Atypical lipomatous tumor mimicking giant fibrovascular polyp of the esophagus: report of a case and a critical review of literature

被引:17
作者
Boni, Andrea [1 ,2 ]
Lisovsky, Mikhail [1 ,2 ]
Dal Cin, Paola [3 ,4 ]
Rosenberg, Andrew E. [5 ,6 ]
Srivastava, Amitabh [3 ,4 ]
机构
[1] Dartmouth Hitchcock Med Ctr, Lebanon, NH 03766 USA
[2] Geisel Sch Med Dartmouth, Lebanon, NH USA
[3] Brigham & Womens Hosp, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Boston, MA USA
[5] Univ Miami Hosp, Miami, FL USA
[6] Univ Miami, Miller Sch Med, Miami, FL 33136 USA
关键词
Atypical lipomatous tumor; Liposarcoma; Esophagus; Fibrovascular polyp; MDM2; CDK4; WELL-DIFFERENTIATED LIPOSARCOMA; PEDUNCULATED LIPOSARCOMA;
D O I
10.1016/j.humpath.2012.10.023
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
An 81-year-old man presented to the emergency department with a mass protruding from his mouth after an episode of emesis. A computed tomography scan showed a hypodense, polypoid structure with a fatty component. The long polyp was attached by a narrow stalk to the cervical esophagus. A 14.0-cm slender mass resembling a giant fibrovascular polyp (GFP) of the esophagus was resected. The microscopic, immunohistochemical, and molecular findings were, however, those of an atypical lipomatous tumor (ALT). Atypical lipomatous tumor of the esophagus is a rare, low-grade malignant neoplasm, with a potential for local recurrence and, in most instances, presents as a large intraluminal polyp mimicking a GFP. Cases reported in the literature as primary myxoid liposarcomas of the esophagus are in all likelihood examples of ALT with myxoid change. A recent case reported as a GFP with karyotypic abnormalities on comparative genomic hybridization is also most likely to be an ALT mimicking a GFP. Pathologists need to be aware of the pitfalls in the diagnosis of ALT of the esophagus and should carefully evaluate the adipocytic component of these lesions. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:1165 / 1170
页数:6
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