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Merkel 细胞癌在 COVID-19 住院后表现为恶性胸腔积液:病例报告和文献复习。

Merkel cell carcinoma presenting as a malignant pleural effusion post-COVID-19 hospitalization: A case report and literature review.

机构信息

Department of Pathology and Laboratory Medicine, Northwell Health-Staten Island University Hospital, New York City, New York, USA.

出版信息

Diagn Cytopathol. 2022 Jan;50(1):E37-E41. doi: 10.1002/dc.24882. Epub 2021 Oct 5.

Abstract

Merkel cell carcinoma (MCC) is a rare, highly aggressive neuroendocrine carcinoma of the skin, associated with immunosuppression, UV light exposure, and the Merkel cell polyomavirus (MCPyV). Cases of metastatic MCC diagnosed in body fluid cytology are extremely rare; only five cases have been reported previously in the English literature. We present a case of a 65-year-old male with acute respiratory failure and an enlarged right pleural effusion. He had two hospitalizations for COVID-19 pneumonia 2 months prior, for which he received steroid treatment and tocilizumab. Emergent thoracentesis was done, with pleural fluid sent for cytologic evaluation. Both the Papanicolaou stained ThinPrep slide and cell block demonstrated clusters of predominantly small to medium sized blue round cells with hyperchromatic nuclei, scant cytoplasm and fine chromatin, in a background of rare mesothelial cells, macrophages and numerous lymphocytes. Tumor cells were positive for CD56, chromogranin, synaptophysin, SAT2B, MCPyV, and CK20 in perinuclear dot like pattern, while negative for TTF-1 and CD45 immunostains. Ki67 proliferative index was approximately 40%. The patient had a history of MCC of the right ulnar forearm 4 years before the current presentation, which was unknown to us at the time of cytologic evaluation. To the best of our knowledge, this is the sixth case of metastatic MCC diagnosed by fluid cytology and the first reported in a patient receiving immunosuppressive treatment for COVID-19. Further reporting of such cases may increase awareness, especially when prior history is not readily available, such as in our case.

摘要

默克尔细胞癌(Merkel cell carcinoma,MCC)是一种罕见的、高度侵袭性的皮肤神经内分泌癌,与免疫抑制、紫外线暴露和默克尔细胞多瘤病毒(Merkel cell polyomavirus,MCPyV)有关。在体液细胞学中诊断转移性 MCC 的病例极为罕见;在英文文献中之前仅报道过五例。我们报告了一例 65 岁男性,因急性呼吸衰竭和右侧胸腔大量积液就诊。他在 2 个月前因 COVID-19 肺炎住院两次,接受了类固醇治疗和托珠单抗治疗。紧急进行了胸腔穿刺,将胸腔积液送检细胞学检查。巴氏染色的 ThinPrep 涂片和细胞块均显示出簇状的小至中等大小的蓝色圆形细胞,细胞核深染,细胞质稀少,染色质细,背景中有罕见的间皮细胞、巨噬细胞和大量淋巴细胞。肿瘤细胞 CD56、嗜铬粒蛋白、突触素、SAT2B、MCPyV 和 CK20 呈核周点样阳性,而 TTF-1 和 CD45 免疫染色阴性。Ki67 增殖指数约为 40%。该患者在当前就诊前 4 年曾有右侧尺骨前臂 MCC 病史,但在细胞学评估时我们并不知道这一点。据我们所知,这是第六例通过液体细胞学诊断的转移性 MCC 病例,也是首例报告在 COVID-19 接受免疫抑制治疗的患者中。进一步报告此类病例可能会提高认识,尤其是在我们的病例中,当无法轻易获得既往病史时。

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本文引用的文献

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A rare case of pleural localisation of both metastatic Merkel cell carcinoma and chronic lymphocytic leukaemia.
Cytopathology. 2021 May;32(3):367-370. doi: 10.1111/cyt.12947. Epub 2020 Dec 20.
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