慢性血液透析患者左眼严重头痛及视力恶化,蝶窦棕色肿瘤。

IF 3.2 Q2 CLINICAL NEUROLOGY
Hicham Esselmani, Abdelmohcine Aimrane, Hicham Chatoui, Omar El Hiba, Mustapha Najimi, Mohamed Merzouki
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引用次数: 0

摘要

背景/目的:棕色肿瘤是一种罕见的与慢性肾衰竭患者甲状旁腺功能亢进相关的骨病变,尤其是继发性甲状旁腺功能亢进(SHPT)。虽然棕色肿瘤通常影响富含骨髓的骨骼,但累及蝶窦极为罕见,并可表现为神经系统症状。本研究报告一例血液透析患者的蝶窦棕色肿瘤,强调其临床表现和诊断挑战。方法:一名31岁的女性接受慢性血液透析,表现为严重头痛、复视和左眼进行性视力丧失。实验室检查显示高钙血症、低磷血症和甲状旁腺激素(PTH)水平升高,与SHPT一致。通过临床检查和磁共振成像(MRI)确诊。结果:临床检查证实左眼视力下降。实验室结果显示血清钙15.5 mg/dL,磷酸盐1.0 mg/dL,甲状旁腺激素2000 pg/mL,与SHPT一致。影像学检查发现蝶窦内一棕色肿瘤对邻近结构产生肿块效应。该病例强调了棕色肿瘤在该部位的罕见性,文献中很少有类似的报道。结论:棕色肿瘤虽然罕见,但在有神经系统症状或颅脑病变的SHPT患者中应考虑棕色肿瘤。通过生化和影像学检查进行早期诊断对于预防严重并发症至关重要。治疗包括治疗潜在的甲状旁腺功能亢进,在神经压迫的情况下进行手术干预。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Severe Headache and Deterioration of Vision in Left Eye in a Chronic Hemodialysis Patient Revealing a Brown Tumor of Sphenoid Sinus.

Background/objectives: Brown tumors are rare bone lesions associated with hyperparathyroidism, particularly secondary hyperparathyroidism (SHPT), in chronic renal failure. While brown tumors commonly affect bones rich in marrow, the involvement of the sphenoid sinus is extremely rare and can present with neurological symptoms. This study reports a case of a sphenoid sinus brown tumor in a patient on hemodialysis, highlighting its clinical presentation and diagnostic challenges.

Methods: A 31-year-old woman undergoing chronic hemodialysis presented with a severe headache, diplopia, and progressive vision loss in her left eye. Laboratory tests revealed hypercalcemia, hypophosphatemia, and elevated parathyroid hormone (PTH) levels, consistent with SHPT. The diagnosis was confirmed through a clinical examination and magnetic resonance imaging (MRI).

Results: The clinical examination confirmed decreased visual acuity in the left eye. The laboratory results revealed serum calcium of 15.5 mg/dL, phosphate of 1.0 mg/dL, and PTH of 2000 pg/mL, consistent with SHPT. The imaging studies identified a brown tumor in the sphenoid sinus exerting a mass effect on adjacent structures. This case underscores the rarity of brown tumors in this location, with very few similar reports in the literature.

Conclusions: Although rare, brown tumors should be considered in patients with SHPT who present with neurological symptoms or cranial lesions. An early diagnosis through biochemical and imaging studies is crucial to prevent severe complications. The management involves treating the underlying hyperparathyroidism, with surgical intervention indicated in cases of neural compression.

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来源期刊
Neurology International
Neurology International CLINICAL NEUROLOGY-
CiteScore
3.70
自引率
3.30%
发文量
69
审稿时长
11 weeks
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