Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

A retrospective clinical analysis of pediatric paragonimiasis in a Chinese children’s hospital from 2011 to 2019

Abstract

Diagnosis of pediatric paragonimiasis is difficult because of its non-specific clinical manifestations. We retrospectively reviewed the records of pediatric paragonimiasis in Children’s Hospital of Fudan University from January 2011 to May 2019. The confirmed diagnosis of paragonimiasis was based on positive anti-parasite serological tests from the local Center for Disease Control (CDC). A total of 11 patients (mean age: 7.7 ± 3.1, male–female ratio: 7:4) diagnosed as paragonimiasis were included. 81.8% were from endemic areas such as Sichuan and Yunnan, and 36% had a clear history of raw crab or crayfish consumption. The characteristic clinical features of pediatric paragonimiasis were eosinophilia (100%), pleural effusion (81.8%), hepatomegaly (54.5%), ascites (54.5%), and subcutaneous nodules (45.5%). Misdiagnosed with other diseases including tuberculosis (18.2%), pneumonia (9.1%), intracranial space-occupying lesions (9.1%) and brain abcess (9.1%) led to rehospitalization and prolonged hospitalization. For treatment, a 3-day course of 150 mg/kg praziquantel (PZQ) didn’t show ideal treatment effectivity and 63.6% needed more than one course of PZQ, while triclabendazole in a total dose of 10 mg/kg had a better efficacy to stubborn manifestations. This study indicated that pediatric paragonimiasis was often misdiagnosed, and the treatment with a 3-day course of 150 mg/kg PZQ had a high rate of failure.

Introduction

Paragonimiasis is a food-borne parasitic infestation caused by the lung flukes of the genus Paragonimus spp.1. Infestation mainly occurs through the consumption of improperly cooked crab, crayfish, or raw meat of wild boar or deer infected with Paragonimus metacercariae2. According to the World Health Organization in 2015, the global burden of Paragonimus spp. was about 1.0 million disability-adjusted life years (DALYs)3. Human paragonimiasis has always been a serious medical problem in Africa, Asia and Latin America4. China, with a nationwide paragonimiasis prevalence rate of 1.7%5, has several epidemic areas such as Chongqing, Sichuan, Zhejiang, Yunnan and the region of the Three Gorges Reservoir6. Meanwhile, a large number of Paragonimus spp. was reported from China and the most predominant infections are P. westermani and P. skrjabini7.

According to the Chinese Center for Disease Control (CDC), information is limited in the symptoms, diagnosis and treatment for pediatric paragonimiasis. Diagnosis is often difficult in the cases of paragonimiasis for its vague and non-specific symptoms, especially in children who cannot accurately describe their symptoms and dietary history. It is easily confused with tuberculosis, fungal infection, malignant diseases, purulent meningitis and brain tumors8,9,10,11,12. However, misdiagnosis can lead to unnecessary medical treatments and procedures that can cause serious illness. Thus, our objective was to summarize the clinical manifestations of pediatric paragonimiasis, which are related to early diagnosis and treatment. Moreover, praziquantel (PZQ) and triclabendazole are two WHO-recommended drugs for the treatment of paragonimiasis for their curative effect and little adverse reaction. However, the Chinese CDC hasn’t differentiated doses and courses of treatment between children and adults13. So we try to find a suitable treatment regimen towards different severity and courses of pediatric paragonimiasis.

We retrospectively reviewed 11 cases of pediatric paragonimiasis who were diagnosed and treated at the Department of Infectious Diseases, Children's Hospital of Fudan University. Clinical information, treatment regimens and follow-up outcomes were collected. We aim to raise the awareness and understanding of clinicians towards this rare and neglected disease and give a discussion about the treatment of pediatric paragonimiasis.

Results

Patient demographics and clinical manifestations

Patient demographics and clinical manifestations for 11 patients were summarized in Tables 1 and 2. Among 11 patients included during a period of 8 years, 7 patients were males and 4 patients were females, with an average age of 7.7 ± 3.1 years (range, 3–12 years). The majority of them came from mountainous areas including Sichuan (54.5%), Yunnan (27.3%) and Zhejiang (9.1%), while 1 patient lived in the seaside of Zhejiang province. 45.5% presented with a history of consuming raw or undercooked crabs or crayfish or drinking unboiled stream water, 2 patients had swum in a river and 1 patient liked eating seafood, while 27.2% had no clear history associated with the disease.

Table 1 Characteristics of 11 patients infected with Paragonimus, China, January 2011–May 2019.
Table 2 The clinical manifestations of patients.

In this group, 45.5% (5/11) were misdiagnosed as other diseases at other hospitals, including tuberculosis (18.2%, 2/11), eosinophilic pneumonia (9.1%, 1/11), brain abscess (9.1%, 1/11) and intracranial space-occupying lesions (9.1%, 1/11). Besides, the median hospital stay of patients misdiagnosed was 21 days (range 9–50), much longer than that of patients correctly diagnosed initially (7, 2–11). Before the diagnosis of paragonimiasis, patients received multiple unnecessary medications and treatments, and these were sometimes associated with serious illness.

Symptoms of the patients were summarized in Table 2. The common reasons for patients seeking hospital treatment were fever (45.5%, 5/11), cough (36.4%, 4/11) and abdominal pain (27.3%, 3/11), while neurological symptoms such as vomiting, headache, nausea, or localized myasthenia were relatively rare. Subcutaneous nodules (45.5%, 5/11) and hepatomegaly (45.5%, 5/11) were easy to find during physical examination.

Laboratory findings

Blood routine examinations (RBTs) were performed in all patients. 90.9% (10/11) were detected with elevated peripheral blood WBC with an average of 13.90 × 103/mm3 (range, 5.64–26.20) and the elevation of peripheral blood eosinophilia levels was present in 11 patients (100%) with the mean percentages of 38.25% (range, 5.80–74.00%) at admission. Anti-parasite serological tests were performed in 9 patients, and all of them showed positive serologic results for Paragonimus infection.

Imaging findings

All the patients received imaging examination, abdominal ultrasonography for 8 patients, including cerebral CT for 5 patients, chest CT for 5 patients, chest X-rays for 4 patients, abdominal CT for 1 patient and echocardiogram (ECHO) for 4 patients. As a result, chest and abdominal CT had a higher detection rate, while ECHO had a lower detection rate (Table 3). Chest X-rays, coupled with chest CT have high sensitivity and accuracy for the diagnosis of paragonimiasis. Among 4 patients accepted chest X-rays, pleural effusion was the most common finding. For patients without abnormalities on X-ray plain films, chest CT would be used for more detailed anatomical observations including pleural effusion, alveolar opacification and ill-defined nodules (Fig. 1A–E). For hepatic paragonimiasis, hepatomegaly and ascites were easily found through abdominal ultrasonography and multiple lesions with low density or calcifications in the liver were found through abdominal CT (Fig. 1F). Patients with cerebral paragonimiasis were diagnosed through cerebral CT and MRI (Fig. 2). Brain edema, cerebral calcifications, abscess, nodules and cerebral hemorrhage were common signs for cerebral paragonimiasis (Table 2). Detailed imaging findings are presented in Table 2.

Table 3 Common imaging scans and its positive detection rate.
Figure 1
figure1

A 7-year-old girl presented with abdominal pain and subcutaneous nodules. (A) Chest X-ray showed pulmonary exudation in the right lower lung lobe; (BE) Chest CT showed the alveolar opacification and ill-defined nodules in bilateral lungs, pleural effusion in both thoracic cavities; (F) Abdominal CT showed the multiple lesions with low density or calcifications in the liver.

Figure 2
figure2

A 4-year-old boy presented with paroxysmal headache and vomiting. (AD) Characteristic ring-like lesions with surrounding edema (white arrowhead) and calcifications (black arrowhead) located in the left frontoparietal lobe showed by cranial CT (A), T1WI (B), T2WI (C) and enhanced MRI (D); (EF) Chest MRI indicated the nodules in the lower lobe of the right lung.

Treatment and follow-up outcomes

All 11 patients were treated with at least a standard course of PZQ. However, 63.6% didn’t respond well with a single course of PZQ treatment and needed another course of 3-day PZQ therapy. All patients were required to return for outpatient follow-up, however, 3 of them were lost to follow-up. Hematological, serological or imageological improvements were detected in the follow-up period of most patients with several courses of praziquantel therapy. Nevertheless, a patient treated with three courses of PZQ in a total dose of 150 mg / kg, three times a day, given orally for 3 days still had subcutaneous and penial nodules and eosinophilia (Table 4). Then, the patient accepted a course of triclabendazole in a total dose of 10 mg/kg orally, and as a result, subcutaneous and penial nodules eliminated and eosinophils count returned to normal. 3 patients required rehospitalization and 2 of them were misdiagnosed with lower age, 3 years and 4 years respectively.

Table 4 Changes in peripheral blood of a patient with subcutaneous and penial nodules and eosinophilia after 3 courses of PZQ.

Discussion

Data are limited in the incidence, diagnosis and treatment of children with paragonimiasis. After infection with Paragonimus spp., clinical symptoms usually appear after 2–20 days. When metacercariae migrate to different parts of the body, patients will present with fever, fatigue, diarrhea or upper abdominal pain and eosinophilia14. Immature forms migrate through the duodenal wall, peritoneal cavity, and diaphragm to become encapsulated and mature within the lungs, or other ectopic tissues including the liver, brain, kidneys, adrenal glands and peritoneal and mesenteric lymph nodes2,5,7. Therefore, symptoms of paragonimiasis were usually variable, as agents of a “neglected tropical disease.” Our study concluded the clinical and imaging findings of paragonimiasis and its treatment course to improve the awareness of this disease.

In this study, among all 11 cases of paragonimiasis in children, all of them came from epidemic areas including Sichuan, Zhejiang and Yunnan and none of them came from Shanghai, which was inconsistent with the report that big city had higher incidences of paragonimiasis15. Dietary habits of raw or undercooked food are also prevalent in these cities16. In our study, 45.5% of the patients presented with a history of consuming raw or undercooked crabs or crayfish, and 2 patients may be contacted with metacercariae-contaminated stream when swimming, while 27.2% of the patients had no clear history associated with the disease. Our findings are consistent with other two large reports of pediatric paragonimiasis in China13,16. Gong et al. reported that 58.5% (72/123) had a history of consuming freshwater crabs and Xu et al. reported that 79.3% (46/58) admitted a history of raw water or food ingestion. Changing dietary patterns are having a profound effect on the epidemiology of paragonimiasis17,18. Hence, it is necessary to appeal to change risky eating habits and strengthen the awareness of not taking raw water or food.

Diagnosis is difficult in paragonimiasis because of its non-specific and vague symptoms. Fever and subcutaneous nodules are two main complaints of patients at admission instead of gastrointestinal symptoms or respiratory symptoms reported by Gong et al.13. Fever is regarded as a sign of early infection of Paragonimus, which can appear in as little as 2–4 days after ingestion of metacercariae19. Subcutaneous nodules, especially migratory subcutaneous nodules, are an important manifestation of extra-pulmonary paragonimiasis, which is caused by the aberrant migration of juvenile worms. For imaging findings, pleural effusion as an important clinical manifestation of pulmonary paragonimiasis appeared in 81.8% of patients in our group, suggesting that most pediatric patients with extra-pulmonary paragonimiasis also had pulmonary paragonimiasis in our group. Moreover, patients with cerebral paragonimiasis showed characteristic ring-like lesions with surrounding edema in MRI and they often had neural symptoms including vomiting, dizziness or cephalalgia, which is different from Xu et al.’s results16. Also, eosinophilia is a very frequent finding in parasite infections. Many functions and properties have been attributed to eosinophils such as exocytic attacks on helminths via released substances, pro-inflammatory effects as well as mechanisms to modulate immune processes20. In our study, eosinophilia was noted in 11(100%) patients and elevated WBC count in 10(90.9%) patients, higher than data reported by Xu et al.16 and may related to the severity of the disease. The change in peripheral blood eosinophil was related to the course of the disease, as seen in Table 3, suggesting that the change in the eosinophil level may be used as a sign for the evaluation of anti-infection therapy.

Misdiagnosis is common, especially in children who cannot exactly describe dietary history and symptoms. In our study, the misdiagnosis rate at admission was 45.5%, and the most commonly confused disease was tuberculosis due to their similar symptoms and signs. Moreover, some clinical manifestation of extra-pulmonary paragonimiasis such as space-occupying lesions in the liver, cerebrum or spinal canal can be easily misdiagnosed with tumors11,21,22. Delayed diagnosis is associated with serious illness, as shown in our results via median hospital stay and rehospitalization. The reason for a prolonged hospital stay can be unnecessary medications and treatments patients received before the diagnosis of paragonimiasis. Therefore, there is a need for a better understanding of relatively rare lung paragonimiasis infection in pediatric patients. Paragonimiasis should be considered in patients with symptoms of intermittent fever, cough or subcutaneous nodule, especially in those come from epidemic regions, have a history of raw crabs or crayfish consumption, or present elevated eosinophil counts.

PZQ and triclabendazole are two WHO-recommended drugs for the treatment of human paragonimiasis. According to the recommendations of the American Academy of Pediatrics, PZQ is the first line of treatment for paragonimiasis and the recommended course is a total amount of 150 mg/kg given three times a day orally for three days23. In our study, a 3-day course was used to alleviate side effects such as allergic reactions and brain edema, brain herniation after high-dose therapy. However, the 3-day course didn’t show ideal treatment effectivity and 63.6% patients needed more than one course of PZQ, much higher than that reported by Gong et al. (23.6%)13. The high rate of misdiagnosis and severe symptoms of patients in our group may be also related to low response to PZQ. It has been reported that paragonimiasis associated with effusions have unsatisfactory responses to the initial PZQ treatment24,25, then 81.8% in our group had pleural effusions. One patient whose subcutaneous nodules still existed after 3 courses of PZQ treatment received a total dose of 10 mg/kg triclabendazole. Furthermore, triclabendazole treatment had a satisfactory therapeutic effect for eliminating subcutaneous nodules. We were the first medical institution in China who had reported using triclabendazole for a pediatric patient with paragonimiasis.

Our study had several limitations. First of all, our sample size was small and it was from one pediatric center, thus the results had extrapolation biases. Besides, the case history of some patients transferred to another hospital in the midway was not detailed. Future studies of pediatric paragonimiasis should be investigated over the country.

In conclusion, the clinical manifestations of paragonimiasis are lack specificity, thus commonly leading to misdiagnosis. Therefore, the diagnosis should be combined with epidemiological history, clinical manifestations and laboratory results. Treatment strategy should be refined to different severity and course of the disease and more investigation on the treatment regimen is needed to improve the curative. When a 3-day course of 150 mg/kg PZQ had a high rate of failure. Triclabendazole would be another choice.

Methods

Data collection

The records of patients diagnosed with paragonimiasis between January 2011 and May 2019 in the Department of Infectious Diseases, Children's Hospital of Fudan University were retrospectively collected.

Patient evaluation and diagnosis

The diagnostic criteria for paragonimiasis were based on epidemiological history: eating raw or improper cooked freshwater crab or crayfish, or drinking raw stream water; clinical manifestations: cough, chest pain, blood phlegm or pleural lesions, etc.; the elevated proportion and absolute value of peripheral eosinophil; positive anti-parasite serological test; radiographical findings; positive parasitological examination results.

Treatment and follow-up management

A total dosage of 150 mg/kg praziquantel (PZQ) taken three times daily with meals for 3 days was recommended as a standard course. Hematological and serological examinations and imageological examinations were performed after treatment to evaluate patient recovery from the infection. Another course of PZQ or triclabendazole was used in patients with unsatisfactory responses.

Ethics declarations

This study was conducted in accordance with the International Council for Harmonisation Guidelines for Good Clinical Practice and the Declaration of Helsinki. This study was approved by the Research Ethics Board of Children’s Hospital of Fudan University ((2020)506), with a waiver regarding informed consent.

Data availability

The datasets used and analyzed during the current study are available from the corresponding author on reasonable request.

References

  1. 1.

    Kalhan, S. et al. Paragonimus westermani infection in lung: A confounding diagnostic entity. Lung India 32, 265–267. https://doi.org/10.4103/0970-2113.156248 (2015).

    Article  PubMed  PubMed Central  Google Scholar 

  2. 2.

    Cumberlidge, N. et al. Paragonimus and paragonimiasis in West and Central Africa: Unresolved questions. Parasitology 145, 1748–1757. https://doi.org/10.1017/s0031182018001439 (2018).

    Article  PubMed  Google Scholar 

  3. 3.

    World Health Organization (WHO). WHO Estimates of the global Burden of Foodborne Diseases. Geneva (2015).

  4. 4.

    Furst, T., Keiser, J. & Utzinger, J. Global burden of human food-borne trematodiasis: A systematic review and meta-analysis. Lancet Infect. Dis. 12, 210–221. https://doi.org/10.1016/S1473-3099(11)70294-8 (2012).

    Article  PubMed  Google Scholar 

  5. 5.

    Liu, Q., Wei, F., Liu, W., Yang, S. & Zhang, X. Paragonimiasis: An important food-borne zoonosis in China. Trends Parasitol. 24, 318–323. https://doi.org/10.1016/j.pt.2008.03.014 (2008).

    Article  PubMed  Google Scholar 

  6. 6.

    Zhang, X. et al. Distribution and clinical features of Paragonimiasis skrjabini in Three Gorges Reservoir Region. Parasitol. Int. 61, 645–649. https://doi.org/10.1016/j.parint.2012.06.007 (2012).

    Article  PubMed  Google Scholar 

  7. 7.

    Yoshida, A., Doanh, P. N. & Maruyama, H. Paragonimus and paragonimiasis in Asia: An update. Acta Trop. 199, 105074. https://doi.org/10.1016/j.actatropica.2019.105074 (2019).

    Article  PubMed  Google Scholar 

  8. 8.

    Zarrinkhameh, N., Citron, D. R., Stager, C. E. & Laucirica, R. Pulmonary paragonimiasis diagnosed by fine-needle aspiration biopsy. J. Clin. Microbiol. 46, 2137–2140. https://doi.org/10.1128/JCM.02424-07 (2008).

    Article  Google Scholar 

  9. 9.

    Nagayasu, E., Yoshida, A., Hombu, A., Horii, Y. & Maruyama, H. Paragonimiasis in Japan: A twelve-year retrospective case review (2001–2012). Internal Med. 54, 179–186. https://doi.org/10.2169/internalmedicine.54.1733 (2015).

    Article  Google Scholar 

  10. 10.

    Tshibwabwa, E. T., Richenberg, J. L. & Aziz, Z. Lung radiology in the tropics. Clin. Chest Med. 23, 309–328. https://doi.org/10.1016/S0272-5231(02)00008-4 (2002).

    Article  PubMed  Google Scholar 

  11. 11.

    Yong, X., Yan, J., Jing, C. & Chao, Y. Cerebral paragonimiasis: A retrospective analysis of 27 cases. J. Neurosurg. 15, 101–106. https://doi.org/10.3171/2014.10.PEDS14208 (2015).

    Article  Google Scholar 

  12. 12.

    Zhi, C. et al. Angiographic findings in 2 children with cerebral paragonimiasis with hemorrhage. J. Neurosurg. 11, 564–567. https://doi.org/10.3171/2013.1.PEDS12475 (2013).

    Article  Google Scholar 

  13. 13.

    Gong, Z. et al. Paragonimiasis in children in southwest China: A retrospective case reports review from 2005 to 2016. Medicine 96, e7265. https://doi.org/10.1097/MD.0000000000007265 (2017).

    Article  PubMed  PubMed Central  Google Scholar 

  14. 14.

    Cho, A., Lee, H., Lee, K., Lee, S. & Lee, S. A case of pulmonary paragonimiasis with involvement of the abdominal muscle in a 9-year-old girl. Korean J. Parasitol. 49, 409–412. https://doi.org/10.3347/kjp.2011.49.4.409 (2011).

    Article  PubMed  PubMed Central  Google Scholar 

  15. 15.

    Zhou, P., Chen, N., Zhang, R., Lin, R. & Zhu, X. Food-borne parasitic zoonoses in China: Perspective for control. Trends Parasitol. 24, 190–196. https://doi.org/10.1016/j.pt.2008.01.001 (2008).

    Article  PubMed  Google Scholar 

  16. 16.

    Xu, H. Z., Tang, L. F., Zheng, X. P. & Chen, Z. M. Paragonimiasis in Chinese children: 58 cases analysis. Iran J. Pediatr. 22, 505–511 (2012).

    PubMed  PubMed Central  Google Scholar 

  17. 17.

    Yoonuan, T. et al. Paragonimiasis prevalences in Saraburi province, Thailand, measured 20 years apart. SE Asian J. Trop. Med. 39, 593–600 (2008).

    Google Scholar 

  18. 18.

    Uttah, E. C. Paragonimiasis and renewed crab-eating behavior in six communities from two ethnocultural clusters in southeastern Nigeria. Int. Scholar. Res. Not. 1–5, 2013. https://doi.org/10.5402/2013/569485 (2013).

    Article  Google Scholar 

  19. 19.

    Zhong, H. L., He, L. Y., Xu, Z. B. & Cao, W. J. Recent progress in studies of paragonimus and paragonimiasis control in China. Chin. Med. J. (Engl.) 94, 483–494 (1981).

    CAS  Google Scholar 

  20. 20.

    Rosenberg, H. F., Dyer, K. D. & Foster, P. S. Eosinophils: Changing perspectives in health and disease. Nat. Rev. Immunol. 13, 9–22. https://doi.org/10.1038/nri3341 (2013).

    CAS  Article  PubMed  Google Scholar 

  21. 21.

    Qin, Y. et al. Intraspinal paragonimiasis in children: MRI findings and suggestions for pathogenesis. Am. J. Neuroradiol. 40, 2166–2171. https://doi.org/10.3174/ajnr.A6296 (2019).

    CAS  Article  PubMed  Google Scholar 

  22. 22.

    Lu, C., Hu, Y. & Chen, W. Characteristic MR and CT imaging findings of hepatobiliary paragonimiasis and their pathologic correlations. Acta Radiol. 53, 481–484. https://doi.org/10.1258/ar.2012.110539 (2012).

    Article  PubMed  Google Scholar 

  23. 23.

    Diseases, A. C. O. I. Red Book, 29th Edition (2012). (American Academy of Pediatrics, 2012).

  24. 24.

    Obara, A., Nakamurauchiyama, F., Hiromatsu, K. & Nawa, Y. Paragonimiasis cases recently found among immigrants in Japan. Internal Med. 43, 388–392. https://doi.org/10.2169/internalmedicine.43.388 (2004).

    Article  Google Scholar 

  25. 25.

    Oh, I. et al. Can pleuropulmonary paragonimiasis be cured by only the 1st set of chemotherapy? Treatment outcome and clinical features of recently developed pleuropulmonary paragonimiasis. Internal Med. 50, 1365–1370. https://doi.org/10.2169/internalmedicine.50.5093 (2011).

    Article  Google Scholar 

Download references

Funding

All phases of this study were supported by a grant from Science and Technology Commission of Shanghai Municipality (19411972100).

Author information

Affiliations

Authors

Contributions

Dr. M.Q., Y.S. and Prof J.S. conceptualized and designed the study, drafted the initial manuscript, and reviewed and revised the manuscript. Dr. M.Q. and F.L., and Dr. Y.Z. designed the data collection instruments, collected data, carried out the initial analyses, and reviewed and revised the manuscript. Prof. J.S. and Prof. Z.Q. conceptualized and designed the study, coordinated and supervised data collection, and critically reviewed the manuscript for important intellectual content. All authors approved the final manuscript as submitted and agree to be accountable for all aspects of the work.

Corresponding authors

Correspondence to Yingyan Shi or Jun Shen.

Ethics declarations

Competing interests

The authors declare no competing interests.

Additional information

Publisher's note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Qian, M., Li, F., Zhang, Y. et al. A retrospective clinical analysis of pediatric paragonimiasis in a Chinese children’s hospital from 2011 to 2019. Sci Rep 11, 2005 (2021). https://doi.org/10.1038/s41598-021-81694-7

Download citation

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing