{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,1]],"date-time":"2026-09-01T15:28:55Z","timestamp":1788276535955,"version":"build-2803163510"},"reference-count":20,"publisher":"Wiley","issue":"10","license":[{"start":{"date-parts":[[2026,5,10]],"date-time":"2026-05-10T00:00:00Z","timestamp":1778371200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"},{"start":{"date-parts":[[2026,5,10]],"date-time":"2026-05-10T00:00:00Z","timestamp":1778371200000},"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":[[2026,10]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:p>Plasmablastic lymphoma (PBL) is a rare, high\u2010grade large B\u2010cell lymphoma characterized by large atypical cells with plasmablastic or immunoblastic morphology and a terminal B\u2010cell differentiation phenotype. PBL often occurs in patients with immune deficiency or dysregulation, most commonly HIV infection. Cutaneous involvement is rare and occurs most frequently in those with immune deficiency. We report a 73\u2010year\u2010old immunocompetent female presenting with multiple cutaneous lesions and cervical lymphadenopathy. Nasopharyngeal and cutaneous biopsies confirmed EBV\u2010associated PBL with plasmacytic differentiation, mimicking primary cutaneous marginal zone lymphoma (PC\u2010MZL). The patient was treated with multiagent chemotherapy. Her disease progressed and she passed away in 9\u2009months. We reviewed the literature for EBV\u2010associated PBL occurring in the skin and those in immunocompetent patients. A comprehensive systemic evaluation integrating clinical, laboratory, and imaging findings is essential for excluding PC\u2010MZL and plasmablastic multiple myeloma and establishing the correct diagnosis.<\/jats:p>","DOI":"10.1111\/cup.70137","type":"journal-article","created":{"date-parts":[[2026,5,11]],"date-time":"2026-05-11T02:29:28Z","timestamp":1778466568000},"page":"930-936","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Plasmablastic Lymphoma Presenting With Multiple Cutaneous Nodules Mimicking Primary Cutaneous Marginal Zone Lymphoma"],"prefix":"10.1111","volume":"53","author":[{"given":"Bo\u2010Jung","family":"Chen","sequence":"first","affiliation":[{"name":"Department of Pathology, Shuang Ho Hospital Taipei Medical University  New Taipei City Taiwan"},{"name":"Department of Pathology, School of Medicine, College of Medicine Taipei Medical University  Taipei Taiwan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Feng\u2010Jie","family":"Lai","sequence":"additional","affiliation":[{"name":"Department of Dermatology Chi\u2010Mei Medical Centre  Tainan Taiwan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yin\u2010Hsun","family":"Feng","sequence":"additional","affiliation":[{"name":"Division of Hemato\u2010Oncology, Department of Internal Medicine Chi\u2010Mei Medical Centre  Tainan Taiwan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-3971-525X","authenticated-orcid":false,"given":"Shih\u2010Sung","family":"Chuang","sequence":"additional","affiliation":[{"name":"Department of Pathology Chi\u2010Mei Medical Centre  Tainan Taiwan"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2026,5,10]]},"reference":[{"key":"e_1_2_7_2_1","first-page":"506","volume-title":"WHO Classification of Haematolymphoid Tumours 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