Case Report Open Access
Copyright ©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Clin Cases. Jan 26, 2021; 9(3): 666-671
Published online Jan 26, 2021. doi: 10.12998/wjcc.v9.i3.666
Pleural lump after paragonimiasis treated by thoracoscopy: A case report
Yue Xie, Department of Burns and Plastic Surgery, Children’s Hospital of Chongqing Medical University, Chongqing 400010, China
Ya-Rui Luo, Outpatient Department, Chongqing University Three Gorges Hospital, Chongqing 404000, China
Meng Chen, Yi-Min Xie, Qiang Chen, Department of Pediatric Surgery, Chongqing University Three Gorges Hospital, Chongqing 400010, China
Chen-Yu Sun, Department of Internal Medicine, AMITA Health Saint Joseph Hospital Chicago, Chicago, IL 60657, United States
ORCID number: Yue Xie (0000-0002-9831-9567); Ya-Rui Luo (0000-0002-0612-5993); Meng Chen (0000-0003-2722-9940); Yi-Min Xie (0000-0001-6555-3667); Chen-Yu Sun (0000-0003-3812-3164); Qiang Chen (0000-0002-4312-1879).
Author contributions: Xie Y and Luo YR contributed equally to this work and reviewed the literature and contributed to manuscript drafting; Chen M and Xie YM are the patient’s surgeons, performed the surgery, and contributed to manuscript drafting; Sun CY was responsible for the revision of the manuscript for important intellectual content; all authors issued final approval for the version to be submitted.
Informed consent statement: Informed written consent was obtained from the patient for publication of this report and any accompanying images.
Conflict-of-interest statement: The authors declare that they have no conflict of interest to disclose.
CARE Checklist (2016) statement: The authors have read the CARE Cheklist (2016), and the manuscript was prepared and revised according to the CARE Checklist (2016).
Open-Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/
Corresponding author: Qiang Chen, MD, Doctor, Department of Pediatric Surgery, Chongqing University Three Gorges Hospital, No. 165 Xincheng Road, Wanzhou District, Chongqing 404000, China. cqwzchenqiang@163.com
Received: September 1, 2020
Peer-review started: September 1, 2020
First decision: November 8, 2020
Revised: November 16, 2020
Accepted: November 29, 2020
Article in press: November 29, 2020
Published online: January 26, 2021
Processing time: 141 Days and 3.8 Hours

Abstract
BACKGROUND

Paragonimiasis is a parasitic disease that has multiple symptoms, with pulmonary types being common. According to our clinical practices, the pleural effusion of our patients is full of fibrous contents. Drainage, praziquantel, and triclabendazole are recommended for the treatment, but when fibrous contents are contained in pleural effusion, surgical interventions are necessary. However, no related reports have been noted. Herein, we present a case of pulmonary paragonimiasis treated by thoracoscopy.

CASE SUMMARY

A 12-year-old girl presented to our outpatient clinic complaining of shortness of breath after exercise for several days. Enzyme-linked immunosorbent assay revealed positivity for antibodies against Paragonimus westermani, serological test showed eosinophilia, and moderate left pleural effusion and calcification were detected on computed tomography (CT). She was diagnosed with paragonimiasis, and praziquantel was prescribed. However, radiography showed an egg-sized nodule in the left pleural cavity during follow-up. She was then admitted to our hospital again. The serological results were normal except slight eosinophilia. CT scan displayed a cystic-like node in the lower left pleural cavity. The patient underwent a thoracoscopic mass resection. A mass with a size of 6 cm × 4 cm × 3 cm adhered to the pleura was resected. The pathological examination showed that the mass was composed of non-structured necrotic tissue, indicating a granuloma. The patient remainded asymptomatic and follow-up X-ray showed complete removal of the mass.

CONCLUSION

This case highlights that thoracoscopic intervention is necessary when fibrous contents are present on CT scan or chest roentgenogram to avoid later fibrous lump formation in patients with pulmonary paragonimiasis.

Key Words: Pulmonary paragonimiasis; Paragonimus; Thoracoscopy; Pleural lump; Pleural effusion; Case report

Core Tip: Paragonimiasis is a common parasitic disease in south China. Based on our clinical experience, the pleural effusion of our patients contains abundant scrambled egg-like materials, and it is difficult to drain all the fluid because the fibrous materials can block the drainage tube. Therefore, the fibrous material can lead to fibrous lump formation. However, there have been rare reports about surgical interventions performed on patients with pleural effusion, hence we recommend early intervention in pleural effusion to prevent the development of the chronic stage.



INTRODUCTION

Paragonimiasis is a typical parasitic disease caused by foodborne zoonotic helminthiasis named paragonimus. Human infections often happen after the ingestion of freshwater crustaceans, crabs, or crayfishes, which were infected by Paragonimus metacercariae[1]. This disease prevails mainly in Asian, Latin America, and Africa, especially areas where the residents habitually take raw or undercooked water or food[2-4]. The invasion of metacercariae causes different clinical symptoms, including subcutaneous, pleurisy, abdominal, cerebral, and asymptomatic types. The pleurisy type is the most common, which presents as chest pain, cough, and pleural effusion. Praziquantel and triclabendazole are potent for the treatment of paragonimiasis and are recommended by the World Health Organization. However, it has been reported that praziquantel is insufficient in massive pleural effusion cases[1], so drainage is suggested, while surgical intervention has not been narrated. But according to our clinical practices, pleural effusion is hard to be removed by drainage due to the numerous fibrous materials inside the fluid, hence we recommend thoracoscopy in such situations. Here, we report one patient who presented a thoracic lump after standard praziquantel treatment and was cured by thoracoscopic mass resection.

CASE PRESENTATION
Chief complaints

A 12-year-old girl presented to our outpatient clinic with shortness of breath after exercise for several days.

History of present illness

The patient’s symptoms started several days ago with shortness of breath after exercise, without symptoms of cough and thoracalgia.

History of past illness

The patient had a history of ingesting raw crabs and a free previous medical history.

Personal and family history

The patient had no specific personal and family history.

Physical examination

After admission, the patient’s vital signs were normal. The breath sounds of the left lung were reduced; neither wet rales nor dry rales were revealed on both lungs.

Laboratory examinations

Enzyme-linked immunosorbent assay revealed positivity for antibodies against Paragonimus westermani. The serological test showed eosinophilia at the first hospitalization. Serological results (basic metabolic panel and tumor markers) were normal, except slight eosinophilia (absolute eosinophil count, 0.61 × 109 /L) at the second hospitalization.

Imaging examinations

At the first hospitalization, CT scan showed moderate left pleural effusion, left pleural thickening, and calcification (Figure 1). At the second hospitalization, CT scan displayed a cystic-like node (6.0 cm × 2.3 cm) in the lower left pleural cavity (Figure 2).

Figure 1
Figure 1 Computed tomography scan of the patient before the praziquantel treatment. Moderate effusion in the left pleural cavity, left pleural thickening and calcification, and a small amount of patchy and striped shadows was visible on the left lower and upper lobes.
Figure 2
Figure 2 Computed tomography scan of the patient several months after the praziquantel treatment. An uneven hyperdensity cystic nodule with smooth edges was seen on the left inferolateral lobe. The largest transverse section was about 6.0 cm × 2.3 cm, with no obvious enhancement inside; the margin of the nodule calcified and was adhesive to the chest wall, and the corresponding pleural thickened.
FINAL DIAGNOSIS

A diagnosis of paragonimiasis with pleural lump was made by clinical symptoms, laboratory, and imaging examinations.

TREATMENT

Praziquantel was prescribed for the patient at the first hospitalization. At the second admission, the patient underwent a thoracoscopic mass resection. A mass that adhered to the pleura and compressed the lower left lobe, which had a size of 6 cm × 4 cm × 3 cm and curved moon shape and was enveloped by fibrous tissue, was resected during the operation (Figure 3). We postulated that it was the necrotic residue of paragonimus.

Figure 3
Figure 3 Gross specimen and biopsy of the resected mass . A: The gross specimen of the mass showing an encapsulated nodule; B: The cut surface of the mass. The arrowhead indicates the necrotic tissue inside; C: The biopsy of the mass. The cystic wall of the mass consists of fibrous tissue. The blue-stained area indicated by the arrowhead is non-structured necrotic tissue.
OUTCOME AND FOLLOW-UP

The patient was discharged on the fifth day post operation. She was seen for outpatient follow-up after the discharge, at which point the pleural mass appeared resolved on a chest radiograph, and her peripheral blood eosinophil count (0.09 × 109/L) dropped to the normal range.

DISCUSSION

Paragonimiasis is a food-borne parasitic disease caused by paragonimus, and there exist more than 50 species of paragonimus all over the world. Paragonimiasis mainly prevails in Asian, African, and South American countries[1]. Paragonimus westermani and Paragonimus skrjabini are dominant species in south China[2]. Paragonimus miracidiums colonize in a suitable snail host and produce numerous cercariae which later leave the snail and penetrate a crab or crayfish, where they grow and transform into metacercariae. After eaten by a suitable human definitive host, metacercariae excyst in the small intestine and penetrate the wall of the gastrointestinal tract. Juvenile worms migrate through the peritoneal cavity, diaphragm, and pleural space to the lungs. The activity of worms in the pleural cavity can cause pleural effusion and thickening. Worms move into the lung parenchyma where they multiply. Encapsulated worms in the lungs produce typical pulmonary paragonimiasis, and the symptoms are cough, chest pain, fatigue, dyspnea, and fever[5]. Histologically, chronic eosinophilic pneumonia and granulomatous inflammation with associated eosinophils are usually present. Lung parenchyma could present serpiginous zones of necrosis, which sometimes extends to the pleural surface. Paragonimus eggs are generally associated with a granulomatous reaction[6]. Serological tests, such as enzyme-linked immunosorbent assay and peripheral eosinophilic granulocyte test, are the most effective methods for laboratory diagnosis of paragonimiasis, and the diagnosis can be confirmed based on clinical, radiological, echo-graphical, and cytological findings. However, the clinical findings in paragonimiasis may resemble those of pleu-ropulmonary tuberculosis (TB), pneumonia, bronchitis, or bronchiectasis. Several studies reported paragonimiasis mimicking TB and the cases were misdiagnosed and treated as TB[7,8]. The mass in the pleural cavity that forms after standard treatment as our case can also lead to a misdiagnosis as malignant lesions.

After the treatment of praziquantel recommended by the World Health Organization at a high dose of 75 mg/kg /d (divided into three doses per day) for 2 d, the majority of the patients have a satisfactory result[9]. However, in cases with a lump in the pleural cavity, praziquantel has a poor therapeutic effect and surgical intervention should be implemented. Video-assisted thoracoscopy is a minimally invasive surgical technique that has been increasingly applied in pediatric surgery due to its superiority of reduction of tissue trauma, less postoperative pain, and reduction of hospital stay, and thoracoscopy can be applied either primarily or after the failure of medication and drainage[10]. Early intervention in pleural effusion like our case is essential to prevent the development of the chronic stage. Based on our clinical experience, and the observation that the pleural effusion of our patients is always an exudate that contains abundant scrambled egg-like material, drainage in the exudative stage is hard to drain all the fluid because the fibrous material can block the drainage tube and the fibrous material can lead to fibrous lump formation like our reported case. However, no suggestion of surgical intervention has been recommended for the treatment of paragonimiasis pleural effusion. Therefore, we recommend thoracoscopic intervention when fibrous contents are present on CT scan or chest roentgenogram to avoid later fibrous lump formation. Thanks to the minimal invasion of thoracoscopy, patients can recover quickly and pleural exudate could be removed early and thoroughly, thus reducing the hospital stay and improving the treatment outcomes.

CONCLUSION

Thoracoscopic intervention should be performed when fibrous contents are present on CT scan or chest roentgenogram to avoid later fibrous lump formation. Diagnose can also be confirmed by finding paragonimus ova in the pleural fluid removed by thoracoscopy. As for why paragonimiasis could cause such a chronic phase, we postulate that this result is related to the species, and more studies should be conducted on this issue.

Footnotes

Manuscript source: Unsolicited manuscript

Specialty type: Surgery

Country/Territory of origin: China

Peer-review report’s scientific quality classification

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P-Reviewer: Sugimura H S-Editor: Zhang L L-Editor: Wang TQ P-Editor: Zhang YL

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