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颞骨原发性淋巴瘤。

Primary lymphoma of the temporal bone.

作者信息

Tucci D L, Lambert P R, Innes D J

机构信息

Department of Otolaryngology-Head and Neck Surgery, University of Virginia Health Sciences Center, Charlottesville 22908.

出版信息

Arch Otolaryngol Head Neck Surg. 1992 Jan;118(1):83-5. doi: 10.1001/archotol.1992.01880010087021.

Abstract

Involvement of the temporal bone by lymphoreticular neoplasm is rare; all reported cases have been of secondary involvement. This article presents what we believe to be the first two reported cases of primary temporal bone lymphoma. The patients, an elderly man and a boy, both presented with infection of the ear, hearing loss, and facial nerve paresis. In both cases, facial paresis resolved after appropriate chemotherapeutic treatment. Patient presentation and clinical course are discussed in light of published work on temporal bone malignancy. Further investigation, including computed tomography and biopsy, should be considered for patients who present with an apparent middle ear infection unresponsive to medical therapy. The development of facial paralysis in such a patient warrants heightened suspicion of malignancy.

摘要

淋巴网状细胞瘤累及颞骨的情况罕见;所有报道的病例均为继发性累及。本文介绍了我们认为是首例报道的两例原发性颞骨淋巴瘤病例。患者分别为一名老年男性和一名男孩,均表现为耳部感染、听力丧失和面神经麻痹。在这两例病例中,经适当的化疗治疗后面神经麻痹均得到缓解。根据已发表的关于颞骨恶性肿瘤的研究,对患者的临床表现和临床病程进行了讨论。对于出现明显中耳感染且对药物治疗无反应的患者,应考虑进一步检查,包括计算机断层扫描和活检。此类患者出现面瘫应高度怀疑恶性肿瘤。

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