2015
DOI: 10.1590/abd1806-4841.20153466
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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.

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Cited by 8 publications
(5 citation statements)
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“…Glaucoma may be associated in some cases . Naevus of Ota usually presents as a separate entity, but sometimes may accompany naevus of Ito or extensive MSs …”
Section: Classical Variants Of Dermal Melanocytosesmentioning
confidence: 99%
“…Glaucoma may be associated in some cases . Naevus of Ota usually presents as a separate entity, but sometimes may accompany naevus of Ito or extensive MSs …”
Section: Classical Variants Of Dermal Melanocytosesmentioning
confidence: 99%
“… 3 Although NA is not usually associated with other abnormalities, it has been linked to several conditions including neurofibromatosis type I and phacomatosis pigmentovascularis. 4 , 5 Although the differential diagnosis for NA includes common conditions such as vitiligo and tinea versicolor, it also includes nevus depigmentosus (NDP), a cutaneous lesion that shares many clinical features with NA.…”
Section: Discussionmentioning
confidence: 99%
“…The name phacomatosis cesio-flammeo-marmorata has already been proposed in the literature, with seven cases identified to date, 1 which show heterogeneity of characteristics and one case with the described triad associated with nevus of Ota and anemic nevus. 2 …”
mentioning
confidence: 99%