A rare presentation of thyroid malignant peripheral nerve sheath tumor in neurofibromatosis type 1 delineated by FDG PET/CT: A case report and literature review.

Serin Moghrabi, Nabeela Al-Hajaj, Fatimah Abu Aljaaz, Omar Jaber, Akram Al-Ibraheem
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Abstract

Malignant peripheral nerve sheath tumors (MPNST) are rare, aggressive soft tissue sarcomas that arise from peripheral nerves and often present a diagnostic and therapeutic challenge. They can occur sporadically or in association with neurofibromatosis type 1 (NF1), a genetic disorder caused by mutations in the NF1 gene. This report presents the unique case of a 33-year-old male with progressive dry cough, hoarseness, and neck swelling who underwent a total thyroidectomy, revealing a high-grade malignant peripheral nerve sheath tumor invading the thyroid. FDG PET/CT led to the additional diagnosis of NF1. This case stands out due to the rarity of finding an MPNST within the thyroid and the simultaneous identification of NF1. It underscores the importance of screening MPNST patients for NF1 and vice versa, spotlighting the expanding role of FDG PET/CT in comprehensive evaluations. To our knowledge, this report presents the first case of NF1-associated MPNST with thyroid involvement worldwide.

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通过 FDG PET/CT 确定的神经纤维瘤病 1 型甲状腺恶性周围神经鞘瘤的罕见表现:病例报告和文献综述。
恶性周围神经鞘瘤(MPNST)是一种罕见的侵袭性软组织肉瘤,源于周围神经,往往给诊断和治疗带来挑战。恶性神经鞘瘤(MPNST)可能偶发,也可能与 1 型神经纤维瘤病(NF1)伴发,NF1 是一种由 NF1 基因突变引起的遗传性疾病。本报告介绍了一例独特的病例,患者是一名 33 岁男性,患有进行性干咳、声音嘶哑和颈部肿胀,接受了甲状腺全切除术,发现甲状腺内有一个高级别恶性周围神经鞘瘤。经 FDG PET/CT 检查,最终确诊为 NF1。由于在甲状腺内发现 MPNST 并同时发现 NF1 的罕见性,该病例显得尤为突出。它强调了对MPNST患者进行NF1筛查的重要性,反之亦然,突出了FDG PET/CT在综合评估中不断扩大的作用。据我们所知,本报告是全球首例NF1相关的甲状腺受累的MPNST病例。
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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来源期刊
Asia Oceania Journal of Nuclear Medicine and Biology
Asia Oceania Journal of Nuclear Medicine and Biology Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
1.80
自引率
0.00%
发文量
28
审稿时长
12 weeks
期刊最新文献
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