI: 10.1684/ejd.2010.1068     Document Type: Letter

References (6)

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2. Akallal N, Belgnaoui FZ, Benameur H, et al. Pseudoainhum and peripheral neuropathy. Ann Dermatol Venereol 2006; 133: 791-4.
3. Sasaki S, Urano Y, Nakagawa K, Nagae H, Nakanishi H, Arase S. Linear porokeratosis with multiple squamous cell carcinomas: study of p53 expression in porokeratosis and squamous cell carcinoma. Br J Dermatol 1996; 134: 1151-3.
4. Happle R. Mibelli revisited: a case of type 2 segmental porokeratosis from 1893. J Am Acad Dermatol 2010; 62: 136-8.
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