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Epidermolysis bullosa

In medicine (dermatology) Epidermolysis bullosa (EB) is a rare genetic disease characterized by the presence of extremely fragile skin and recurrent blister formation, resulting from minor mechanical friction or trauma. This condition is not contagious. The condition was brought to public attention in the Channel 4 documentary The Boy Whose Skin Fell Off, chronicling the life and death of English sufferer Jonny Kennedy. more...

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Forms

There are three main forms of inherited EB. These different subtypes are defined by the depth of blister location within the skin layers, and the location of the dissolution of the skin.

EB Simplex (EBS) -- ABOVE the basement membrane

Blister formation of EB simplex is within the basal keratinocyte of the epidermis. Sometimes EB simplex is called epidermolytic. There are four subtypes of EBS:

  1. EBS - Weber-Cockayne (EBS-WC)
  2. EBS - Koebner (EBS-K)
  3. EBS - Dowling-Meara (EBS-DM) -- caused by missense mutation in KRT5 (E477K) or one of two missense mutations in KRT14 (R125C and R125H)
  4. EBS - Mottled Pigmentation (EBS-MP) - caused by one missense mutation in KRT5 (I161S) or by missense mutations in the plectin gene (Koss-Harnes et al., 1997;Koss-Harnes et al., 2002).

Junctional EB (JEB) -- THROUGH the basement membrane

Blister formation in Junctional EB is seen at the level of the lamina lucida within the basement membrane zone.

Dystrophic EB (DEB) -- UNDER the basement membrane

Dystrophic EB (DEB) forms which can lead to scarring occur in a deeper tissue level; the sub-lamina densa region(the beneath the lamina densa) within the upper dermis. The disease DEB is caused by genetic defects (or mutations) within the molecule type VII collagen (collagen VII). Collagen VII is a very large molecule (780 nm) that dimerizes to forms a semicircular looping structure: the anchoring fibril. Anchoring fibrils are thought to form a strucutral link between the epidermal basement membrane and the fibrillar collagens in the upper dermis.

Collagen VII is also present in the epithelial tissue of the esophagus, which leads to chronic scarring, webbing, and obstruction. Affected individuals are often severely malnourished due to trauma to the oral and esophageal mucosa and require feeding tubes for nutrition. They also suffer from iron-deficiency anemia of uncertain origin, which leads to chronic fatigue.

Open wounds on the skin heal slowly and are particularly susceptible to infection. Many individuals bathe in a bleach and water mixture to fight off these infections.

The chronic inflammation leads to errors in the DNA of the affected skin cells, which in turn causes squamous cell carcinoma (SCC). The majority of these patients die before the age of 30, either of SCC or complications related to DEB.

Epidemiology

An estimated 2 out of every 100,000 live births are affected with some type of EB. The disorder occurs in every racial and ethnic group throughout the world and affects both sexes equally.

Read more at Wikipedia.org


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Dilation of an esophageal stricture caused by epidermolysis bullosa - Esophagoscopy Clinic - Brief Article
From Ear, Nose & Throat Journal, 2/1/02 by Gregory N. Postma

A 27-year-old man with a history of epidermolysis bullosa came to the clinic complaining of progressive dysphagia. He had been unable to swallow solids or liquids for the previous 24 hours. Physical examination revealed the presence of fluid-filled blisters, scarring, and contractures over the dorsal surface of his hands (figure, A). Transnasal esophagoscopy detected an area of severe inflammation and circumferential sloughing of the mucosa in the middle portion of the esophagus, 24 cm from the nasal vestibule (figure, B). A narrow stricture 1 cm in length was seen just distal to the area of mucosal slough (figure, C).

In light of the significant risk that intubation poses in a patient with active epidermolysis bullosa, we elected to perform esophageal dilation in the clinic with Savary dilators (figure, D). Our technique for in-office dilation involves the direct visualization of the area of stricture with a transnasal esophagoscope. A Savary dilator guidewire is inserted through the instrument's biopsy port. Then the esophagoscope is removed, leaving the wire in place as it passes through the stricture and out the patient's nose. A Kelly clamp is used to reach into the patient's mouth and withdraw the wire transorally. Progressively larger Savary dilators are then advanced over the wire to dilate the stricture. Our patient tolerated the procedure easily and did not require sedation. At the 4-month follow-up, he was still eating without difficulty.

From the Center for Voice Disorders, Department of Otolaryngology, Wake Forest University Medical Center, Winston-Salem, N.C.; www.thevoicecenter.org

COPYRIGHT 2002 Medquest Communications, Inc.
COPYRIGHT 2002 Gale Group

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