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The Skin

  • Peter R. Millard
  • Fraser G. Charlton
Chapter

Keywords

Epidermolysis Bullosa Ectodermal Dysplasia Melanocytic Nevus Epidermolysis Bullosa Simplex Cutis Laxa 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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References

  1. Akiyama M, Sawamura D, Shimizu H (2003) The clinical spectrum of nonbullous congenital ichthyosiform erythroderma and lamellar ichthyosis. Clin Exp Dermatol 28:235–240.PubMedCrossRefGoogle Scholar
  2. Alain G, Carrier C, Beaumier L, Bernard J, Lemay M, Lavoie A (1993) In utero acute graft-versus-host disease in a neonate with severe combined immuno-deficiency. J Am Acad Dermatol 29:862–865.PubMedCrossRefGoogle Scholar
  3. Anton-Lamprecht I (1983) Genetically induced abnormalities of epidermal differentiation and ultrastructure in ichthyoses and epidermolyses; pathogenesis, heterogenicity, fetal manifestations and prenatal diagnosis. J Invest Dermatol 81:1495– 1565.CrossRefGoogle Scholar
  4. Anton-Lamprecht I, Schnyder UW (1973) EB dystro-phica dominant, a defect in anchoring fibrils. Derma-tologica 147:289–298.Google Scholar
  5. Arnold ML, Rauskolb R, Anton-Lamprecht I, Schnizel A, Schmid W (1984) Prenatal diagnosis of anhidrotic ectodermal dysplasia. Prenat Diagn 4:85–98.PubMedCrossRefGoogle Scholar
  6. Arvin AM, Prober CG (1997) Herpes simplex virus type 2—a persistent problem. N Engl J Med 337:1158– 1159.PubMedCrossRefGoogle Scholar
  7. Atherton DJ, Rook A (1986) The newborn. In: Rook A, Wilkinson DS, Ebling FJG, Champion RH, Burton JL (eds) Textbook of Dermatology, 4th ed. Blackwell Scientific Publications, Oxford, pp 229–230.Google Scholar
  8. Baden HP (1982) Keratinization in the harlequin fetus. Arch Dermatol 118: 14–18.PubMedCrossRefGoogle Scholar
  9. Barnhill RL (1998) Childhood melanoma. Semin Diagn Pathol 15: 189–194.PubMedGoogle Scholar
  10. Bassukas ID (1992) Is erythema toxicum neonatorum a mild self-limited acute cutaneous graft versus host reaction form maternal-to-foetal lymphocytes transfer? Med Hypothesis 38:334–338.CrossRefGoogle Scholar
  11. Black CM, Gathercole LJ, Bailey AJ, Beighton P (1980) Ehlers. Danlos syndrome: an analysis of the structure of the collagen fibres of the skin. Br J Dermatol 102:85.PubMedCrossRefGoogle Scholar
  12. Bogdan I, Smolle J, Kerl H, Burg G, Boni R (2003) Melanoma ex naevo: a study of the associated naevus. Melanoma Res 13:213–217.PubMedCrossRefGoogle Scholar
  13. Bonifas JM, Rothman AL, Epstein EH Jr (1991) Epider-molysis bullosa simplex: evidence in two families for keratin gene abnormalities. Science 254:1202– 1205.PubMedCrossRefGoogle Scholar
  14. Bos JD, Kapsenberg ML (1993) The skin immune system: progress in cutaneous biology. Immunol Today 14:75–78.PubMedCrossRefGoogle Scholar
  15. Bos JD, Sillevis-Smith JH, Krieg SR, Bakker PM, Vos GD, van Zaane DJ (1984) Acute disseminated histio-cytosis X. J Cutan Pathol 11:59–64.PubMedCrossRefGoogle Scholar
  16. Breathnach AS (1971) The Herman Beerman lecture: embryology of human skin. J Invest Dermatol 57:133–143.PubMedCrossRefGoogle Scholar
  17. Breathnach AS, Robins J (1969) Ultrastructural features of epidermis of a 14 mm (6 weeks) human embryo. J Dermatol 81:504–516.CrossRefGoogle Scholar
  18. Breathnach AS, Wylie LM (1965) Electron microscopy of melanocytes and Langerhans' cells in human fetal epidermis at 14 weeks (menstrual dates). J Invest Dermatol 44:51–60.PubMedGoogle Scholar
  19. Briggaman RA, Wheeler CE (1975) EB dystrophica recessive. A possible role of anchoring fibrils in the pathogenesis. J Invest Dermatol 65:203–211.PubMedCrossRefGoogle Scholar
  20. Brough AJ, Jones D, Page RH, Mizukami I (1967) Dermal erythropoiesis in neonates. A manifestation of intrauterine viral disease. Pediatrics 40:627–635.PubMedGoogle Scholar
  21. Bruckner-Tuderman L, Mitsuhashi Y, Schnyder UW, Bruckner P (1989) Anchoring fibrils and Type VII collagen are absent from skin in severe recessive dys-trophic epidermolysis bullosa. J Invest Dermatol 93:3–9.PubMedCrossRefGoogle Scholar
  22. Burgdorf WH, Mukai K, Rosai J, Burge SM, Wilkinson JD (1981) Immunohistochemical identification of factor VIII-related antigen in endothelial cells of cutaneous lesions of alleged vascular nature. Am J Clin Pathol 75:167–171.PubMedGoogle Scholar
  23. Burge SM, Wilkinson JD (1992) Darrier-White disease: a review of the clinical features in 163 patients. J Am Acad Dermatol 27:40–50.PubMedCrossRefGoogle Scholar
  24. Burkhart CG, Gohara A (1981) Dermal melanocyte hamartoma. A distinctive new form of dermal mela-nocytosis. Arch Dermatol 117:102–104.PubMedCrossRefGoogle Scholar
  25. Calonje E, Mentzel T, Fletcher CD (1995) Pseudomalig-nant perineurial invasion in cellular (“infantile”) capillary haemangiomas. Histopathology 26:159–164.PubMedCrossRefGoogle Scholar
  26. Canninga-van Dijk MR, Sanders CJ, Verdonck LF, Fijn-heer R, van den Tweel JG (2003) Differential diagnosis of skin lesions after allogeneic haematopoietic stem cell transplantation. Histopathology 42:313– 330.PubMedCrossRefGoogle Scholar
  27. Carney RG (1976) Incontinentia pigmenti—a world statistical analysis. Arch Dermatol 112:535–542.PubMedCrossRefGoogle Scholar
  28. Cramer SF (1988) The melanocytic differentiation pathway in congenital melanocytic nevi: theoretical considerations. Pediatr Pathol 8:253–265.PubMedCrossRefGoogle Scholar
  29. Cribier BJ, Santinelli F, Grosshans E (1999) Lack of clinical-pathological correlation in the diagnosis of congenital naevi. Br J Dermatol 141:1004–1009.PubMedCrossRefGoogle Scholar
  30. Crowe FW, Schull WJ (1953) Diagnostic importance of café au lait spot in neurofibromatosis. Arch Intern Med 91:758–766.Google Scholar
  31. Dale BA, Holbrook KA, Fleckman P, Kimball JR, Brumbaugh S, Sybert VP (1990) Heterogeneity in harlequin ichthyosis, an inborn error of epidermal keratinization: variable morphology and structural protein expression and a defect in lamellar granules. J Invest Dermatol 94:6–18.PubMedCrossRefGoogle Scholar
  32. De Dobbeleer G, Heenen M, Song M, Achten G (1982) Collodion baby skin. Ultrastructural and autoradio-graphic study. J Cutan Pathol 9:196–202.PubMedCrossRefGoogle Scholar
  33. Dompmartin A, Leroy D, Labbé D, Letessier JB, Mandard JC (1989) Dermal malignant melanoma developing from a nevus of Ota. Int J Dermatol 28:535–536.PubMedCrossRefGoogle Scholar
  34. Dorfman DH, Glaser JH (1990) Congenital syphilis presenting in infants after the newborn period. N Engl J Med 323:1299–1302.PubMedGoogle Scholar
  35. Eady RAJ (1987) Babes, blisters and basement membranes: from sticky molecules to epidermolysis bullosa. Clin Exp Dermatol 12:161–170.PubMedCrossRefGoogle Scholar
  36. Elias PM (1989) The stratum corneum as an organ of protection; old and new concepts. In: Fritsch P, Schuler G, Hintner H (eds) Immunodeficiency and Skin. Current Problems in Dermatology, 18th ed. S. Karger AG, Basel pp. 10–21.Google Scholar
  37. Elias PM, Fritsch P, Epstein EH (1977) Review: staphy-lococcal scalded skin syndrome. Arch Dermatol 113:207–219.PubMedCrossRefGoogle Scholar
  38. Emile JF, Wechsler J, Brousse N, et al. (1995) Langer-hans' cell histiocytosis. Definitive diagnosis with the use of monoclonal antibody O10 on routinely paraffin-embedded samples. Am J Surg Pathol 19:636–641.PubMedGoogle Scholar
  39. Epstein EJ, Williams ML, Elias PM (1981) Editorial: steroid sulphatase, X linked ichthyosis and stratum corneum cell cohesion. Arch Dermatol 117:761–763.PubMedCrossRefGoogle Scholar
  40. Farber EM, Mullen RH, Jacobs AH, Nall L (1986) Infantile psoriasis: a follow up study. Pediatr Dermatol 3:237–243.PubMedCrossRefGoogle Scholar
  41. Favara BE (1991) Langerhans' cell histiocytosis: pathology and pathogenesis. Semin Oncol 18:3–7.PubMedGoogle Scholar
  42. Fine J, Couchman JR (1989) Chondroitin-6-sulphate proteoglycan but not heparin-sulphate proteoglycan is abnormally expressed in skin basement membrane from patients with dominant and recessive dystro-phic epidermolysis bullosa. J Invest Dermatol 92:611–616.PubMedCrossRefGoogle Scholar
  43. Fine J, Hintner H, Katz SI (1987) Immunofluorescent studies in epidermolysis bullosa utilising polyclonal and monoclonal antibodies. In: Beutner EH, Chorzelski TP, Kumar V (eds) Immunopathology of the Skin, 3rd ed. John Wiley and Sons, Chichester, pp. 399–405.Google Scholar
  44. Finlay JL, Noe JM, Arndt KA, Rosen S (1984) Port wine stains. Arch Dermatol 120:1453–1455.CrossRefGoogle Scholar
  45. Francis DP, Herrmann KL, MacMahon, JR, Chaviguy KJ, Sanderlin KC (1975) Nosocomial and maternally acquired herpes virus hominis infections. Am J Dis Child 129:889–893.PubMedGoogle Scholar
  46. Francois J (1984) Incontinentia pigmenti and retinal change. Br J Ophthalmol 68:19–25.PubMedCrossRefGoogle Scholar
  47. Frieden IJ (1986) Aplasia cutis congenital: a clinical review and proposal for classification. J Am Acad Dermatol 14:646–660.PubMedCrossRefGoogle Scholar
  48. Frieden IJ (1989) Blisters and pustules in the newborn. Curr Probl Pediatr 19:551–614.CrossRefGoogle Scholar
  49. Friedman SJ, Winkelmann RK (1989) Subcutaneous fat necrosis of the newborn: light, ultrastructural and histochemical microscopic studies. J Cutan Pathol 16:99–105.PubMedCrossRefGoogle Scholar
  50. Frost P, van Scott EJ (1966) Ichthyosiform dermatoses. Arch Dermatol 94:113–126.PubMedCrossRefGoogle Scholar
  51. Fulk CS (1984) Primary disorders of hyperpigmenta-tion. J Am Acad Dermatol 10:1–16.PubMedCrossRefGoogle Scholar
  52. Gari LM, Rivers JK, Kopf AW (1988) Melanomas arising in large congenital nevocytic nevi; a prospective study. Pediatr Dermatol 5:151–158.PubMedCrossRefGoogle Scholar
  53. Gellis SS (1977) Constrictive bands in the human. Birth Defects 13:259–265.PubMedGoogle Scholar
  54. Golkar L, Bernhard JD (1997) Mastocytosis. Lancet 349:1379–1385.PubMedCrossRefGoogle Scholar
  55. Goltz RW, Henderson RR, Hitch JM, Ott JE (1970) Focal dermal hypoplasia. Arch Dermatol 101:1–11.PubMedCrossRefGoogle Scholar
  56. Gorlin RJ, Anderson RC, Blaw M (1969) Multiple len-tigines syndrome. Am J Dis Child 117:652–662.PubMedGoogle Scholar
  57. Gottlieb SK, Fisher BK, Violin GA (1973) Focal dermal hypoplasia, 9 year follow-up. Arch Dermatol 108:551–553.PubMedCrossRefGoogle Scholar
  58. Groh V, Gadner H, Radaszkiewicz T, et al. (1988) The phenotypic spectrum of histiocystosis X-cells. J Invest Dermatol 90:441–447.PubMedCrossRefGoogle Scholar
  59. Gross BD, Forman D, Ansell PE, et al. (1990) The prevalence and characteristics of congenital pigmented lesions in newborn babies in Oxford. Paediatr Perinat Epidemiol 4:448–457.CrossRefGoogle Scholar
  60. Guerrier CJW, Wong CK (1974) Ultrastructural evolution of the skin in incontinentia pigmenti. Dermato-logica 149:10–22.Google Scholar
  61. Hamada T, McLean WH, Ramsay M, et al. (2002) Lipoid proteinosis maps to 1q21 and is caused by mutations in the extracellular matrix protein 1 gene (ECM1). Hum Mol Genet 11:833–840.PubMedCrossRefGoogle Scholar
  62. Hansen RC (1983) Staphylococcal scalded skin syndrome, toxic shock syndrome and Kawasaki disease. Pediatr Clin North Am 30:533–544.PubMedGoogle Scholar
  63. Hashimoto K, Gross BG, DiBella RJ, Lever WF (1966) The ultrastructure of the skin of human embryos. IV. Epidermis. J Invest Dermatol 47:317–335.PubMedGoogle Scholar
  64. Hazell M, Marks R (1985) Clinical, histologic, and cell kinetic discriminants between lamellar ichthyosis and nonbullous ichthyosiform erythroderma. Arch Dermatol 121:489–493.PubMedCrossRefGoogle Scholar
  65. Held JL, Haber RS, Silvers DN, Grossman ME (1990) Benign neonatal hemangiomatosis: review and description of a patient with unusually persistent lesions. Pediatr Dermatol 7:63–66.PubMedCrossRefGoogle Scholar
  66. Holbrook KA, Byers PH (1982) Structural abnormalities of the dermal collagen and elastic matrix from the skin of patients with inherited connective tissue disorders. J Invest Dermatol 7:7s–16s.CrossRefGoogle Scholar
  67. Holbrook KA, Odland GF (1975) The fine structure of developing human epidermis: light, scanning and transmission electron microscopy of the periderm. J Invest Dermatol 65:16–38.PubMedCrossRefGoogle Scholar
  68. Honig PJ (1983) Diaper dermatitis. Postgrad Med 74: 79–84.PubMedGoogle Scholar
  69. Honour JW, Goolamali SK, Taylor NF (1985) Prenatal diagnosis and variable presentation of recessive X-linked ichthyosis. Br J Dermatol 112: 423–430.PubMedCrossRefGoogle Scholar
  70. Horn TD (1994) Acute cutaneous eruptions after marrow ablation: roses by other names? J Cutan Pathol 21:385–392.PubMedCrossRefGoogle Scholar
  71. Hoyes AD (1968) Electron microscopy of the surface layer (periderm) of human foetal skin. J Anat 103:321–336.PubMedGoogle Scholar
  72. Hurwitz S (1983) Epidermal nevi and tumours of epidermal origin. Pediatr Clin North Am 30:483–494.PubMedGoogle Scholar
  73. Jacobs AH, (1983) Vascular nevi. Pediatr Clin North Am 30:465–482.PubMedGoogle Scholar
  74. Jacobs AH, Walton RG (1976) The incidence of birthmarks in the neonate. Pediatrics 58: 218–222.PubMedGoogle Scholar
  75. Jungbluth AA, Busam KJ, Gerald WL, et al. (1998) A103: An anti-Melan-A monoclonal antibody for the detection of malignant melanoma in paraffin-embedded tissues. Am J Surg Pathol 22:595–602.PubMedCrossRefGoogle Scholar
  76. Kellum RE, Ray TL, Brown GR (1968) Sclerema neona-torum. Report of a case and analysis of subcutaneous and epidermal-dermal lipids by chromatographic methods. Arch Dermatol 97:372–380.PubMedCrossRefGoogle Scholar
  77. Kere J, Srivastava AK, Montonen O, et al. (1996) X-linked anhidrotic (hypohidrotic) ectodermal dyspla-sia is caused by mutations in a novel transmembrane protein. Nat Genet 73:409–416.CrossRefGoogle Scholar
  78. Khakoo A, Thomas R, Trompeter R, Duffy P, Price R, Pope FM (1997) Congenital cutis laxa and lysyl oxidase deficiency. Clin Genet 51:109–114.PubMedGoogle Scholar
  79. Kimyai-Asadi A, Kotcher LB, Jih MH (2002) The molecular basis of hereditary palmoplantar keratodermas. J Am Acad Dermatol 47:327–343.PubMedCrossRefGoogle Scholar
  80. Kruisinski PA, Saurat J (1989) Transplacentally transferred dermatosis. Pediatr Dermatol 6:166–177.CrossRefGoogle Scholar
  81. Lamartine J (2003) Towards a new classification of ecto-dermal dysplasias. Clin Exp Dermatol 28:351–355.PubMedCrossRefGoogle Scholar
  82. Lamartine J, Munhoz Essenfelder G, Kibar Z, et al. (2000) Mutations in GJB6 cause hidrotic ectodermal dysplasia. Nat Genet 26:142–144.PubMedCrossRefGoogle Scholar
  83. Lawler F, Holmes SC (1989) Focal dermal hypoplasia syndrome in the neonate. J R Soc Med 82:165–166.Google Scholar
  84. Ledoux-Corbusier M (1983) Cutis laxa, congenital form with pulmonary emphysema; an ultrastructural study. J Cutan Pathol 10:340–349.PubMedCrossRefGoogle Scholar
  85. Lee CW, Park MH, Lee H (1988) Recurrent cutaneous Langerhans' cell histiocytosis in infancy. Br J Derma-tol 119:259–265.CrossRefGoogle Scholar
  86. Lee LA (1993) Neonatal lupus erythematosus. J Invest Dermatol 100:9–13S.CrossRefGoogle Scholar
  87. Leung AKC, Telmesani AMA (1989) Salmon patches in Caucasian children. Pediatr Dermatol 6:185–187.PubMedCrossRefGoogle Scholar
  88. Lim W, Sadick N, Gupta A, Kaplin M, Pahwa S (1990) Skin diseases in children with HIV infection and their association with degree of immunosuppression. Int J Dermatol 29:24–30.PubMedCrossRefGoogle Scholar
  89. Luders D (1960) Histologic observations in erythema toxicum neonatorum. Pediatrics 26:219–224.PubMedGoogle Scholar
  90. Mao JR, Bristow J (2001) The Ehlers-Danlos syndrome: on beyond collagens. J Clin Invest 107:1063–1069.PubMedCrossRefGoogle Scholar
  91. Marghoob AA, Schoenbach SP, Kopf AW, et al. (1996) Large congenital naevi and the risk for the development of malignant melanoma. Arch Dermatol 132:170–175.PubMedCrossRefGoogle Scholar
  92. Mark GJ, Mihm MC, Liteplo MG, Reed RJ, Clark WH (1973) Congenital melanocytic naevi of small and garment type; clinical, histologic and ultrastructural studies. Hum Pathol 4:395–418.PubMedCrossRefGoogle Scholar
  93. Martin-Pascual A, de Unamuno P, Aparicio M, Herreros V (1977) Anhidrotic (or hypohidrotic) ectodermal dysplasia. Dermatologica 154:235–243.PubMedGoogle Scholar
  94. McCarthy T, Sanders P (1978) The origin and circulation of the amniotic fluid. In: Fairweather DVI, Eskes TKAB (eds) Amniotic Fluid Research and Clinical Application, 2nd ed. Excerpta Medica, Amsterdam, pp 1–17.Google Scholar
  95. McDonald CJ (1988) Structure and function of the skin: are there differences between black and white skin? Dermatol Clin 6:343–368.PubMedGoogle Scholar
  96. McLaurin CI (1988) Pediatric dermatology in black patients. Dermatol Clin 6:457–473.PubMedGoogle Scholar
  97. Mellerio JE, Dunnill MGS, Allison W, et al. (1997) Recurrent mutations in the Type VII collagen gene (COL 7AI) in patients with recessive dystrophic epi-dermolysis bullosa. J Invest Dermatol 109:246–249.PubMedCrossRefGoogle Scholar
  98. Merlob P, Metzker A, Hazaz B, Rogovin H, Reisner SH (1986) Neonatal pemphigus vulgaris. Pediatrics 78:1102–1105.PubMedGoogle Scholar
  99. Milner ME, O'Guin WM, Holbrook KA, et al. (1992) Abnormal lamellar granules in harlequin ichthyosis. J Invest Dermatol 99:824–829.PubMedCrossRefGoogle Scholar
  100. Moller LB, Tumer Z, Lund C, et al. (2000) Similar splice-site mutations of the ATP7A gene lead to different phenotypes: classical Menkes disease or occipital horn syndrome. Am J Hum Genet 66:1211–1220.PubMedCrossRefGoogle Scholar
  101. Moss C, Savin JA (1995) Dermatology and the New Genetics. Oxford Science, Oxford.Google Scholar
  102. Nanda A, Kaur, S, Bhakoo ON, Dhall K (1989) Survey of cutaneous lesions in Indian newborns. Paediatr Dermatology 6:39–42.CrossRefGoogle Scholar
  103. Nickoloff BJ, Walton R, Pregerson-Rodnan K, Jacobs AH, Cox AJ (1986) Immunohistologic patterns of congenital nevocellular nevi. Arch Dermatol 122:1263–1268.PubMedCrossRefGoogle Scholar
  104. Norwood-Galloway A, Lebwohl M, Phelps RG, Raucher H (1987) Subcutaneous fat necrosis of the newborn with hypercalcemia. J Am Acad Dermatol 16:435– 439.PubMedCrossRefGoogle Scholar
  105. Olson NY, Lindsley CB (1987) Neonatal lupus syndrome. Am J Dis Child 141:908–910.PubMedGoogle Scholar
  106. Osburn K, Schosser RH, Evertt MA (1987) Congenital pigmented and vascular lesions in newborn infants. J Am Acad Dermatol 16:788–792.PubMedCrossRefGoogle Scholar
  107. Owen DR, Chu ML, Kitto J (1988) Expression of basement membrane zone genes coding for type IV pro-collagen and laminin by human skin fibroblasts in vitro; elevated a1 (IV) collagen mRNA levels in lipoid proteinosis. J Invest Dermatol 90:734–738.CrossRefGoogle Scholar
  108. Paller AS, Syder AJ, Chan YM, et al. (1994) Genetic and clinical mosaicism in a type of epidermal nevus. N Engl J Med 331:1408–1415.PubMedCrossRefGoogle Scholar
  109. Pierard GE, van Neste D, Letot B (1979) Hidrotic ecto-dermal dysplasia. Dermatologica 158:168–174.PubMedCrossRefGoogle Scholar
  110. Pinheiro M, Freire-Maia N (1983) Dermoodontodyspla-sia: an eleven number, four generation pedigree with an apparently hitherto undescribed pure ectodermal dysplasia. Clin Genet 24:58–68.PubMedCrossRefGoogle Scholar
  111. Pollard ZE, Harley RD, Calhoun J (1976) Dermoid cysts in children. Pediatrics 57:379–382.PubMedGoogle Scholar
  112. Pope FM, Nicholls AC (1986) Collagen genes and proteins in human diseases. In: Chapman PH (ed) Recent advances in dermatology. Churchill Livingstone, Edinburgh.Google Scholar
  113. Pope FM, Narcisi P, Nicholls AC, Liberman N, Oorthuys JWE (1988) Clinical presentation of Ehlers–Danlos syndrome type IV. Arch Dis Child 63:1016–1025.PubMedCrossRefGoogle Scholar
  114. Prussick R, Brain MC, Walker IR, Sauder DN (1991) Polymyositis: a manifestation of chronic graft-versus-host disease. J Am Acad Dermatol 25:560– 562.PubMedCrossRefGoogle Scholar
  115. Rasmussen HB, Teisner B, Chemnitx J, Rasmussen JM, Brandrup F (1989) Localisation of fetal antigen 2 (FA-2) in fetal and adult human skin. Br J Dermatol 121:433–442.PubMedCrossRefGoogle Scholar
  116. Rehfield SJ, Palchy WZ, Williams ML, Elias PM (1988) Calorimetric and electron spin resonance examination of lipid phase transitions in human stratum corneum: molecular basis for normal cohesion and abnormal desquamation in recessive X-linked ich-thyosis. J Invest Dermatol 91:499–505.CrossRefGoogle Scholar
  117. Rhodes AR (1983) Pigmented birthmarks and precursor melanocytic lesions of cutaneous melanoma identifiable in childhood. Pediatr Clin North Am 30:435–463.PubMedGoogle Scholar
  118. Rhodes AR (1986) Congenital nevomelanocytic nevi: histologic patterns in the first year of life and evolution during childhood. Arch Dermatol 122:1257–1262.PubMedCrossRefGoogle Scholar
  119. Rhodes AR, Melski J (1982) Small congenital nevocel-lular nevi and the risk of cutaneous melanoma. J Pediatr 100:219–224.PubMedCrossRefGoogle Scholar
  120. Rhodes AR, Silverman RA, Harrist TJ, Melski JW (1985) A histologic comparison of congenital and acquired nevomelanocytic nevi. Arch Dermatol 121:1266– 1273.PubMedCrossRefGoogle Scholar
  121. Rodriguez-Revenga L, Iranzo P, Badenas C, Puig S, Carrio A, Mila M (2004) A novel elastin gene mutation resulting in an autosomal dominant form of cutis laxa. Arch Dermatol 140:1135–1139.PubMedCrossRefGoogle Scholar
  122. Roth RR, James WD (1989) Microbiology of the skin: resident flora, ecology, infection. J Am Acad Derma-tol 20:367–390.CrossRefGoogle Scholar
  123. Rothnagel JA, Domney AM, Demsey, et al. (1992) Mutations in the rod domain of keratin 1 and 10 in epidermolytic hyperkeratosis. Science 257:1128– 1130.PubMedCrossRefGoogle Scholar
  124. Rusenko KW, Gammon WR, Fine J, Briggaman RA (1989) The carboxyl-terminal domain of type VII collagen is present at the basement membrane in recessive dystrophic epidermolysis bullosa. J Invest Dermatol 92:623–627.PubMedCrossRefGoogle Scholar
  125. Sagebiel RW, Odland GF (1970) Ultrastructural identi-fication of melanocytes in early human embryos. J Invest Dermatol 54:96(abstr).Google Scholar
  126. Sakuntabhai A, Ruiz-Perez V, Carter S, et al. (1999) Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease. Nat Genet 21:271–277.PubMedCrossRefGoogle Scholar
  127. Sandler A, Snedeker JD (1987) Cytomegalovirus infection in an infant presenting with cutaneous vasculi-tis. Pediatr Infect Dis J 6:422–423.PubMedGoogle Scholar
  128. Satoh T, Tokura Y, Katsumata M, Sonoda T, Takigawa M (1990) Histological diagnostic criteria for accessory tragi. J Cutan Pathol 17:206–210.PubMedCrossRefGoogle Scholar
  129. Saurat JH, Gluckman E (1977) Lichen-planus-like eruption following bone marrow transplantation: a manifestation of the graft-versus-host disease. Clin Exp Dermatol 2:335–344.PubMedGoogle Scholar
  130. Schachner L, Lazarus GS, Dembitzer H (1977) Epider-molysis bullosa herditaria letalis; pathology, natural history and therapy. Br J Dermatol 96:51–58.PubMedCrossRefGoogle Scholar
  131. Schamburg-Lever G, Lever WF (1973) Electron microscopy of incontinentia pigmenti. J Invest Dermatol 61:151–158.PubMedCrossRefGoogle Scholar
  132. Shapiro LJ, Weiss R, Webster D, France JT (1978) X linked ichthyosis due to steroid sulphatase defi-ciency. Lancet I:70–72.Google Scholar
  133. Shimada S, Katz SI (1988) The skin as an immunologic organ. Arch Pathol Lab Med 112:231–234.PubMedGoogle Scholar
  134. Shimizu H, Niizeki H, Suzumori K, et al. (1994) Prenatal diagnosis of oculocutaneous albinism by analysis of the fetal tyrosinase gene. J Invest Dermatol 103:104–106.PubMedCrossRefGoogle Scholar
  135. Shornick JK (1987) Herpes gestationis. J Am Acad Dermatol 17:539–556.PubMedCrossRefGoogle Scholar
  136. Sigg C, Pelloni F, Schnyder UW (1990) Frequency of congenital nevi, nevi spili and café au lait spots and their relation to nevus count and skin complexion in 939 children. Dermatologica 180:118–123.PubMedGoogle Scholar
  137. Slaughter JC, Hardman JM, Kempe LG, Earle KM (1969) Neurocutaneous melanosis and leptomeningeal mel-anomatosis in children. Arch Pathol 88:298–304.PubMedGoogle Scholar
  138. Smahi A, Hyden-Granskog C, Peterlin B, et al. (1994) The gene for the familial form of incontinentia pig-menti (IP2) maps to the distal part of Xq28. Hum Mol Genet 3:273–278.PubMedCrossRefGoogle Scholar
  139. Smith LT, Holbrook KA (1986) Embryogenesis of the dermis in human skin. Pediatr Dermatol 3:271–280.PubMedCrossRefGoogle Scholar
  140. Smith LT, Sakai LY, Burgeson RE, Holbrook KA (1988) Ontogenesis of structural components of the dermal– epidermal junction in human embryonic and fetal skin: the appearance of anchoring fibrils and type VII collagen. J Invest Dermatol 90:480–485.PubMedCrossRefGoogle Scholar
  141. Solomon LM, Keuer EJ (1980) The ectodermal dyspla-sias. Problems of classification and some newer syndromes. Arch Dermatol 116:1295–1299.PubMedCrossRefGoogle Scholar
  142. Sontheimer RD, McCauliffe DP (1990) Pathogenesis of anti-Ro/SS-A autoantibody-associated cutaneous lupus erythematosus. Dermatol Clin 8:751–758.PubMedGoogle Scholar
  143. Stingl G, Steiner G (1989) Immunological host defence of the skin. In: Fritsch P, Schuler G, Hintner H (eds) Immunodeficiency and Skin. Current Problems in Dermatology, 18th ed. S. Karger AG, Basel pp. 22–30.Google Scholar
  144. Straka BF, Whitaker DL, Morrison SH, Oleske JM, Grant-Kels JM (1988) Cutaneous manifestations of the acquired immunodeficiency syndrome in children. J Am Acad Dermatol 18:1089–1102.PubMedCrossRefGoogle Scholar
  145. Sulica VI, Cooper PH, Pope FM, Hambrick GW, Gerson BM, McKusick VA (1979) Cutaneous histologic features in Ehlers-Danlos syndrome: study of 21 patients. Arch Dermatol 115:40–42.PubMedCrossRefGoogle Scholar
  146. Swerdlow AJ, English JSC, Qiao Z (1995) The risk of melanoma in patients with congenital naevi: a cohort study. J Am Acad Dermatol 32:595–599.PubMedCrossRefGoogle Scholar
  147. Sybert VP, Dale BA, Holbrook KA (1988) Palmar– plantar keratoderma. A clinical, ultrastructural and biochemical study. J Am Acad Dermatol 18:75–86.PubMedCrossRefGoogle Scholar
  148. Takematsu H, Terui T, Torinuki W, et al. (1986) Incon-tinentia pigmenti: eosinophilic chemotactic activity of the crusted scales in the vesiculo-bullous stage. Br J Dermatol 115:61–66.PubMedCrossRefGoogle Scholar
  149. Terasaki K, Kanekura T, Setoyama M, Kanzaki T (2003) A pediatric case of sclerodermatous chronic graft-versus-host disease. Pediatr Dermatol 20:327–331.PubMedCrossRefGoogle Scholar
  150. Tomita Y (1994) The molecular genetics of albinism and piebaldism. Arch Dermatol 130:355–358.PubMedCrossRefGoogle Scholar
  151. Travis WD, Li C, Bergstralh EJ, Yam LT, Swee RG (1988) Systemic mast cell disease: analysis of 58 cases and literature review. Medicine 67:345–368.PubMedCrossRefGoogle Scholar
  152. Tunnessen WW (1983) Cutaneous infections. Pediatr Clin North Am 30(3):515–532.PubMedGoogle Scholar
  153. Vandersteen PR, Muller SA (1972) Lamellar ichthyosis. Enzyme histochemical, light and EM study. Arch Dermatol 106:694–701.PubMedCrossRefGoogle Scholar
  154. Walsh SS, Robson WJ (1988) Granuloma gluteale infan-tum: an unusual complication of napkin dermatitis. Arch Emerg Med 5:113–115.PubMedGoogle Scholar
  155. Wessells NK (1967) Differentiation of epidermis and epidermal derivatives. N Engl J Med 277(1):21–33.PubMedCrossRefGoogle Scholar
  156. Whimster IW (1976) The pathology of lymphangioma circumscriptum. Br J Dermatol 94:473–486.PubMedCrossRefGoogle Scholar
  157. Williams ML (1992) Ichthyosis: mechanisms of disease. Paediatric Dermatol 9:365–368.CrossRefGoogle Scholar
  158. Williams ML, Elias PM (1985) Heterogeneity in autoso-mal recessive ichthyosis. Arch Dermatol 121:477– 488.PubMedCrossRefGoogle Scholar
  159. Williams ML, Elias PM (1987) Genetically transmitted generalised disorders of cornification. The Ichthyo-ses. Dermatol Clin 5:155–178.PubMedGoogle Scholar
  160. Wolfson SL, Botero F, Hurwitz S, Pearson HA (1981) “Pure” cutaneous histiocytosis X. Cancer 48:2236– 2238.PubMedCrossRefGoogle Scholar
  161. Yancey KB (1995) Adhesion molecules: II interactions of keratinocytes with epidermal basement membrane. Prog Dermatol 104:1008–1014.Google Scholar

Copyright information

© Springer-Verlag London Limited 2007

Authors and Affiliations

  • Peter R. Millard
    • 1
  • Fraser G. Charlton
    • 2
  1. 1.Department of HistopathologyJohn Radcliffe HospitalOxfordUK
  2. 2.Department of Cellular PathologyRoyal Victoria InfirmaryNewcastle Upon TyneUK

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