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1例宫崎并殖吸虫病累及肺部且感染7年后才确诊的罕见病例:病例报告及文献复习

A rare case of paragonimiasis miyazakii with lung involvement diagnosed 7 years after infection: A case report and literature review.

作者信息

Yatera Kazuhiro, Hanaka Minako, Hanaka Tetsuya, Yamasaki Kei, Nishida Chinatsu, Kawanami Toshinori, Kawanami Yukiko, Ishimoto Hiroshi, Kanazawa Tamotsu, Mukae Hiroshi

机构信息

Department of Respiratory Medicine, University of Occupational and Environmental Health, Japan, 1-1, Iseigaoka, Yahatanishiku, Kitakyushu City, Fukuoka 807-8555, Japan.

Department of Respiratory Medicine, University of Occupational and Environmental Health, Japan, 1-1, Iseigaoka, Yahatanishiku, Kitakyushu City, Fukuoka 807-8555, Japan.

出版信息

Parasitol Int. 2015 Oct;64(5):274-80. doi: 10.1016/j.parint.2015.02.009. Epub 2015 Mar 11.

DOI:10.1016/j.parint.2015.02.009
PMID:25771073
Abstract

We report a rare case of pulmonary paragonimiasis caused by Paragonimus miyazakii that showed pulmonary manifestations and a long-term clinical course after infection. A 45-year-old Japanese male developed cough and dyspnea in 2004 and was diagnosed with eosinophilic pneumonia. He had been treated with low-dose oral corticosteroid for 7 years. He recalled that he had consumed a large amount of raw freshwater crab (Geothelphusa dehaani) several weeks before he had been admitted for the first time, and that had been the only occasion when he had eaten this meat. The patient was referred to our hospital due to persistent hemoptysis, and his chest computed tomography scan showed pulmonary nodules and cavities, and his serum total IgE level was elevated. Bronchoscopy was performed, and ova were detected in the bronchoalveolar lavage fluid. The morphological examination of the ova and immunoserological examination yielded typical findings of P. miyazakii. Treatment with praziquantel improved his chest radiographic findings and a decrease of serum total IgE, as well as the values of immunoserological examination for P. miyazakii. The clinical course of this patient indicated that he had been infected with P. miyazakii for 7 years at least, which is unusual for paragonimiasis miyazakii.

摘要

我们报告了一例由宫崎并殖吸虫引起的罕见肺型并殖吸虫病病例,该病例在感染后出现肺部表现及长期临床病程。一名45岁日本男性于2004年出现咳嗽和呼吸困难,被诊断为嗜酸性粒细胞性肺炎。他接受低剂量口服糖皮质激素治疗达7年。他回忆首次入院前几周曾大量食用生淡水蟹(日本绒螯蟹),且仅此一次食用这种食物。患者因持续咯血转诊至我院,胸部计算机断层扫描显示肺部有结节和空洞,血清总IgE水平升高。进行了支气管镜检查,在支气管肺泡灌洗液中检测到虫卵。虫卵的形态学检查和免疫血清学检查得出宫崎并殖吸虫的典型结果。吡喹酮治疗改善了他的胸部影像学表现,降低了血清总IgE水平以及宫崎并殖吸虫免疫血清学检查的值。该患者的临床病程表明他感染宫崎并殖吸虫至少7年,这在宫崎并殖吸虫病中并不常见。

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