Science

EPIDERMOLISE BOLHOSA SIMPLES PDF

July 11, 2019

16 mar. Diagnóstico Sintomas – 3 tipos de epidermólise bolhosa → Simples → Distrófica → Juncional Causas – incidência → 1 em 50, 3 jun. Epidermólise Bolhosa (EB) O que é? Doença rara e grave caracterizada pela intensa sensibilidade da pele, causando bolhas desencadeadas. Epidermólise bolhosa hereditária: aspectos clínicos e terapêuticos. Vanessa Lys Simas Yamakawa d) Simple clinical and histopathological examination.

Author: Shakanos Moogukus
Country: Lesotho
Language: English (Spanish)
Genre: Marketing
Published (Last): 26 February 2014
Pages: 335
PDF File Size: 14.10 Mb
ePub File Size: 8.10 Mb
ISBN: 482-4-44685-564-8
Downloads: 38904
Price: Free* [*Free Regsitration Required]
Uploader: Voodoole

Am J Clin Dermatol.

With respect to the treatment of lesions, blister puncturing to prevent dissemination and use of sterile dressings are recommended. Despite such a close similarity, monoclonal antibodies have been developed that are capable of marking each CK.

Portal Regional da BVS

Pulkkinen L, Uitto J. Correction of junctional epidermolysis bullosa by transplantation of genetically modified epidermal stem cells. The clinical spectrum of dystrophic epidermolysis bullosa. A systematic review of randomized epidermolies trials of treatments for inherited forms of epidermolysis bullosa.

Epidermólise Bolhosa by Leonor Sá Pinto on Prezi

Arch Dermatol Res ; No carcinoma de Merkel. Our aim was to develop a comprehensive instrument that is easy to use in the context of interventional studies. Staphylococcus aureus and Streptococcus pyogenes are often the etiological agents, although infections with gram-negative bacteria may also occur.

Along with poor nutritional status, there is decreased resistance to infections. Na bainha radicular interna encontram-se variantes da CQ 6. However, the mechanism and the risk and benefits of this aggressive treatment in the long term need to be better understood.

Related Articles  EL DIOS CRUCIFICADO MOLTMANN PDF

As genetic differentiation is not available in most Brazilian cities, subtypes are usually distinguished by immunological and ultra-structural analysis. Cases of JEB with congenital pyloric atresia and, more rarely, of other portions of the gastrointestinal tract, have been described in the literature.

It is believed that the slow healing observed in patients with Herlitz JEB is due to a deficiency of: The peak of incidence of SCC increases dramatically in the second and third decades of life.

Assessment of mobility, activities and pain in different subtypes of epidermolysis bullosa. However, the presence of scar tissue in patients with chronic Herlitz JEB cannot explain this phenomenon alone, because SCC that affect scar tissue are not usually as aggressive as those involving patients with RDEB, suggesting that other factors may be involved in its pathogenesis.

Acquired melanocytic naevus in childhood vulval pemphigoid. Mutations of CK 9, since it is found in the palmoplantar epidermis, are accompanied by a degeneration restricted to that area, typical of epidermolytic palmoplantar keratoderma; likewise, in this disease the mutations have been found at the beginning of segment 1 A. Am J Clin Dermatol ; 4: Information for all members: Curr Opin Ophthalmol ; Gastrointestinal complications of inherited epidermolysis bullosa: Medical management of epidermolysis bullosa: Patents with Herlitz JEB heal slowly, probably due to deficiency of laminin J Dermatol Sci ; Enamel hypoplasia, which facilitates the formation of cavities and tooth loss, is a pathognomonic characteristic of all types of JEB, while microstomia and ankyloglossia are typical of RDEB.

Related Articles  EXACT CONSTRAINT BLANDING PDF

Nutritional support plays a critical role in the resolution of wounds. They have a perforated surface, allowing the passage of exudate into the dressing If there is significant bleeding or exudate, the dressing will adhere Epidermollse layers Inert protection material, which allows the non-traumatic removal of the dressing Biosynthetic cellulose Dressing composed of cellulose, water, 0.

Mutation-based prenatal diagnosis of Herlitz junctional epidermolysis bullosa. In the last decade, several mutations were described in CK genes, which lead to structural changes in its molecule.

Due to their hydration capacity, they have a cooling effect and may help to relieve pain, itching and discomfort. In some patients with cryptogenic cirrhosis, which occurs without viral hepatitis, alcoholism or any other known cause, mutations have been described in CK 8 and Both can occur in childhood, causing scarring and progressive visual impairment, if not treated. Which type of genetic inheritance is observed in EBS? Support Center Support Center.

Which type of inheritance is observed in JEB? The information obtained in the last two decades on CK epider,olise brought countless advances in the understanding of various cutaneous diseases, thereby demonstrating the importance of laboratorial research and its subsequent application in daily practice.