{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,15]],"date-time":"2026-10-15T01:45:29Z","timestamp":1792028729997,"version":"4.4.0"},"reference-count":18,"publisher":"Wiley","issue":"11","license":[{"start":{"date-parts":[[2026,6,7]],"date-time":"2026-06-07T00:00:00Z","timestamp":1780790400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"},{"start":{"date-parts":[[2026,6,7]],"date-time":"2026-06-07T00:00:00Z","timestamp":1780790400000},"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":["J Cutan Pathol"],"published-print":{"date-parts":[[2026,11]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:p>T\u2010cell rich angiomatoid polypoid pseudolymphoma (TRAPP) is a rare skin condition with important clinical and histological differentials. We report a case arising on the left cheek of a 31\u2010year\u2010old pregnant female, first noticed at 7\u2009months of pregnancy. By the time of excision soon after delivery, it was 6\u2009mm in diameter. Histology showed a relatively circumscribed dermal proliferation of high endothelial venule\u2010like vessels, surrounded and densely infiltrated by non\u2010atypical CD4 positive T lymphocytes. A diagnosis of TRAPP was made. To our knowledge this is only the second case in the literature to arise during pregnancy. We review the literature on TRAPP, discuss its histological and immunohistochemical features, recently proposed changes to its nomenclature, and distinguishing features that separate it from its main differential diagnoses.<\/jats:p>","DOI":"10.1111\/cup.70160","type":"journal-article","created":{"date-parts":[[2026,6,8]],"date-time":"2026-06-08T00:10:38Z","timestamp":1780877438000},"page":"1051-1054","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["A Rare Case of a T\u2010Cell Rich Angiomatoid Polypoid Pseudolymphoma in a 31\u2010Year\u2010Old Pregnant Woman"],"prefix":"10.1111","volume":"53","author":[{"ORCID":"https:\/\/orcid.org\/0009-0008-1088-570X","authenticated-orcid":false,"given":"Jasmine","family":"Zaremba","sequence":"first","affiliation":[{"name":"Histopathology University Hospital North Midlands  Stoke on Trent UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Olumide","family":"Adebambo","sequence":"additional","affiliation":[{"name":"Histopathology University Hospital North Midlands  Stoke on Trent UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Vivek","family":"Mudaliar","sequence":"additional","affiliation":[{"name":"Dermatopathology University Hospitals North Midlands  Stoke on Trent UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-8748-695X","authenticated-orcid":false,"given":"Shahd","family":"Nour","sequence":"additional","affiliation":[{"name":"Plastic Surgery University Hospital North Midlands  Stoke on Trent UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Wayne","family":"Jaffe","sequence":"additional","affiliation":[{"name":"Plastic and Reconstructive Surgery University Hospital North Midlands  Stoke on Trent UK"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2026,6,7]]},"reference":[{"issue":"4","key":"e_1_2_11_2_1","article-title":"T\u2010Cell\u2010Rich Angiomatoid Polypoid Pseudolymphoma: A Case Report and Comparison With Key Differential Diagnoses","volume":"15","author":"Xu K. 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