Academic Journal

Angiomatoid fibrosis histiocytoma in the pulmonary artery: A case report

التفاصيل البيبلوغرافية
العنوان: Angiomatoid fibrosis histiocytoma in the pulmonary artery: A case report
المؤلفون: Shuji Mishima, Osamu Mishima, Koji Azuhata, Hisashi Shimojo, Nobuo Ito, Kenji Misawa, Kimihiro Shimizu
المصدر: Thoracic Cancer, Vol 12, Iss 9, Pp 1453-1456 (2021)
بيانات النشر: Wiley, 2021.
سنة النشر: 2021
المجموعة: LCC:Neoplasms. Tumors. Oncology. Including cancer and carcinogens
مصطلحات موضوعية: angiomatoid fibrosis histiocytoma, case report, EWSR1‐CREB1 fusion, pulmonary artery, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
الوصف: Abstract Angiomatoid fibrosis histiocytoma (AFH) is a rare neoplastic disease. Only one report has demonstrated an intraluminal tumor of the pulmonary artery (PA) corresponding to AFH to date. We describe the case of AFH with EWSR1‐CREB1 fusion occurring in the ascending artery. A 42‐year‐old man exhibited an abnormal nodule on chest computed tomography (CT) during checkup. It revealed an intraluminal mass in the ascending artery with significant metabolic uptake in positron emission tomography (PET)/CT. Therefore, right upper lobectomy with wedge resection of the PA trunk was performed. Histologically, the tumor was multinodular and surrounded by a dense lymphoplasmacytic cuff. Each nodule was composed of myxoid stroma and comprised ovoid or spindle cell fascicles with mild atypia. Fluorescent in situ hybridization (FISH) analysis confirmed EWSR1‐CREB1 fusion. A diagnosed as AFH was made. This report widens the spectrum of differential diagnoses of primary tumors occurring in the PA.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1759-7714
1759-7706
Relation: https://doaj.org/toc/1759-7706; https://doaj.org/toc/1759-7714
DOI: 10.1111/1759-7714.13929
URL الوصول: https://doaj.org/article/3f3db651a369422d9805cb933b078cb9
رقم الانضمام: edsdoj.3f3db651a369422d9805cb933b078cb9
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:17597714
17597706
DOI:10.1111/1759-7714.13929