Nigam S, Singh T, Mishra A, Chaturvedi K U
Department of Pathology, Maulana Azad Medical College, Bahadurshah Zafar Marg, C-367 Saraswati Vihar, Pitampura, Delhi, 34 India.
Head Neck. 2001 Jun;23(6):497-9. doi: 10.1002/hed.1066.
Cysticercosis cellulosae rarely involves the oral region in humans.
Six cases of oral cysticercosis were diagnosed, three each in lips and buccal mucosa. Diagnosis was made by characteristic gross and histopathologic appearances.
Of 146 cases of cysticercosis, 6 (4.1%) were of the oral cavity. All 6 cases were initially seen with painless swellings. Clinical differential diagnosis ranged from retention cyst, lipoma, fibroma, neurofibroma, and angular stomatitis. Histopathologic examination revealed cysticercus larvae.
The oral cavity is a rare site of involvement by cysticercosis, even in an endemic area. Histopathologic findings of the excised cyst are diagnostic of the lesion.
人体囊尾蚴病很少累及口腔区域。
诊断出6例口腔囊尾蚴病，唇部和颊黏膜各3例。通过特征性大体表现和组织病理学表现进行诊断。
在146例囊尾蚴病病例中，6例（4.1%）为口腔囊尾蚴病。所有6例最初均表现为无痛性肿胀。临床鉴别诊断包括潴留性囊肿、脂肪瘤、纤维瘤、神经纤维瘤和口角炎。组织病理学检查发现囊尾蚴幼虫。
即使在流行地区，口腔也是囊尾蚴病罕见的受累部位。切除囊肿的组织病理学检查结果可确诊该病变。
