Giant cell tumour of the larynx-a diagnostic challenge.

IF 0.5 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING BJR Case Reports Pub Date : 2025-02-10 eCollection Date: 2025-01-01 DOI:10.1093/bjrcr/uaaf006
Vitor H Fraga de Abreu, Ricardo Pacheco, Fernando Cunha, Alexandra Borges
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Abstract

Giant cell tumours (GCTs) of the larynx are extremely rare. The most affected structure is the thyroid cartilage and only 44 cases are reported in the literature.1 Clinically, their first manifestation is usually a palpable neck mass, often accompanied by hoarseness, dyspnoea, and/or dysphagia depending on size and location. GCTs are benign neoplasms, yet awareness of this entity is crucial as their aggressive local behaviour can cause significant morbidity with airway obstruction and can simulate a malignancy. The differential diagnosis is broad and remains a clinical and radiological challenge. Indeed, the final diagnosis is established by histology postoperatively. Surgery is the preferred treatment but may impair voice quality. For incomplete surgical resections and high surgical risk lesions, denosumab treatment is a valuable option. We share our experience on GCTs in a young adult presenting as a supraglottic mass.

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喉巨细胞瘤(GCT)极为罕见。受影响最大的结构是甲状软骨,文献中仅报道了 44 个病例。1 在临床上,它们的首发症状通常是可触及的颈部肿块,根据肿块的大小和位置,通常伴有声音嘶哑、呼吸困难和/或吞咽困难。GCT 属于良性肿瘤,但由于其侵袭性局部表现可导致气道阻塞,并可模拟恶性肿瘤,因此对这种实体的认识至关重要。鉴别诊断的范围很广,仍然是临床和放射学上的难题。事实上,最终诊断要通过术后组织学检查来确定。手术是首选的治疗方法,但可能会影响嗓音质量。对于手术切除不彻底和手术风险较高的病变,地诺单抗治疗是一种有价值的选择。我们将与大家分享我们对一名表现为声门上肿块的年轻成人 GCT 的治疗经验。
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BJR Case Reports
BJR Case Reports RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING-
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审稿时长
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