S100-positive stroma in salivary gland basal cell adenomas: a neoplastic component with CTNNB1 mutations.

IF 3.4 3区 医学 Q1 PATHOLOGY Virchows Archiv Pub Date : 2024-12-26 DOI:10.1007/s00428-024-04021-1
Eiichi Sasaki, Yasuko Fujita, Katsuhiro Masago, Akari Iwakoshi, Nobuhiro Hanai, Hirokazu Matsushita
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Abstract

Basal cell adenomas (BCAs) are benign epithelial tumors of the salivary gland, characterized by the proliferation of basaloid and luminal cells. In addition, a distinctive spindle cell stroma, that is immunohistochemically-positive for S100, is often observed in BCAs. Based on the ultrastructural findings, the S100-positive stroma was presumed to originate from neoplastic myoepithelial cells. However, immunohistochemical studies do not provide strong evidence supporting a myoepithelial origin, and the true nature of this stroma remains elusive. The aim of this study was to determine whether the S100-positive stroma was neoplastic through a molecular analysis. We selected 2 cases involving BCAs with at least one S100-positive stromal area within the tumor, measuring ≥ 0.2 × 0.2 mm. CTNNB1 I35T mutations were detected in both tumors by Sanger sequencing. Two areas of S100-positive stroma from these two tumors were successfully dissected by manual microdissection using a stereomicroscope without contamination from the surrounding neoplastic bilayered epithelial cells. Because of the small number of dissected stromal cells, the mutation status of these two areas was analyzed using digital PCR, and CTNNB1 I35T mutations were detected in both. In conclusion, this study demonstrated that the S100-positive stroma of BCAs exhibits a neoplastic nature from a molecular perspective. While future studies are needed to confirm whether the S100-positive stroma originates from myoepithelial cells, BCAs morphologically display tricellular differentiation, with neoplastic spindle-shaped stromal cells along with a bilayered neoplastic epithelium.

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唾液腺基底细胞腺瘤中的s100阳性基质:CTNNB1突变的肿瘤成分
基底细胞腺瘤(bca)是涎腺的良性上皮性肿瘤,以基底细胞和腔细胞增生为特征。此外,在bca中经常观察到一种独特的梭形细胞基质,其免疫组化S100阳性。根据超微结构结果,推测s100阳性基质来源于肿瘤肌上皮细胞。然而,免疫组织化学研究并没有提供强有力的证据支持肌上皮起源,并且这种基质的真实性质仍然难以捉摸。本研究的目的是通过分子分析确定s100阳性基质是否为肿瘤。我们选择了2例bca,肿瘤内至少有一个s100阳性间质区,面积≥0.2 × 0.2 mm。Sanger测序在两种肿瘤中检测到CTNNB1 I35T突变。在没有周围肿瘤双层上皮细胞污染的情况下,通过体视显微镜成功地解剖了这两个肿瘤的两个s100阳性间质区域。由于解剖的间质细胞数量较少,采用数字PCR分析这两个区域的突变状态,在这两个区域均检测到CTNNB1 I35T突变。综上所述,本研究从分子角度证明了s100阳性bca基质具有肿瘤性。虽然需要进一步的研究来证实s100阳性基质是否来源于肌上皮细胞,但bca在形态学上表现为三细胞分化,具有肿瘤梭形基质细胞和双层肿瘤上皮。
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来源期刊
Virchows Archiv
Virchows Archiv 医学-病理学
CiteScore
7.40
自引率
2.90%
发文量
204
审稿时长
4-8 weeks
期刊介绍: Manuscripts of original studies reinforcing the evidence base of modern diagnostic pathology, using immunocytochemical, molecular and ultrastructural techniques, will be welcomed. In addition, papers on critical evaluation of diagnostic criteria but also broadsheets and guidelines with a solid evidence base will be considered. Consideration will also be given to reports of work in other fields relevant to the understanding of human pathology as well as manuscripts on the application of new methods and techniques in pathology. Submission of purely experimental articles is discouraged but manuscripts on experimental work applicable to diagnostic pathology are welcomed. Biomarker studies are welcomed but need to abide by strict rules (e.g. REMARK) of adequate sample size and relevant marker choice. Single marker studies on limited patient series without validated application will as a rule not be considered. Case reports will only be considered when they provide substantial new information with an impact on understanding disease or diagnostic practice.
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