肺鳞状细胞癌放化疗后与Durvalumab相关的肺结节样肉芽肿病

Seigo Minami, Hironao Yasuoka, Nao Shoshihara, Daisuke Ishida, Yasushi Sakamaki
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摘要

在接受免疫检查点抑制剂(ICIs)治疗的癌症患者中,结节样肉芽肿病是一种独特的免疫相关不良事件(irAE)。这种irAE并不常见,据报道,ICI治疗的黑色素瘤发生率为2%至22.2%。对于局限于肺部的肉芽肿病,很难区分肉芽肿病与癌症进展或转移。在此,我们报告一例ci诱导的肺结节样肉芽肿病,与原发性肺癌的局部复发相混淆。1例56岁女性右下叶c期肺鳞状细胞癌患者接受顺铂和长春瑞滨两疗程化疗放疗及同期胸部放疗,随后接受1年杜伐单抗巩固治疗。在杜伐单抗治疗后1.5年,右侧S6的肿瘤生长并表现出氟脱氧葡萄糖正电子发射断层扫描(FDG-PET)的异常摄取。计算机断层扫描(CT)和FDG-PET均未发现纵隔和远处转移。她接受了右下肺叶切除术。病理组织学上,肿瘤及淋巴结未见癌细胞残留,呈弥漫性上皮样肉芽肿伴炎性细胞浸润,部分坏死灶及多核巨细胞。免疫组化染色以CD3+、CD8+ T细胞为主浸润,CD4+ T细胞较少,CD20+ B细胞少量。我们在没有类固醇和其他免疫抑制药物的情况下跟踪她。结节样肉芽肿病是一种罕见的恶性肿瘤,很难与癌症进展相鉴别,应引起重视。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Sarcoid-Like Granulomatosis of the Lung Related to Durvalumab After Chemoradiation for Pulmonary Squamous Cell Carcinoma.

Sarcoid-like granulomatosis is a unique immune-related adverse event (irAE) in cancer patients treated with immune checkpoint inhibitors (ICIs). This irAE is infrequent, reported to range from 2% to 22.2% of melanoma treated with ICI. In a case of granulomatosis localized in the lung, it is difficult to differentiate granulomatosis from cancer progression or metastases. Herein, we report a case of ICI-induced sarcoid-like granulomatosis of the lung, which was confusable with localized recurrence of the primary lung cancer. A 56-year-old woman with c-stage IIIA of pulmonary squamous cell carcinoma in the right lower lobe received chemo-radiotherapy with two courses of cisplatin and vinorelbine and concurrent thoracic irradiation, followed by 1-year durvalumab consolidation therapy. The tumor in the right S6 grew and presented abnormal uptake by fluorodeoxyglucose positron emission tomography (FDG-PET), 1.5 years after durvalumab. Neither computed tomography (CT) nor FDG-PET found mediastinal and distant metastases. She underwent right lower lobe lobectomy. Histopathologically, the tumor and sampled lymph nodes contained no residue of carcinoma cells but presented diffuse epithelioid granuloma with infiltration of inflammatory cells, partial necrotic lesions and many multinucleated giant cells. In immunohistochemical stains, CD3+ and CD8+ T cells predominantly infiltrated, while there were few CD4+ T cells and a small number of CD20+ B cells. We followed her without steroid and other immunosuppressant drug. We should pay attention to the development of sarcoid-like granulomatosis as a rare irAE, which is difficult to be differentiated from cancer progression.

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