Mazhari N J, Kumar N, Jain S
Department of Pathology, Maulana Azad Medical College and LN Hospital, New Delhi, India.
J Oral Pathol Med. 2001 Mar;30(3):187-9. doi: 10.1034/j.1600-0714.2001.300309.x.
Oral mucosa is a rare site for cysticercosis. This paper describes eight cases of cysticercosis involving the oral cavity: four in the buccal mucosa, two in the lips, one in the tongue and one in the gums. All of the patients presented with a solitary superficial mucosal nodule, with duration varying from one month to three years. Larval fragments of cysticercus cellulosae on an inflammatory background were seen in cytologic smears in all cases. Diagnosis of cysticercosis was clinically unsuspected in all these cases prior to aspiration cytologic diagnosis.
口腔黏膜是囊尾蚴病的罕见发病部位。本文描述了8例累及口腔的囊尾蚴病病例：4例发生于颊黏膜，2例发生于唇部，1例发生于舌部，1例发生于牙龈。所有患者均表现为单个浅表黏膜结节，病程从1个月至3年不等。所有病例的细胞学涂片均可见在炎症背景下的猪囊尾蚴幼虫碎片。在细针穿刺细胞学诊断之前，所有这些病例的囊尾蚴病临床诊断均未被怀疑。
