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Nagashima-type palmoplantar keratosis with melanoma: absence of epidermal Langerhans cells in hyperkeratotic skin
- Source :
- European Journal of Dermatology. 27:210-212
- Publication Year :
- 2017
- Publisher :
- John Libbey Eurotext, 2017.
-
Abstract
- Nagashima-type palmoplantar keratosis (PPK) is characterised by transgressive PPK with an autosomal recessive trait [1]. We describe a case of melanoma in a patient with Nagashima-type PPK.A 63-year-old Japanese woman presented with erythematous hyperkeratotic lesions on her palms and soles that had persisted since infancy. The lesions extended to the dorsal surfaces of the hands and feet and the Achilles tendon area, showing a whitish appearance after bathing. There was no family member with similar [...]
- Subjects :
- Dorsum
Achilles tendon
medicine.medical_specialty
Pathology
business.industry
Melanoma
Dermatology
medicine.disease
Palmoplantar Keratosis
030207 dermatology & venereal diseases
03 medical and health sciences
Autosomal recessive trait
Family member
0302 clinical medicine
medicine.anatomical_structure
030220 oncology & carcinogenesis
Medicine
business
Keratoderma
Skin pathology
Subjects
Details
- ISSN :
- 19524013 and 11671122
- Volume :
- 27
- Database :
- OpenAIRE
- Journal :
- European Journal of Dermatology
- Accession number :
- edsair.doi...........4db93e567d4b478d49413e470f5c5ce9
- Full Text :
- https://doi.org/10.1684/ejd.2016.2960