Diebold J, Audouin J, Viry B, Ghandour C, Betti P, D'Ornano G
Service Central J. Delarue d'Anatomie et de Cytologie Pathologiques Hôtel-Dieu, Paris, France.
Ann Otol Rhinol Laryngol. 1990 Jul;99(7 Pt 1):577-80. doi: 10.1177/000348949009900716.
Laryngoscopy carried out in a 46-year-old man revealed a left paralaryngeal tumor. The mass was entirely removed by left pharyngolaryngotomy. Microscopic study showed a diffuse malignant lymphoma of low-grade malignancy, exhibiting all the criteria of the MALT-type lymphoma: the proliferation of centrocyte-like and lymphoplasmacytic cells, lymphoepithelial lesions, and the presence of germinal centers. Primary lymphoma of the larynx is a rare condition. Most of the reported low-grade lymphomas and the pseudolymphomas probably belong to the category of MALT-type lymphoma. Remission can be obtained by surgery, radiotherapy, and polychemotherapy.
对一名46岁男性进行的喉镜检查发现左侧喉旁肿瘤。通过左侧咽侧喉切开术将肿块完全切除。显微镜检查显示为低级别恶性弥漫性恶性淋巴瘤，具备黏膜相关淋巴组织型淋巴瘤的所有特征：中心细胞样细胞和淋巴浆细胞增殖、淋巴上皮病变以及生发中心的存在。原发性喉淋巴瘤是一种罕见疾病。大多数报道的低级别淋巴瘤和假性淋巴瘤可能属于黏膜相关淋巴组织型淋巴瘤范畴。通过手术、放疗和多药化疗可实现缓解。
