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首页> 外文期刊>APMIS: Acta Pathologica, Microbiologica et Immunologica Scandinavica >Clinicopathological features of five unusual cases of intraosseous myoepithelial carcinomas, mimicking conventional primary bone tumours, including EWSR1 rearrangement in one case
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Clinicopathological features of five unusual cases of intraosseous myoepithelial carcinomas, mimicking conventional primary bone tumours, including EWSR1 rearrangement in one case

机译:五例罕见的骨内肌上皮癌罕见病例的临床病理特征,模仿了传统的原发性骨肿瘤,其中一例包括EWSR1重排

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摘要

Primary intraosseous myoepithelial tumours, including carcinomas are rare tumours. The concept of histopathological spectrum of these tumours is evolving. We describe clinicopathological and immunohistochemical features of five myoepithelial carcinomas, including molecular cytogenetic results in one case. There were five male patients within age-range of 8-40 years (median = 26). Four tumours occurred in the long bones, including two tumours, each, in the femur and fibula, respectively, while a single tumour occurred in the proximal phalanges. Tumour size (n = 3 cases) varied from 5.6 to 8.6 cm. On radiological imaging, most tumours appeared as expansile, lytic and destructive lesions. Two tumours appeared as sclerotic lesions. Two cases were referred with diagnoses of chondrosarcomas and a single case was referred with two different diagnoses, including an adamantinoma and an osteosarcoma. Histopathological examination in all these cases showed multinodular tumours comprising mostly polygonal cells, exhibiting moderate nuclear atypia and interspersed mitotic figures within a stroma containing variable amount of myxoid, chondroid, hyalinised and osteoid-like material. Three tumours revealed prominent squamous differentiation. By immunohistochemistry, tumour cells were positive for EMA (5/5), pan CK (AE1/AE3) (3/3), CK5/6 (4/4), CK MNF116 (1/1), S100 protein (5/5) and GFAP (3/5). The first tumour revealed EWSR1 rearrangement. The first patient, 10 months after tumour resection and a simultaneous lung metastatectomy, is free-of-disease (FOD). The second patient, 11 months after tumour resection is FOD. The third and fourth patients underwent wide resections and are on follow-up. The fifth patient underwent resections, including a lung metastatectomy. Primary intraosseous myoepithelial carcinomas are rare and mimic conventional primary bone tumours. Some primary intraosseous myoepithelial carcinomas display EWSR1 rearrangement. Squamous differentiation may be considered as an addition to their evolving histopathological spectrum. Immunohistochemical stains constitute as a necessary tool for arriving at the correct diagnosis in such cases, which has treatment implications. Surgical resection remains the treatment mainstay.
机译:原发性骨内肌上皮肿瘤,包括癌是罕见的肿瘤。这些肿瘤的组织病理学谱的概念正在发展。我们描述了五例肌上皮癌的临床病理和免疫组织化学特征,包括在一例中的分子细胞遗传学结果。年龄在8-40岁(中位数= 26)之间的男性患者为5名。长骨中有四个肿瘤,其中两个分别在股骨和腓骨中发生,而单个肿瘤在近端指骨中发生。肿瘤大小(n = 3例)从5.6到8.6 cm不等。在放射成像上,大多数肿瘤表现为扩张性,溶解性和破坏性病变。两种肿瘤表现为硬化性病变。 2例转诊为软骨肉瘤,1例转诊为两种不同的诊断,包括金刚烷瘤和骨肉瘤。在所有这些病例中的组织病理学检查均显示多结节性肿瘤,主要由多角形细胞组成,在基质中表现出中等程度的核非典型性和散布的有丝分裂形态,其中基质中含有可变数量的类固醇,软骨,透明质和类骨质。三种肿瘤显示出突出的鳞状分化。通过免疫组织化学,肿瘤细胞阳性EMA(5/5),pan CK(AE1 / AE3)(3/3),CK5 / 6(4/4),CK MNF116(1/1),S100蛋白(5 / 5)和GFAP(3/5)。第一个肿瘤显示EWSR1重排。肿瘤切除并同时进行肺转移瘤切除术后10个月的第一例患者为无病(FOD)。肿瘤切除后11个月的第二名患者是FOD。第三和第四例患者接受了广泛的切除术并接受随访。第五名患者接受了包括肺转移切除术在内的切除术。原发性骨内肌上皮癌很少见,可模仿传统的原发性骨肿瘤。一些原发性骨内肌上皮癌表现出EWSR1重排。鳞状分化可以被认为是其不断发展的组织病理学光谱的补充。在这种情况下,免疫组织化学染色是获得正确诊断的必要工具,这对治疗有影响。手术切除仍然是治疗的主体。

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