男性大汗腺乳腺癌伴沙粒体1例。

HCA healthcare journal of medicine Pub Date : 2024-12-01 eCollection Date: 2024-01-01 DOI:10.36518/2689-0216.1768
Alena Bashinskaya, Eric W Baum, Michael B Morgan
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引用次数: 0

摘要

导读:虽然男性乳腺癌是一种相对罕见的疾病,但其发病率正在上升,可能归因于零星的病理生理机制,主要涉及激素失衡。侵袭性大汗腺癌占全球乳腺恶性肿瘤的一小部分,文献中报道的男性患者病例有限。大汗腺乳腺癌的临床表现与其他乳腺癌亚型非常相似,因为它最常被描述为占据乳房乳晕后区域的孤立性溃疡性结节性病变。在这里,我们描述了一个新的情况下,一个大汗腺男性乳腺癌转移到皮肤,鉴于过去的病例已经提出从头开始在皮下乳房组织。此外,我们讨论了在这种实体中遇到的不寻常的组织病理学,例如沙砾瘤体的存在。病例介绍:在本病例报告中,我们概述了一位80岁男性的临床表现,既往有乳腺癌和乳房切除术史,在此皮肤科会诊前9年。在体格检查中,在他的右乳房上发现了一个单一的结节性病变,因此进行了活组织检查。随后的组织学分析确定了以大量沙粒小体为特征的大汗腺细胞癌,这在乳腺组织中是不寻常的。因此,该患者被诊断为复发性乳腺大汗腺癌。结论:大汗腺乳腺癌引起的皮肤转移在男性患者中并不常见。浸润性大汗腺乳腺癌的准确诊断取决于免疫组织化学标志物的准确识别和清晰的形态学特征。观察到明显的相关性,特别是在囊性疾病液蛋白-15 (GCDFP-15)和雄激素受体的阳性表达中。然而,由于这种表现的罕见性,关于治疗方式的数据有限。正在进行的研究正在调查抗雄激素在治疗大汗腺乳腺癌中的潜在作用。
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Apocrine Breast Cancer With Psammoma Bodies in a Male Patient.

Introduction: While male breast carcinoma is a relatively uncommon occurrence, its incidence is on the rise, potentially attributed to sporadic pathophysiological mechanisms, primarily involving hormonal imbalances. Invasive apocrine carcinoma represents a small fraction of global breast malignancies, with limited instances reported among male patients in the literature. The clinical presentation of an apocrine breast carcinoma closely resembles that of other breast cancer subtypes, as it is most often described as a solitary ulcerative nodular lesion occupying a retro-areolar region of the breast. Herein, we describe a novel case of an apocrine male breast carcinoma metastasizing to the skin, given that past cases had presented ab initio in the subcutaneous breast tissue. Furthermore, we discuss the unusual histopathology encountered in this entity such as the presence of psammoma bodies.

Case presentation: In this case report, we outline the clinical presentation of an 80-year-old male with a history of prior breast cancer and mastectomy, performed 9 years before this dermatologic consultation. Upon a physical examination, a singular nodular lesion on his right breast was discovered, leading to a biopsy. Subsequent histological analysis identified an apocrine cell carcinoma characterized by numerous psammoma bodies, an unusual occurrence in breast tissue. Consequently, the patient received a diagnosis of relapsing breast apocrine carcinoma.

Conclusion: Cutaneous metastases arising from apocrine breast carcinoma are infrequent in male patients. The precise diagnosis of invasive apocrine breast carcinoma hinges on the accurate identification of immunohistochemical markers and a clear morphological profile. A notable correlation has been observed, particularly in positive expressions of gross cystic disease fluid protein-15 (GCDFP-15) and androgen receptor. However, due to the rarity of this presentation, there is limited data on treatment modalities. Ongoing studies are investigating the potential role of anti-androgens in the treatment of apocrine breast carcinomas.

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