{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,30]],"date-time":"2026-06-30T03:04:45Z","timestamp":1782788685051,"version":"3.54.5"},"reference-count":24,"publisher":"Wiley","license":[{"start":{"date-parts":[[2022,6,24]],"date-time":"2022-06-24T00:00:00Z","timestamp":1656028800000},"content-version":"unspecified","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Case Reports in Pathology"],"published-print":{"date-parts":[[2022,6,24]]},"abstract":"<jats:p>Epithelioid hemangioendothelioma is a rare tumor of endothelial differentiation most commonly arising in soft tissue, liver, and lung, following a variable clinical course. Most cases are characterized by a t(1;3)(p36;q23-25) resulting in WWTR1-CAMTA1 fusion. Only five epithelioid hemangioendothelioma have been previously reported arising in the salivary glands. None have presented as Bell\u2019s palsy. In the current case, a 37-year-old female presented with a longstanding complaint of pain and fullness in the right preauricular region and progressive episodes of Bell\u2019s palsy and facial nerve weakness. Surgical resection showed a tumor comprised of atypical cells with occasional intracytoplasmic vacuoles in a fibromyxoid stroma. Immunohistochemical stains demonstrated the neoplastic cells expressed ERG, CD31, and CD34, confirming vascular differentiation. Fluorescence in situ hybridization revealed a t(1;3)(p36;q25), confirming a diagnosis of epithelioid hemangioendothelioma. At 12-month follow-up, the patient has no evidence of disease.<\/jats:p>","DOI":"10.1155\/2022\/5687190","type":"journal-article","created":{"date-parts":[[2022,6,24]],"date-time":"2022-06-24T22:50:19Z","timestamp":1656111019000},"page":"1-6","source":"Crossref","is-referenced-by-count":3,"title":["Epithelioid Hemangioendothelioma with WWTR1-CAMTA1 Fusion in the Parotid Gland Presenting as Bell\u2019s Palsy"],"prefix":"10.1155","volume":"2022","author":[{"given":"Landon J.","family":"Kunzelman","sequence":"first","affiliation":[{"name":"University of New Mexico, Department of Pathology, MSC08 4640, Reginald Heber Fitz Hall, Room 335, 1 University of New Mexico, Albuquerque, NM 87131, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-3026-6040","authenticated-orcid":true,"given":"Shweta","family":"Agarwal","sequence":"additional","affiliation":[{"name":"University of New Mexico, Department of Pathology, MSC08 4640, Reginald Heber Fitz Hall, Room 335, 1 University of New Mexico, Albuquerque, NM 87131, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nathan","family":"Boyd","sequence":"additional","affiliation":[{"name":"University of New Mexico, Department of Surgery-Division of Otolaryngology-Head and Neck Surgery, MSC10 5610, 1 University of New Mexico, Albuquerque, NM 87131, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-9755-4832","authenticated-orcid":true,"given":"Cory J.","family":"Broehm","sequence":"additional","affiliation":[{"name":"University of New Mexico, Department of Pathology, MSC08 4640, Reginald Heber Fitz Hall, Room 335, 1 University of New Mexico, Albuquerque, NM 87131, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","reference":[{"key":"1","doi-asserted-by":"publisher","DOI":"10.1002\/hed.23203"},{"key":"2","doi-asserted-by":"publisher","DOI":"10.1097\/00000478-199704000-00001"},{"key":"3","doi-asserted-by":"publisher","DOI":"10.1126\/scitranslmed.3002409"},{"key":"4","doi-asserted-by":"publisher","DOI":"10.1097\/00000478-200105000-00019"},{"key":"5","doi-asserted-by":"publisher","DOI":"10.1002\/gcc.20886"},{"issue":"3","key":"6","first-page":"457","article-title":"Epithelioid haemangioendothelioma of the parotid salivary gland: a case report","volume":"56","author":"L. 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