2017, Number 3
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Rev Méd Electrón 2017; 39 (3)
Epidermolysis bullosa: butterfly skin. Apropos of a case
del Rosario MOC, Smith OY, González JAL, González DA, Arcis RA, Fernández LY
Language: Spanish
References: 18
Page: 552-560
PDF size: 543.74 Kb.
ABSTRACT
The epidermolysis bullosa includes a heterogeneous group of bullous skin and
mucous diseases of congenital and hereditary origin. Diagnosing them is not
difficult if the specialist has dermatologic experience, but their classification is
complex and it is necessary to take into account the clinical, genetic and
microscopic factors, and the laboratory assessment. The treatment of this disease
is also difficult and it is necessary to take certain measures to protect the patient,
avoid the onset of lesions and the complications derived from them. The treatment
of these lesions in a newborn is described. Prophylactic antibiotics were
administered and bandages were put on the lesions. All the cares and
recommendations to avoid rubbings and pressures on these lesions, and also the
high temperatures, are described. To develop the current term, 18 materials
(journals and pediatric books) were consulted. The reported case was the case of a
newborn with epidermolysis bullosa attended in the University Hospital “Dr. Mario
Muñoz Monroy” of Colon, Matanzas. It was demonstrated the low frequency and
rarity of this pathology for the specialists of the theme.
REFERENCES
1- McKenna K, Walsh M, Bingham E. Epidermolysis bullosa in Northern Ireland. Br j dermatol [Internet]. 1992 [citado 15 Sep 2015];127(4):318-21. Disponible en: http://onlinelibrary.wiley.com/doi/10.1111/j.1365-2133.1992.tb00448.x/full
2- Horn H, Tidman M. The clinical spectrum of dystrophic epidermolysis bullosa. Br j Dermatol [Internet]. 2002 [citado 15 Sep 2015];146(2):267-74. Disponible en: http://onlinelibrary.wiley.com/doi/10.1046/j.1365-2133.2002.04607.x/pdf
3- Chung Jin H, Uitto J. Epidermolysis bullosa with pyloric atresia. Dermatologic clinics [Internet]. 2010 [citado 28 May 2015];28(1):43-54. Disponible en: http://www.sciencedirect.com/science/article/pii/S0733863509000795
4- Sánchez Macias LR, García Retana PP, Viego Romero ME. Epidermólisis bullosa congénita (piel de cristal). Acta méd centro [Internet]. 2012 [citado 28 May 2015];6(4). Disponible en: http://www.medigraphic.com/pdfs/medicadelcentro/mec-2012/mec124n.pdf
5- Gupta R, Woodley DT, Chen M. Epidermolysis bullosa acquisita. Clinics in dermatology [Internet]. 2012 [citado 28 May 2015];30(1):60-9. Disponible en: http://www.sciencedirect.com/science/article/pii/S0738081X11000873
6- Intong LR, Murrell DF. Inherited epidermolysis bullosa: new diagnostic criteria and classification. Clinics in dermatology [Internet]. 2012 [citado 28 May 2015];30(1):70-7. Disponible en: http://www.sciencedirect.com/science/article/pii/S0738081X11000885
7- Fine JD, Eady RA, Bauer EA, et al. Revised classification system for inherited epidermolysis bullosa: Report of the Second International Consensus Meeting on diagnosis and classification of epidermolysis bullosa. AAD [Internet]. 2000 [citado 15 Sep 2015];42(6):1051-66. Disponible en: http://scholar.google.com.cu/scholar?q=Revised+classification+system+for+inherited+epidermolysis+bullosa%3A+report+of+the+second+international+consenses+meeting+on+diagnosis+and+classification+of+epidermolysis+bullosa&btnG=&hl=es&as_sdt=0%2C5#
8- Itoh M, Kiuru M, Cairo MS, et al. Generation of keratinocytes from normal and recessive dystrophic epidermolysis bullosa-induced pluripotent stem cells. Proceedings of the National Academy of Sciences [Internet]. 2011 [citado 28 May 2015];108(21):8797-802. Disponible en: http://www.pnas.org/content/108/21/8797.short
9- Pope E, Lara-Corrales I, Mellerio J, et al. A consensus approach to wound care in epidermolysis bullosa. JAAD [Internet]. 2012 [citado 28 May 2015];67(5):904-17. Disponible en: http://www.sciencedirect.com/science/article/pii/S0190962212001016
10- Sawamura D, Nakano H, Matsuzaki Y. Overview of epidermolysis bullosa. The Journal of dermatology [Internet]. 2010 [citado 28 May 2015];37(3):214-9. Disponible en: http://onlinelibrary.wiley.com/doi/10.1111/j.1346-8138.2009.00800.x/full
11- Sprecher E. Epidermolysis bullosa simplex. Dermatologic clinics [Internet]. 2010 [citado 28 May 2015];28(1):23-32. Disponible en: http://www.sciencedirect.com/science/article/pii/S0733863509000771
12- Schober Flores C. Epidermolysis bullosa: a nursing perspective. Dermatol nurs [Internet]. 1999 [citado 15 Sep 2015];11(4):243-8, 53-6. Disponible en: http://europepmc.org/abstract/med/10670355
13- Vargas A, Palomer L, Palisson F. Manifestaciones orales de la epidermólisis bulosa en el niño. Rev chil pediatr [Internet]. 2005 [citado 15 Sep 2015];76(6):612-6. Disponible en: http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0370-41062005000600009
14- Smith LT. Ultrastructural findings in epidermolysis bullosa. Arch Dermatol [Internet]. 1993 [citado 15 Sep 2015];129(12):1578-84. Disponible en: http://archderm.jamanetwork.com/article.aspx?articleid=555415
15- Hovnanian A, Christiano AM, Vitto J. The molecular genetics of dystrophic epidermolysis bullosa. Archi Dermatol [Internet]. 1993 [citado 15 Sep 2015];129(12):1566-70. Disponible en: http://archderm.jamanetwork.com/article.aspx?articleid=555397
16- Tolar J, Xia L, Riddle MJ, et al. Induced pluripotent stem cells from individuals with recessive dystrophic epidermolysis bullosa. Journal of Investigative Dermatology [Internet]. 2011 [citado 28 May 2015];131(4):848-56. Disponible en: http://www.sciencedirect.com/science/article/pii/S0022202X15352301
17- Uitto J, McGrath JA, Rodeck U, et al. Progress in epidermolysis bullosa research: toward treatment and cure. Journal of Investigative Dermatology [Internet]. 2010 [citado 28 May 2015];130(7):1778-84. Disponible en: http://encedirect.com/science/article/pii/S0022202X15348818
18- Wagner JE, Ishida Yamamoto A, McGrath JA, et al. Bone marrow transplantation for recessive dystrophic epidermolysis bullosa. New England Journal of Medicine [Internet]. 2010 [citado 28 May 2015];363(7):629-39. Disponible en: http://www.nejm.org/doi/full/10.1056/NEJMoa0910501