{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,18]],"date-time":"2026-08-18T01:12:40Z","timestamp":1787015560291,"version":"build-2736575974"},"reference-count":20,"publisher":"Wiley","issue":"9","license":[{"start":{"date-parts":[[2018,3,23]],"date-time":"2018-03-23T00:00:00Z","timestamp":1521763200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Acad Dermatol Venereol"],"published-print":{"date-parts":[[2018,9]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>\n                      Diagnosis of bullous pemphigoid (\n                      <jats:styled-content style=\"fixed-case\">BP<\/jats:styled-content>\n                      ) and pemphigus is based on clinical features, histology, immunofluorescence and laboratory data.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Objectives<\/jats:title>\n                    <jats:p>\n                      To evaluate features of\n                      <jats:styled-content style=\"fixed-case\">BP<\/jats:styled-content>\n                      and pemphigus at reflectance confocal microscopy (\n                      <jats:styled-content style=\"fixed-case\">RCM<\/jats:styled-content>\n                      ) and optical coherence tomography (\n                      <jats:styled-content style=\"fixed-case\">OCT<\/jats:styled-content>\n                      ) in order to provide a rapid non\u2010invasive bed\u2010side diagnosis. Secondary objective was to evaluate the detectability of clinically non\u2010visible lesions.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      This was an observational, retrospective, multicentre study in which patients with suspicious lesions for\n                      <jats:styled-content style=\"fixed-case\">BP<\/jats:styled-content>\n                      or pemphigus underwent clinical assessment,\n                      <jats:styled-content style=\"fixed-case\">RCM<\/jats:styled-content>\n                      ,\n                      <jats:styled-content style=\"fixed-case\">OCT<\/jats:styled-content>\n                      , blood tests and skin biopsy for histological and direct immunofluorescence examinations from January 2014 to December 2015. A total of 72 lesions in 24 selected patients were evaluated. Additionally, apparently unaffected skin at two different distances [near (1\u20132 cm) and far (2\u20133 cm)] from each lesion was examined to test subclinical lesion detectability.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      RCM was able to detect subepidermal and intra\u2010epidermal blisters, respectively, in 75% and 50% of the patients affected by\n                      <jats:styled-content style=\"fixed-case\">BP<\/jats:styled-content>\n                      and pemphigus. At\n                      <jats:styled-content style=\"fixed-case\">OCT<\/jats:styled-content>\n                      , the exact blister level was identified in all patients. Acantholytic cells were observed only at\n                      <jats:styled-content style=\"fixed-case\">RCM<\/jats:styled-content>\n                      in pemphigus (62.5%). Fibrin deposition inside the blisters was only found in\n                      <jats:styled-content style=\"fixed-case\">BP<\/jats:styled-content>\n                      , evidenced both at\n                      <jats:styled-content style=\"fixed-case\">RCM<\/jats:styled-content>\n                      and\n                      <jats:styled-content style=\"fixed-case\">OCT<\/jats:styled-content>\n                      . Among patients with\n                      <jats:styled-content style=\"fixed-case\">BP<\/jats:styled-content>\n                      , subclinical blisters were detected in nine (9.4%) clinically healthy skin, while among patients with pemphigus were observed in 10 (20.8%) apparently unaffected skin.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>\n                      RCM and\/or\n                      <jats:styled-content style=\"fixed-case\">OCT<\/jats:styled-content>\n                      provide useful information for a rapid diagnosis of\n                      <jats:styled-content style=\"fixed-case\">BP<\/jats:styled-content>\n                      and pemphigus and for the identification of biopsy site. Combined use of\n                      <jats:styled-content style=\"fixed-case\">RCM<\/jats:styled-content>\n                      and\n                      <jats:styled-content style=\"fixed-case\">OCT<\/jats:styled-content>\n                      is optimal because associates the higher resolution of\n                      <jats:styled-content style=\"fixed-case\">RCM<\/jats:styled-content>\n                      with the greater penetration depth of\n                      <jats:styled-content style=\"fixed-case\">OCT<\/jats:styled-content>\n                      .\n                      <jats:styled-content style=\"fixed-case\">OCT<\/jats:styled-content>\n                      could be an optimal tool for treatment monitoring, especially in the cases of subclinical lesions. However, histopathologic and immunologic examinations remain the gold standard for establishing the final diagnosis.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/jdv.14795","type":"journal-article","created":{"date-parts":[[2018,1,16]],"date-time":"2018-01-16T18:56:39Z","timestamp":1516128999000},"page":"1562-1569","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":33,"title":["Reflectance confocal microscopy and optical coherence tomography for the diagnosis of bullous pemphigoid and pemphigus and surrounding subclinical lesions"],"prefix":"10.1111","volume":"32","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-0682-6148","authenticated-orcid":false,"given":"V.D.","family":"Mandel","sequence":"first","affiliation":[{"name":"Dermatology Unit Surgical, Medical and Dental Department of Morphological Sciences related to Transplant, Oncology and Regenerative Medicine University of Modena and 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