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Clinical Presentation and Treatment Options for Clear Cell Lung Cancer: University of Cincinnati A Case Series and Literature Review of Clear Cell Lung Cancer

机译:透明细胞肺癌的临床表现和治疗选择:辛辛那提大学一系列病例和透明细胞肺癌的文献综述

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摘要

Clear cell carcinomas are common finding in renal, ovarian and uterine carcinomas. However, clear cell lung cancer (CCLC), first described by Liebow and Castleman in 1963, is considered an extremely rare variant of lung tumors. The 2011 WHO classification of lung tumors considered CCLC as a rare cytologic feature of squamous cell or adenocarcinomas. It is no longer recognized as a formal subtype, albeit it can be referred to in the pathological diagnosis as “with clear cell features” even with marginal fractions of the tumor cells. Such recognition is needed since the variation in clinical features and outcome in this subset of patients. The disease has a clinically vague natural history, is characterized by slight female predominance and is often seen in the elderly. As frequently encountered with rare diseases, its clinical course and treatment options have many questions still yet to be answered. In this paper, we review both the natural history and treatment options mentioned in literature, in the light of our experience by reporting a case series of four patients diagnosed with CCLC and highlight their aspects.
机译:透明细胞癌是肾癌,卵巢癌和子宫癌的常见发现。然而,透明细胞肺癌(CCLC)(最早由Liebow和Castleman在1963年描述)被认为是极为罕见的肺部肿瘤变体。 2011年WHO对肺肿瘤的分类认为CCLC是鳞状细胞癌或腺癌的罕见细胞学特征。尽管它在病理学诊断中甚至被称为“具有清晰的细胞特征”,即使肿瘤细胞的边缘部分也被认为是正式的亚型。由于该患者子集中临床特征和预后的变化,因此需要这种识别。该病具有临床上模糊的自然病史,其特征是女性占主导地位,常在老年人中见到。作为罕见疾病的常见病,其临床病程和治疗选择还有许多问题尚待解答。在本文中,根据我们的经验,我们通过报告四例确诊为CCLC的患者的病例系列并重点介绍其方面,回顾了文献中提到的自然病史和治疗选择。

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