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一例罕见的着色性干皮病病例:纳武利尤单抗治疗三种皮肤恶性肿瘤并与临床和代谢影像相关分析

A Rare Case of Xeroderma Pigmentosum: Nivolumab Treatment for Three Cutaneous Malignancies with Clinical and Metabolic Imaging Correlation.

作者信息

Proietti Ilaria, Pirisino Riccardo, Azzella Giulia, Coppolelli Vincenzo, Greco Maria Elisabetta, Casciani Emanuele, Potenza Concetta, Filippi Luca

机构信息

Dermatology Unit "Daniele Innocenzi", "A. Fiorini" Hospital, Via Firenze, 1, 04019 Terracina, Italy.

Department of Nuclear Medicine, Santa Maria Goretti Hospital, AUSL Latina, 04100 Latina, Italy.

出版信息

Diagnostics (Basel). 2025 Apr 12;15(8):979. doi: 10.3390/diagnostics15080979.

Abstract

Xeroderma pigmentosum (XP) is a rare autosomal recessive disorder characterized by extreme ultraviolet (UV) sensitivity, predisposing patients to multiple cutaneous malignancies. We present the case of a 26-year-old male with XP diagnosed with three distinct skin cancers: superficial spreading melanoma (SSM), basal cell carcinoma (BCC), and squamous cell carcinoma (SCC). Among these, the melanoma had metastasized. A computed tomography (CT) scan revealed a suspicious pulmonary nodule, prompting further metabolic characterization via positron emission tomography/computed tomography (PET/CT) with F-fluorodeoxyglucose ([F]FDG). The scan detected significant hypermetabolism not only in the lung lesion but also in an unsuspected right parotid gland lesion, refining disease staging and guiding treatment decisions. The patient underwent immunotherapy with nivolumab, achieving a complete metabolic response in both metastatic lesions, as confirmed by follow-up PET/CT. This case underscores the critical role of [F]FDG PET/CT in staging and treatment monitoring for selected patients with XP, a population in which advanced imaging is rarely employed. Moreover, the patient's remarkable response to immunotherapy suggests a potential link between XP-related DNA repair defects and increased sensitivity to PD-1 blockade. These findings highlight the importance of integrating metabolic imaging into XP management and warrant further investigation into the immunogenicity of XP-associated malignancies.

摘要

着色性干皮病(XP)是一种罕见的常染色体隐性疾病,其特征为对紫外线(UV)极度敏感,使患者易患多种皮肤恶性肿瘤。我们报告了一例26岁患有XP的男性病例,其被诊断患有三种不同的皮肤癌:浅表扩散性黑色素瘤(SSM)、基底细胞癌(BCC)和鳞状细胞癌(SCC)。其中,黑色素瘤已发生转移。计算机断层扫描(CT)显示一个可疑的肺结节,促使通过使用F - 氟脱氧葡萄糖([F]FDG)的正电子发射断层扫描/计算机断层扫描(PET/CT)进行进一步的代谢特征分析。该扫描不仅在肺部病变中检测到显著的高代谢,还在一个未被怀疑的右腮腺病变中检测到,从而完善了疾病分期并指导了治疗决策。该患者接受了纳武单抗免疫治疗,后续的PET/CT证实两个转移病灶均实现了完全代谢缓解。本病例强调了[F]FDG PET/CT在特定XP患者的分期和治疗监测中的关键作用,而这一人群很少使用先进成像技术。此外,患者对免疫治疗的显著反应表明XP相关的DNA修复缺陷与对PD - 1阻断的敏感性增加之间可能存在联系。这些发现凸显了将代谢成像纳入XP管理的重要性,并值得进一步研究XP相关恶性肿瘤的免疫原性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cccc/12025773/f9c69659ece3/diagnostics-15-00979-g001.jpg

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