Spiny keratoderma (SK) was first described by Brown in 1871 and is characterized by numerous 1-2 mm spines of keratin on the palms and soles, usually sparing the dorsal surfaces, or disseminated over the trunk. Histologically, the "spine" represents a column of hyperkeratosis. Several different forms are known, including familial, sporadic, post-inflammatory and paraneoplastic. Although an association of SK with melanoma has been reported, the significance of such co-occurrence remains unclear due to the limited number of cases. To increase the body of knowledge and shed further light on this rare condition, we present a case of SK in a patient with a recent history of melanoma in situ.
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http://dx.doi.org/10.3390/dermatopathology10020021 | DOI Listing |
Cureus
November 2024
Dermatology, Institute for Social Security and Services for State Workers Regional Hospital "Lic. Adolfo Lopez Mateos", Mexico City, MEX.
A 14-year-old male with disseminated superficial porokeratosis and a family history of the same lesions on his maternal side presented with spiny keratoderma. Spiny keratoderma is a dermatosis characterized by multiple punctate keratotic neoformations on the palms and soles. It is considered a rare disease, with fewer than 84 cases reported in the world medical literature to date.
View Article and Find Full Text PDFInt J Dermatol
October 2024
Department of Dermatology, Faculty of Medicine and Medical Sciences, Sana'a University, Sana'a, Yemen.
Medicina (B Aires)
October 2024
Servicio de Clínica Médica, Hospital Británico de Buenos Aires, Buenos Aires, Argentina.
Am J Dermatopathol
July 2024
Department of Dermatology, Yale School of Medicine, New Haven, CT.
JAAD Case Rep
March 2024
Division of Dermatology, University of Kansas Medical Center, Kansas City, Kansas.
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