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结外鼻型自然杀伤/T 细胞淋巴瘤伪装成难治性鼻窦炎。

Extranodal nasal-type natural killer/T-cell lymphoma masquerading as recalcitrant sinusitis.

机构信息

Department of Otolaryngology-Head and Neck Surgery, University of Missouri-School of Medicine, Columbia, Missouri, USA.

出版信息

Head Neck. 2010 Feb;32(2):268-73. doi: 10.1002/hed.21068.

Abstract

BACKGROUND

Extranodal nasal-type natural killer (NK)/T-cell lymphoma is a very uncommon disease process often mimicking refractory sinusitis. The diagnosis may be discovered after an extensive exclusion process. Careful immunohistochemical evaluation is crucial to differentiate NK/T-cell lymphoma from other malignancies.

METHODS AND RESULTS

We describe a 46-year-old white man presenting with a 4-month history of refractory sinusitis and new onset visual field loss in his right eye, right facial tingling, and pain. Examination revealed right periorbital edema and scleritis, and necrotic appearing turbinates with purulence and fibrinous debris. CT/MRI delineated extensive paranasal sinus involvement. Immunohistopathology demonstrated extranodal nasal-type NK/T-cell lymphoma. Additional radiography revealed widespread involvement.

CONCLUSION

Severe recalcitrant sinusitis with orbital involvement may be the initial presentation of NK/T-cell lymphoma. Ulcerative or necrotic lesions in the midline of the head and neck should raise concern for this disease. In addition to radiographic and laboratory testing, large biopsies should be taken for immunohistochemical analysis to achieve diagnosis and guide further management.

摘要

背景

结外鼻型自然杀伤(NK)/T 细胞淋巴瘤是一种非常罕见的疾病过程,常模仿难治性鼻窦炎。诊断可能是在广泛的排除过程后发现的。仔细的免疫组织化学评估对于将 NK/T 细胞淋巴瘤与其他恶性肿瘤区分开来至关重要。

方法和结果

我们描述了一名 46 岁的白人男性,他有 4 个月的难治性鼻窦炎病史,右眼新出现视野丧失、右侧面部刺痛和疼痛。检查发现右眼眶周水肿和巩膜炎,以及坏死的鼻甲,伴有脓性和纤维蛋白碎片。CT/MRI 描绘了广泛的副鼻窦受累。免疫组织病理学显示结外鼻型 NK/T 细胞淋巴瘤。其他射线照相显示广泛受累。

结论

伴有眼眶受累的严重难治性鼻窦炎可能是 NK/T 细胞淋巴瘤的首发表现。头颈部中线的溃疡性或坏死性病变应引起对这种疾病的关注。除了影像学和实验室检查外,还应进行大活检以进行免疫组织化学分析,以实现诊断并指导进一步治疗。

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