一例罕见的皮脂腺肿瘤中出现微乳头状结构和 Apocrine 分化的腺癌。

IF 1.1 4区 医学 Q4 DERMATOLOGY American Journal of Dermatopathology Pub Date : 2024-08-01 Epub Date: 2024-06-14 DOI:10.1097/DAD.0000000000002766
Naoko Shojiguchi, Eiichi Arai, Anna Kamimura, Masanori Yasuda
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摘要

摘要:一名 77 岁的日本男子因右上臂和腋窝皮下肿瘤来我院就诊。活组织检查显示,该患者患有皮肤附件肿瘤,呈腺垂体分化,并伴有腋窝淋巴结转移。化疗缩小肿瘤后,两个病灶均被切除。手臂肿瘤的切除标本显示出不同的组织学特征:(1)典型的皮脂腺瘤,具有类器官形态和皮脂腺细胞;(2)皮脂腺瘤,细胞不典型;(3)乳头管状瘤,表现为双相形态的苍白嗜酸性细胞,具有凋亡分化和基底细胞;(4)浸润性腺癌,具有微乳头状结构,让人联想到乳腺浸润性微乳头状癌。腋窝肿瘤已消退。据我们所知,这是首例在皮脂腺肿瘤中出现的具有浸润性微乳头状结构的皮肤附件肿瘤。
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A Rare Case of Adenocarcinoma With Micropapillary Structure and Apocrine Differentiation Arising in a Sebaceous Tumor.

Abstract: A 77-year-old Japanese man presented to our hospital with subcutaneous tumors of the right upper arm and axilla. A biopsy revealed a cutaneous adnexal tumor, showing apocrine differentiation, and axillary lymph node metastasis. After chemoradiotherapy to shrink the tumors, both lesions were resected. A resected specimen of the arm tumor showed a variegated histology: (1) a classic sebaceoma with an organoid pattern and sebocytes; (2) a sebaceous tumor with cellular atypia; (3) a papillotubular tumor showing a biphasic pattern of pale eosinophilic cells with apocrine differentiation and basaloid cells; and (4) an invasive adenocarcinoma with a micropapillary structure, reminiscent of an invasive micropapillary carcinoma of the breast. The axillary tumor was regressed. To our knowledge, this is the first reported case of an adnexal tumor of the skin with an invasive micropapillary structure arising in a sebaceous tumor.

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来源期刊
CiteScore
1.80
自引率
9.10%
发文量
453
审稿时长
3 months
期刊介绍: The American Journal of Dermatopathology offers outstanding coverage of the latest diagnostic approaches and laboratory techniques, as well as insights into contemporary social, legal, and ethical concerns. Each issue features review articles on clinical, technical, and basic science advances and illuminating, detailed case reports. With the The American Journal of Dermatopathology you''ll be able to: -Incorporate step-by-step coverage of new or difficult-to-diagnose conditions from their earliest histopathologic signs to confirmatory immunohistochemical and molecular studies. -Apply the latest basic science findings and clinical approaches to your work right away. -Tap into the skills and expertise of your peers and colleagues the world over peer-reviewed original articles, "Extraordinary cases reports", coverage of practical guidelines, and graphic presentations. -Expand your horizons through the Journal''s idea-generating forum for debating controversial issues and learning from preeminent researchers and clinicians
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