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原发性内镜切除术后帕博利珠单抗治疗下扩张性破坏性鼻窦黏膜黑色素瘤从明显的假性进展到持久完全缓解:一例报告

From apparent pseudoprogression to durable complete remission of expansile destructive sinonasal mucosal melanoma under pembrolizumab after primary endoscopic resection: A case report.

作者信息

Lu Hung-Chun, Shen Ping-Hung, Kok Victor C

机构信息

Department of Otolaryngology, Kuang-Tien General Hospital, Taichung, Taiwan.

Division of Medical Oncology, Cancer Center of Kuang Tien General Hospital, Taichung, Taiwan.

出版信息

SAGE Open Med Case Rep. 2024 May 12;12:2050313X241253471. doi: 10.1177/2050313X241253471. eCollection 2024.

Abstract

Head and neck mucosal melanoma is a rare but highly aggressive malignant tumor that usually has a poor prognosis. We describe a 53-year-old male patient, having no any medical history, with left maxillary sinus mucosal melanoma causing bilateral lung metastasis. Rapid tumor regrowth was observed on the 49th day after radical tumor resection. Subsequent pembrolizumab immunotherapy initially elicited pseudoprogression, for which add-on radiation therapy was carried out during maintenance pembrolizumab. A gradual decrease in tumor volume and complete remission were observed by a series of magnetic resonance imaging scans and lung windows of a computer tomography scan of chest. At the 29-month follow-up, the patient was rendered disease-free. In conclusion, head and neck mucosal melanoma may regrow rapidly after surgical resection and pseudoprogression could be frightening during immunotherapy. Subsequent single-agent pembrolizumab plus localized radiation therapy aiming to release more tumor antigens may offer the possibility of long-term remission.

摘要

头颈部黏膜黑色素瘤是一种罕见但侵袭性很强的恶性肿瘤,预后通常较差。我们描述了一名53岁男性患者,无任何病史,患有左上颌窦黏膜黑色素瘤并导致双侧肺转移。在肿瘤根治性切除术后第49天观察到肿瘤迅速复发。随后的帕博利珠单抗免疫治疗最初引发了假性进展,在维持使用帕博利珠单抗期间进行了追加放射治疗。通过一系列磁共振成像扫描以及胸部计算机断层扫描的肺部窗观察到肿瘤体积逐渐减小并完全缓解。在29个月的随访中,患者实现了无病状态。总之,头颈部黏膜黑色素瘤在手术切除后可能迅速复发,免疫治疗期间假性进展可能令人恐惧。随后使用单药帕博利珠单抗联合局部放射治疗以释放更多肿瘤抗原,可能提供长期缓解的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/468c/11089941/682ea16c48a5/10.1177_2050313X241253471-fig1.jpg

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