Résumé
Abstract Phacomatosis pigmentovascularis is a rare syndrome, defined as the simultaneous presence of vascular nevus and melanocytic nevus in the same patient. We report the case of a 53-year-old woman presented with dermal melanosis and extensive vascular nevus, which match the typical manifestations of phakomatosis pigmetovascularis of cesioflammea type, according to Happle's classification. The rare occurrence of this genodermatosis and the clinical exuberance of the skin lesions motivated this case report.
Sujets)
Humains , Femelle , Adulte d'âge moyen , Tumeurs cutanées/anatomopathologie , Syndromes neurocutanés/anatomopathologie , Mélanose/anatomopathologie , Naevus pigmentaire/anatomopathologie , Peau/anatomopathologie , Tache lie de vin/anatomopathologie , Maladies rares/anatomopathologieRésumé
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.
.Sujets)
Humains , Mâle , Jeune adulte , Tache mongoloïde/anatomopathologie , Syndromes neurocutanés/anatomopathologie , Naevus de Ota/anatomopathologie , Tache lie de vin/anatomopathologie , Dermatoses vasculaires/anatomopathologie , Tumeurs cutanées/anatomopathologie , Télangiectasie/congénital , Syndromes neurocutanés/classification , Télangiectasie/anatomopathologieRésumé
We present an interesting case report of two sarcoid-like lesions on a port-wine stain (PWS) birthmark in a Brazilian patient which on investigation proved to be cutaneous leishmaniasis.
Sujets)
Adulte , Femelle , Humains , Leishmaniose cutanée/anatomopathologie , Tache lie de vin/anatomopathologie , Biopsie , Immunohistochimie , Peau/anatomopathologieRésumé
Pyogenic granuloma is a common benign vascular lesion of the skin and mucosa. There are a few reports on the rare association between it and port wine stain, but there is no clear description of an association with neurofibromatosis type 1 in the literature. This report presents a 29-year-old Saudi male with Von Recklinghausen's disease with recurrent pyogenic granuloma on the nevus flammeus over his neck. He was treated with shave excision and electrocautery with clearance and no recurrence of pyogenic granuloma for the last 5 years follow-up