Kojima Masaru, Sugihara Shiro, Iijima Misa, Ono Takayuki, Yoshizumi Takashi, Masawa Nobuhide
Department of Pathology and Clinical Laboratories, Gunma Cancer Center Hospital, Ohta, Japan.
J Oral Pathol Med. 2006 May;35(5):314-6. doi: 10.1111/j.1600-0714.2006.00408.x.
We report here a case of mucosa-associated lymphoid tissue (MALT)-type lymphoma arising from the minor salivary gland of the oral cavity exhibiting tumor-forming amyloidosis. The patient was a 64-year-old Japanese woman who presented with 4-year history of a left soft palate mass. Despite multiple and multifocal recurrences including the lip, soft palate, tongue, oral base and vocal code and soft palate, the tumor remained localized in the upper aerodigestive tract, and the patient did not develop multiple myeloma during the course of disease. Histologically, the majority of the lesion was occupied by amyloid deposition. Only the periphery of the lesion contained numerous plasmacytoid cells, along with occasional centrocyte-like cells. In addition, lymphoepithelial lesion and follicular colonization were noted. The present case indicates that primary minor salivary gland MALT-type lymphoma appears to be the cause of tumor-forming amyloidosis of the upper aerodigestive tract including the larynx.
我们在此报告一例起源于口腔小唾液腺的黏膜相关淋巴组织(MALT)型淋巴瘤,该肿瘤呈现肿瘤性淀粉样变性。患者为一名64岁的日本女性,有4年左侧软腭肿物病史。尽管出现多次多灶性复发,累及唇部、软腭、舌、口底及声门和软腭,但肿瘤仍局限于上消化道,且患者在病程中未发生多发性骨髓瘤。组织学上,病变大部分被淀粉样沉积占据。仅病变周边含有大量浆细胞样细胞,偶尔可见中心细胞样细胞。此外,还观察到淋巴上皮病变和滤泡植入。本病例表明,原发性小唾液腺MALT型淋巴瘤似乎是包括喉部在内的上消化道肿瘤性淀粉样变性的病因。