One delayed diagnosis of paragonimiasis case and literature review.
Luxia KongLijuan HuaQian LiuChen BaoJiannan HuShuyun XuPublished in: Respirology case reports (2021)
Human paragonimiasis has been appearing all over the world due to increased human migration, international travel, and worldwide food trading. However, delayed and missed diagnosis rates are also increasing due to atypical clinical manifestations and the lack of disease understanding by clinical workers. We describe the case of a 43-year-old man, who was hospitalized with cough and chest pain for two months. Chest computed tomography (CT) revealed bilateral emphysema, left pleural effusion, and bilateral atelectasis. The hypereosinophilia gave us a clue; ultimately, the diagnosis of paragonimiasis was made through a diet history and a positive result of serum Paragonimus sp. immunoglobulin (Ig) G antibody. Moreover, 27 misdiagnosed paragonimiasis cases in the past decade have been reported. We draw conclusions by summarizing their characteristics for suspicious eosinophilic paragonimiasis patients; we should inquire diet history carefully, test serum IgG antibodies, and try to detect eggs. Once diagnosed, praziquantel is preferred for treatment.
Keyphrases
- computed tomography
- endothelial cells
- case report
- end stage renal disease
- weight loss
- physical activity
- induced pluripotent stem cells
- ejection fraction
- newly diagnosed
- magnetic resonance imaging
- contrast enhanced
- dual energy
- pluripotent stem cells
- chronic kidney disease
- magnetic resonance
- peritoneal dialysis
- single cell
- cystic fibrosis
- risk assessment
- patient reported outcomes
- climate change
- combination therapy