References
Iwata M, Tanizaki H, Endo Y, et al. Malignant melanoma arising in the skin lesions of Nagashima-type palmoplantar keratosis. Eur J Dermatol 2014; 24: 259–60.
Kubo A, Shiohama A, Sasaki T, et al. Mutations in SERPINB7, encoding a member of the serine protease inhibitor superfamily, cause Nagashima-type palmoplantar keratosis. Am J Hum Genet 2013; 93: 945–56.
Kabashima K, Sakabe J, Yamada Y, Tokura Y. “Nagashima-type” keratosis as a novel entity in the palmoplantar keratoderma category. Arch Dermatol 2008; 144: 375–9.
Adachi A, Komine M, Maekawa T, et al. Multiple primary acral lentiginous melanoma on the feet developing in lesions of Nagashimatype palmoplantar keratoderma. Acta Derm Venereol 2017; 97: 756–8.
Tsutsumi R, Yoshida Y, Yamada N, et al. Nagashima-type palmoplantar keratosis with melanoma: absence of epidermal Langerhans cells in hyperkeratotic skin. Eur J Dermatol 2017; 27: 210–2.
Nakajima K, Nakano H, Takiyoshi N, et al. Papillon-Lefèvre syndrome and malignant melanoma. A high incidence of melanoma development in Japanese palmoplantar keratoderma patients. Dermatology 2008; 217: 58–62.
Bullón P, Morillo JM, Thakker N, et al. Confirmation of oxidative stress and fatty acid disturbances in two further Papillon-Lefèvre syndrome families with identification of a new mutation. J Eur Acad Dermatol Venereol 2014; 28: 1049–56.
Kerns ML, Hakim JM, Lu RG, et al. Oxidative stress and dysfunctional NRF2 underlie pachyonychia congenita phenotypes. J Clin Invest 2016; 126: 2356–66.
Asagoe K, Takahashi K, Yoshino T, et al. Numerical, morphological and phenotypic changes in Langerhans cells in the course of murine graft-versus-host disease. Br J Dermatol 2001; 145: 918–27.
Author information
Authors and Affiliations
Corresponding author
About this article
Cite this article
Kogame, T., Kaku, Y., Endo, Y. et al. A follow-up report of acral melanoma in a patient with Nagashima-type palmoplantar keratosis: validation of SERPINB7 mutation and local recurrence. Eur J Dermatol 28, 519–520 (2018). https://doi.org/10.1684/ejd.2018.3317
Published:
Issue Date:
DOI: https://doi.org/10.1684/ejd.2018.3317