2021
DOI: 10.1007/s00428-020-03000-6
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Common and rare carcinomas of the thymus

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Cited by 7 publications
(18 citation statements)
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“…Generally, most of the histotypes such as squamous or mucoepidermoid are morphological (at histology and immunohistochemistry) to the counterpart of another organ. Therefore, searching for a clinical-radiological correlation and for immunomarkers of thymic origin is mandatory to exclude mediastinal metastases from cancers of other sites [35]. Squamous cell carcinoma (SCC) is the most common histotype of thymic carcinoma accounting for 70-80% of all TC, similar to what emerged from our case series [2, 34,36].…”
Section: Thymic Carcinomasupporting
confidence: 73%
“…Generally, most of the histotypes such as squamous or mucoepidermoid are morphological (at histology and immunohistochemistry) to the counterpart of another organ. Therefore, searching for a clinical-radiological correlation and for immunomarkers of thymic origin is mandatory to exclude mediastinal metastases from cancers of other sites [35]. Squamous cell carcinoma (SCC) is the most common histotype of thymic carcinoma accounting for 70-80% of all TC, similar to what emerged from our case series [2, 34,36].…”
Section: Thymic Carcinomasupporting
confidence: 73%
“…Importantly, in the differential from thymic carcinoma, type B3 cells are CD5‐ and CD117‐negative, with rarely at most focal expression of GLUT1 and MUC1, 44 and also negative for CD20, which is typically positive in thymoma type A. Conversely, positivity for CD5, CD117, GLUT‐1, Muc1, or a combination thereof is typical of thymic squamous carcinomas, although these are neither completely sensitive nor entirely specific 44‐47 . Recently, it has been shown that proteasome subunit beta5t may be a good marker in the distinction between thymic carcinoma (negative) and B3 thymomas (positive), and in combination with Muc1 (positive in carcinomas) has been shown to reach impressive sensitivities and specificities 45,47‐49 . Moreover, including TdT in a panel also containing BAP1, MTAP (both of which can be lost in thymic carcinoma), and CD117 (using a cutoff of >10% tumour cell expression for carcinomas) may be useful in the distinction between thymomas and thymic carcinomas 50 .…”
Section: Type B3 Thymomamentioning
confidence: 99%
“…Like other carcinomas, they tend to occur in a slightly higher age group than thymomas (median age 54–65.5 years), but with a broad age range (12–96 years old) and a male predominance 52,90‐97 . They are usually invasive, with an aggressive course of disease, and often present at advanced stages (most patients presenting at TNM stage III, IVA, or IVB, with lymph node metastases in 1/3 at presentation), with a median time to death (3 years) considerably shorter than in thymomas 48,89‐92,97 . Paraneoplastic/autoimmune diseases are rarely seen in patients with thymic carcinomas (1.5%–2%), setting them apart for thymomas 99‐101 .…”
Section: Thymic Carcinomasmentioning
confidence: 99%
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“…These tumors share morphological and immunophenotypic features with squamous cell cancers of the lung, which constitute approximately 20% of all non-small cell lung cancers (NSCLCs) ( 1 , 4 ). Although clinical and radiological features along with morphologic and immunophenotypic findings ( 2 ) can help to distinguish between thymic carcinomas and NSCLCs, in some cases it can be difficult to make a distinction between these tumors. Nevertheless, it is important to distinguish between thymic carcinoma and NSCLC due to differences in the clinical presentation, natural history, and management of these diseases.…”
mentioning
confidence: 99%