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乳腺实性乳头状癌中肌上皮的缺失情况不一。

Loss of myoepithelium is variable in solid papillary carcinoma of the breast.

作者信息

Nicolas M M, Wu Y, Middleton L P, Gilcrease M Z

机构信息

Department of Pathology, University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.

出版信息

Histopathology. 2007 Nov;51(5):657-65. doi: 10.1111/j.1365-2559.2007.02849.x.

Abstract

AIMS

Reports on the frequency of myoepithelial loss in solid papillary carcinoma (SPC) of the breast, an unusual variant of papillary carcinoma with a solid pattern of expansile growth, have been strikingly contradictory. The aim was to clarify the frequency of myoepithelial loss in cases of SPC diagnosed at our institution.

METHODS AND RESULTS

Eleven cases of SPC with available blocks or unstained slides were retrieved from the M. D. Anderson archives or obtained from outside contributors. Immunohistochemistry for smooth muscle actin (SMA) and p63 was evaluated on the circumscribed nests that appeared to be non-invasive by haematoxylin and eosin morphology. Three of the 11 cases (27%) were positive for both SMA and p63 at the periphery of all such foci, whereas eight cases (73%) lacked staining for both myoepithelial markers in at least one focus. Of these eight cases, one was diagnosed with only microinvasion, yet metastatic tumour resembling the circumscribed primary SPC was identified in two ipsilateral axillary lymph nodes.

CONCLUSIONS

SPC of the breast frequently lacks myoepithelial markers at the tumour-stromal interface in spite of a circumscribed non-invasive appearance. Metastases from such tumours are infrequent, but can occur in cases that lack myoepithelial marker expression by immunohistochemistry.

摘要

目的

乳腺实性乳头状癌(SPC)是乳头状癌的一种不常见变体,具有实性膨胀性生长模式,关于其肌上皮丢失频率的报道存在显著矛盾。本研究旨在明确在本机构诊断的SPC病例中肌上皮丢失的频率。

方法与结果

从MD安德森癌症中心档案库中检索出11例有可用组织块或未染色玻片的SPC病例,或从外部捐赠者处获得病例。对苏木精和伊红染色形态学显示为边界清楚的、看似无侵袭性的巢状结构进行平滑肌肌动蛋白(SMA)和p63免疫组织化学评估。11例病例中有3例(27%)在所有此类病灶周边SMA和p63均呈阳性,而8例(73%)至少在一个病灶中两种肌上皮标志物均无染色。在这8例病例中,1例仅诊断为微侵袭,但在两个同侧腋窝淋巴结中发现了类似边界清楚的原发性SPC的转移瘤。

结论

尽管乳腺SPC外观边界清楚且无侵袭性,但在肿瘤-基质界面处常缺乏肌上皮标志物。此类肿瘤转移罕见,但在免疫组织化学显示缺乏肌上皮标志物表达的病例中可能发生转移。

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