Bullous Systemic Lupus Erythematosus: Case report

Summary Introduction: Bullous systemic lupus erythematosus (BSLE) is an autoantibody-mediated disease with subepidermal blisters. It is a rare form of presentation of SLE that occurs in less than 5% of cases of lupus. Case Report: A 27-year-old, female, FRS patient reported...

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Main Authors: Ivan Dieb Miziara, Ali Mahmoud, Azis Arruda Chagury, Ricardo Dourado Alves
Format: Article
Language:English
Published: Thieme Revinter Publicações Ltda. 2013-07-01
Series:International Archives of Otorhinolaryngology
Subjects:
Online Access:http://www.thieme-connect.de/DOI/DOI?10.7162/S1809-977720130003000016
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spelling doaj-783f663582fd4bc8a6db65b78960347d2020-11-25T03:16:22ZengThieme Revinter Publicações Ltda.International Archives of Otorhinolaryngology1809-97771809-48642013-07-01170334434610.7162/S1809-977720130003000016Bullous Systemic Lupus Erythematosus: Case reportIvan Dieb Miziara0Ali Mahmoud1Azis Arruda Chagury2Ricardo Dourado Alves3Associate Professor in the Department of Otorhinolaryngology, School of Medicine, University of São Paulo, São Paulo, Brazil.Otolaryngologist in the Department of Otorhinolaryngology, School of Medicine, University of São Paulo, São Paulo, Brazil.Specialist in Otolaryngology, School of Medicine, University of São Paulo, São Paulo, Brazil.Resident in Otolaryngology, School of Medicine, University of São Paulo, São Paulo, Brazil.Summary Introduction: Bullous systemic lupus erythematosus (BSLE) is an autoantibody-mediated disease with subepidermal blisters. It is a rare form of presentation of SLE that occurs in less than 5% of cases of lupus. Case Report: A 27-year-old, female, FRS patient reported the appearance of painful bullous lesions in the left nasal wing and left buccal mucosa that displayed sudden and rapid growth. She sought advice from emergency dermatology staff 15 days after onset and was hospitalized with suspected bullous disease. Intravenous antibiotics and steroids were administered initially, but the patient showed no improvement during hospitalization. She displayed further extensive injuries to the trunk, axillae, and vulva as well as disruption of the bullous lesions, which remained as hyperemic scars. Incisional biopsy of a lesion in the left buccal mucosa was performed, and pathological results indicated mucositis with extensive erosion and the presence of a predominantly neutrophilic infiltrate with degeneration of basal cells and apoptotic keratinocytes. Under direct immunofluorescence, the skin showed anti-IgA, anti-IgM, and anti-IgG linear fluorescence on the continuous dermal side of the cleavage. Indirect immunofluorescence of the skin showed conjugated anti-IgA, was anti-IgM negative, and displayed pemphigus in conjunction with anti-IgG fluorescence in the nucleus of keratinocytes, consistent with a diagnosis of bullous lupus erythematosus. Discussion: BSLE is an acquired autoimmune bullous disease caused by autoantibodies against type VII collagen or other components of the junctional zone, epidermis, and dermis. It must be differentiated from the secondary bubbles and vacuolar degeneration of the basement membrane that may occur in acute and subacute cutaneous lupus erythematosus.http://www.thieme-connect.de/DOI/DOI?10.7162/S1809-977720130003000016lupus erythematosussystemicstomatitismucositis
collection DOAJ
language English
format Article
sources DOAJ
author Ivan Dieb Miziara
Ali Mahmoud
Azis Arruda Chagury
Ricardo Dourado Alves
spellingShingle Ivan Dieb Miziara
Ali Mahmoud
Azis Arruda Chagury
Ricardo Dourado Alves
Bullous Systemic Lupus Erythematosus: Case report
International Archives of Otorhinolaryngology
lupus erythematosus
systemic
stomatitis
mucositis
author_facet Ivan Dieb Miziara
Ali Mahmoud
Azis Arruda Chagury
Ricardo Dourado Alves
author_sort Ivan Dieb Miziara
title Bullous Systemic Lupus Erythematosus: Case report
title_short Bullous Systemic Lupus Erythematosus: Case report
title_full Bullous Systemic Lupus Erythematosus: Case report
title_fullStr Bullous Systemic Lupus Erythematosus: Case report
title_full_unstemmed Bullous Systemic Lupus Erythematosus: Case report
title_sort bullous systemic lupus erythematosus: case report
publisher Thieme Revinter Publicações Ltda.
series International Archives of Otorhinolaryngology
issn 1809-9777
1809-4864
publishDate 2013-07-01
description Summary Introduction: Bullous systemic lupus erythematosus (BSLE) is an autoantibody-mediated disease with subepidermal blisters. It is a rare form of presentation of SLE that occurs in less than 5% of cases of lupus. Case Report: A 27-year-old, female, FRS patient reported the appearance of painful bullous lesions in the left nasal wing and left buccal mucosa that displayed sudden and rapid growth. She sought advice from emergency dermatology staff 15 days after onset and was hospitalized with suspected bullous disease. Intravenous antibiotics and steroids were administered initially, but the patient showed no improvement during hospitalization. She displayed further extensive injuries to the trunk, axillae, and vulva as well as disruption of the bullous lesions, which remained as hyperemic scars. Incisional biopsy of a lesion in the left buccal mucosa was performed, and pathological results indicated mucositis with extensive erosion and the presence of a predominantly neutrophilic infiltrate with degeneration of basal cells and apoptotic keratinocytes. Under direct immunofluorescence, the skin showed anti-IgA, anti-IgM, and anti-IgG linear fluorescence on the continuous dermal side of the cleavage. Indirect immunofluorescence of the skin showed conjugated anti-IgA, was anti-IgM negative, and displayed pemphigus in conjunction with anti-IgG fluorescence in the nucleus of keratinocytes, consistent with a diagnosis of bullous lupus erythematosus. Discussion: BSLE is an acquired autoimmune bullous disease caused by autoantibodies against type VII collagen or other components of the junctional zone, epidermis, and dermis. It must be differentiated from the secondary bubbles and vacuolar degeneration of the basement membrane that may occur in acute and subacute cutaneous lupus erythematosus.
topic lupus erythematosus
systemic
stomatitis
mucositis
url http://www.thieme-connect.de/DOI/DOI?10.7162/S1809-977720130003000016
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