乳房皮肤默克尔细胞癌1例。

IF 1.7 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
American journal of translational research Pub Date : 2025-05-15 eCollection Date: 2025-01-01 DOI:10.62347/YFTJ3672
Xinming Hou, Qian Lv, Zhaobao Lv
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引用次数: 0

摘要

默克尔细胞癌(MCC)是一种罕见的侵袭性神经内分泌皮肤恶性肿瘤,其特点是高复发和转移率。在此,我们报告一例65岁女性患者的原发性乳房皮肤MCC,她最初表现为右乳花生大小的肿块,随后迅速发展为花菜样肿块并伴有间歇性疼痛。患者接受根治性手术(右侧乳房切除术和右侧腋窝淋巴结清扫),术后化疗。免疫组化检查显示细胞角蛋白20 (CK20)、突触素(Syn)、分化簇蛋白56 (CD56)、嗜铬粒蛋白A (CgA)染色阳性,诊断为MCC。随后的正电子发射断层扫描-计算机断层扫描(PET-CT)显示继发性肝转移。尽管最初对化疗有有效反应,但患者出现严重的骨髓抑制,需要改用卡培他滨维持治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Breast skin merkel cell carcinoma: a case report.

Merkel cell carcinoma (MCC) is a rare and aggressive neuroendocrine skin malignancy characterized by high recurrence and metastasis rates. Here, we present a case of primary breast skin MCC in a 65-year-old female patient who initially presented with a peanut-sized lump on her right breast, which rapidly developed into a cauliflower-like mass accompanied by intermittent pain. The patient underwent radical surgery (right mastectomy and right axillary lymph node dissection), followed by postoperative chemotherapy. Immunohistochemical examination revealed positive staining for Cytokeratin 20 (CK20), Synaptophysin (Syn), Cluster of Differentiation 56 (CD56), and Chromogranin A (CgA), confirming the diagnosis of MCC. A subsequent Positron Emission Tomography - Computed Tomography (PET-CT) scan revealed secondary liver metastasis. Despite an initial effective response to chemotherapy, the patient developed severe bone marrow suppression, necessitating a switch to maintenance therapy with capecitabine.

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来源期刊
American journal of translational research
American journal of translational research ONCOLOGY-MEDICINE, RESEARCH & EXPERIMENTAL
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