| Literature DB >> 32128196 |
Joji Samejima1, Hiroyuki Ito1, Tomoyuki Yokose2, Takuya Nagashima1.
Abstract
Desmoid-type fibromatosis following thoracotomy is rare and has been previously reported only in <20 cases; however, it might mimic chest wall recurrence of previous cancer and needs differential diagnosis. When the tumor location corresponded to the thoracotomy incision, we should consider desmoid-type fibromatosis as a differential diagnosis.Entities:
Keywords: chest wall; desmoid‐type; fibromatosis; thoracotomy
Year: 2019 PMID: 32128196 PMCID: PMC7044401 DOI: 10.1002/ccr3.2634
Source DB: PubMed Journal: Clin Case Rep ISSN: 2050-0904
Figure 1A, Chest computed tomography (CT) revealed a chest wall mass measuring 33 × 23 mm 19 mo after surgery. B, We could identify a mass measuring 14 × 8 mm at the same site on a CT scan taken 11 mo after surgery. C, 18F‐fluorodeoxyglucose positron emission tomography showed a maximum standardized uptake value of 4.7 in the tumor
Figure 2A, Histopathological examination showing tumor cells composed of spindle‐shaped cells arranged in a fascicular pattern (hematoxylin and eosin stain, original magnification ×100). B, Immunohistochemical examination showing spindle cells positive for nuclear ß‐catenin (original magnification ×400) and negative for desmin, S100, and CD34. The MIB‐1 index was <5%