Skip to main content
Top
Published in: Orphanet Journal of Rare Diseases 1/2019

Open Access 01-12-2019 | Mucous Membrane Pemphigoid | Research

Linear IgA bullous dermatosis in adults and children: a clinical and immunopathological study of 38 patients

Authors: Giovanni Genovese, Luigia Venegoni, Daniele Fanoni, Simona Muratori, Emilio Berti, Angelo Valerio Marzano

Published in: Orphanet Journal of Rare Diseases | Issue 1/2019

Login to get access

Abstract

Background

Linear IgA bullous dermatosis (LABD) is a rare autoimmune subepithelial vesiculobullous disease due to IgA autoantibodies directed against different antigens of the basement membrane zone (BMZ) of the skin and/or mucosae. It affects mainly preschool-aged children and adults, with only few studies on large series. The aim of this study was to assess possible differences between adults and children regarding clinical presentation, immunopathologic features, management and course of the disease.

Methods

A retrospective review of 38 LABD patients, followed-up from November 2006 to September 2018, was performed.

Results

Of 38 patients, 27 were adults and 11 children. Mean age at diagnosis was 5.4 years and 60.6 years in the pediatric and adult group, respectively. Considering both groups, limbs were the most commonly involved site (73.7%), followed by trunk (55.3%), head (36.8%) and buttocks (13.2%). Interestingly, head (p = 0.008), particularly perioral (p = 0.001), involvement, as well as “string of pearls” arrangement (p = 0.03), were more prevalent in children. Mucosal involvement was seen in 9 (23.7%) patients and was more frequent in children than adults (45.5% vs 14.8%, respectively, p = 0.09). Linear IgA deposits along the BMZ were observed in 30 patients (78.9%), while linear/granular IgA deposits in 8 patients (21.1%). Dapsone was the most commonly used drug (78.9%) and complete remission was achieved in most cases (81.6%).

Conclusions

Our epidemiological and clinicopathological findings relative to a large cohort of LABD patients are mostly consistent with the literature data. Interestingly, head, notably perioral, involvement and “string of pearls” arrangement occurred more frequently in the paediatric than adult group. The above clinical parameters may be regarded as diagnostic tools for LABD in children.
Appendix
Available only for authorised users
Literature
1.
go back to reference Fortuna G, Marinkovich MP. Linear immunoglobulin a bullous dermatosis. Clin Dermatol. 2012;30:38–50.CrossRef Fortuna G, Marinkovich MP. Linear immunoglobulin a bullous dermatosis. Clin Dermatol. 2012;30:38–50.CrossRef
2.
go back to reference Egan CA, Zone JJ. Linear IgA bullous dermatosis. Int J Dermatol. 1999;38:818–27.CrossRef Egan CA, Zone JJ. Linear IgA bullous dermatosis. Int J Dermatol. 1999;38:818–27.CrossRef
3.
go back to reference Ohata C, Ishii N, Koga H, Nakama T. A clinical and serological study of linear IgA bullous dermatosis without linear immunoglobulin deposition other than IgA at the basement membrane zone using direct immunofluorescence. Br J Dermatol. 2017;177:152–7.CrossRef Ohata C, Ishii N, Koga H, Nakama T. A clinical and serological study of linear IgA bullous dermatosis without linear immunoglobulin deposition other than IgA at the basement membrane zone using direct immunofluorescence. Br J Dermatol. 2017;177:152–7.CrossRef
4.
go back to reference Kong YL, Lim YL, Chandran NS. Retrospective study on autoimmune blistering disease in Paediatric patients. Pediatr Dermatol. 2015;32:845–52.CrossRef Kong YL, Lim YL, Chandran NS. Retrospective study on autoimmune blistering disease in Paediatric patients. Pediatr Dermatol. 2015;32:845–52.CrossRef
5.
go back to reference Jabłońska S, Chorzelski TP, Rosinska D, Maciejowska E. Linear IgA bullous dermatosis of childhood (chronic bullous dermatosis of childhood). Clin Dermatol. 1991;9:393–401.CrossRef Jabłońska S, Chorzelski TP, Rosinska D, Maciejowska E. Linear IgA bullous dermatosis of childhood (chronic bullous dermatosis of childhood). Clin Dermatol. 1991;9:393–401.CrossRef
6.
go back to reference Wojnarowska F, Marsden RA, Bhogal B, Black MM. Chronic bullous disease of childhood, childhood cicatricial pemphigoid, and linear IgA disease of adults. A comparative study demonstrating clinical and immunopathologic overlap. J Am Acad Dermatol. 1988;19:792–805.CrossRef Wojnarowska F, Marsden RA, Bhogal B, Black MM. Chronic bullous disease of childhood, childhood cicatricial pemphigoid, and linear IgA disease of adults. A comparative study demonstrating clinical and immunopathologic overlap. J Am Acad Dermatol. 1988;19:792–805.CrossRef
7.
go back to reference Kanwar AJ, Sandhu K, Handa S. Chronic bullous dermatosis of childhood in North India. Pediatr Dermatol. 2004;21:610–2.CrossRef Kanwar AJ, Sandhu K, Handa S. Chronic bullous dermatosis of childhood in North India. Pediatr Dermatol. 2004;21:610–2.CrossRef
8.
go back to reference Nanda A, Dvorak R, Al-Sabah H, Alsaleh QA. Linear IgA bullous disease of childhood: an experience from Kuwait. Pediatr Dermatol. 2006;23:443–7.CrossRef Nanda A, Dvorak R, Al-Sabah H, Alsaleh QA. Linear IgA bullous disease of childhood: an experience from Kuwait. Pediatr Dermatol. 2006;23:443–7.CrossRef
9.
go back to reference Kharfi M, Khaled A, Karaa A, Zaraa I, Fazaa B, Kamoun MR. Linear IgA bullous dermatosis: the more frequent bullous dermatosis of children. Dermatol Online J. 2010;16(2). Kharfi M, Khaled A, Karaa A, Zaraa I, Fazaa B, Kamoun MR. Linear IgA bullous dermatosis: the more frequent bullous dermatosis of children. Dermatol Online J. 2010;16(2).
10.
go back to reference Kenani N, Mebazaa A, Denguezli M, Ghariani N, Sriha B, Belajouza C, Nouira R. Childhood linear IgA bullous dermatosis in Tunisia. Pediatr Dermatol. 2009;26:28–33.CrossRef Kenani N, Mebazaa A, Denguezli M, Ghariani N, Sriha B, Belajouza C, Nouira R. Childhood linear IgA bullous dermatosis in Tunisia. Pediatr Dermatol. 2009;26:28–33.CrossRef
11.
go back to reference Bertram F, Brocker EB, Zillikens D, Schmidt E. Prospective analysis of the incidence of autoimmune bullous disorders in lower Franconia, Germany. J Dtsch Dermatol Ges. 2009;7:434–40.PubMed Bertram F, Brocker EB, Zillikens D, Schmidt E. Prospective analysis of the incidence of autoimmune bullous disorders in lower Franconia, Germany. J Dtsch Dermatol Ges. 2009;7:434–40.PubMed
12.
go back to reference Mulyowa GK, Jaeger G, Kabakyenga J, Bröcker EB, Zillikens D, Schmidt E. Autoimmune subepidermal blistering diseases in Uganda: correlation of autoantibody class with age of patients. Int J Dermatol. 2006;45:1047–52.CrossRef Mulyowa GK, Jaeger G, Kabakyenga J, Bröcker EB, Zillikens D, Schmidt E. Autoimmune subepidermal blistering diseases in Uganda: correlation of autoantibody class with age of patients. Int J Dermatol. 2006;45:1047–52.CrossRef
13.
go back to reference Kelly SE, Frith PA, Millard PR, Wojnarowska F, Black MM. A clinicopathological study of mucosal involvement in linear IgA disease. Br J Dermatol. 1988;119:161–70.CrossRef Kelly SE, Frith PA, Millard PR, Wojnarowska F, Black MM. A clinicopathological study of mucosal involvement in linear IgA disease. Br J Dermatol. 1988;119:161–70.CrossRef
14.
go back to reference Gottlieb J, Ingen-Housz-Oro S, Alexandre M, et al. Idiopathic linear IgA bullous dermatosis: prognostic factors based on a case series of 72 adults. Br J Dermatol. 2017;177:212–22.CrossRef Gottlieb J, Ingen-Housz-Oro S, Alexandre M, et al. Idiopathic linear IgA bullous dermatosis: prognostic factors based on a case series of 72 adults. Br J Dermatol. 2017;177:212–22.CrossRef
15.
go back to reference Garel B, Ingen-Housz-Oro S, Afriat D, et al. Drug-induced linear IgA bullous dermatosis: a French retrospective pharmacovigilance study of 69 cases. Br J Clin Pharmacol. 2019;85:570–9.CrossRef Garel B, Ingen-Housz-Oro S, Afriat D, et al. Drug-induced linear IgA bullous dermatosis: a French retrospective pharmacovigilance study of 69 cases. Br J Clin Pharmacol. 2019;85:570–9.CrossRef
16.
go back to reference Chanal J, Ingen-Housz-Oro S, Ortonne N, et al. Linear IgA bullous dermatosis: comparison between the drug-induced and spontaneous forms. Br J Dermatol. 2013;169:1041–8.CrossRef Chanal J, Ingen-Housz-Oro S, Ortonne N, et al. Linear IgA bullous dermatosis: comparison between the drug-induced and spontaneous forms. Br J Dermatol. 2013;169:1041–8.CrossRef
17.
go back to reference Fortuna G, Salas-Alanis JC, Guidetti E, Marinkovich MP. A critical reappraisal of the current data on drug-induced linear immunoglobulin a bullous dermatosis: a real and separate nosological entity? J Am Acad Dermatol. 2012;66:988–94.CrossRef Fortuna G, Salas-Alanis JC, Guidetti E, Marinkovich MP. A critical reappraisal of the current data on drug-induced linear immunoglobulin a bullous dermatosis: a real and separate nosological entity? J Am Acad Dermatol. 2012;66:988–94.CrossRef
18.
go back to reference Fuligni A, Di Blasi A, Borgogni L, Pimpinelli N, Moretti S, Fabbri P. A peculiar case of linear IgA bullous dermatosis. Arch Dermatol. 1991;127:126–7.CrossRef Fuligni A, Di Blasi A, Borgogni L, Pimpinelli N, Moretti S, Fabbri P. A peculiar case of linear IgA bullous dermatosis. Arch Dermatol. 1991;127:126–7.CrossRef
19.
go back to reference Zambruno G, Manca V, Kanitakis J, Cozzani E, Nicolas JF, Giannetti A. Linear IgA bullous dermatosis with autoantibodies to a 290 kd antigen of anchoring fibrils. J Am Acad Dermatol. 1994;31:884–8.CrossRef Zambruno G, Manca V, Kanitakis J, Cozzani E, Nicolas JF, Giannetti A. Linear IgA bullous dermatosis with autoantibodies to a 290 kd antigen of anchoring fibrils. J Am Acad Dermatol. 1994;31:884–8.CrossRef
20.
go back to reference Zambruno G, Kanitakis J. Linear IgA dermatosis with IgA antibodies to type VII collagen. Br J Dermatol. 1996;135:1004–5.CrossRef Zambruno G, Kanitakis J. Linear IgA dermatosis with IgA antibodies to type VII collagen. Br J Dermatol. 1996;135:1004–5.CrossRef
21.
go back to reference Pellicano R, Lomuto M, Cozzani E, Iannantuono M, De Simone C. Linear IgA bullous dermatosis after contact with sodium hypochlorite. Dermatology. 1997;194:284–6.CrossRef Pellicano R, Lomuto M, Cozzani E, Iannantuono M, De Simone C. Linear IgA bullous dermatosis after contact with sodium hypochlorite. Dermatology. 1997;194:284–6.CrossRef
22.
go back to reference De Simone C, Guerriero C, Pellicano R. Linear IgA disease and ulcerative colitis. Eur J Dermatol. 1998;8:48–50.PubMed De Simone C, Guerriero C, Pellicano R. Linear IgA disease and ulcerative colitis. Eur J Dermatol. 1998;8:48–50.PubMed
23.
go back to reference Viglizzo G, Cozzani E, Nozza P, Occella C, Parodi A. A case of linear IgA disease in a child with IgA and IgG circulating antibodies directed to BPAg2. Int J Dermatol. 2007;46:1302–4.CrossRef Viglizzo G, Cozzani E, Nozza P, Occella C, Parodi A. A case of linear IgA disease in a child with IgA and IgG circulating antibodies directed to BPAg2. Int J Dermatol. 2007;46:1302–4.CrossRef
24.
go back to reference Marzano AV, Ramoni S, Spinelli D, Alessi E, Berti E. Refractory linear IgA bullous dermatosis successfully treated with mycophenolate sodium. J Dermatolog Treat. 2008;19:364–7.CrossRef Marzano AV, Ramoni S, Spinelli D, Alessi E, Berti E. Refractory linear IgA bullous dermatosis successfully treated with mycophenolate sodium. J Dermatolog Treat. 2008;19:364–7.CrossRef
25.
go back to reference Antiga E, Bellandi S, Bianchi B, et al. A further case of subacute prurigo-like linear IgA bullous dermatosis: growing evidence of a new subset. Int J Dermatol. 2012;51:1500–1.CrossRef Antiga E, Bellandi S, Bianchi B, et al. A further case of subacute prurigo-like linear IgA bullous dermatosis: growing evidence of a new subset. Int J Dermatol. 2012;51:1500–1.CrossRef
26.
go back to reference Paloni G, Shardlow A, Maschio M, Berti I, Taddio A, Ventura A. A child with bullous skin lesions. Linear IgA dermatosis. JAMA Pediatr. 2013;167:975–6.CrossRef Paloni G, Shardlow A, Maschio M, Berti I, Taddio A, Ventura A. A child with bullous skin lesions. Linear IgA dermatosis. JAMA Pediatr. 2013;167:975–6.CrossRef
27.
go back to reference Romani L, Diociaiuti A, D'Argenio P, et al. A case of neonatal linear IgA bullous dermatosis with severe eye involvement. Acta Derm Venereol. 2015;95:1015–7.CrossRef Romani L, Diociaiuti A, D'Argenio P, et al. A case of neonatal linear IgA bullous dermatosis with severe eye involvement. Acta Derm Venereol. 2015;95:1015–7.CrossRef
28.
go back to reference Diociaiuti A, Zambruno G, Diomedi Camassei F, et al. IgA tracheobronchial deposits underlie respiratory compromise in neonatal linear IgA bullous dermatosis. J Eur Acad Dermatol Venereol. 2017;31:e333–5.CrossRef Diociaiuti A, Zambruno G, Diomedi Camassei F, et al. IgA tracheobronchial deposits underlie respiratory compromise in neonatal linear IgA bullous dermatosis. J Eur Acad Dermatol Venereol. 2017;31:e333–5.CrossRef
29.
go back to reference Gatto A, Guerriero C, Moretta G, et al. Linear IgA bullous dermatosis in a two-year-old child: possible association with aspirin. Eur J Dermatol. 2017;27:417–8.PubMed Gatto A, Guerriero C, Moretta G, et al. Linear IgA bullous dermatosis in a two-year-old child: possible association with aspirin. Eur J Dermatol. 2017;27:417–8.PubMed
30.
go back to reference Leonard JN, Haffenden GP, Ring NP, et al. Linear IgA disease in adults. Br J Dermatol. 1982;107:301–16.CrossRef Leonard JN, Haffenden GP, Ring NP, et al. Linear IgA disease in adults. Br J Dermatol. 1982;107:301–16.CrossRef
31.
go back to reference Chan LS, Ahmed AR, Anhalt GJ, et al. The first international consensus on mucous membrane pemphigoid: definition, diagnostic criteria, pathogenic factors, medical treatment, and prognostic indicators. Arch Dermatol. 2002;138:370–9. Chan LS, Ahmed AR, Anhalt GJ, et al. The first international consensus on mucous membrane pemphigoid: definition, diagnostic criteria, pathogenic factors, medical treatment, and prognostic indicators. Arch Dermatol. 2002;138:370–9.
32.
go back to reference Naranjo CA, Busto U, Sellers EM, et al. A method for estimating the probability of adverse drug reactions. Clin Pharmacol Ther. 1981;30:239–45.CrossRef Naranjo CA, Busto U, Sellers EM, et al. A method for estimating the probability of adverse drug reactions. Clin Pharmacol Ther. 1981;30:239–45.CrossRef
33.
go back to reference Horiguchi Y, Ikoma A, Sakai R, Masatsugu A, Ohta M, Hashimoto T. Linear IgA dermatosis: report of an infantile case and analysis of 213 cases in Japan. J Dermatol. 2008;35:737–43.CrossRef Horiguchi Y, Ikoma A, Sakai R, Masatsugu A, Ohta M, Hashimoto T. Linear IgA dermatosis: report of an infantile case and analysis of 213 cases in Japan. J Dermatol. 2008;35:737–43.CrossRef
34.
go back to reference Lings K, Bygum A. Linear IgA bullous dermatosis: a retrospective study of 23 patients in Denmark. Acta Derm Venereol. 2015;95:466–71.CrossRef Lings K, Bygum A. Linear IgA bullous dermatosis: a retrospective study of 23 patients in Denmark. Acta Derm Venereol. 2015;95:466–71.CrossRef
35.
go back to reference Shipman AR, Reddy H, Wojnarowska F. Association between the subepidermal autoimmune blistering diseases linear IgA disease and the pemphigoid group and inflammatory bowel disease: two case reports and literature review. Clin Exp Dermatol. 2012;37:461–8.CrossRef Shipman AR, Reddy H, Wojnarowska F. Association between the subepidermal autoimmune blistering diseases linear IgA disease and the pemphigoid group and inflammatory bowel disease: two case reports and literature review. Clin Exp Dermatol. 2012;37:461–8.CrossRef
36.
go back to reference Walker SL, Banerjee P, Harland CC, Black MM. Remission of linear IgA disease associated with ulcerative colitis following panproctocolectomy. Br J Dermatol. 2000;143:1341–2.CrossRef Walker SL, Banerjee P, Harland CC, Black MM. Remission of linear IgA disease associated with ulcerative colitis following panproctocolectomy. Br J Dermatol. 2000;143:1341–2.CrossRef
37.
go back to reference Paige DG, Leonard JN, Wojnarowska F, Fry L. Linear IgA disease and ulcerative colitis. Br J Dermatol. 1997;136:779–82.CrossRef Paige DG, Leonard JN, Wojnarowska F, Fry L. Linear IgA disease and ulcerative colitis. Br J Dermatol. 1997;136:779–82.CrossRef
38.
go back to reference Trallori G, Palli D, Saieva C, et al. A population-based study of inflammatory bowel disease in Florence over 15 years (1978–92). Scand J Gastroenterol. 1996;31:892–9.CrossRef Trallori G, Palli D, Saieva C, et al. A population-based study of inflammatory bowel disease in Florence over 15 years (1978–92). Scand J Gastroenterol. 1996;31:892–9.CrossRef
39.
go back to reference Kartan S, Shi VY, Clark AK, Chan LS. Paraneoplastic pemphigus and autoimmune blistering diseases associated with neoplasm: characteristics, diagnosis, associated neoplasms, proposed pathogenesis, treatment. Am J Clin Dermatol. 2017;18:105–26.CrossRef Kartan S, Shi VY, Clark AK, Chan LS. Paraneoplastic pemphigus and autoimmune blistering diseases associated with neoplasm: characteristics, diagnosis, associated neoplasms, proposed pathogenesis, treatment. Am J Clin Dermatol. 2017;18:105–26.CrossRef
40.
go back to reference Willsteed E, Bhogal BS, Black MM, McKee P, Wojnarowska F. Use of 1M NaCl split skin in the indirect immunofluorescence of the linear IgA bullous dermatoses. J Cutan Pathol. 1990;17:144–8.CrossRef Willsteed E, Bhogal BS, Black MM, McKee P, Wojnarowska F. Use of 1M NaCl split skin in the indirect immunofluorescence of the linear IgA bullous dermatoses. J Cutan Pathol. 1990;17:144–8.CrossRef
41.
go back to reference Lally A, Chamberlain A, Allen J, Dean D, Wojnarowska F. Dermal-binding linear IgA disease: an uncommon subset of a rare immunobullous disease. Clin Exp Dermatol. 2007;32:493–8.CrossRef Lally A, Chamberlain A, Allen J, Dean D, Wojnarowska F. Dermal-binding linear IgA disease: an uncommon subset of a rare immunobullous disease. Clin Exp Dermatol. 2007;32:493–8.CrossRef
42.
go back to reference Tsuchisaka A, Ohara K, Ishii N, et al. Type VII collagen is the major autoantigen for sublamina densa-type linear IgA bullous dermatosis. J Invest Dermatol. 2015;135:626–9.CrossRef Tsuchisaka A, Ohara K, Ishii N, et al. Type VII collagen is the major autoantigen for sublamina densa-type linear IgA bullous dermatosis. J Invest Dermatol. 2015;135:626–9.CrossRef
43.
go back to reference Vodegel RM, de Jong MC, Pas HH, Jonkman MF. IgA-mediated epidermolysis bullosa acquisita: two cases and review of the literature. J Am Acad Dermatol. 2002;47:919–25.CrossRef Vodegel RM, de Jong MC, Pas HH, Jonkman MF. IgA-mediated epidermolysis bullosa acquisita: two cases and review of the literature. J Am Acad Dermatol. 2002;47:919–25.CrossRef
44.
go back to reference Koga H, Prost-Squarcioni C, Iwata H, Jonkman MF, Ludwig RJ, Bieber K. Epidermolysis bullosa Acquisita: the 2019 update. Front Med (Lausanne). 2019;5:362.CrossRef Koga H, Prost-Squarcioni C, Iwata H, Jonkman MF, Ludwig RJ, Bieber K. Epidermolysis bullosa Acquisita: the 2019 update. Front Med (Lausanne). 2019;5:362.CrossRef
45.
go back to reference Antiga E, Caproni M, Fabbri P. Linear immunoglobulin a bullous dermatosis: need for an agreement on diagnostic criteria. Dermatology. 2013;226:329–32.CrossRef Antiga E, Caproni M, Fabbri P. Linear immunoglobulin a bullous dermatosis: need for an agreement on diagnostic criteria. Dermatology. 2013;226:329–32.CrossRef
46.
go back to reference Di Zenzo G, Carrozzo M, Chan LS. Urban legend series: mucous membrane pemphigoid. Oral Dis. 2014;20:35–54.CrossRef Di Zenzo G, Carrozzo M, Chan LS. Urban legend series: mucous membrane pemphigoid. Oral Dis. 2014;20:35–54.CrossRef
Metadata
Title
Linear IgA bullous dermatosis in adults and children: a clinical and immunopathological study of 38 patients
Authors
Giovanni Genovese
Luigia Venegoni
Daniele Fanoni
Simona Muratori
Emilio Berti
Angelo Valerio Marzano
Publication date
01-12-2019
Publisher
BioMed Central
Published in
Orphanet Journal of Rare Diseases / Issue 1/2019
Electronic ISSN: 1750-1172
DOI
https://doi.org/10.1186/s13023-019-1089-2

Other articles of this Issue 1/2019

Orphanet Journal of Rare Diseases 1/2019 Go to the issue