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男性患者的肛门叶状肿瘤:独特的病例报告及文献复习。

Anal phyllodes tumor in a male patient: a unique case presentation and literature review.

机构信息

Department of Pathology and Laboratory Medicine, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan.

出版信息

Diagn Pathol. 2013 Mar 26;8:49. doi: 10.1186/1746-1596-8-49.

Abstract

UNLABELLED

Lesions of anogenital mammary-like glands are rare, and only 44 female cases have been reported. Herein, we describe a particularly rare case of phyllodes tumor of anogenital mammary-like glands in a 41-year-old male presenting anal bleeding. Papillectomy was performed. The excised tumor was circumscribed in shape, and after it was sliced into sections, it was noted that there were leaf-like slits on the surface of cut side. Under the microscope, the tumor was found to be biphasic, with a bland glandular epithelium and low-to-intermediate cellular stroma, which together created the leaf-like slits. Gynecomastoid hyperplasia was evident at the periphery. The epithelium showed immuno-activity for ER, PR(focal), AR, and GCDFP-15. The stromal cells showed positive staining for CD34 and vimentin. The morphology and immunophenotype were similar to benign phyllodes tumors of breast. To the best of our knowledge, this case report represents the first case of phyllodes tumor of anogenital mammary-like glands with gynecomastoid hyperplasia at the periphery in a male patient. To make a diagnosis, we had to differentiate this lesion from hidradenoma papilliferum of skin appendage, phyllodes tumor of ectopic prostatic tissue, and other tumors of anogenital mammary-like glands analogous to the breast tumor (e.g., fibroadenoma phyllodes, periductal stromal sarcoma, and spindle cell carcinoma). While gynecomastia of male breast is usually a result of hormone imbalance, our patient's tumor did not seem to be related to peripheral hormone status in the anogenital mammary-like glands. Nevertheless, because hormone imbalance has been strongly related to male breast cancer, hormone levels may need to be followed in male patients who have this rare malady.

VIRTUAL SLIDES

The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/1509145815899177.

摘要

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肛门生殖器乳腺样腺体的病变较为罕见,仅有 44 例女性病例报告。在此,我们描述了一例非常罕见的肛门生殖器乳腺样腺体叶状肿瘤病例,患者为 41 岁男性,表现为肛门出血。行乳头切除术。切除的肿瘤边界清楚,切开后可见切面有叶状裂隙。显微镜下,肿瘤呈双相性,有温和的腺上皮和低到中等细胞基质,共同形成叶状裂隙。周边可见乳腺样增生。上皮组织 ER、PR(局灶性)、AR 和 GCDFP-15 免疫活性阳性。基质细胞 CD34 和波形蛋白阳性染色。形态学和免疫表型与良性乳腺叶状肿瘤相似。据我们所知,这是首例男性肛门生殖器乳腺样腺体叶状肿瘤伴周边乳腺样增生的病例报告。为做出诊断,我们必须将该病变与皮肤附属器的汗管乳头状瘤、异位前列腺组织的叶状肿瘤以及其他与乳腺肿瘤类似的肛门生殖器乳腺样腺体肿瘤(如纤维腺瘤叶状肿瘤、导管周围间质肉瘤和梭形细胞癌)相鉴别。虽然男性乳腺的乳腺增生通常是由于激素失衡引起的,但我们患者的肿瘤似乎与肛门生殖器乳腺样腺体的周边激素状态无关。然而,由于激素失衡与男性乳腺癌密切相关,对于患有这种罕见疾病的男性患者,可能需要监测激素水平。

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