Bilateral Sudden Sensorineural Hearing Loss in Waldenström’s Macroglobulinemia: Case Report and Review of the Literature

N. Shoman, Thamir Aldahmashi
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Abstract

Abstract Objective Waldenström’s macroglobulinemia (WM) is a rare indolent B-cell lymphoproliferative disorder, representing 1 to 2% of all hematological malignancies. Involvement of the inner ear is rare with only case reports published over the past six decades. Methods The occurrence of bilateral sudden sensorineural hearing loss is exceeding rare, with limited published data in the literature. We present a case of a 62-year-old man diagnosed with WM who presented with bilateral sequential sudden sensorineural hearing loss. Results A few months following his WM diagnosis, he experienced sudden hearing loss in his left ear. He was treated with a course of oral steroids with no improvement. Three months following this incident, he experienced a similar sudden loss of hearing in his right ear. Treatment for WM was initiated. A repeat hearing test, done 1 week later, did not show any significant improvement in his right hearing. Conclusion The clinical course of WM is highly variable, with relatively infrequent involvement of lymph nodes, spleen, or liver. The inner ear is rarely involved. In this article, otologic clinical presentation is discussed, along with a review of the literature on hearing loss in WM.
Waldenström巨球蛋白血症患者双侧突发性感音神经性听力损失:病例报告及文献回顾
摘要目的Waldenström巨球蛋白血症(WM)是一种罕见的惰性b淋巴细胞增生性疾病,占所有血液系统恶性肿瘤的1%至2%。累及内耳是罕见的,只有病例报告发表在过去的六十年。方法双侧突发性感音神经性听力损失的发生极为罕见,文献资料有限。我们提出一个病例62岁的男子诊断为WM谁提出了双侧顺序突发性感音神经性听力损失。结果在确诊WM后数月,患者左耳突然失聪。他接受了一个疗程的口服类固醇治疗,但没有任何改善。这件事发生三个月后,他的右耳也出现了类似的突然失聪。开始治疗WM。一周后再次进行听力测试,他的右侧听力没有明显改善。结论WM的临床病程变化多端,累及淋巴结、脾脏和肝脏的病例相对较少。内耳很少受累。在这篇文章中,我们讨论了耳科的临床表现,并对WM听力损失的文献进行了回顾。
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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