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

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...

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Published inAnais brasileiros de dermatología Vol. 90; no. 3 Suppl 1; pp. 10 - 12
Main Authors Ma, Han, Liao, Mengsi, Qiu, Shu, Luo, Ruijun, Lu, Rongbiao, Lu, Chun
Format Journal Article
LanguageEnglish
Published Brazil Sociedade Brasileira de Dermatologia 01.06.2015
Subjects
Case Report
DERMATOLOGY
Hemangioma
Humans
Male
Mongolian spot
Mongolian Spot - pathology
Neurocutaneous Syndromes - classification
Neurocutaneous Syndromes - pathology
Nevus of ota
Nevus of Ota - pathology
Nevus, pigmented
Port-Wine Stain
Port-Wine Stain - pathology
Skin Diseases, Vascular - pathology
Skin Neoplasms - pathology
Telangiectasis - congenital
Telangiectasis - pathology
Young Adult
Nevus, pigmented
Hemangioma
Port-Wine Stain
Nevus of ota
Mongolian spot
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Summary: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.
Bibliography:ObjectType-Case Study-2
SourceType-Scholarly Journals-1
ObjectType-Feature-4
content type line 23
ObjectType-Report-1
ObjectType-Article-3
Conflict of Interest: None.
ISSN:0365-0596
1806-4841
1806-4841
0365-0596
DOI:10.1590/abd1806-4841.20153466