The case of a boy with nevus of Ota, extensive Mongolian spot, nevus flammeus, nevus anemicus and cutis marmorata telangiectatica congenita: a unique instance of phacomatosis pigmentovascularis.

Abstract

Phacomatosis pigmentovascularis is a rare, congenital condition characterized by a combination of cutaneous melanocytic lesions and vascular malformation. We discuss an entirely unique case of Phacomatosis pigmentovascularis with nevus of Ota, extensive Mongolian spot, nevus flammeus, nevus anemicus and cutis marmorata telangiectatica congenita, which may represent a heretofore undescribed variant of phacomatosis pigmentovascularis.

• Authors: Han Ma, Mengsi Liao, Shu Qiu, Ruijun Luo, Rongbiao Lu, Chun Lu
• Journal: Anais brasileiros de dermatologia (An Bras Dermatol) Vol. 90 Issue 3 Suppl 1 Pg. 10-2 ( 2015) ISSN: 1806-4841 [Electronic] Spain
• PMID: 26312661 (Publication Type: Case Reports, Journal Article)

Topics

• Humans
• Livedo Reticularis
• Male
• Mongolian Spot (pathology)
• Neurocutaneous Syndromes (classification, pathology)
• Nevus of Ota (pathology)
• Port-Wine Stain (pathology)
• Skin Diseases, Vascular (pathology)
• Skin Neoplasms (pathology)
• Telangiectasis (congenital, pathology)
• Young Adult