One delayed diagnosis of paragonimiasis case and literature review

Autor: Lijuan Hua, Chen Bao, Jiannan Hu, Luxia Kong, Qian Liu, Shuyun Xu
Rok vydání: 2021
Předmět:
Zdroj: Respirology Case Reports, Vol 9, Iss 5, Pp n/a-n/a (2021)
Respirology Case Reports
ISSN: 2051-3380
DOI: 10.1002/rcr2.750
Popis: 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.
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. Here, we present a case of delayed diagnosis in a 43‐year‐old male. The key findings for correct diagnosis were patient's living in mountainous areas with streams with the presence of host, hypereosinophilia, and careful diet history. Once diagnosed, praziquantel is preferred for treatment.
Databáze: OpenAIRE