▶Epidermolysis bullosa (EB) is a group of rare genetic skin disorders characterized by fragile skin and the formation of vesicles or bullae in response to mild frictional trauma.
▶Occurs in approximately 1 per 50,000 births.
▶Genders affected equally.
▶Classified into 3 general categories, based on the level of the cleavage plane within the dermal-epidermal junction
■Epidermolysis bullosa simplex (EBS)
– Autosomal dominant
– Due to defects in keratin genes K5 or K14
– Three major forms: localized, generalized intermediate, and generalized severe
– Also, EBS with muscular dystrophy (autosomal recessive; caused by mutation in plectin) and some rarer forms due to mutations in transglutaminase 5, plakophilin-1, desmoplakin, and plakoglobin
■Junctional EB (JEB)
– Autosomal recessive
– Due to defects in
•Laminin 332 (formerly laminin 5) (Herlitz type; JEB, generalized severe)
•Integrin α6ß4 (JEB with pyloric atresia)
•Collagen XVII (non-Herlitz type; JEB, generalized intermediate)
■Dystrophic EB (DEB)
– Autosomal dominant and recessive forms
– Due to defects in collagen VII
▶EBS
■EBS, localized (Weber-Cockayne type)
– Blisters primarily on the hand s and feet (Figure 83.1)
– May not present until adolescence or early adulthood in some patients
– Hyperhidrosis common
■EBS, generalized intermediate (Koebner type)
– Generalized blisters from birth or during infancy, especially on the arms and legs
– Mild mucosal involvement
– Occasional nail dystrophy
■EBS, generalized severe (Dowling-Meara type)
– Vesicles arranged in a herpetiform pattern.
– Blisters may be large during infancy, with significant oral mucosal involvement.
– Blistering tends to become milder with age.
■EBS with muscular dystrophy
– Resembles mild EBS.
■Muscular dystrophy may develop anytime between infancy and third decade.
▶JEB
■JEB, generalized severe (Herlitz type)
– 50% of affected children die in infancy, usually from sepsis, dehydration, or respiratory complications.
– Lesions are typically seen at birth or soon after (Figure 83.2).
– Blisters occur anywhere on the body, including mucous membranes.
– Granulation tissue in perioral area is common.
– Laryngeal involvement may be present, with hoarseness.
– Growth retardation and anemia are common.
– Nail dystrophy or anonychia often are present.
■JEB with pyloric atresia (Figure 83.3)
– Pyloric atresia and genitourinary anomalies are possible.
– Prognosis is poor.
■JEB, generalized intermediate (non-Herlitz type)
– Similar to Herlitz type but milder.
– Mucosal involvement is less severe.
▶DEB
■Dominant DEB
– Blistering most prominent on distal extremities, elbows, and knees.
– Milia are common (Figure 83.4).
– Scarring is present at prior blister sites.
– Nail dystrophy is common.
■Recessive DEB
– Blisters are noted at birth and involve the skin and mucous membranes.
– Widespread scarring is present.
– Mitten deformities of hand s and feet develop with digital fusion (Figure 83.5).
– Teeth often are carious; delayed eruption may be noted.
– Microstomia develops from scarring.
– Other complications include difficulty swallowing (esophageal scarring), chronic anemia, growth failure, conjunctival scarring, and predisposition to squamous cell carcinoma.
Look-alikes
Disorder | Differentiating Features |
•Blisters may be present soon after birth, similar to EB. •Thickened areas of skin with ridging often present during infancy or develop with time. •Eventuates into an ichthyosis disorder (epidermolytic hyperkeratosis), with less propensity toward blistering. | |
•Small vesicles occur in clusters. •Blisters are arranged in a linear or whorled pattern, along Blaschko lines. •Subsequent to blister stage, skin lesions appear verrucous or hyperpigmented. •Most patients are female (X-linked dominant). •Blisters not trauma-induced. | |
•Does not usually present as a recurrent or chronic condition. •Involvement more focal. •Mucous membranes not involved. •Blisters rupture easily, leaving superficial erosions with peripheral collarettes of scale. •Blisters not trauma-induced. | |
Herpes simplex virus infection | •Most often clustered vesicles and erosions with an erythematous surround. •Usually more focal. •Blisters not trauma-induced. |
•Urticarial plaques present in addition to tense blisters. •Blisters not trauma-induced. •Pruritus common with early lesions. •Direct fluorescence and immunoblotting studies will help confirm diagnosis. | |
•Usually presents as tiny vesicles and erosions. •Most often clustered on elbows, knees, shoulders, sacrum, and buttocks. •Blisters not trauma-induced. •Pruritus is intense. •May be associated with gluten sensitivity. | |
Erythema multiforme major | •Typical target lesions may be present. •Only occasionally bullous, and bullae are not trauma-induced. •Oral mucous membrane erosions common. •Palms and soles usually involved. •History of herpes simplex virus infection or drug ingestion may be present. |
•Acquired autoimmune blistering disease, not genetic. •Direct fluorescence and immunoblotting studies will help confirm diagnosis. | |
•Acquired autoimmune blistering disorder, not genetic. •“Cluster of jewels” pattern (annular grouping of bullae) often noted. •Blisters not trauma-induced. •Mucosal involvement not as extensive as in EB. |
▶Genetic testing (mutation analysis) is recommended to confirm the diagnosis and aid in prognosis and decision-making.
▶Skin biopsy for immunomapping may provide for more prompt diagnosis, when available.
▶Electron microscopy may be helpful when genetic testing or immunomapping is not available or does not provide conclusive results, but this is rarely used in the current era.
▶Prenatal genetic testing is possible and should be considered when applicable.
▶Treatment is palliative and supportive.
▶Avoidance of trauma, treatment of infections, pain control, and nutritional counseling are all vital.
▶Bullae may be drained with sterile needle and syringe for pain control.
▶Antibiotic ointment and protective dressings can be applied to areas of open or blistered skin to promote healing and prevent secondary infection.
▶Patient/family education, psychologic support, and referral to support group organizations are important.
Treating Associated Conditions
▶Multidisciplinary treatment teams are important to decrease morbidities associated with EB.
▶Care teams may include representation from primary care/pediatrics, dermatology, nursing, plastic surgery, ophthalmology, gastroenterology, general surgery, hematology, dentistry, genetics, and nutrition.
▶Growth failure is treated with aggressive nutritional rehabilitation; gastrostomy tube placement may be required for infants with severe forms of EB.
▶Esophageal involvement with dysphagia may require dietary modifications or dilatation procedures.
▶Mitten deformities of the hand require physical therapy and surgical intervention (degloving procedures).
▶Prognosis depends on the subtype of EB.
▶Children with most forms of EBS, non-Herlitz JEB, and dominant DEB tend to have a fairly good prognosis.
▶EBS, generalized severe (Dowling-Meara) subtype, may be severe during infancy and is occasionally fatal.
▶Herlitz JEB and JEB with pyloric atresia have a poor prognosis.
▶Patients with recessive DEB have a chronic course marked by complications and diminished quality of life. Squamous cell carcinoma, if it occurs, is usually rapidly progressive and invasive, leading to death in most of these patients.
▶Patients with possible EB should be referred to an experienced dermatologist for confirmation of the diagnosis and coordination of multidisciplinary care.
▶Because of the increased risk of cutaneous squamous cell carcinoma, any suspicious lesion in patients with recessive DEB should be biopsied.
▶American Academy of Dermatology: Epidermolysis bullosa: overview.
https://www.aad.org/public/diseases/a-z/epidermolysis-bullosa-overview
▶Dystrophic Epidermolysis Bullosa Research Association (debra) of America: Provides information, support, and resources for patients who have epidermolysis bullosa and their families.
▶Dystrophic Epidermolysis Bullosa Research Association (debra) UK: Located in the United Kingdom, this organization provides information for patients who have epidermolysis bullosa and their families.
▶Epidermolysis Bullosa Medical Research Foundation: Dedicated to supporting research in EB. Provides information for patients and families.