626 results match your criteria Linear IgA Dermatosis


Neonatal Autoimmune Subepidermal IgG/IgA Blistering Disease With Severe Laryngeal and Esophageal Involvement: A Report of a Case and Review of the Literature.

Am J Dermatopathol 2020 Jun 15. Epub 2020 Jun 15.

Department of Dermatology, Rambam Health Care Campus, Haifa, Israel.

Neonatal autoimmune subepidermal blistering disease is rare. Mucosal involvement is more common in neonatal linear immunoglobulin A (IgA) bullous dermatosis. We describe a neonate with subepidermal cutaneous blistering disease with severe laryngeal and esophageal involvement leading to acute respiratory distress. Read More

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http://dx.doi.org/10.1097/DAD.0000000000001700DOI Listing

Linear IgA Bullous Dermatosis.

N Engl J Med 2020 Jun;382(23):2248

Hospital Universitario 12 de Octubre, Madrid, Spain

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http://dx.doi.org/10.1056/NEJMicm1913412DOI Listing

IgA pemphigus and linear IgA bullous dermatosis in a patient with ulcerative colitis.

Australas J Dermatol 2020 May 17. Epub 2020 May 17.

Division of Dermatology, Department of Medicine, University of Louisville, Louisville, Kentucky, USA.

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http://dx.doi.org/10.1111/ajd.13341DOI Listing

Bullous lesions in a young adolescent postrenal transplant.

Saudi J Kidney Dis Transpl 2020 Mar-Apr;31(2):553-555

Division of Pediatric Nephrology, Sheikh Khalifa Medical City, Abu Dhabi, United Arab Emirates.

Kidney transplant recipients frequently suffer from skin infections and malignancies. New dermatosis can appear after transplantation. Although children are maintained on varying degrees of chronic immunosuppression, there is still a possibility of autoimmune blistering skin conditions, which can pose a diagnostic challenge in terms of clinical presentation. Read More

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http://dx.doi.org/10.4103/1319-2442.284037DOI Listing

Transient and zosteriform vancomycin-induced linear IgA bullous dermatosis in a patient undergoing haemodialysis: drug-mediated IgA immunoreactivity against type VII collagen.

Eur J Dermatol 2020 Apr 16. Epub 2020 Apr 16.

Department of Dermatology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama,, Dermatology Division, Fukushima Rosai Hospital, Iwaki, Japan.

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http://dx.doi.org/10.1684/ejd.2020.3729DOI Listing

A Case of Drug-induced Linear IgA Bullous Dermatosis.

Cureus 2020 Mar 4;12(3):e7175. Epub 2020 Mar 4.

Internal Medicine, Marshall University, Huntington, USA.

Linear immunoglobulin A (IgA) bullous dermatosis (LABD) presents as a rare autoimmune disease that can either occur spontaneously or induced by certain drugs, the most common of which is vancomycin. LABD is a subepidermal blistering disease that is diagnosed by detecting linear IgA bands along the basement membrane. We present a case of a 59-year-old man with worsening blistering skin rash who was treated with vancomycin and piperacillin-tazobactam for pneumonia. Read More

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http://dx.doi.org/10.7759/cureus.7175DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7117611PMC

A case of concurrent intercellular IgA dermatosis and linear IgA/IgG bullous dermatosis.

Australas J Dermatol 2020 Mar 1. Epub 2020 Mar 1.

Department of Dermatology, Osaka City University Graduate School of Medicine, Osaka, Japan.

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http://dx.doi.org/10.1111/ajd.13264DOI Listing

Autoantibody Profile of a Cohort of 54 Italian Patients with Linear IgA Bullous Dermatosis: LAD-1 Denoted as a Major Auto-antigen of the Lamina Lucida Subtype.

Acta Derm Venereol 2020 02 29;100(4):adv00070. Epub 2020 Feb 29.

Section of Dermatology, Department of Health Sciences (Di.S.Sal.), University of Genoa, 16132 Genoa, Italy.

Linear IgA bullous dermatosis (LABD) is characterized by presence of multiple IgA autoantibodies, and a comparatively lesser number of IgG antibodies, directed against different hemidesmosomal antigens. The main autoantigens are LAD-1, LABD-97, BP180 and BP230, type VII collagen and laminin 332. We retrospectively studied the serology of 54 Italian patients with LABD using enzyme-linked immunosorbent assay (ELISA), immunoblotting assay, and indirect immunofluorescence on monkey oesophagus and salt-split skin. Read More

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http://dx.doi.org/10.2340/00015555-3415DOI Listing
February 2020

Successful treatment of a case of idiopathic linear IgA bullous dermatosis with oral sulfasalazine.

Dermatol Ther 2020 Mar 14;33(2):e13210. Epub 2020 Jan 14.

Department of Dermatology, Affiliated Hangzhou Third Hospital, Anhui Medical University, Hangzhou, China.

Linear IgA bullous dermatosis (LABD) is a rare acquired autoimmune chronic vesiculobullous dermatosis affecting primarily young children and older adults. We report a 17-year-old Chinese boy with a 2-month history of intense itching erythema or tense vesicles on healthy skin or on an erythematous base, with parts of lesions arising a characteristic "cluster of jewels" pattern. With the characteristics of vesicles or blisters on the skin, subepidermal blisters with neutrophilic infiltrate on histology, and linear IgA deposits on the basement membrane zone and absence of other immunoglobulins on direct immunofluorescence, LABD was dignosized. Read More

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http://dx.doi.org/10.1111/dth.13210DOI Listing

Image Gallery: Onychomadesis in linear IgA bullous dermatosis.

Br J Dermatol 2020 May 22;182(5):e160. Epub 2019 Dec 22.

Shandong Provincial Hospital for Skin Diseases, Shandong First Medical University, 27397 Jingshi Road, Shandong 250022, China.

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http://dx.doi.org/10.1111/bjd.18744DOI Listing

Vancomycin-induced linear Immunoglobulin A bullous dermatosis.

BMJ Case Rep 2019 Dec 9;12(12). Epub 2019 Dec 9.

Internal Medicine, University of Iowa Hospitals and Clinics, Iowa City, Iowa, USA.

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http://dx.doi.org/10.1136/bcr-2019-233281DOI Listing
December 2019
5 Reads

Linear IgA bullous dermatosis with laryngeal involvement.

Acta Otorrinolaringol Esp 2020 May - Jun;71(3):190-192. Epub 2019 Nov 25.

Servicio de Otorrinolaringología, Hospital Universitario Miguel Servet, Zaragoza, España.

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http://dx.doi.org/10.1016/j.otorri.2019.05.006DOI Listing
November 2019

Linear IgA dermatosis of the childhood-Report of an amoxicillin-induced case.

Dermatol Ther 2020 01 4;33(1):e13173. Epub 2019 Dec 4.

Institute of Pathology, School of Medicine, University of Belgrade, Belgrade, Serbia.

Linear IgA dermatosis (LAD) is a rare autoimmune disorder in children. A 9-year-old boy was presented with blisters on the intact skin (face, body, arms, hands, soles, perigenital and perianal area) after amoxicillin treatment. Systemic corticosteroids and dapsone treatment for 6 weeks was successful. Read More

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http://dx.doi.org/10.1111/dth.13173DOI Listing
January 2020

Linear IgA bullous dermatosis successfully treated with omalizumab: A case report.

JAAD Case Rep 2019 Nov 24;5(11):966-969. Epub 2019 Oct 24.

Université de Sherbrooke, Sherbrooke, QC, Canada.

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http://dx.doi.org/10.1016/j.jdcr.2019.08.019DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6820281PMC
November 2019
1 Read

Response to "Linear IgA bullous dermatosis protracted by vancomycin-loaded bone cement".

JAAD Case Rep 2019 Oct 3;5(10):904-905. Epub 2019 Oct 3.

Department of Dermatology, Norfolk and Norwich University Hospital NHS Trust.

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http://dx.doi.org/10.1016/j.jdcr.2019.07.017DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6820365PMC
October 2019

Linear IgA/IgG bullous dermatosis with autoantibodies directing the native and processed forms of BP180.

Br J Dermatol 2020 Apr 4;182(4):1061-1062. Epub 2019 Dec 4.

Department of Dermatology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, North 15 West 7, Sapporo, 060-8638, Japan.

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http://dx.doi.org/10.1111/bjd.18642DOI Listing
April 2020
1 Read

Skin lesions and vancomycin use in a hemodialysis patient.

Hemodial Int 2019 10 3;23(4):E127-E129. Epub 2019 Oct 3.

AURA Paris Plaisance, Paris, France.

Vancomycin is a widely used antibiotic in hemodialysis patients. The main complications include renal toxicity and skin lesions. Herein, we report the case of a 29-year-old hemodialysis patient who presented a bullous pruriginous dermatosis after vancomycin treatment. Read More

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http://dx.doi.org/10.1111/hdi.12786DOI Listing
October 2019

Unilateral vancomycin-induced linear IgA bullous dermatosis.

Indian J Dermatol Venereol Leprol 2019 Nov-Dec;85(6):621-622

Department of Dermatology, Fattouma Bourguiba Hospital, Monastir, Tunisia.

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http://dx.doi.org/10.4103/ijdvl.IJDVL_899_18DOI Listing

Ten-year follow-up study of linear immunoglobulin A dermatosis complicated with ulcerative colitis.

Clin J Gastroenterol 2020 Apr 25;13(2):164-169. Epub 2019 Sep 25.

Department of Internal Medicine II, Faculty of Medicine, Shimane University, Izumo, Japan.

Linear immunoglobulin A dermatosis (LAD) is rarely complicated in patients with ulcerative colitis (UC), though the long-term prognosis in those with concurrent LAD and UC is not fully understood. Here, we report findings obtained in follow-up examinations performed over a 10-year period of a UC patient initially complicated with LAD. We treated an 18-year-old male for relapse of UC with deteriorating blisters diagnosed as LAD. Read More

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http://dx.doi.org/10.1007/s12328-019-01047-wDOI Listing
April 2020
1 Read

Linear IgA dermatosis in association with angioimmunoblastic T-cell lymphoma infiltrating the skin: A case report with literature review.

J Cutan Pathol 2020 Mar 27;47(3):251-256. Epub 2019 Oct 27.

Dermatology Department, Cliniques Universitaires Saint-Luc, Brussels, Belgium.

Angioimmunoblastic T-cell lymphoma (AITL) is an aggressive form of peripheral T-cell lymphoma, characterized by systemic symptoms, diffuse lymphadenopathy, hepatosplenomegaly and immunodysregulation. Half of AITL is associated with cutaneous symptoms, but only few cases with bullous eruption have been described. Association with a linear IgA dermatosis is extremely rare. Read More

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http://dx.doi.org/10.1111/cup.13576DOI Listing
March 2020
3 Reads

Linear IgA Disease: A Rare Complication of Vancomycin.

Cureus 2019 Jun 6;11(6):e4848. Epub 2019 Jun 6.

Internal Medicine, St. Francis Medical Center, Seton Hall University, Trenton, USA.

Linear immunoglobulin A (IgA) bullous dermatosis, also known as linear IgA disease, is a rare disorder with an incidence of about 0.5 to 2.3 cases per million individuals per year. Read More

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http://dx.doi.org/10.7759/cureus.4848DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6684112PMC

Vancomycin-induced linear IgA bullous dermatosis presenting as generalized fixed drug eruption.

J Cutan Pathol 2019 Dec 21;46(12):979-981. Epub 2019 Aug 21.

Kaplan-Amonette Department of Dermatology, University of Tennessee Health Science Center, Memphis, Tennessee.

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http://dx.doi.org/10.1111/cup.13563DOI Listing
December 2019
5 Reads

Topical imiquimod-induced linear IgA bullous dermatosis.

BMJ Case Rep 2019 Jul 19;12(7). Epub 2019 Jul 19.

Unit of Dermatology, University of Padua, Padova, Italy.

A 68-year-old woman was referred to the unit of dermatology for a large basal cell carcinoma on the chin. She was treated with imiquimod cream 5%, and 4 weeks after she developed isolated and grouped tense serum-filled vesicles and bullae on lips, nose, scalp, ankles and lumbar area, and then expanded to the whole body. Histological examination was consistent with a subepidermal bullous dermatosis. Read More

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http://dx.doi.org/10.1136/bcr-2019-230037DOI Listing
July 2019
4 Reads

Linear IgA bullous dermatosis associated with ulcerative colitis: A case report and literature review.

Australas J Dermatol 2020 Feb 18;61(1):e82-e86. Epub 2019 Jul 18.

Department of Dermatology, Nippon Medical School, Tokyo, Japan.

We report the case of a 59-year-old Japanese woman who developed linear IgA bullous dermatosis during treatment for ulcerative colitis that manifested as pruritic vesicles with erythema on the trunk and scalp. Histopathological examination revealed subepidermal bulla with neutrophil and eosinophil infiltration in the upper dermis. Direct immunofluorescence revealed linear IgA deposits at the basement membrane zone, and indirect immunofluorescence using split skin revealed IgA reaction to the epidermal side (lamina lucida type). Read More

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http://dx.doi.org/10.1111/ajd.13121DOI Listing
February 2020
2 Reads

Lichen Planus Pemphigoides: From Lichenoid Inflammation to Autoantibody-Mediated Blistering.

Front Immunol 2019 2;10:1389. Epub 2019 Jul 2.

Department of Dermatology, University of Lübeck, Lübeck, Germany.

Lichen planus pemphigoides (LPP) is a very rare autoimmune sub-epidermal blistering disease associated with lichenoid skin changes. Initially thought to be a mere variant of more common inflammatory dermatoses, particularly Bullous Pemphigoid (BP) or Lichen Planus (LP), a growing body of evidence suggests that it is a disease entity in its own right. In common with a range of autoimmune blistering diseases, including BP, pemphigoid gestationis (PG), mucous membrane pemphigoid (MMP) and linear IgA dermatosis (LAD), a key feature of the disease is the development of autoantibodies against type XVII collagen (COL17). Read More

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http://dx.doi.org/10.3389/fimmu.2019.01389DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6614382PMC
July 2019
4 Reads

Complement Activation in Autoimmune Bullous Dermatoses: A Comprehensive Review.

Front Immunol 2019 26;10:1477. Epub 2019 Jun 26.

Department of Pathology, Erasmus Medical Center Rotterdam, Rotterdam, Netherlands.

Autoimmune bullous dermatoses (AIBD) are characterized by circulating autoantibodies that are either directed against epidermal antigens or deposited as immune complexes in the basement membrane zone (BMZ). The complement system (CS) can be activated by autoantibodies, thereby triggering activation of specific complement pathways. Local complement activation induces a pathogenic inflammatory response that eventually results in the formation of a sub- or intraepidermal blister. Read More

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http://dx.doi.org/10.3389/fimmu.2019.01477DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6606728PMC
June 2019
3 Reads

[Pitfall cryothermic dermatitis artefacta].

Hautarzt 2019 Nov;70(11):883-887

Klinik für Dermatologie, Venerologie und Allergologie, Universitätsmedizin Leipzig, Philipp-Rosenthal-Str. 23, 04103, Leipzig, Deutschland.

We present four clinicopathological correlated cases of young patients with cryothermic dermatitis artefacta. They were initially misdiagnosed as primary bullous dermatoses or fixed drug eruptions. Cryothermic dermatitis artefacta can imitate authentic dermatoses such as linear IgA bullous dermatosis, herpes virus infection, bullous pemphigoid or fixed drug eruption. Read More

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http://dx.doi.org/10.1007/s00105-019-4443-3DOI Listing
November 2019
13 Reads

Consensus on the treatment of autoimmune bullous dermatoses: dermatitis herpetiformis and linear IgA bullous dermatosis - Brazilian Society of Dermatology.

An Bras Dermatol 2019 Apr 3;94(2 Suppl 1):48-55. Epub 2019 Jun 3.

Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brazil.

Dermatitis herpetiformis and linear IgA bullous dermatosis are autoimmune diseases that present with pruritic urticarial papules and plaques, with formation of vesicles and blisters of subepidermal location, mediated by IgA antibodies. Mucosal lesions are present only in linear IgA bullous dermatosis. The elaboration of this consensus consisted of a brief presentation of the different aspects of these dermatoses and, above all, of an updated literature review on the various therapeutic options that were discussed and compared with the authors' experience, aiming at the treatment orientation of these diseases in Brazil. Read More

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http://dx.doi.org/10.1590/abd1806-4841.2019940208DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6544034PMC
April 2019
23 Reads

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

Orphanet J Rare Dis 2019 05 24;14(1):115. Epub 2019 May 24.

Dermatology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Via Pace, 9, 20122, Milan, Italy.

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. Read More

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http://dx.doi.org/10.1186/s13023-019-1089-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6534856PMC
May 2019
16 Reads

Vancomycin-induced linear IgA bullous dermatosis (LABD)-an atypical presentation.

Clin Case Rep 2019 May 22;7(5):1091-1093. Epub 2019 Apr 22.

State University of Campinas (UNICAMP) Campinas Brazil.

We report an uncommon presentation of bullous dermatosis by linear IgA. There are few cases reported in the literature with this form of presentation starting with mucosal lesions and then evolving into a similar bullous pemphigoid pattern. In addition, we emphasize the importance of direct immunofluorescence for the definitive diagnosis. Read More

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http://dx.doi.org/10.1002/ccr3.2039DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6509886PMC
May 2019
5 Reads

Pemphigoid variants affecting the skin.

Clin Exp Dermatol 2019 Oct 16;44(7):721-727. Epub 2019 May 16.

Department of Dermatology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.

Pemphigoid diseases are autoimmune subepidermal blistering diseases affecting the skin and mucous membranes, which are caused by autoantibodies targeting structural hemidesmosomal proteins or hemidesmosome-associated proteins. Variants of pemphigoid can be differentiated based on targeted antigens and clinical aspects. In this review, we will discuss pemphigoid variants that predominantly affect the skin, and provide clinicians with clues to diagnosis. Read More

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http://dx.doi.org/10.1111/ced.13984DOI Listing
October 2019
2 Reads

Linear IgA Bullous Dermatosis: A Series of 17 Cases.

Actas Dermosifiliogr 2019 Oct 20;110(8):673-680. Epub 2019 Apr 20.

Sector Dermatología Pediátrica, Hospital Ramos Mejía, Buenos Aires, Argentina; Servicio de Dermatología, Hospital Alemán, Buenos Aires, Argentina.

Linear IgA bullous dermatosis is an acquired subepidermal immunoglobulin-mediated vesiculobullous disease. In this retrospective, observational, descriptive study, we describe the clinical characteristics, treatments, and outcomes of 17 patients with linear IgA bullous dermatosis. Two children had been vaccinated 2 weeks before the onset of symptoms, 2 had had bronco-obstructive respiratory symptoms, and 1 had received intravenous antibiotic therapy. Read More

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http://dx.doi.org/10.1016/j.ad.2018.06.017DOI Listing
October 2019
3 Reads

Bullous dermatosis suspected in an 8-month-old child in Guinea-Bissau.

Oxf Med Case Reports 2019 Apr 15;2019(4):omz004. Epub 2019 Apr 15.

Buenos Aires, Argentina.

An 8-month-old child was admitted to a paediatric intensive care unit in Guinea-Bissau with severe blistering dermatosis. He was treated with broad spectrum antibiotics and dressings, without improvement. After 2 weeks, linear IgA bullous dermatosis was suspected. Read More

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http://dx.doi.org/10.1093/omcr/omz004DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6464016PMC
April 2019
11 Reads

Cephalosporin-induced linear IgA dermatosis in a child: Case report and literature review.

Dermatol Ther 2019 07 3;32(4):e12927. Epub 2019 Jun 3.

Faculty of Medicine, Department of Dermatology, Trakya University, Edirne, Turkey.

Linear IgA dermatosis (LAD) is a rare, subepidermal blistering disease with mucocutaneous involvement. It may be idiopathic or drug induced. We describe a 4-year-old girl who presented with a vesiculobullous eruption after she had been treated with cefixime for urinary tract infection. Read More

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https://onlinelibrary.wiley.com/doi/abs/10.1111/dth.12927
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http://dx.doi.org/10.1111/dth.12927DOI Listing
July 2019
19 Reads

Direct Immunofluorescence Studies in Lichen Planus.

Turk Patoloji Derg 2019 ;35(3):193-197

Department of Pathology, Bharati Vidyapeeth (deemed to be university) Medical College and Hospital, SANGLI, INDIA.

Objective: Lichen planus is a common, usually intensely pruritic, symmetrical, papulosquamous dermatosis. Direct immunofluorescence studies in patients with lichen planus shows deposition of multiple immunoglobulins and fibrin at the dermoepidermal junction and in the colloid bodies.

Material And Method: Histopathological features were analysed in 100 cases of lichen planus which were sent for routine histology. Read More

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http://dx.doi.org/10.5146/tjpath.2018.01455DOI Listing
February 2020
3 Reads

Erythrodermic linear IgA/IgG bullous dermatosis.

Eur J Dermatol 2019 04;29(2):220-221

Department of Dermatology, Osaka City University Graduate School of Medicine, Osaka, Abeno-ku, Osaka 545-8585, Japan.

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http://dx.doi.org/10.1684/ejd.2019.3503DOI Listing
April 2019
3 Reads

A case of recalcitrant linear IgA bullous dermatosis: Successfully treated with rituximab.

Dermatol Ther 2019 05 25;32(3):e12911. Epub 2019 Apr 25.

Faculty of Medicine, Department of Dermatology, Selcuk University, Konya, Turkey.

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http://dx.doi.org/10.1111/dth.12911DOI Listing
May 2019
3 Reads

Clinical, pathologic, and immunologic features of pemphigus herpetiformis: a literature review and proposed diagnostic criteria.

Int J Dermatol 2019 Sep 22;58(9):997-1007. Epub 2019 Mar 22.

Department of Dermatology, Mayo Clinic, Jacksonville, FL, USA.

Pemphigus herpetiformis (PH), a rare type of pemphigus, is characterized by immunologic findings consistent with pemphigus but with a unique clinical and pathologic presentation. PH was first described as resembling dermatitis herpetiformis clinically, but because of its variable presentation, it can also resemble linear immunoglobulin A bullous dermatosis and bullous pemphigoid. We reviewed reported cases to analyze the most frequent clinical, pathologic, and immunologic characteristics and to propose corresponding diagnostic criteria. Read More

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http://dx.doi.org/10.1111/ijd.14395DOI Listing
September 2019
7 Reads

[Linear IgA bullous dermatosis].

Hautarzt 2019 Apr;70(4):254-259

Klinik für Dermatologie, Venerologie und Dermatoonkologie, Fakultät für Medizin, Semmelweis Universität, Budapest, Ungarn.

Linear IgA bullous dermatosis is a rare autoimmune blistering disease that occurs in both children and adults. Strings of pearls, crowns of jewels, rosettes and urticarial plaques can occur on the whole integument with emphasis on the face (particularly perioral area) and genitalia. Pruritus is common and may be severe. Read More

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http://dx.doi.org/10.1007/s00105-019-4377-9DOI Listing
April 2019
7 Reads

Linear IgA bullous dermatosis protracted by vancomycin-loaded bone cement.

JAAD Case Rep 2019 Mar 22;5(3):234-236. Epub 2019 Feb 22.

Department of Dermatology, MetroHealth Medical System, Case Western University, Cleveland, Ohio.

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http://dx.doi.org/10.1016/j.jdcr.2019.01.011DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6389549PMC
March 2019
2 Reads

Drug-induced Linear IgA Bullous Dermatosis: A Case Report and Review of the Literature.

Acta Derm Venereol 2019 May;99(6):508-515

Department of Dermatology and Allergology, Technical University Munich, DE-80802 Munich, Germany.

Linear IgA bullous dermatosis (LABD) is a rare subepidermal autoimmune blistering disease characterized by linear deposition of IgA along the basement membrane zone. Although most reported cases are idiopathic, there is a subset of patients with drug-induced LABD. Various drugs have been associated with the drug-induced form of the disease. Read More

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http://dx.doi.org/10.2340/00015555-3154DOI Listing
May 2019
6 Reads

Different presentations of linear IgA disease in a father and daughter.

J Eur Acad Dermatol Venereol 2019 07 8;33(7):e260-e261. Epub 2019 Apr 8.

Department of Dermatology, Hospital Infantil Universitario Niño Jesús, Av de Menéndez Pelayo 65, Madrid, 28009, Spain.

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http://dx.doi.org/10.1111/jdv.15532DOI Listing
July 2019
1 Read

Widespread Erythematous and Bullous Plaques Associated With Nasolabial Fold Ulceration: Answer.

Am J Dermatopathol 2019 Mar;41(3):237-238

Dermatology Department, Complejo Hospitalario Universitario de Pontevedra, Pontevedra, Spain.

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http://dx.doi.org/10.1097/DAD.0000000000001051DOI Listing
March 2019
13 Reads

Linear immunoglobulin A/immunoglobulin G bullous dermatosis with autoantibodies to LAD-1 and laminin-γ1.

Clin Exp Dermatol 2019 04 28;44(3):e44-e46. Epub 2019 Jan 28.

Department of Dermatology, Tokushima University Graduate School of Medical Science, Tokushima, 3-15-18 Kuramoto-cho, Tokushima City, Tokushima, 770-8503, Japan.

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http://doi.wiley.com/10.1111/ced.13921
Publisher Site
http://dx.doi.org/10.1111/ced.13921DOI Listing
April 2019
1 Read

Linear IgA bullous dermatosis treated with rituximab.

JAAD Case Rep 2019 Feb 12;5(2):124-126. Epub 2019 Jan 12.

Dermatology Department, Institute for Research and Innovation in Biomedicine, Rouen University Hospital, University of Normandy, Rouen, France.

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http://dx.doi.org/10.1016/j.jdcr.2018.11.004DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330365PMC
February 2019
5 Reads

Systemic Lupus Erythematosus with Linear IgA Bullous Dermatosis and Renal Vascular Lesions: An Extremely Rare Association.

Indian J Nephrol 2018 Nov-Dec;28(6):465-467

Department of Pathology, St. John's Medical College, Bengaluru, Karnataka, India.

We report a rare case of systemic lupus erythematosus presenting initially with cutaneous manifestations of linear IgA bullous dermatosis. Later the patient developed renal abnormalities due to thrombotic microangiopathy and lupus nephritis with inflammatory necrotizing vasculitis. Paucity of immune deposits was observed on Immunofluorescence. Read More

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http://dx.doi.org/10.4103/ijn.IJN_200_17DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6309391PMC
January 2019
7 Reads

Childhood sclerosing cholangitis associations in a Tunisian tertiary care hospital: a many-faceted disease.

Turk J Pediatr 2019 ;61(6):905-914

Departments of Pediatric, Sahloul Hospital.

Tfifha M, Kamoun T, Mama N, Mestiri S, Hassayoun S, Zouari N, Jemni H, Abroug S. Childhood sclerosing cholangitis associations in a Tunisian tertiary care hospital: a many-faceted disease. Turk J Pediatr 2019; 61: 905-914. Read More

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http://dx.doi.org/10.24953/turkjped.2019.06.012DOI Listing
January 2019

Drug-induced linear immunoglobulin A bullous dermatosis: A French retrospective pharmacovigilance study of 69 cases.

Br J Clin Pharmacol 2019 03 4;85(3):570-579. Epub 2019 Jan 4.

EA 7379 EpiDermE, Université Paris Est Créteil Val de Marne UPEC, Créteil, France.

Aims: Linear immunoglobin A (IgA) bullous dermatosis is a rare autoimmune dermatosis considered spontaneous or drug-induced (DILAD). We assessed all DILAD cases, determined the imputability score of drugs and highlighted suspected drugs.

Methods: Data for patients with DILAD were collected retrospectively from the French Pharmacovigilance network (from 1985 to 2017) and from physicians involved in the Bullous Diseases French Study Group and the French Investigators for Skin Adverse Reactions to Drugs. Read More

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http://dx.doi.org/10.1111/bcp.13827DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6379232PMC
March 2019
57 Reads

Linear IgA Bullous Dermatosis Preceding the Diagnosis of Primary Sclerosing Cholangitis and Ulcerative Colitis: A Case Report.

Am J Dermatopathol 2019 Jul;41(7):498-501

Gastroenterology, Hepatology, and Nutrition, University of Pittsburgh Medical Center, Pittsburgh, PA.

Linear IgA bullous dermatosis (LABD) is a rare autoimmune blistering disorder seen in the pediatric and adult populations that is often linked to a medication, infection, or underlying gastrointestinal, hepatobiliary, or autoimmune disease. In this study, we describe the case of a 23-year-old white man whose presentation and diagnosis of LABD ultimately led to the discovery of underlying primary sclerosing cholangitis (PSC) and ulcerative colitis (UC). His dermatitis resolved with topical steroids and dapsone, and he is undergoing systemic treatment for his UC and PSC. Read More

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http://dx.doi.org/10.1097/DAD.0000000000001313DOI Listing
July 2019
7 Reads

["Decoratively figured blisters" on the whole integument in initially diagnosed ulcerative colitis].

Hautarzt 2019 Mar;70(3):210-214

Klinik- und Poliklinik für Haut- und Geschlechtskrankheiten, Universitätsmedizin Greifswald, Greifswald, Deutschland.

The rare case of a 61-year-old patient suffering from linear IgA dermatosis is presented. The patient was previously hospitalized with chronic inflammatory bowel disease. The correct diagnosis of the disease was based on clinical and histological findings. Read More

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http://dx.doi.org/10.1007/s00105-018-4314-3DOI Listing
March 2019
27 Reads