Linear IgA Dermatosis and Chronic Bullous Dermatosis of Childhood (Linear IgA Disease, linear IgA bullous dermatosis [LABD], Chronic Bullous Dermatosis of Childhood)
Are You Confident of the Diagnosis?
What you should be alert for in the history
Patients with pruritic (itchy) blisters should alert the physician. The disease onset can be in adulthood or in childhood, even in the neonate. The disease onset in childhood has been termed chronic bullous dermatosis of childhood, which is now considered to be the same disease as LABD in adulthood.
Characteristic findings on physical examination
The most useful finding is a group of blisters lining up in a circle, creating a “string of pearls” configuration (
A group of blisters forming a ring in this patient with LABD
Expected results of diagnostic studies
Lesional skin biopsy of LABD characteristically exhibits a sub-epidermal blister with prominent neutrophil infiltration. Direct immunofluorescence microscopy performed on a peri-lesional skin biopsy typically shows a linear deposition of IgA (
Immunofluorescence showing liner IgA along the basement membrane zone. (Courtesy of Bryan Anderson, MD)
Clinical differential diagnoses: Patients with pruritic blistering diseases can also develop dermatitis herpetiformis and bullous pemphigoid.
Histologic differential diagnoses: The histopathologic findings of subepidermal blister with prominent neutrophil infiltration can also be observed in dermatitis herpetiformis, epidermolysis bullosa acquisita, bullous lupus erythematosus and two partially characterized autoimmune blistering skin diseases: anti-p105 pemphigoid and anti-p200 pemphigoid. ELISA testing for autoantibodies present in linear IgA dermatosis is currently not available on a commercial basis.
Who is at Risk for Developing this Disease?
As a rare disease, LABD is observed in patients of all races and genders. Accurate epidemiologic data for LABD is currently not available. Many drug-induced cases have been reported. The drug-induced form of disease is commonly due to vancomycin. Other reported cases are apparently associated with other antibiotics, phenytoin, angiotensin-converting enzyme inhibitor, acetaminophen, carbamazepine, naproxen, and piroxicam.
A study has reported a significant association of HLA Cw7, B8, and DR3 with the disease.
What is the Cause of the Disease?
The disease is mediated by IgA class autoantibodies targeting one of the many skin epithelial basement membrane proteins named BP180 (type XVII collagen); its antigenic epitope is located in the upper/mid-lamina lucida level.
It is commonly hypothesized that the IgA autoantibodies bind to the target antigen in the lamina lucida, leading to complement activation, followed by chemoattraction of neutrophils into the target site. The subsequent release of enzymes by the reactive neutrophils may lead to the weakening of the binding structure of lamina lucida, resulting in clefting between the epidermis and dermis leading to the formation of a subepidermal blister. The pathogenesis of the IgA autoantibodies, ie, how the autoantibodies come about, however, is not understood at the present time.
Systemic Implications and Complications
It is now recognized that some inflammatory diseases (such as coeliac disease, inflammatory bowel disease, IgA nephropathy), internal malignancies (such as renal cell carcinoma, leukemia) and monoclonal gammopathy are associated with the onset of LABD. However, these associations randomly occur without any particular HLA pattern identified. Thus, physicians who care for patients suffering from LABD should perform a careful review of systems and order appropriate laboratory studies (CBC, urinalysis) or refer to appropriate specialists when indicated. A full physical examination by the patient's primary care physician is recommended.
MEDICAL TREATMENT FOR ADULT PATIENTS:
Topical: Topical corticosteroids may be used as an adjunct treatment for LABD.
Most patients affected by LABD require systemic treatment. The initial treatment regimen should be dapsone, with an average dose of 100mg per day. In some cases, a low dose (10 to 20mg per day) of systemic corticosteroids (prednisone) is also needed to control the disease. In case dapsone treatment results in intolerable side effects (such as peripheral neuropathy or a low red-cell count), it can be substituted with other sulfur-containing medication (such as trimethoprim/sulfamethoxazole).
The next treatment option would be mycophenolate mofetil. Other successful treatments reported in the literature include cyclosporin, colchicine, and intravenous immunoglobulin G (IVIG). If the patient fails to respond completely, rituximab (anti-B cell antibody) in combination with IVIG would be a good option.
MEDICAL TREATMENT FOR PEDIATRIC PATIENTS
In general the dose must be carefully adjusted according to the age or weight of the patients. Topical corticosteroids, if used, must be used for short-term only to avoid the skin thinning effect of corticosteroid on immature skin.
Dapsone should be initiated unless otherwise contraindicated. Colchicine should be tried if dapsone is not tolerated or if it is contraindicated (as in G6PD-deficiency or drug allergy). Other drugs from the sulfa group can be tried as well, such as sulfapyridine, trimethoprim/sulfamethoxazole. Rare reports of successful treatment with dicloxacillin provide yet another option. Erythromycin is somewhat effective, but sustained improvement has not been the outcome.
Systemic corticosteroids or other immunosuppressives (such as mycophenolate mofetil) should be used only if other medications failed in cases of generalized disease; these agents should be used with the full consent from the patients' pediatricians.
Rituximab, an antibody against a B-cell surface marker, CD20, is an option that should be used only if all other medications failed in cases of generalized disease.
SURGICAL TREATMENT: None available.
PHYSICAL MODALITIES: None available.
Optimal Therapeutic Approach for this Disease
Topical corticosteroids (mid to high potency) should be initiated. For adult patients, medium to high potency corticosteroid could be used. One good choice would be betamethasone diproprionate 0.05% cream twice daily. For pediatric patients, low-to-medium potency corticosteroid would be a better choice, such as mometasone furoate 0.1% cream twice daily. If the disease is not completely controlled, the addition of dapsone (50 to 100mg per day, adult dose) may be sufficient.
Stop any offending agents. Initial treatment option will be dapsone (50 to 100 mg per day, adult dose). Since the histologic finding of LABD is characteristic of neutrophil infiltration and dapsone has direct antagonistic effect on neutrophils, this is the first line of treatment. If dapsone treatment results in intolerable side effects, substitution with another sulfur-containing medication is appropriate, since other sulfur medications also possess antagonistic effects to neutrophils. One option is trimethoprim-sulfamethoxasole (Bactrim), double strength, twice daily. Sulfapyridine or sulfasalazine are other sulfa-containing medications that could be beneficial, but their availability in the United States is unreliable.
If dapsone or a sulfur-containing medication alone does not completely control the disease, the addition of low dose prednisone (10 to 20mg per day, adult dose) would be appropriate, as it provides an additional anti-inflammatory effect.
In case the combination of low-dose prednisone and dapsone (or other sulfur-containing drug) does not achieve complete control of the disease, the addition of an immunosuppressive agent (azathioprine or mycophenolate mofetil) should be considered. Azathioprine (100mg per day, adult dose) or mycophenolate mofetil (1g per day, adult dose) will be average initial doses for the additional regimen. These immunosuppressives provide direct countering effect to the immune system, for both B and T cells.
Rituximab, an antibody directly against B cells (CD20), is a new treatment, which, although expensive, may be available for those rare cases that are unresponsive to standard treatments (alone or in combination). Rituximab is probably best used in combination with IVIG. One such protocol for adult patients, proven to be useful in treating pemphigus vulgaris, is the following:
Initial courses: For the first two months: Rituximab 375mg/m2 body surface every week for the first three weeks, followed by IVIG 2 g/kg body weight for the fourth week, then this 4-week therapy will be repeated for a second month.
Maintenance courses: For the next 4 months: Rituximab 375mg/m2 body surface one dose per month and IVIG 2g/kg body weight one dose per month.
Other treatment options reported to be useful in only a small number of patients may be considered in individual cases, such as cyclosporine or colchicine.
Patients receiving only topical treatments should be monitored on a monthly basis initially. As the disease resolves, the frequency of patient visits can be reduced to every other month, and then to every 3 months. Physicians need to monitor for possible skin atrophy induced by the chronic use of topical steroids. Thus, the use of a high-potency steroid should be limited in duration and should be changed to medium- or low-potency steroids when clinically appropriate.
Patients receiving prednisone treatment should be monitored for common steroid side effects on a regular basis (at least every other month). The use of prednisone should be restricted to a minimal level for the shortest possible duration. Tapering the prednisone dose should be considered as the disease resolves.
Patients receiving immunosuppressive agents should be monitored for bone marrow suppression on a regular basis, at least every other month. An absolute lymphocyte count usually is the most sensitive parameter in assessing bone marrow suppression by these medications.
Patients receiving azathioprine or mycophenolate mofetil should be monitored for liver toxicity on a regular basis, at least every other month.
Since malignancies have been associated with the onset of LABD, a careful review of systems should be performed regularly in all patients, although thus far these cases were found in adult patients. No single malignancy is seen to be particularly prominent. If a symptom suggests a problem in a particular organ system, appropriate screening diagnostic studies should be requested to investigate the possibility of a malignancy, and referral to the appropriate specialist..
Unusual Clinical Scenarios to Consider in Patient Management
Even though initially chronic bullous dermatosis of childhood was recognized as a disease distinct from the adult form of LABD, it is now understood that these are the same disorder for these four reasons: 1) Both diseases manifest with itchy blisters that tend to form a “string of pearls” pattern; 2) Both diseases manifest histologically as sub-epidermal blister with predominantly neutrophil infiltration; 3) Both diseases are characterized by linear IgA deposition on the skin basement membrane and by circulating IgA autoantibodies that bind to the epidermal side of high salt-split human skin substrate; and 4) Both diseases are characterized by IgA autoantibodies that target the BP180 protein.
Even though association of LABD with internal malignancies is predominantly identified in adult patients with LABD, physicians should be alerted to this possibility when a pediatric patient affected by LABD presents with an unusual symptom or sign suggesting an internal malignancy.
What is the evidence?
Farrant, P, Darley, C, Carmichael, A. "Is erythromycin an effective treatment for chronic bullous disease of childhood? A national survey of members of the British Society for Paediatric Dermatology". Pediatr Dermatol. vol. 25. 2008. pp. 479-82.(By survey, among the 40 patients treated in a 2-year period, 5 patients received erythromycin as the first-line drug. Although three of these patients obtained initial improvement or complete resolution, only one of these patients had sustained benefits and the other two patients had their diseases relapsed in 4 to 12 weeks. Thus, erythromycin may be a good initial medication of choice, especially in a clinically supported case awaiting diagnostic test confirmation.)
Collier, PM, Wojnaroska, F, Welsh, K, McGuire, W, Black, MM. "Adult linear IgA disease and chronic bullous dermatosis of childhood: the association with human lymphocyte antigens Cw7, B8, DR3 and tumor necrosis factor influences disease expression". Br J Dermatol. vol. 141. 1999. pp. 867-75.(In an HLA study of 60 patients [26 had chronic bullous dermatosis of childhood; 34 had adult LABD] using lymphocyte microtoxicity assay, the disease was found to be significantly associated with HLA Cw7 (P=.001), B8 (P=.04), and DR3 (P=.014).
Schumann, H, Baetge, J, Tasanen, K, Wojnarowska, F, Schacke, H, Zillikens, D. "The shed ectodomain of collagen XVII/BP180 is targeted by autoantibodies in different blistering skin disease". Am J Pathol. vol. 156. 2000. pp. 85-95.(In adult LABD and chronic bullous dermatosis of childhood, serum IgA autoantibodies recognized the BP180 but targeted the soluble ectodomain more efficiently than the full-length protein of BP180.)
Zone, JJ, Taylor, TB, Kadunce, DP, Chorzelski, TP, Schachner, LA, Huff, JC. "IgA antibodies in chronic bullous disease of childhood react with 97 kDa basement membrane zone protein". J Invest Dermatol. vol. 106. 1996. pp. 1277-80.(In a study of 12 sera obtained from patients of chronic bullous dermatosis of childhood, 8 of these sera bound to the epidermal roof of high-salt-split skin substrate also reacted with a 97-kDa protein that co-migrated with a 97-kDa protein reacted by IgA autoantibodies from adult patients affected by LABD, strongly suggesting that the target antigens for both of these forms of disease are the same.)
Talhari, C, Mahnke, N, Ruzicka, T, Megahed, M. "Successful treatment of linear IgA disease with mycophenolate mofetil as a corticosteroid sparing agent". Clin Exp Dermatol. vol. 30. 2005. pp. 297-8.(Mycophenolate mofetil is an option for the treatment of LABD.)
Peterson, JD, Chan, LS. "Linear IgA dermatosis responsive to trimethoprim-sulfamethoxazole". Clin Exp Dermatol. vol. 32. 2007. pp. 756-8.(An adult patient who failed to respond completely to mycophenolate mofetil and systemic corticosteroid, and was not able to tolerate dapsone, was completely controlled by adding a dose of trimethoprim-sulfamethoxazole.)
Cummings, JE, Snyder, RR, Kelly, EB, Raimer, SS. "Drug-induced linear immunoglobulin A bullous dermatosis mimicking Stevens-Johnson syndrome: a case report". Cutis. vol. 79. 2007. pp. 203-7.(The drug-induced form of LABD can resemble Stevens-Johnson syndrome, thus,physician should be alerted to this possibility, as removal of the offending drug is essential for managing this form of disease.)
Coelho, S, Tellechea, O, Reis, JP, Mariano, A, Figueiredo, A. "Vancomycin-associated linear IgA bullous dermatosis mimicking toxic epidermal necrolysis". Int J Dermatol. vol. 45. 2006. pp. 995-6.(Vancomycin-induced LABD can resemble a life-threatening dermatosis toxic epidermal necrolysis and physicians should be alerted to this possibility and obtain appropriate diagnostic tests such as direct immunofluorescence microscopy to rule out this possibility.)
Zeharia, A, Hodak, E, Mukamel, M, Danziger, Y, Mimouni, M. "Successful treatment of chronic bullous dermatosis of childhood with colchicine". J Am Acad Dermatol. vol. 30. 1994. pp. 660-1.(Colchicine is an option to treat pediatric patients affected by LABD.)
Copyright © 2017, 2012 Decision Support in Medicine, LLC. All rights reserved.
No sponsor or advertiser has participated in, approved or paid for the content provided by Decision Support in Medicine LLC. The Licensed Content is the property of and copyrighted by DSM.
Next Article in Dermatology
Neurology Advisor Articles
- OCD in Duchenne Muscular Dystrophy Features Distinct Phenotype, Associated Symptoms
- History of Migraine Associated With Higher Risk for Cochlear Disorders
- Patent Foramen Ovale Closure for Stroke Prevention: Key Principles for Clinical Practice
- Vagus Nerve Stimulation in Pediatric Epilepsy: Weighing the Risks and Benefits
- A Model for Predicting Quality of Life Improvements After Deep Brain Stimulation
- Some Statins May Be Associated With Cognition, Memory Deficits
- Neuropathic Pain Treatments
- Cannabis for Multiple Sclerosis: Prescriber's Perspective
- New Monoclonal Antibody BAN2401 Reduces Amyloid Plaques, Improves Cognition in Alzheimer's
- Nonpharmacologic Interventions for Alzheimer's Have Greater Impact on Outcomes Than Currently Available Medications
- Apomorphine Infusions Improves Off Time Associated With Parkinson Disease
- FDA Grants Orphan Drug Status to Angelman Syndrome Treatment
- Treatment of New-Onset Epilepsy: AAN, AES Update Practice Guidelines
- Clinical, Radiologic Markers Predictive of Cortical Superficial Siderosis in ICH Identified
- Migraine Pain Location May Not Have Clinical Implications