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皮肤假性黏液瘤;一种新的疾病实体。

Pseudomyxoma cutis; a new entity.

作者信息

Terada Tadashi

机构信息

Department of Pathology, Shizuoka City Shimizu Hospital, Shimizu, Shizuoka, Japan.

出版信息

Int J Clin Exp Pathol. 2013 May 15;6(6):1169-76. Print 2013.

Abstract

Pseudomyxoma (PM) implies an accumulation of a large amount of mucins which show myxomatous appearances. PM Peritonei (PMP) is famous and the only example of PM. PMP means excessive accumulation of mucins and mucin-secreting cells in the peritoneal cavity. The causes of PMP are mostly mucinous tumors, both benign and malignant, of ovaries and vermiform appendix. The author experienced excessive accumulation of mucins and mucin-producing cells in the subcutis and deep soft tissue. This situation very resembled PMP. Thus, the author termed the lesion as PM cutis (PMC). A 57-year-old man admitted to our hospital because of multiple subcutaneous large tumors in the perianal skin. The tumors were deeply seated and soft. No biopsy was performed. Very large skin and subcutis resection of the perianal region was done. Grossly, the material was skin and sot tissue flap measuring 25x25x5cm. The subcutis and deep soft tissue were resected. On cut surface, the tumor was slimy liquid. Microscopical examination revealed a large amount of mucins pools and mucin-producing intestinal epithelium with mild atypia. The author diagnosed it metastatic extremely well differentiated adenocarcinoma producing mucins, and pointed out anorectal primary. Thus, Miles operation was performed, which showed tumor formation in the anus. The tumor was located from the submucosa to adventitia, and composed of mucin pools and mucins producing intestinal-type epithelium with atypia. Mucins histochemistry showed that the mucin pools and epithelial cytoplasm contained neutral, carboxylated, and sulfated mucins. Immunohistochemically, the tumor cells were positive for CKAE1/3, CKCAM5.2, CK7, CK8, CK19, CK20, CEA, CA19-9,CD68, MET, p53, MUC2, MUC5AC, KIT, PDGFRA, chromogranin, and Ki-67 (76%). They were negative for CK34BE12, CK5/6, CK14, CK18, EMA, vimentin, desmin, smooth muscle actin, p63, CD34, ER, PgR, CA125, MUC1, MUC6, CD45, CD10, synaptophysin, surfactant Apo-A, TTF-1, NCAM, bcl-2, CDX-2. Although the atypia is mild, the author diagnosed primary anorectal extremely well differentiated adenocarcinoma with excessive production of mucins. The author considers the cutaneous mucins and tumor cells are metastatic or directly invading lesions of the anal tumor. Thus, the author termed pseudomyxoma cutis (PMC) for the cutaneous lesion.

摘要

黏液瘤(PM)意味着大量呈现黏液瘤样外观的黏蛋白积聚。腹膜黏液瘤(PMP)是黏液瘤中为人熟知且唯一的例子。PMP指的是腹膜腔内黏蛋白和黏蛋白分泌细胞的过度积聚。PMP的病因大多是卵巢和阑尾的黏液性肿瘤,包括良性和恶性。作者遇到了皮下和深部软组织中黏蛋白及黏蛋白产生细胞的过度积聚。这种情况与PMP非常相似。因此,作者将该病变称为皮肤黏液瘤(PMC)。一名57岁男性因肛周皮肤多发皮下大肿瘤入住我院。肿瘤位置较深且质地柔软。未进行活检。对肛周区域进行了非常大的皮肤和皮下组织切除。大体上,切除的组织是一块大小为25×25×5cm的皮肤和软组织瓣。皮下组织和深部软组织被切除。切面显示肿瘤为黏液样液体。显微镜检查发现大量黏液池和产生黏液的肠上皮,有轻度异型性。作者诊断为转移性高分化黏液腺癌,并指出原发部位在肛肠。于是进行了腹会阴联合切除术,术中发现肛门处有肿瘤形成。肿瘤位于黏膜下层至外膜,由黏液池和产生黏液的异型肠型上皮组成。黏液组织化学显示黏液池和上皮细胞质中含有中性、羧化和硫酸化黏蛋白。免疫组化结果显示,肿瘤细胞对CKAE1/3、CKCAM5.2、CK7、CK8、CK19、CK20、CEA、CA19 - 9、CD68、MET、p53、MUC2、MUC5AC、KIT、PDGFRA、嗜铬粒蛋白和Ki - 67(76%)呈阳性。它们对CK3BE12、CK5/6、CK14、CK18、EMA、波形蛋白、结蛋白、平滑肌肌动蛋白、p63、CD34、ER、PgR、CA125、MUC1、MUC6、CD45、CD10、突触素、表面活性剂Apo - A、TTF - l、NCAM、bcl - 2、CDX - 2呈阴性。尽管异型性较轻,但作者诊断为原发性肛肠高分化黏液腺癌伴黏液过度产生。作者认为皮肤中的黏液和肿瘤细胞是肛门肿瘤的转移或直接侵犯性病变。因此,作者将皮肤病变称为皮肤黏液瘤(PMC)。

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