Primary small cell neuroendocrine carcinoma of the breast: The histogenetic diatribe

D. Cabibi, C. Cipolla
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Abstract

cell neuroendocrine carcinoma of the breast: a report of two cases and review of the literature” by Spinelli et al. [1]. The authors stated that “the histogenesis is still unclear because the presence of neuroendocrine cells in normal breast has not been proved conclusively”. Moreover they reported two histogenetic hypotheses, the first one stating that “small cell neuroendocrine carcinoma (SCNC) is a variant of metaplastic carcinoma arising from a lobular or ductal carcinoma”, the second one claiming that “it is a distinct type of breast carcinoma different from the usual type”. We appreciate this case report and we agree with the authors on the histogenetic diatribe of this rare type of breast neoplasia. In this background, we would highlight our previous case report about a solid variant of mammary adenoid cystic carcinoma merging with "small cell carcinoma" [2] in which we found positivity for CD10 and S100 and negativity for estrogen receptors, both in sbACC and in SCC, in keeping with a myoepithelial origin of both neoplastic areas [3] supporting the hypothesis that the “two components share the same histogenetic myoepithelial origin and represent an example of dedifferentiation along neuroendocrine phenotype lines occurring in a multipotential neoplastic stem line, already committed towards a myoepithelial phenotype”. These findings are in keeping with the first hypothesis about the metaplastic, divergent histogenetic nature of SNSC and we think that this rare SNSC, albeit arising from a different tumor, could be introduced in this case review of the literature, also for its contribute to the histogenetic diatribe.
乳腺原发性小细胞神经内分泌癌:组织发生差异
乳腺细胞神经内分泌癌:附2例报告及文献复习”,Spinelli等[1]。作者指出,“组织发生尚不清楚,因为正常乳腺中存在神经内分泌细胞尚未得到确凿证明”。此外,他们还报告了两种组织遗传学假说,第一个假说认为“小细胞神经内分泌癌(SCNC)是由小叶癌或导管癌引起的化生癌的一种变体”,第二个假说认为“它是一种不同于通常类型的乳腺癌”。我们赞赏这一病例报告,并同意作者对这种罕见乳腺肿瘤的组织遗传学特征。在此背景下,我们将强调我们之前关于乳腺腺样囊性癌合并“小细胞癌”的病例报告[2],我们发现在sbACC和SCC中CD10和S100呈阳性,雌激素受体呈阴性。这与两个肿瘤区域的肌上皮起源一致[3],支持了“两个成分具有相同的组织发生性肌上皮起源,并代表了神经内分泌表型线沿多潜能肿瘤干系发生的去分化的例子,已经倾向于肌上皮表型”的假设。这些发现与第一个关于SNSC化生的假设一致,我们认为这种罕见的SNSC,尽管起源于不同的肿瘤,也可以在这个病例中引入,因为它有助于组织遗传变异。
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