Matsushita Michiko, Kuwamoto Satoshi
Department of Pathobiological Science and Technology, School of Health Science, Faculty of Medicine, Tottori University, Yonago, Japan.
Division of Molecular Pathology, Faculty of Medicine, Tottori University, Yonago, Japan.
Acta Cytol. 2018;62(5-6):456-462. doi: 10.1159/000493335. Epub 2018 Oct 4.
SMARCA4-deficient thoracic sarcoma is a recently proposed entity of soft tissue tumors associated with an extremely poor prognosis. Its cytologic features have not been well described in the literature yet.
A woman in her early 30s who presented with chest pain was found to have a tumor in the right chest wall. Cytologic smears revealed numerous atypical round-to-polygonal cells appearing singly or in loosely cohesive clusters. These cells had a well-defined cell border, scant-to-moderate cytoplasm, and enlarged vesicular nuclei with prominent nucleoli. In addition, some cells with eosinophilic globular intracytoplasmic inclusions and eccentrically located nuclei, consistent with rhabdoid cells, were observed. Immunocytochemically, the cells were at least focally positive for cytokeratin CAM5.2 and CD34 and showed a significantly reduced BRG1/SMARCA4 expression. The diagnosis was confirmed by histological, immunohistochemical, and genetic analysis of a metastatic lesion to the left axillary lymph node.
Although the cytologic features of SMARCA4-deficient thoracic sarcoma are not fully unique, they are sufficiently characteristic to suspect this tumor in cases of supporting clinical and radiological features, which may promote additional immunological or molecular testing to establish a definitive diagnosis.
SMARCA4缺陷型胸壁肉瘤是一种最近提出的软组织肿瘤实体,预后极差。其细胞学特征在文献中尚未得到充分描述。
一名30岁出头的女性因胸痛就诊,发现右胸壁有一个肿瘤。细胞学涂片显示大量非典型圆形至多边形细胞,单个或呈松散聚集状出现。这些细胞具有清晰的细胞边界、少量至中等量的细胞质,以及增大的泡状核和明显的核仁。此外,还观察到一些具有嗜酸性球状胞质内包涵体和偏心核的细胞,符合横纹肌样细胞。免疫细胞化学检测显示,这些细胞至少局灶性表达细胞角蛋白CAM5.2和CD34,且BRG1/SMARCA4表达显著降低。通过对左腋窝淋巴结转移灶的组织学、免疫组织化学和基因分析确诊。
尽管SMARCA4缺陷型胸壁肉瘤的细胞学特征并非完全独特,但在具有支持性临床和放射学特征的病例中,这些特征足以怀疑该肿瘤,这可能会促使进行额外的免疫或分子检测以明确诊断。