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Неонатальная и детская эритродермия
Неонатальная и детская эритродермия
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Полный текст
Список литературы
1. Dogra S, De D. Disorders of keratinization: Erythroderma in Children. In: Inamdar AC, Sacchidanand S (eitors). Textbook of Pediatric Dermatology. 1st ed. New Delhi: Jaypee Brothers Medical Publishers (P) Ltd, 2009; p. 341–8.
2. Hoeger PH, Harper JI. Neonatal erythroderma: Differential diagnosis and management of red baby. Arch Dis Child 1998; 79: 186–91.
3. Sehgal VN, Srivastava G. Erythroderma/generalized exfoliative dermatitis in pediatric practice: an overview. Int J Dermatol 2006; 45: 831–9.
4. Sarkar R, Sharma RC, Koranne RV et al. Erythroderma in children – a clinico-etiological study. J Dermatol (Tokyo) 1999; 26: 507–11.
5. Pruskowsky A, Bodmer C, Fraitog S. Neonatal and infantile erythroderma – a retrospective study of 51 patients. Arch Dermatol 2000; 136: 875–80.
6. Sarkar R, Basu S, Sharma RC. Neonatal and infantile erythroderma. Arch Dermatol 2001; 137: 822–3.
7. Spraker MK. Differential diagnosis of neonatal erythroderma. In: Harper J, Orange A, Prose N (eds). Textbook of Pediatric Dermatology. 1st ed. London Blackwell Science Ltd, 2007; p. 92–103.
8. Dyke MP, Marlow N, Berry PJ. Omenn’s Disease. Arc Dis Child 1991; 66: 1247–8.
9. Glover MT, Atherton DJ, Levinsky RJ. Syndrome of erythroderma failure to thrive and
diarrhoea in infancy – a manifestation of immuno-deficiency. Pediatrics 1988; 81: 66–72.
10. Alain G, Carrier C, Beaumier L et al. In utero acute graph versus host disease in a neonate with severe combined immuno-deficiency. J Am Acad Dermatol 1993; 29: 862–5.
11. Conley ME, Beckwith JB, Mancer JFK. The spectrum of the Di-georg’s syndrome. J Pediatrics 1979; 94: 883–90.
12. Archer E, Chuan TY, Hong R. severe eczema in a patient with Di-georg’s syndrome. Cutis 1990; 45: 455–9.
13. Llorente CP, Amors JT, Frutur FJO. Cutaneous lesions in severe combined immuno-deficiency. Pediatr Dermatol 1991; 8: 314–21.
14. Leiner C. Erythroderma desquamative (universal dermatitis of children at the breast). Brt J Child Dis 1908; 5: 244–51.
15. Muller FB, Hausser I, Berg D et al. Genetic analysis of a severe case of Netherton syndrome and application for prenatal testing. Br J Dermatol 2002; 146: 495–9.
16. Chang SE, Choi JH, Kon JK. Congenital erythrodemic psoriasis. Br J Dermatol 1999; 140: 538–9.
17. Kumar S, Sehgal VN, Sharma RC. Common genodermatoses. Int J Dermatol 1996; 35: 685–94.
18. Wolff K, Komar M, Petzelbauer P. Clinical and hystopathological aspects of cutaneous mastocytosis. Leuk Res 2001; 25: 519–28.
2. Hoeger PH, Harper JI. Neonatal erythroderma: Differential diagnosis and management of red baby. Arch Dis Child 1998; 79: 186–91.
3. Sehgal VN, Srivastava G. Erythroderma/generalized exfoliative dermatitis in pediatric practice: an overview. Int J Dermatol 2006; 45: 831–9.
4. Sarkar R, Sharma RC, Koranne RV et al. Erythroderma in children – a clinico-etiological study. J Dermatol (Tokyo) 1999; 26: 507–11.
5. Pruskowsky A, Bodmer C, Fraitog S. Neonatal and infantile erythroderma – a retrospective study of 51 patients. Arch Dermatol 2000; 136: 875–80.
6. Sarkar R, Basu S, Sharma RC. Neonatal and infantile erythroderma. Arch Dermatol 2001; 137: 822–3.
7. Spraker MK. Differential diagnosis of neonatal erythroderma. In: Harper J, Orange A, Prose N (eds). Textbook of Pediatric Dermatology. 1st ed. London Blackwell Science Ltd, 2007; p. 92–103.
8. Dyke MP, Marlow N, Berry PJ. Omenn’s Disease. Arc Dis Child 1991; 66: 1247–8.
9. Glover MT, Atherton DJ, Levinsky RJ. Syndrome of erythroderma failure to thrive and
diarrhoea in infancy – a manifestation of immuno-deficiency. Pediatrics 1988; 81: 66–72.
10. Alain G, Carrier C, Beaumier L et al. In utero acute graph versus host disease in a neonate with severe combined immuno-deficiency. J Am Acad Dermatol 1993; 29: 862–5.
11. Conley ME, Beckwith JB, Mancer JFK. The spectrum of the Di-georg’s syndrome. J Pediatrics 1979; 94: 883–90.
12. Archer E, Chuan TY, Hong R. severe eczema in a patient with Di-georg’s syndrome. Cutis 1990; 45: 455–9.
13. Llorente CP, Amors JT, Frutur FJO. Cutaneous lesions in severe combined immuno-deficiency. Pediatr Dermatol 1991; 8: 314–21.
14. Leiner C. Erythroderma desquamative (universal dermatitis of children at the breast). Brt J Child Dis 1908; 5: 244–51.
15. Muller FB, Hausser I, Berg D et al. Genetic analysis of a severe case of Netherton syndrome and application for prenatal testing. Br J Dermatol 2002; 146: 495–9.
16. Chang SE, Choi JH, Kon JK. Congenital erythrodemic psoriasis. Br J Dermatol 1999; 140: 538–9.
17. Kumar S, Sehgal VN, Sharma RC. Common genodermatoses. Int J Dermatol 1996; 35: 685–94.
18. Wolff K, Komar M, Petzelbauer P. Clinical and hystopathological aspects of cutaneous mastocytosis. Leuk Res 2001; 25: 519–28.
Авторы
В.П.Адаскевич
УО Витебский государственный ордена Дружбы народов медицинский университет
УО Витебский государственный ордена Дружбы народов медицинский университет
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