Isolated Sphenoid Fungal Sinusitis With Mucocele Mistaken for Chordoma: A Study of Two Unique Cases.

Journal of Rhinology Pub Date : 2024-03-01 Epub Date: 2024-03-31 DOI:10.18787/jr.2023.00070
Kukjin Nam, Min Young Seo
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Abstract

Isolated sphenoid fungal sinusitis (ISFS) is a rare condition characterized by fungal infection of the sphenoid sinus. It often presents with non-specific symptoms, which can lead to misdiagnosis. This study presents two unique cases of ISFS with mucocele that were initially misdiagnosed as chordoma based on preoperative radiographic findings. Two cases of ISFS were thoroughly investigated, including clinical examinations, radiological assessments, and surgical explorations. The patients' symptoms, radiographic findings, surgical procedures, and postoperative outcomes were documented. In both cases, radiographic assessments raised suspicion of chordoma due to bony destruction and soft tissue lesions involving the sphenoid sinus and clivus. However, endoscopic sinus surgery revealed fungal balls and mucoceles, confirming the diagnosis of ISFS. Postoperative pathology confirmed the presence of aspergilloma. The patients recovered well with appropriate treatment. ISFS is challenging to diagnose due to its deep anatomical location and non-specific symptoms. Visual disturbances, particularly affecting the abducens nerve, are common. Sphenoid sinus mucocele, though rare, can be present. Surgical exploration plays a crucial role in establishing an accurate diagnosis and initiating appropriate treatment. ISFS can mimic other skull base lesions, such as chordoma, on preoperative radiography. These cases underscore the value of surgical exploration in reaching an accurate diagnosis and highlight the need for the cautious interpretation of radiological findings in sphenoid sinus lesions to ensure optimal patient care.

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孤立性蝶窦真菌性鼻窦炎伴黏液囊肿误诊为脊索瘤:两例独特病例的研究。
孤立性蝶窦真菌性鼻窦炎(ISFS)是一种罕见的疾病,其特征是蝶窦真菌感染。它通常表现为非特异性症状,这可能导致误诊。本研究报告了两个独特的ISFS伴粘液囊肿的病例,根据术前的影像学表现,最初被误诊为脊索瘤。我们对2例ISFS进行了全面的调查,包括临床检查、放射学评估和手术探查。记录了患者的症状、影像学表现、手术过程和术后结果。在这两个病例中,由于骨破坏和涉及蝶窦和斜坡的软组织病变,x线检查怀疑脊索瘤。然而,内窥镜鼻窦手术发现真菌球和粘液囊肿,证实了ISFS的诊断。术后病理证实存在曲菌瘤。经适当治疗,患者恢复良好。ISFS由于其深层解剖位置和非特异性症状,诊断具有挑战性。视觉障碍,特别是影响外展神经,是常见的。蝶窦黏液囊肿虽罕见,但仍可存在。手术探查在建立准确诊断和开始适当治疗方面起着至关重要的作用。ISFS可以在术前影像学上模仿其他颅底病变,如脊索瘤。这些病例强调了手术探查在准确诊断中的价值,并强调了在蝶窦病变中谨慎解释影像学表现以确保最佳患者护理的必要性。
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自引率
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发文量
23
审稿时长
8 weeks
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