Phakomatosis pigmentovascularis;La facomatosi pigmento-vascolare

Minerva Pediatrica

Volumn 48, Issue 5, 1996, Pages 225-228

  Cincinnati, P ^a,b   Carucci, T ^a   Rutiloni, C ^a  

^a Ospedale Civile   (Italy)

^b NONE   (Italy)

Author keywords

Nevus flammeus; Pigmentation disorder

Indexed keywords

ARTICLE; CASE REPORT; CHILD; EYE; FEMALE; HUMAN; MELANOSIS; NEVUS FLAMMEUS; PATHOPHYSIOLOGY; PHENOTYPE; PIGMENT DISORDER;

CHILD; EYE; FEMALE; HUMANS; MELANOSIS; PHENOTYPE; PIGMENTATION DISORDERS; PORT-WINE STAIN;

EID: 0030135211     PISSN: 00264946     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (20)

1. Ota M, Kawamura T, Ito N Phakomatosis pigmentovascularis (Ota) Jpn J Dermatol 1947;52.1-3.
2. Ortonne JP, Floret D, Coiffet J et al. Syndrome de Sturge-Weber associé à une mélanose oculocutanée. Ann Dermatol Venereol 1978,105:1019-31
3. Noriega-Sanchez A, Markand ON, Herndon JH Oculocutaneous melanosis associated with the Sturge-Weher syndrome. Neurology 1972;22:256-62.
4. Toda K. A new type of phacomatosis pigmentovascularis. Ota Jpn J Dermatol 1966;76 47-51.
5. Hasegawa Y, Yasuhara M. Phacomatosis pigmentovascularis type IVa Arch Dermatol 1985,121:651-5.
6. Prigent F, Kahn A, Martinet C et al. Phacomatose pigmentovasculaire IIIa. Ann Dermatol Venereol 1991;118:531-3
7. Guiglia MC, Prendiville JS Multiple granular cell tumors associated with giant speckled lentiginous nevus and nevus flammeus in a child J Am Acad Dermatol 1991;24:359-63-
8. Kaise M, Watanabe A, Kobayashi Y. A case of phacomatosis pigmentovascularis accompanied with esophageal varices due to hypoplasia of the portal veins. Gastroenterol Jpn 1992;27 546-9.
9. Peyron N, Dereure O, Bessis D et al La phacomatose pigmentovasculaire. A propos de 2 cas associés à une angiodysplasie. J Mal Vasc 1993,18:336-9.
10. Libow LF. Phacomatosis pigmentovascularis type IIIb J Am Acad Dermatol 1993;29:305-7
11. Gilliam AC, Ragge NK, Perez MI et al. Phakomatosis pigmentovascularis type IIb with iris mammillations. Arch Dermatol 1993,129:340-2.
12. Furukawa T, Igata A, Toyokura Y et al. Sturge-Weber and Klippel-Trénaunay syndrome with nevus of Ota and Ito. Arch Dermatol 1970;102:640-5
13. Adrien A, Lacour JP, Rostain G et al. Phacomatose pigmentovasculaire type IIb. Ann Dermatol Venereol 1986,113:915-6.
14. Enjolras O, Riché MC, Merland JJ. Facial port-wine stains and Sturge-Weber syndrome Pediatrics 1985;76:48-51.
15. Kitamura W, Iwai M, Sakamoto K. A case of phacomatosis pigmentovascularis. Rinsho Dermatol 1981;35:399-405.
16. Smoller BR, Rosen S. Port-wine stains, a disease of altered neural modulation of blood vessels? Arch Dermatol 1986.122:177-9.
17. Happle R Allelic somatic mutations may explain vascular twin nevi. Hum Genet 1991,86.321-2
18. Calvani M. Neurocristopatie: dalla biologia alla clinica. Atti II Congresso Niazionale di Pediatria Ospedaliera (SIP). Roma, 13-15 gennaio 1994:221-41.
19. Langman J Embriologia medica. Padova: Ed. Piccin, 1967.262.
20. Stevenson RF, Thomson HG, Morin JD. Unrecognized ocular problems associated with port-wine stains of the face in children. Can Med Assoc J 1974;111:953-5.