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出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2013/05/21 00:27:50」(JST)
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Porokeratosis |
Classification and external resources |
A porokeratosis lesion in a patient with disseminated superficial actinic porokeratosis. |
DiseasesDB |
31356 |
eMedicine |
article/1059123 |
MeSH |
D017499 |
Porokeratosis is a specific disorder of keratinization that is characterized histologically by the presence of a cornoid lamella, a thin column of closely stacked, parakeratotic cells extending through the stratum corneum with a thin or absent granular layer.[1]:532
Contents
- 1 Types
- 2 Pathology
- 3 See also
- 4 References
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Types [edit]
Porokeratosis may be divided into the following clinical types:[1]:532
-
- Classic porokeratosis Mibelli
- Disseminated superficial actinic porokeratosis
- Disseminated superficial porokeratosis
- Porokeratosis palmaris et plantaris disseminata
- Linear porokeratosis
- Punctate porokeratosis
However, additional types have also been described:[2]:213,566
-
- Porokeratosis plantaris discreta
Pathology [edit]
Micrograph of a case of porokeratosis showing a characteristic cornoid lamella (dark pink/red structure in the right/upper portion of the image). H&E stain.
Porokeratosis has a characteristic histomorphologic feature known as a cornoid lamella.
See also [edit]
- List of cutaneous conditions
- List of cutaneous conditions associated with increased risk of nonmelanoma skin cancer
References [edit]
- ^ a b Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN 0-07-138076-0.
- ^ James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0-7216-2921-0.
UpToDate Contents
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English Journal
- Altered gene expression in squamous cell carcinoma arising from congenital unilateral linear porokeratosis.
- Scola N, Skrygan M, Wieland U, Kreuter A, Gambichler T.SourceDepartment of Dermatology, Venereology and Allergology, Ruhr-University Bochum, Germany Institute of Virology, National Reference Centre for Papilloma- and Polyomaviruses, University of Cologne, Cologne, Germany.
- Clinical and experimental dermatology.Clin Exp Dermatol.2012 Oct;37(7):781-5. doi: 10.1111/j.1365-2230.2012.04393.x.
- Congenital unilateral linear porokeratosis (CULP) is a rare disorder of keratinization that shares clinical and molecular similarities with psoriasis. It also has an increased risk for malignant transformation to cutaneous squamous cell carcinoma (SCC). We investigated the expression of psoriasin, h
- PMID 22998543
Japanese Journal
- 治療 日光表在播種型汗孔角化症の1例 : イミキモドクリームによる治療の試み
- 基底細胞癌を発生した表在播種型汗孔角化症の1例 (特集 角化症・炎症性角化症)
- 5%イミキモドクリーム外用が奏効したと考えられた汗孔角化症の1例 (特集 角化症・炎症性角化症)
Related Links
- 26 Oct 2012 ... Porokeratosis. Porokeratosis is a clonal disorder of keratinization characterized by one or more atrophic patches surrounded by a clinically and histologically distinctive hyperkeratotic ridgelike border called the cornoid ...
- Porokeratosis is a specific disorder of keratinization that is characterized histologically by the presence of a cornoid lamella, a thin column of closely stacked, parakeratotic cells extending through the stratum corneum with a thin or absent ...
Related Pictures