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Differential Diagnosis of Inflammatory Myofibroblastic Tumour and Low-Grade Myofibroblastic Sarcoma: Two Case Reports with a Literature Review

机译:炎症性肌纤维母细胞瘤和低度肌纤维母细胞肉瘤的鉴别诊断:两例报道并文献复习

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Inflammatory myofibroblastic tumour (IMT) and low-grade myofibroblastic sarcoma (LGMS) have similar morphological and immunophenotypic features, but LGMS is more malignant than IMT and the treatment requires a wider surgical margin plus post-operative chemotherapy or radiotherapy. To date, only 28 cases of IMT and two cases of LGMS have been reported in the laryngopharynx. Recent studies have suggested that anaplastic lymphoma kinase (ALK) and cytokeratin are important markers for differentiating between the two tumours. Here, two cases involving different myofibroblastic tumours of the larynx are reported. Based on the histological and immunohistochemical results, case 1 was diagnosed as IMT involving the right arytenoepiglottic fold, while case 2 was diagnosed as LGMS involving the epiglottic–glossal surface. There was no recurrence or metastasis in either case after post-operative follow-up (12 and 14 months, respectively). It is difficult to distinguish IMT from LGMS; both morphological and immunohistological analyses are required.
机译:炎性肌纤维母细胞瘤(IMT)和低度肌纤维母细胞肉瘤(LGMS)具有相似的形态学和免疫表型特征,但LGMS的恶性程度要高于IMT,并且该疗法需要更广泛的手术切缘以及术后化疗或放疗。迄今为止,在喉咽中仅报道了28例IMT和2例LGMS。最近的研究表明,间变性淋巴瘤激酶(ALK)和细胞角蛋白是区分两种肿瘤的重要标志。在此,报道了两个涉及不同的喉肌纤维母细胞瘤的病例。根据组织学和免疫组化结果,病例1被诊断为IMT并累及右咽ep上褶皱,病例2被诊断为LGMS累及会厌-舌上表面。术后随访(分别为12和14个月)中,两种情况均无复发或转移。很难将IMT与LGMS区别开来;形态学和免疫组织学分析都是必需的。

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