Phacomatosis pigmentovascularis revisited and reclassified

Archives of Dermatology

Volumn 141, Issue 3, 2005, Pages 385-388

  Happle, Rudolf ^a  

^a PHILIPPS UNIVERSITY MARBURG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

DATA ANALYSIS; DISEASE CLASSIFICATION; HUMAN; PHACOMATOSIS CESIOFLAMMEA; PHACOMATOSIS CESIOMARMORATA; PHACOMATOSIS PIGMENTOVASCULARIS; PHACOMATOSIS SPILOROSEA; PHAKOMATOSIS; PIGMENTED NEVUS; PRIORITY JOURNAL; REVIEW;

BIOPSY, NEEDLE; FEMALE; HUMANS; IMMUNOHISTOCHEMISTRY; INCIDENCE; INFANT; INFANT, NEWBORN; MALE; NEUROCUTANEOUS SYNDROMES; PIGMENTATION DISORDERS; PROGNOSIS; RISK ASSESSMENT; SEX DISTRIBUTION; SURVIVAL RATE;

EID: 14944378165     PISSN: 0003987X     EISSN: None     Source Type: Journal    
DOI: 10.1001/archderm.141.3.385     Document Type: Review

References (27)

1. Hasegawa Y, Yasuhara M. Phakomatosis pigmentovascularis type IVa. Arch Dermatol. 1985;121:651-655.
2. Happle R, Steijlen PM. Phacomatosis pigmentovascularis gedeutet als ein Phänomen der Zwillingsflecken. Hautarzt. 1989;40:721-724.
3. Happle R. Loss of heterozygosity in human skin. J Am Acad Dermatol. 1999;41:143-161.
4. Enjolras O, Mulliken JB. Vascular malformations. In: Harper J, Oranje A, Prose N, eds. Textbook of Pediatric Dermatology. Oxford, England: Blackwell; 2000:975-996.
5. Torrelo A, Zambrano A, Happle R. Cutis marmorata telangiectatica congenita and extensive mongolian spots: type 5 phacomatosis pigmentovascularis. Br J Dermatol. 2003;148:342-345.
6. Happle R. Neurocutaneous diseases. In: Freedberg IM, Eisen AZ, Wolff K, Austen KF, Goldsmith LA, Katz SI, eds. Fitzpatrick's Dermatology in General Medicine. 6th ed. New York, NY: McGraw-Hill; 2003:1806-1821.
7. Vidaurri-de la Cruz H, Tamayo-Sanchez L, Duran-McKinster C, Orozco-Covarrubias ML, Ruiz-Maldonado R. Phacomatosis pigmentovascularis IIA and IIB: clinical findings in 24 patients. J Dermatol. 2003;30:381-388.
8. Di Landro A, Tadini GL, Marchesi L, Cainelli T. Phakomatosis pigmentovascularis: a new case with renal angiomas and some considerations about the classification. Pediatr Dermatol. 1999;16:25-30.
9. Mandt N, Blume-Peytavi U, Pfrommer C, Krengel S, Goerdt S. Phakomatosis pigmentovascularis type IIa. J Am Acad Dermatol. 1999;40:318-321.
10. Ruiz-Maldonado R, Tamayo L, Laterza AM, Brawn G, Lopez A. Phacomatosis pigmentovascularis: a new syndrome? report of four cases. Pediatr Dermatol. 1987;4:189-196.
11. Bhat J, Batta K, Shah P, Bissenden J, Moss C. Phakomatosis pigmentovascularis type 2β: a case report [abstract]. Br J Dermatol. 2002;147(suppl 62):92.
12. Furukawa T, Igata A, Toyokura Y, Ikeda S. Sturge-Weber and Klippel-Trenaunay syndrome with nevus of Ota and Ito. Arch Dermatol. 1970;102:640-645.
13. Larralde ML, Barquin MA, Casas JG, Sidelsky S. Phacomatosis pigmentovascularis with a selective IgA deficiency. Pediatr Dermatol. 1995;12:159-163.
14. Chekroun-Le Du L, Delaporte E, Catteau B, Destée A, Piette F. Phacomatosis pigmentovascularis type II. Eur J Dermatol. 1998;8:569-572.
15. Van Gysel D, Oranje AP, Stroink H, Simonsz HJ. Phacomatosis pigmentovascularis. Pediatr Dermatol. 1996;13:33-35.
16. 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;24:359-363.
17. Libow LF. Phakomatosis pigmentovascularis type IIIb. J Am Acad Dermatol. 1993;29:305-307.
18. Mahroughan M, Mehregan AH, Mehregan DA. Phakomatosis pigmentovascularis: report of a case. Pediatr Dermatol. 1996;13:36-38.
19. Eichenfield LF, Gibbs NF. Hyperpigmentation disorders. In: Eichenfield LF, Frieden IJ, Esterly NB, eds. Textbook of Neonatal Dermatology. Philadelphia, Pa: WB Saunders; 2001:370-394.
20. Fishman SJ, Mulliken JB. Vascular anomalies: a primer for pediatricians. Pediatr Clin North Am. 1998;45:1455-1477.
21. Tsuruta D, Fukai K, Seto M, et al. Phakomatosis pigmentovascularis type IIIb associated with Moyamoya disease. Pediatr Dermatol. 1999;16:35-38.
22. Sigg C, Pelloni F. Oligosymptomatic form of Klippel-Trenaunay-Weber syndrome associated with giant nevus spilus. Arch Dermatol. 1989;125:1284-1285.
23. Joshi A, Garg VK, Agrawal S, Agarwalla A, Thakur A. Port-wine-stain (nevus flammeus), congenital Becker's nevus, café-au-lait-macule and lentigines: phakomatosis pigmentovascularis type Ia - a new combination. J Dermatol. 1999;26:834-836.
24. De las Heras E, Boixeda JP, Ledo A, Happle R. Paired melanotic and achromic macules in a case of phacomatosis pigmentovascularis: a further example of twin spotting? Am J Med Genet. 1997;70:336-337.
25. Dippel E, Utikal J, Feller G, et al. Nevi flammei affecting two contralateral quadrants and nevus depigmentosus: a new type of phacomatosis pigmentovascularis? Am J Med Genet. 2003;119A:228-230.
26. Chen W, Happle R. Phacomatosis pigmentovasculosebacea: an unusual case of phacomatosis multiplex. Eur J Dermatol. 2003;13:231-233.
27. Bielsa I, Paradelo C, Ribera M, Ferrándiz C. Generalized nevus spilus and nevus anemicus in a patient with a primary lymphedema: a new type of phakomatosis pigmentovascularis? Pediatr Dermatol. 1998;15:293-295.