{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,26]],"date-time":"2026-08-26T10:23:57Z","timestamp":1787739837720,"version":"build-2784847793"},"reference-count":20,"publisher":"Wiley","license":[{"start":{"date-parts":[[2026,8,26]],"date-time":"2026-08-26T00:00:00Z","timestamp":1787702400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"},{"start":{"date-parts":[[2026,8,26]],"date-time":"2026-08-26T00:00:00Z","timestamp":1787702400000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Histopathology"],"abstract":"<jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>\n                      A peripheral nerve sheath tumour composed predominantly of Wagner\u2010Meissner (W\u2010M) bodies is typically regarded as a variant of schwannoma and has been considered rare. Interestingly, a\n                      <jats:italic>SH3PXD2A::HTRA1<\/jats:italic>\n                      fusion was found which is described in schwannomas with a so\u2010called \u201cserpentine\u201d palisading pattern comprising short palisades of Schwann cells.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      We describe a case of plexiform W\u2010M schwannoma with a\n                      <jats:italic>SH3PXD2A::HTRA1<\/jats:italic>\n                      fusion demonstrated on RNA\u2010based next generation sequencing and review the relevant histological, immunohistochemical and molecular findings and discuss differential diagnoses.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      The lesion arose in the distal volar pulp of the right middle finger in a 37\u2010year\u2010old female. It had a plexiform architecture and was composed predominantly of densely packed, repetitive Wagner\u2010Meissner bodies which expressed S100, SOX10, Calretinin and CD56, with intervening S100, SOX10, CD34 and patchy EMA staining. It showed no NF1 expression. A\n                      <jats:italic>SH3PXD2A::HTRA1<\/jats:italic>\n                      fusion was present.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>\n                      The case presented suggests that so\u2010called W\u2010M schwannomas may be driven by\n                      <jats:italic>SH3PXD2A::HTRA1<\/jats:italic>\n                      fusions and that W\u2010M bodies in this context correlate with the \u2018serpentine\u2019 palisading pattern described in schwannomas with\n                      <jats:italic>HTRA1 rearrangements<\/jats:italic>\n                      . Analysis of further cases of W\u2010M rich or predominant lesions including schwannoma, neurilemmoma and perhaps even neurotised melanocytic naevi may warrant consideration.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/his.70270","type":"journal-article","created":{"date-parts":[[2026,8,26]],"date-time":"2026-08-26T10:00:12Z","timestamp":1787738412000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Plexiform Wagner\u2010Meissner schwannoma with a\n                    <scp>\n                      <i>SH3PXD2A::HTRA1<\/i>\n                    <\/scp>\n                    fusion: a twisted sister?"],"prefix":"10.1111","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-7959-9671","authenticated-orcid":false,"given":"Mark James","family":"Wilsher","sequence":"first","affiliation":[{"name":"North West London Pathology Imperial College Healthcare NHS Trust  London UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-4835-2422","authenticated-orcid":false,"given":"Onur","family":"Berber","sequence":"additional","affiliation":[{"name":"Royal Free London, NHS Foundation Trust  London UK"},{"name":"OS Clinic  London UK"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2026,8,26]]},"reference":[{"key":"e_1_2_9_2_1","doi-asserted-by":"crossref","first-page":"856","DOI":"10.2174\/1871527311201070856","article-title":"Clinical implication of Meissner's corpuscles","volume":"11","author":"Vega JA","year":"2012","journal-title":"CNS Neurol. 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