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首页> 外文期刊>The Internet Journal of Tropical Medicine >Cysticercosis Of The Cheek
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Cysticercosis Of The Cheek

机译：面颊囊虫病

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The cheek is a rare site for cysticercosis cellulosae. Very few cases of solitary cysticercosis of cheek have been reported. We report one such case and discuss the review of literature, etoipathogenesis, clinical course and management. Case Report An 11-year old male presented to ENT OPD with a swelling on left cheek 8 months. The swelling was around 2cm x 2cm, firm and non-tender and mobile. FNAC of swelling showed only blood. An excisional biopsy was done from intraoral route and specimen was sent for histopathological examination, which revealed cysticercosis. Patient was then taken up for CT scan head and thorough clinical examination to rule out cysticercocis elsewhere. Stool examination for ova and cyst and blood examination for eosinophilia was with in normal limits. Patient was given tablet albendazole 400mg daily for 8 days. Review of personal history revealed that the patient was not a meat eater.
机译：脸颊是囊尾rc病纤维素的罕见部位。很少有面颊囊尾虫病的报道。我们报告了一种这样的情况，并讨论了文献综述，病因，临床过程和管理。病例报告一名11岁男性出现在ENT OPD，左脸红肿8个月。肿胀约2cm x 2cm，结实且不嫩且可移动。肿胀的FNAC仅显示血液。从口内途径进行切除活检，并将标本送去进行组织病理学检查，发现囊尾rc病。然后，将患者接受CT扫描头检查和彻底的临床检查，以排除其他地方的囊尾co。正常检查卵和囊肿的大便检查和嗜酸性粒细胞的血液检查。每天给患者服用阿苯达唑片剂400mg，持续8天。对个人病史的回顾表明，该患者不是吃肉者。

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