Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters










Database
Language
Publication year range
1.
Eur J Dermatol ; 30(5): 516-523, 2020 Oct 01.
Article in English | MEDLINE | ID: mdl-32972911

ABSTRACT

BACKGROUND: Mucosal involvement in autoimmune subepidermal blistering disorders (ASBD) may represent the only or predominant localization. Circulating autoantibodies are detected in 50% cases. OBJECTIVE: The aim of this study was to evaluate the usefulness of fluorescence overlay antigen mapping by laser-scanning confocal microscopy (FOAM-LSCM) to identify ASBD with mucosal involvement in oral mucosa specimens. MATERIALS & METHODS: Thirty-two ASBD patients, diagnosed based on direct immunofluorescence between 2006 and 2016, were enrolled. Localization of IgG deposits bound at the basement membrane zone, relative to laminin-332 and collagen IV localization, was assessed in vivo. RESULTS: FOAM-LSCM disclosed four different immunofluorescence patterns. IgG deposits were located above laminin-332, as in bullous pemphigoid (BP-type), in 19% cases and co-localized with laminin-332 (anti-laminin-332-type) in 6% cases. IgG deposits were found below laminin-332 and above collagen IV (mucous membrane pemphigoid-type) in 59% cases, and below collagen IV (epidermolysis bullosa acquisita-type) in 16%. Circulating antibodies were found in 56% cases. CONCLUSION: The FOAM-LSCM method should be used in order to obtain a definitive diagnosis of ASBD with mucosal involvement, particularly in the presence of negative circulating antibodies.


Subject(s)
Epidermolysis Bullosa Acquisita/diagnostic imaging , Epidermolysis Bullosa Acquisita/immunology , Fluorescent Antibody Technique, Direct , Microscopy, Confocal , Mouth Mucosa/diagnostic imaging , Mouth Mucosa/immunology , Adult , Aged , Aged, 80 and over , Autoantibodies/blood , Basement Membrane/immunology , Cell Adhesion Molecules/immunology , Collagen Type IV/immunology , Female , Humans , Immunoglobulin G/analysis , Male , Middle Aged , Kalinin
2.
Int J Med Inform ; 122: 27-36, 2019 02.
Article in English | MEDLINE | ID: mdl-30623781

ABSTRACT

Direct immunofluorescence (DIF) microscopy of a skin biopsy is used by physicians and pathologists to diagnose autoimmune bullous dermatoses (AIBD). This technique is the reference standard for diagnosis of AIBD, which is used worldwide in medical laboratories. For diagnosis of subepidermal AIBD (sAIBD), two different types of serrated pattern of immunodepositions can be recognized from DIF images, namely n- and u-serrated patterns. The n-serrated pattern is typically found in the most common sAIBD bullous pemphigoid. Presence of the u-serrated pattern indicates the sAIBD subtype epidermolysis bullosa acquisita (EBA), which has a different prognosis and requires a different treatment. The manual identification of these serrated patterns is learnable but challenging. We propose an automatic technique that is able to localize u-serrated patterns for automated computer-assisted diagnosis of EBA. The distinctive feature of u-serrated patterns as compared to n-serrated patterns is the presence of ridge-endings. We introduce a novel ridge-ending detector which uses inhibition-augmented trainable COSFIRE filters. Then, we apply a hierarchical clustering approach to detect the suspicious u-serrated patterns from the detected ridge-endings. For each detected u-serrated pattern we provide a score that indicates the reliability of its detection. In order to evaluate the proposed approach, we created a data set with 180 DIF images for serration pattern analysis. This data set consists of seven subsets which were obtained from various biopsy samples under different conditions. We achieve an average recognition rate of 82.2% of the u-serrated pattern on these 180 DIF images, which is comparable to the recognition rate achieved by experienced medical doctors and pathologists.


Subject(s)
Autoimmune Diseases/diagnosis , Epidermolysis Bullosa Acquisita/diagnosis , Fluorescent Antibody Technique, Direct/instrumentation , Fluorescent Antibody Technique, Direct/methods , Image Interpretation, Computer-Assisted/methods , Autoimmune Diseases/diagnostic imaging , Diagnosis, Differential , Epidermolysis Bullosa Acquisita/diagnostic imaging , Humans , Reproducibility of Results
SELECTION OF CITATIONS
SEARCH DETAIL
...