Kahraman Devrim, Karakoyunlu Berkem, Karagece Ulker, Ertas Umit, Gunhan Omer
TOBB ETU School of Medicine, Department of Pathology, Beştepe, Yaşam Cd. No:5, 06560 Yenimahalle, Ankara, Turkey.
TOBB ETU School of Medicine, Beştepe, Yaşam Cd. No:5, 06560 Yenimahalle, Ankara, Turkey.
J Bone Oncol. 2020 Oct 21;26:100333. doi: 10.1016/j.jbo.2020.100333. eCollection 2021 Feb.
Desmoplastic fibroma (DF) is an intraosseous counterpart of desmoid-type soft tissue fibromatosis. It is most frequently seen in the jawbones. The clinical and radiological features of the present cases were nonspecific. The accumulation of beta-catenin in the nuclei of neoplastic cells which is a diagnostic feature of desmoid-type soft tissue fibromatosis could not be detectED in the present DF series. The aim of this study is to report a series of 22 cases of DF involving either mandible or maxilla. A retrospective evaluation of desmoplastic fibroma and beta-catenin, smooth muscle actin, nestin, cyclin D1 immunostaining's patterns. Most of the DF cases expressed only cytoplasmic beta-catenin immunostainings. We suggest that nuclear beta-catenin staining may not be used as a corroborating the diagnosis of DF. Immunohistochemical staining difference of jaw bone desmoplastic fibromas from other soft tissue and bone lesions may be related to the origination of jaw bone from The neural crest. Strong nestin and cyclin D1 positivity in our series supported this. A combined clinical, radiological, and histopathological analysis of the DF cases is essential in the diagnosis and management.
促纤维增生性纤维瘤(DF)是韧带样型软组织纤维瘤病的骨内对应物。它最常见于颌骨。本病例的临床和放射学特征不具有特异性。在本系列促纤维增生性纤维瘤中未检测到β-连环蛋白在肿瘤细胞核中的积聚,而这是韧带样型软组织纤维瘤病的诊断特征。本研究的目的是报告一系列22例累及下颌骨或上颌骨的促纤维增生性纤维瘤病例。对促纤维增生性纤维瘤以及β-连环蛋白、平滑肌肌动蛋白、巢蛋白、细胞周期蛋白D1免疫染色模式进行回顾性评估。大多数促纤维增生性纤维瘤病例仅表现为β-连环蛋白免疫染色呈细胞质阳性。我们认为,细胞核β-连环蛋白染色可能不能用于辅助促纤维增生性纤维瘤的诊断。颌骨促纤维增生性纤维瘤与其他软组织和骨病变在免疫组化染色上的差异可能与颌骨起源于神经嵴有关。我们系列病例中巢蛋白和细胞周期蛋白D1呈强阳性支持了这一点。对促纤维增生性纤维瘤病例进行临床、放射学和组织病理学综合分析对于诊断和治疗至关重要。