Epidermal nevus syndromes: Clinical findings in 35 patients

Pediatric Dermatology

Volumn 21, Issue 4, 2004, Pages 432-439

  Vidaurri De La Cruz, Helena ^a   Tamayo Sánchez, Lourdes ^a   Durán McKinster, Carola ^a   Orozco Covarrubias, María De La Luz ^a   Ruiz Maldonado, Ramón ^a  

^a INSTITUTO NACIONAL DE PEDIATRÍA   (Mexico)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BECKER NEVUS; CANCER SUSCEPTIBILITY; CELL MIGRATION; CHILD; CLINICAL FEATURE; COMEDO NEVUS; DISEASE CLASSIFICATION; DISEASE COURSE; FEMALE; HUMAN; MAJOR CLINICAL STUDY; MALE; MULTIPLE CANCER; NERVE CELL; NEVUS; NEVUS UNIUS LATERIS; PHAKOMATOSIS; PIGMENTOKERATOTICA; PRIORITY JOURNAL; SEBACEOUS NEVUS;

ABNORMALITIES, MULTIPLE; CHILD; FEMALE; HUMANS; LONGITUDINAL STUDIES; MALE; MEXICO; NEVUS; PREVALENCE; RETROSPECTIVE STUDIES; SKIN NEOPLASMS; SYNDROME;

EID: 4043149952     PISSN: 07368046     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.0736-8046.2004.21402.x     Document Type: Article

References (36)

1. Oranje AP, Przyrembel H, Meradji M, Loonen MCB, Klerk JBC. Solomon's epidermal nevus syndrome (type: linear nevus sebaceus) and hypophosphatemic vitamin D-resistant rickets. Arch Dermatol 1994;130:1167-1171.
2. Solomon LM, Esterly NB. Epidermal and other congenital organoid nevi. Curr Prob Pediatr 1975;6:3-56.
3. Happle R. Epidermal nevus syndromes. Semin Dermatol 1995;4:111-121.
4. Happle R, Hoffmann R, Restano L, Caputo R, Tadini G. Phacomatosis pigmentokeratotica: a melanocytic epidermal twin nevus syndrome. Am J Med Genet 1996;65:363-365.
5. Atherton DJ. Naevi and other developmental defects. The epidermal naevus syndrome. In: Champion RH, Burton JL, Burns DA, Breathnach SM, eds. Rook/Wilkinson/Ebling. textbook of dermatology on CD-ROM, 6th ed. London: Blackwell, 1999.
6. Rogers M. Epidermal nevi. In: Harper J, Oranje A, Prose N. Textbook of pediatric dermatology. London: Blackwell, 2000:955-972.
7. Rogers M. Epidermal nevi and the epidermal nevus syndromes: a review of 233 cases. Pediatr Dermatol 1992;9:342-344.
8. Ivker R, Resnick S, Skidmore RA. Hypophosphatemic vitamin D-resistant rickets, precocious puberty, and the epidermal nevus syndrome. Arch Dermatol 1997;133:1557-1561.
9. Tay YK, Weston WL, Ganong CA, Klingensmith GJ. Epidermal nevus syndrome: association with central precocious puberty and woolly hair nevus. J Am Acad Dermatol 1996;35:839-842.
10. Stosiek N, Hornstein OP, Hiller D, Peters KP. Extensive linear epidermal nevus associated with hemangiomas of bones and vitamin-D-rickets. Dermatology 1994;189:278-282.
11. Moss C, Parkin JM, Comaish JS. Precocious puberty in a boy with a widespread linear epidermal naevus. Br J Dermatol 1991;125:178-182.
12. Aschinberg LC, Solomon LM, Zeis PM, Justice P, Rosenthal IM. Vitamin D-resistant rickets associated with epidermal nevus syndrome: demonstration of a phosphaturic substance in the dermal lesions. J Pediatr 1977;91:56-60.
13. Happle R. Elattoproteus syndrome: delineation of an inverse form of Proteus syndrome. Am J Med Genet 1999;84:25-28.
14. Koopman RJJ. Concept of twin spotting. Am J Med Genet 1999;85:355-358.
15. Gordon PL, Wilroy RS, Lasater OE, Cohen MM. Neoplasms in Proteus syndrome. Am J Med Genet 1995;57:74-78.
16. Online Mendelian Inheritance in Man OMIM™. Johns Hopkins University, Baltimore, MD. MIM number *601728 (updated to December 13, 2001). Phosphatase and tensin homolog; PTEN. Available at http://www.ncbi.nih. gov/omim/.
17. Zhou XP, Marxh DJ, Hampel H, Mulliken JB, Gimm O, Eng C. Germline and germline mosaic PTEN mutations associated with a Proteus-like syndrome of hemihypertrophy, lower limb asymmetry, arteriovenous malformations and lipomatosis. Hum Mol Genet 2000;9:765-768.
18. Pavone L, Curatolo P, Rizzo R, et al. Epidermal nevus syndrome: a neurologic variant with hemimegalencephaly, gyral malformation, mental retardation, seizures and facial hemihypertrophy. Neurology 1991;41:266-271.
19. El-Shanti H, Bell WE, Waziri MH. Epidermal nevus syndrome: subgroup with neuronal migration defects. J Child Neurol 1992;7:29-34.
20. Prayson RA, Kotagal P, Wyllie E, Bingaman W. Linear epidermal nevus and nevus sebaceus syndromes. A clinico-pathologic study of 3 patients. Arch Pathol Lab Med 1999;123:301-305.
21. Kang WH, Koh YJ, Chun SI. Nevus sebaceus syndrome associated with intracranial arteriovenous malformation. Int J Dermatol 1987;26:382-384.
22. Ogata H, Ebihara S, Mukai K. Salivary gland neoplasms in children. Jpn J Clin Oncol 1994;24:88-93.
23. Pinkston JA, Cole P. Incidence rates of salivary gland tumors: results from a population-based study. Otolaryngol Head Neck Surg 1999;120:834-840.
24. Xin H, Matt D, Qin JZ, Burg G, Böni R. The sebaceous nevus: a nevus with deletions of the PTCH gene. Cancer Res 1999;59:1834-1836.
25. Munro CS, Wilkie AOM. Epidermal mosaicism producing localised acne: somatic mutation in FGFR2. Lancet 1998;352:704-705.
26. Online Mendelian Inheritance in Man OMIM™. Johns Hopkins University, Baltimore, MD. MIM number 101200 (updated to April 21, 2000). Apert syndrome. Available at http://www.ncbi.nih.gov/omim/.
27. Online Mendelian Inheritance in Man OMIM™. Johns Hopkins University, Baltimore, MD. MIM number *176943 (updated to February 28, 2002). Fibroblast growth factor receptor 2; FGFR2. Available at http://www.ncbi.nih.gov/omim/.
28. Rott HD. Extracutaneous analogies of Blaschko lines. Am J Med Genet 1999;85:338-341.
29. Dimond RL, Amon RB. Epidermal nevus and rhabdomyosarcoma. Arch Dermatol 1976;112:1424-1426.
30. Wexler LH, Helman LJ. Rhabdomyosarcoma and the undifferentiated sarcomas. In: Pizzo PA, Poplack DG, eds. Principles and practice of pediatric oncology. Philadelphia: Lippincott-Raven, 1997:799-801.
31. Rubio-Muñoz A, Bono-Arino A, Berne-Manero JM, et al. Leiomioma de la vejiga. Arch Esp Urol 2000;53:934-937.
32. Alapont-Pérez FM, Gil-Salom M, Chuan-Nuez P, et al. Leiomioma vesical. Revisión y reporte de un caso. Arch Esp Urol 1995;48:1035-1037.
33. Greco A, Baima C, Piana P. Leiomyoma of the bladder. Report of a case and review of the literature. Minerva Urol Nefrol 1999;51:33-38.
34. Horie Y, Fujita H, Mano S, Kuwajima M, Ogawa K. Regional Proteus syndrome: report of an autopsy case. Pathol Int 1995;45:530-535.
35. Happle R, Mittag H, Küster W. The CHILD nevus: a distinct skin disorder. Dermatology 1995;191:210-216.
36. König A, Happle R, Bornholdt D, Engel H, Grzeschik WH. Mutations in the NSDHL gene, encoding a 3beta-hydroxysteroid dehydrogenase, cause CHILD syndrome. Am J Med Genet 2000;90:339-346.