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眼皮肤嗜酸性细胞瘤:2例临床病理及免疫组化研究并文献复习

Oculocutaneous oncocytic tumors: clinicopathologic and immunohistochemical study of 2 cases with literature review.

作者信息

George Evan, Swanson Paul E, Newman Brian K, Wick Mark R

机构信息

Department of Pathology, University of Washington, Seattle, Washington, USA.

出版信息

Am J Dermatopathol. 2007 Jun;29(3):279-85. doi: 10.1097/DAD.0b013e318053d87c.

Abstract

Oculocutaneous oncocytic tumors (OCOTs) are uncommon neoplasms that have been reported only rarely in the dermatopathology literature and whose immunophenotypic profile has not been well characterized. The clinical, histologic, and immunophenotypic features of 2 cases seen by the authors were assessed, and relevant publications in the literature were reviewed. Both patients with OCOTs were adult women with gradually enlarging, asymptomatic lesions involving the caruncle; they were locally excised. Histologically, the tumors were well-circumscribed nodules comprised of large oxyphilic cells arranged in confluent sheets and forming glandular spaces with secretory material. Microcystic areas and sparse intermingled goblet-cells were also apparent. Nuclear atypia and infiltrative growth were absent. Mitotic activity was absent in one case; a single mitotic figure was identified in the other. Immunostains demonstrated uniform expression of pankeratin and mitochondrial antigens. Both neoplasms were also labeled for markers associated with cutaneous adnexal, lacrimal, and minor salivary glandular tissue, including alpha-1-antitrypsin, gross cystic disease fluid protein-15, carcinoembryonic antigen, lysozyme and MUC1; each case expressed 4 of the 5 substances. Some cells expressed cytokeratins 5/6 and p63 consistent with the presence of basal-type differentiation in a subset of cells. No definite evidence of myoepithelial differentiation was demonstrated, as stains for smooth muscle actin, muscle-specific actin, and S100 protein were negative. Estrogen and progesterone receptor proteins were absent; strong cytoplasmic immunoreactivity for androgen receptor protein was evident, but nuclear staining was absent. The authors conclude that OCOTs show glandular differentiation. A review of the literature disclosed that none of these lesions arising in the caruncle behaved aggressively, in contrast to occasional tumors in other oculocutaneous sites.

摘要

眼皮肤嗜酸性细胞瘤(OCOTs)是一种罕见的肿瘤,在皮肤病理学文献中仅有极少的报道,其免疫表型特征尚未得到充分描述。作者对所观察的2例OCOTs的临床、组织学和免疫表型特征进行了评估,并对文献中的相关出版物进行了回顾。2例OCOTs患者均为成年女性,病变位于泪阜,逐渐增大且无症状,均接受了局部切除。组织学上,肿瘤为边界清楚的结节,由大的嗜酸性细胞组成,呈融合片状排列,形成含有分泌物质的腺腔。微囊区和稀疏散在的杯状细胞也很明显。未见核异型性和浸润性生长。1例未见有丝分裂活性,另1例仅见1个有丝分裂象。免疫组化显示全角蛋白和线粒体抗原呈均匀表达。两种肿瘤均标记了与皮肤附属器、泪腺和小涎腺组织相关的标志物,包括α1-抗胰蛋白酶、巨大囊肿病液体蛋白-15、癌胚抗原、溶菌酶和MUC1;每例均表达了5种物质中的4种。部分细胞表达细胞角蛋白5/6和p63,提示部分细胞存在基底样分化。未显示明确的肌上皮分化证据,因为平滑肌肌动蛋白、肌特异性肌动蛋白和S100蛋白染色均为阴性。雌激素和孕激素受体蛋白缺失;雄激素受体蛋白呈强细胞质免疫反应,但无核染色。作者得出结论,OCOTs显示腺性分化。文献回顾显示,与其他眼皮肤部位偶尔出现的肿瘤不同,泪阜发生的这些病变均无侵袭性表现。

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