Katayama syndrome disguised as eosinophilic asthma with acute systemic symptoms and pulmonary nodules

IF 0.8 Q4 RESPIRATORY SYSTEM
Femke Demolder , Samuel De Bontridder , Shane Hanon
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引用次数: 0

Abstract

Background

Katayama syndrome is an acute manifestation of schistosomiasis, a parasitic infection that manifests itself through a hypersensitivity reaction to migrating larvae and early egg deposition. Left undiagnosed and untreated, acute schistosomiasis can develop into chronic schistosomiasis which can lead to debilitating morbidity such as pulmonary hypertension. This case highlights that Katayama syndrome can also been seen in regions where the parasite is not endemic, as it occurs in travelers returning from endemic regions or in immigrants.

Case presentation

We describe the case of a 26-year-old asthmatic male, who presented with systemic symptoms including fever, myalgia, night sweats as well as gastro-intestinal and pulmonary complaints since five days. At presentation, there was a raised blood eosinophil count and nodular lesions were seen on computed tomography. After considering diagnoses such as tuberculosis, vasculitis and hypereosinophilic syndrome, it was repeated history taking that revealed that the patient had suffered from swimmer’s itch during a stay in Guinea. A stool sample showed microscopic presence of Schistosoma mansoni eggs, confirming the diagnosis of Katayama syndrome. The patient was treated with tapered corticosteroids to suppress the hypersensitivity reaction and praziquantel was added to cure the parasitic infection. This led to a complete resolution of the patients' symptoms and radiological abnormalities. Negative stool samples confirmed the eradication of the schistosomes.

Conclusions

Swimmer’s itch and Katayama syndrome are manifestations of acute schistosomiasis. It is important to recognize the syndrome, because early diagnosis and adequate treatment can prevent chronic disease and significant morbidity.

伪装成嗜酸性粒细胞性哮喘的片山综合征,伴有急性全身症状和肺部结节
研究背景 卡塔亚马综合征是血吸虫病的一种急性表现,血吸虫病是一种寄生虫感染,表现为对移行幼虫和早期虫卵沉积的超敏反应。如果不及时诊断和治疗,急性血吸虫病可发展为慢性血吸虫病,导致肺动脉高压等致残性疾病。本病例强调,片山综合征也可出现在非寄生虫流行地区,因为它发生在从寄生虫流行地区返回的旅行者或移民身上。病例介绍 我们描述了一个 26 岁男性哮喘病人的病例,他出现全身症状,包括发热、肌痛、盗汗以及胃肠道和肺部不适 5 天。发病时,血液中嗜酸性粒细胞计数升高,计算机断层扫描显示有结节性病变。在考虑了肺结核、血管炎和嗜酸性粒细胞过多综合征等诊断后,医生反复询问病史,发现患者在几内亚逗留期间曾患过游泳瘙痒症。粪便样本在显微镜下显示存在曼氏血吸虫虫卵,确诊为片山综合征。患者接受了渐进式皮质类固醇治疗,以抑制超敏反应,并加入吡喹酮治疗寄生虫感染。这使得患者的症状和放射学异常完全消失。结论斯维默氏痒和片山综合征是急性血吸虫病的表现。认识这种综合征非常重要,因为早期诊断和适当治疗可以预防慢性疾病和重大疾病的发生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Respiratory Medicine Case Reports
Respiratory Medicine Case Reports RESPIRATORY SYSTEM-
CiteScore
2.10
自引率
0.00%
发文量
213
审稿时长
87 days
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