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具有蜕膜样形态的间皮瘤:一种形态学谱系及一种不限于年轻女性的变体。

Mesotheliomas with deciduoid morphology: a morphologic spectrum and a variant not confined to young females.

作者信息

Shanks J H, Harris M, Banerjee S S, Eyden B P, Joglekar V M, Nicol A, Hasleton P S, Nicholson A G

机构信息

Department of Histopathology, Christie Hospital, Manchester, England.

出版信息

Am J Surg Pathol. 2000 Feb;24(2):285-94. doi: 10.1097/00000478-200002000-00015.

Abstract

Deciduoid mesotheliomas are rare with only four previously reported cases, all affecting the peritoneum of young females. We describe another six cases (three men and three women; age range 52-65 yrs, median 55 yrs; five peritoneal and one pleural). Three patients had an occupational history of asbestos exposure. The deciduoid appearance predominated in four cases, whereas in two it represented a minor component within conventional tubulopapillary epithelioid mesothelioma. All tumors were strongly cytokeratin-positive (including CK5/6) and all showed at least focal staining for thrombomodulin, HBME-1, and calretinin. All were negative for epithelial mucin (D/PAS), CEA, BerEP4, LeuM1 (CD15), CD21, CD35, and S100 protein. Five of six cases (83%) were vimentin-positive and two (33%) were focally positive for alpha-smooth muscle actin. A differential diagnosis of gastrointestinal autonomic nerve tumor (GANT) had been initially considered from the morphology of one case, and we found positivity for some of the "neuronal" markers described in GANTs. This prompted us to apply such a panel to the other five tumors, accepting that the cytokeratin positivity encountered in all of our cases would exclude GANT. All cases of deciduoid mesothelioma (100%) were positive for PGP 9.5 and NSE and four of six (66%) were positive for NKI/C3. Weak focal staining (<5% cells) for synaptophysin was seen in two of six tumors. All cases were chromogranin-negative. All cases examined by electron microscopy showed desmosomes and smooth microvilli without rootlets but no neuroendocrine granules. In conclusion, a deciduoid morphology appears to be part of the histopathologic spectrum encountered in epithelioid mesothelioma. This variant is not confined to female patients and occurs over a wider age range than previously recognized. The overlapping immunophenotype with GANTs illustrates that caution should be exercised when interpreting positivity for "neuronal" markers in this context. An immunohistochemical panel that includes cytokeratins should always be used.

摘要

蜕膜样间皮瘤很罕见,此前仅报道过4例,均累及年轻女性的腹膜。我们描述了另外6例(3名男性和3名女性;年龄范围52 - 65岁,中位年龄55岁;5例腹膜肿瘤,1例胸膜肿瘤)。3例患者有石棉接触职业史。4例以蜕膜样外观为主,而在另外2例中,它是传统管状乳头状上皮样间皮瘤中的次要成分。所有肿瘤细胞角蛋白均呈强阳性(包括CK5/6),且均至少局灶性表达血栓调节蛋白、HBME - 1和钙视网膜蛋白。上皮黏液(D/PAS)、癌胚抗原(CEA)、BerEP4、LeuM1(CD15)、CD21、CD35和S100蛋白均为阴性。6例中有5例(83%)波形蛋白阳性,2例(33%)α - 平滑肌肌动蛋白局灶性阳性。根据1例的形态学表现,最初考虑鉴别诊断为胃肠道自主神经肿瘤(GANT),我们发现其对一些GANT中描述的“神经元”标志物呈阳性。这促使我们将这样一组标志物应用于其他5例肿瘤,同时我们也清楚我们所有病例中细胞角蛋白阳性这一情况可排除GANT。所有蜕膜样间皮瘤病例(100%)PGP 9.5和NSE呈阳性,6例中有4例(66%)NKI/C3呈阳性。6例肿瘤中有2例可见突触素弱局灶性染色(<5%细胞)。所有病例嗜铬粒蛋白均为阴性。所有经电子显微镜检查的病例均显示有桥粒和无根的平滑微绒毛,但无神经内分泌颗粒。总之,蜕膜样形态似乎是上皮样间皮瘤组织病理学谱的一部分。这种变异并不局限于女性患者,且发生年龄范围比之前认识的更广。与GANTs重叠的免疫表型说明在此背景下解释“神经元”标志物阳性时应谨慎。应始终使用包括细胞角蛋白的免疫组织化学标志物组合。

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