Cordier Fleur, Hoorens Anne, Ferdinande Liesbeth, Van Dorpe Jo, Creytens David
Department of Pathology, Ghent University Hospital, Ghent 9000, Belgium.
World J Clin Cases. 2023 Jul 16;11(20):4734-4739. doi: 10.12998/wjcc.v11.i20.4734.
Inflammatory myofibroblastic tumor (IMT) of the biliary tract is rare, and often difficult to diagnose or to distinguish from other tumors due to its atypical clinical presentation and nonspecific radiological features. Histologically, IMTs are (myo)fibroblastic neoplasms with a prominent inflammatory infiltrate. They are characterized by receptor tyrosine kinase gene rearrangements, most often involving an anaplastic lymphoma kinase () translocation. The final diagnosis of IMT depends on histopathology and immunohistochemical examination. In this manuscript, we provide a clinical and morphomolecular overview of IMT and the difficulties that may arise in using immunohistochemical and molecular techniques in diagnosing IMT.
胆道炎性肌纤维母细胞瘤(IMT)较为罕见,由于其非典型的临床表现和非特异性的放射学特征,常难以诊断或与其他肿瘤相鉴别。组织学上,IMT是具有显著炎性浸润的(肌)纤维母细胞性肿瘤。它们的特征是受体酪氨酸激酶基因重排,最常见的是涉及间变性淋巴瘤激酶(ALK)易位。IMT的最终诊断取决于组织病理学和免疫组化检查。在本手稿中,我们提供了IMT的临床及形态分子概述,以及在使用免疫组化和分子技术诊断IMT时可能出现的困难。