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Angiokeratoma

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Dermatopathology

Part of the book series: Encyclopedia of Pathology ((EP))

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Definition

Angiokeratomas represent a group of unrelated disorders having in common dilated preexistent vascular channels in the superficial (papillary) dermis, usually accompanied by secondary epidermal changes. Angiokeratoma circumscriptum probably represents a capillary-lymphatic malformation.

Clinical Features

Four clinical variants of angiokeratomas can be distinguished:

  • Solitary angiokeratomas. They are the most common variant, representing about 80 % of all angiokeratomas. Solitary angiokeratomas have a wide age distribution, but most commonly develop in the second to fourth decades of life and show a male predominance. Although a solitary angiokeratoma can develop at any site, including mucosal surfaces, sites of predilection are the lower extremities. A solitary angiokeratoma presents clinically as an asymptomatic warty hyperkeratotic papule or nodule, measuring from 2 to 10 mm in diameter. Bleeding following minor trauma is not infrequent. The lesion can occasionally be...

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References and Further Reading

  • Orteu, C. H., Jansen, T., Lidove, O., et al. (2007). Fabry disease and the skin: Data from FOS, the Fabry outcome survey. British Journal of Dermatology, 157, 331–337.

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  • Schiller, P. I., & Itin, P. H. (1996). Angiokeratomas: An update. Dermatology, 19(193), 275–282.

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  • Zaballos, P., Daufi, C., Puig, S., et al. (2007). Dermoscopy of solitary angiokeratomas. A morphological study. Archives of Dermatology, 143, 318–325.

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Correspondence to Eduardo Calonje .

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© 2016 Springer International Publishing Switzerland

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Calonje, E., Luzar, B. (2016). Angiokeratoma. In: Massi, D. (eds) Dermatopathology. Encyclopedia of Pathology. Springer, Cham. https://doi.org/10.1007/978-3-319-30006-1_403

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  • DOI: https://doi.org/10.1007/978-3-319-30006-1_403

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  • Publisher Name: Springer, Cham

  • Print ISBN: 978-3-319-30005-4

  • Online ISBN: 978-3-319-30006-1

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