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伴有梭形细胞的导管原位癌:乳腺病变评估中潜在的诊断陷阱。

Ductal carcinoma in situ with spindle cells: a potential diagnostic pitfall in the evaluation of breast lesions.

作者信息

Tan P H, Lui G G, Chiang G, Yap W M, Poh W T, Bay B H

机构信息

Department of Pathology, Singapore General Hospital, Singapore.

出版信息

Histopathology. 2004 Oct;45(4):343-51. doi: 10.1111/j.1365-2559.2004.01947.x.

Abstract

AIMS

To evaluate the morphological features of 11 cases of breast ductal carcinoma in situ (DCIS) with spindle cells and to propose an approach to distinguish it from benign mimics. The association with neuroendocrine differentiation was also investigated.

METHODS

Cases of breast DCIS with a spindle cell component diagnosed in the Department of Pathology, Singapore General Hospital, between June 1996 and January 2003, were included in the study. The histological characteristics were documented, and immunohistochemistry for neuroendocrine markers, hormone receptors, cerbB2, smooth muscle actin (SMA) and high-molecular-weight (HMW) cytokeratins, was carried out. Electron microscopy was carried out on reprocessed paraffin-embedded material in three cases.

RESULTS

Of 11 women diagnosed with DCIS with spindle cells, four presented with nipple discharge, six with a breast lump, while one was discovered to have a screen detected density. The tumour size ranged from 3 to 41 mm. The proportion of spindle cells varied from 10% to 80% of the in-situ tumour cell population. Nuclear grade was low in seven cases and intermediate in four. Necrosis was observed in two cases. Architectural pattern was papillary in six cases, and mixed in the rest. Microinvasion was present in two cases, with possible microinvasion in another two. Immunohistochemistry for neuroendocrine markers synaptophysin and chromogranin showed positive reactivity for at least one marker in all but three cases; one of these latter cases demonstrated ultrastructural neurosecretory granules. Oestrogen and progesterone receptors were expressed in 10 and nine cases, respectively, while cerbB2 was positive in only one case. HMW cytokeratin immunoprofile revealed a general lack of immunostaining within the abnormal cell population; likewise, no positivity for SMA of the cellular proliferation was detected.

CONCLUSIONS

Almost all DCIS lesions with spindle cells disclose neuroendocrine differentiation. Although the distinction from benign florid usual hyperplasia may pose a diagnostic histological problem, the presence of diffuse neuroendocrine expression, in conjunction with the pattern of HMW keratin profile on immunohistochemistry, supports an in-situ neoplastic process. The absence of SMA immunostaining, in conjunction with negative reactivity for cytokeratins 5/6 and 14, makes the possibility of a myoepithelial proliferation unlikely.

摘要

目的

评估11例伴有梭形细胞的乳腺导管原位癌(DCIS)的形态学特征,并提出一种将其与良性模仿病变相鉴别的方法。同时研究其与神经内分泌分化的关系。

方法

纳入1996年6月至2003年1月在新加坡总医院病理科诊断的伴有梭形细胞成分的乳腺DCIS病例。记录组织学特征,并进行神经内分泌标志物、激素受体、cerbB2、平滑肌肌动蛋白(SMA)和高分子量(HMW)细胞角蛋白的免疫组织化学检测。对3例病例的重新处理石蜡包埋材料进行电子显微镜检查。

结果

在11例诊断为伴有梭形细胞的DCIS的女性中,4例有乳头溢液,6例有乳腺肿块,1例是在筛查时发现密度异常。肿瘤大小为3至41毫米。梭形细胞在原位肿瘤细胞群体中的比例为10%至80%。7例核分级低,4例为中级。2例观察到坏死。6例的结构模式为乳头状,其余为混合型。2例有微浸润,另外2例可能有微浸润。神经内分泌标志物突触素和嗜铬粒蛋白的免疫组织化学显示,除3例病例外,所有病例中至少有一种标志物呈阳性反应;后一组病例中的1例显示有超微结构的神经分泌颗粒。雌激素和孕激素受体分别在10例和9例中表达,而cerbB2仅在1例中呈阳性。HMW细胞角蛋白免疫表型显示异常细胞群体中普遍缺乏免疫染色;同样,未检测到细胞增殖的SMA阳性。

结论

几乎所有伴有梭形细胞的DCIS病变都显示神经内分泌分化。虽然与良性的小叶性增生相鉴别可能会带来诊断组织学难题,但弥漫性神经内分泌表达的存在,结合免疫组织化学中HMW角蛋白的模式,支持原位肿瘤形成过程。SMA免疫染色阴性,结合细胞角蛋白5/6和14的阴性反应,使得肌上皮增生的可能性不大。

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