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首页> 外文期刊>The Korean Journal of Parasitology >Cutaneous Gnathostomiasis with Recurrent Migratory Nodule and Persistent Eosinophilia: a Case Report from China
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Cutaneous Gnathostomiasis with Recurrent Migratory Nodule and Persistent Eosinophilia: a Case Report from China

机译:皮肤食管角化症伴反复迁徙性结节和持续性嗜酸性粒细胞增多症:中国的一例病例报告

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摘要

The present study reports a human case of cutaneous gnathostomiasis with recurrent migratory nodule and persistent eosinophilia in China. A 52-year-old woman from Henan Province, central China, presented with recurrent migratory reddish swelling and subcutaneous nodule in the left upper arm and on the back for 3 months. Blood examination showed eosinophila (21.2%), and anti-sparganum antibodies were positive. Skin biopsy of the lesion and histopathological examinations revealed dermal infiltrates of eosinophils but did not show any parasites. Thus, the patient was first diagnosed as sparganosis; however, new migratory swellings occurred after treatment with praziquantel for 3 days. On further inquiring, she recalled having eaten undercooked eels and specific antibodies to the larvae of Gnathostoma spinigerum were detected. The patient was definitely diagnosed as cutaneous gnathostomiasis caused by Gnathostoma sp. and treated with albendazole (1,000 mg/day) for 15 days, and the subsequent papule and blister developed after the treatment. After 1 month, laboratory findings indicated a reduced eosinophil count (3.3%). At her final follow-up 18 months later, the patient had no further symptoms and anti-Gnathostoma antibodies became negative. Conclusively, the present study is the first report on a human case of cutaneous gnathostomiasis in Henan Province, China, based on the past history (eating undercooked eels), clinical manifestations (migratory subcutaneous nodule and persistent eosinophilia), and a serological finding (positive for specific anti-Gnathostoma antibodies).
机译:本研究报道了在中国发生的一例人类皮肤破口症并伴有反复迁徙性结节和持续性嗜酸性粒细胞增多的病例。一名来自中国中部河南省的52岁妇女在左上臂和背部表现出反复出现的迁徙性红肿和皮下结节3个月。血液检查显示嗜酸性粒细胞(21.2%),抗石笋抗体呈阳性。病变的皮肤活检和组织病理学检查显示嗜酸性粒细胞真皮浸润,但未显示任何寄生虫。因此,该患者首先被诊断为斯巴德病。然而,吡喹酮治疗3天后出现新的迁徙肿胀。在进一步询问后,她回忆说吃了未煮熟的鳗鱼,并检测到了针对食蟹猴的幼虫的特异性抗体。该患者肯定被诊断为由Gnathostoma sp引起的皮肤破口。并用阿苯达唑(1,000 mg /天)治疗15天,治疗后出现丘疹和水疱。 1个月后,实验室检查结果显示嗜酸性粒细胞减少(3.3%)。在18个月后的最后一次随访中,该患者没有进一步的症状,并且抗Gnhosthostoma抗体变为阴性。最后,本研究是基于中国河南省过去的历史(食用鳗鱼煮熟),临床表现(迁徙性皮下结节和持续性嗜酸性粒细胞增多)和血清学发现(阳性)而在中国河南省发生的一例人类皮肤白皮病的报告。 (针对特定的抗性生殖器瘤抗体)。

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