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. 2023 Feb 20;12:193. [Version 1] doi: 10.12688/f1000research.128900.1

Case Report: A case of a multivisceral echinococcosis with atypical localization

Rania Kaddoussi 1,a, Mohamed Jellazi 2, Abdelkader Mizouni 3, Ikram Chamtouri 4, Mabrouk Abdelaaly 5, Asma Migaou 1, Hager Ben Brahim 6, Nessrine Fahem 1, Ahmed Ben Saad 1, Sameh Joober 1, Saoussen Cheikhmhamed 1, Naceur Rouetbi 1
PMCID: PMC11470981  PMID: 39399295

Abstract

Hydatidosis is a pathology that is still common. The hydatid cyst commonly involves the liver and lung. Cases of multi visceral echinococcosis with atypical localization are rare. We report the case of a 53-year-old Tunisian farmer with a multiple organ hydatidosis that included 13 hydatid cysts: the lungs, the liver, the left heart ventricle, the left kidney, the abdomen cavity, muscles (psoas, adductors), and subcutaneous gluteal area. The majority of these cysts was already treated surgically, and some were due to be removed.

Keywords: Hydtidosis, multi visceral, muscles

Background

Hydatidosis is a human disease caused by the larval form of Echinococcus spp., which live in the gut of dogs, wild canines and other carnivorous animals. Humans become the accidental intermediate hosts by ingesting Taenia spp. eggs. Echinococcus spp. are endemic in many countries where sheep, dogs and man live in close contact.

All organs in the human body may be affected by hydatid disease. The hydatid cyst from Echinococcus granulosus commonly involves the liver and lung but may also be found in other unusual organs, including the brain, heart and bones. Hydatid cysts rupture into left-sided cardiac chambers may cause systemic emboli, and if ruptured into right-sided cardiac chambers may cause pulmonary emboli.

Cases of multi visceral echinococcosis with atypical localization are rare. We report here the case of a male with 13 hydatid cysts including the lung, the heart, the muscles, the liver, the kidney and abdomen cavity.

Case report

This is the case of a 53-year-old maghribian male farmer. This patient, with no personal or family history, was referred to the pulmonology department, for the management of a pulmonary Aspergilloma on a sequelary lung cavity following lung surgery.

At the time of the encounter the patient had no subjective complaints, expect for right lower limb paresthesia. The physical exam showed no abnormalities.

The patient was followed up in the abdominal surgery department for a multiple organ hydatidosis that included 13 hydatid cysts: the lungs, the liver ( Figure 1), the left heart ventricle, the left kidney ( Figure 2), the abdomen cavity, muscles (psoas, adductors), and subcutaneous gluteal area. The majority of these cysts was already treated surgically and some are still pending to be removed ( Table 1). The patient has received oral Albendazole 400 mg twice-daily for 2 years.

Figure 1. Axial chest scan passing through the liver showing a CE1 type hydatid cyst of segment 8 of the liver (yellow arrow).

Figure 1.

Figure 2. Axial computed tomography scans passing through the thorax in the mediastinal window and through the kidneys and coronal through the kidneys after injection of iodinated contrast product: Calcified hydatid cyst of the lateral wall of the left ventricle (blue arrow). Partially calcified multivesicular hydatid cyst with left endo and exo renal development (yellow arrow).

Figure 2.

Table 1. Different types of organ involvement.

Organ Location Size Treatment Notes
Lungs 1) Right lungs 25×20 mm Surgical
a) Left inferior lobe N/A Wedge resection
b) Left superior lobe 60 mm Partially removed surgically
Liver Segment VIII 33×21 mm Partially removed surgically Between superior left and middle hepatic vein.
Segment V 53×40 mm Surgical removal+ Cholecystectomy Tight adhesion with cystic bladder and right portal vein.
Kidney Left kidney 10×80×79 mm Surgical drainage
Heart Left ventricle 30 mm Surgical (thoracotomy)
Muscles Psoas
Adductor
Gluteus
55×34 mm and 40×25 mm
20 mm
Surgical drainage
Subcutaneous Gluteal 15 mm Surgical
Abdomen cavity Parieto colic gutter 60 mm Surgical
Abdomen cavity Parietal peritonum Bilobed Surgical

During a regular post-surgical follow up, a scannographic image of a fluid-density endo-bronchial material in the right superior lobe (lung cavity sequelary to the previous cystectomy) of the lung separated from the cavity wall by an airspace (“air crescent” sign) was found, this image is typical of pulmonary aspergilloma ( Figure 3). Even though the Aspergillus serology showed doubtful results, the clinical context coupled to the CT scan findings were highly suggestive of a pulmonary aspergilloma. Blood work up showed high levels of IgE. A surgical resection of the cavity is programmed but not yet performed.

Figure 3. Axial chest scan passing through the thorax in the parenchymal window and after injection of iodinated contrast product showing a fluid-density endo-bronchial material in the right superior lobe of the lung with an “air crescent” sign: pulmonary aspergilloma (blue arrow).

Figure 3.

Discussion

Hydatid cyst remains an important issue in Tunisian health that affects both humans and animals, especially in rural areas.

The annual incidence of hydatidosis is 11.3 per 100000 inhabitant. 1 Usually, hydatidosis presents as a single cyst usually of the liver or of the lungs, but in certain circumstances multiple organs may be affected. In our case we are reporting multiple atypical locations including heart, kidney, muscles and subcutaneous tissue. The conjunction of cysts in these locations simultaneously has not been described in the literature. We will not focus on the liver and the lung involvement given that they are a classic location of this parasitosis, and they are well commonly cited in the literature, instead we will discuss the other locations separately.

Heart involvement is uncommon and accounts for less than 0.5% of the cases, it is usually part of a disseminated infection. 2 This localization is potentially fatal without surgical treatment but fortunately with the improvement of surgical techniques, its morbidity has declined drastically. Our patient underwent open heart surgery to remove a left ventricular wall cyst without local recurrence and a post-surgical echocardiography without abnormalities.

The invasion of the myocardium usually occurs hematogeniously through the coronary arteries and since the majority of the population have a left dominant circulation, the left ventricle is the most commonly involved part of the heart (60%), 3 other explanation is the dissemination from the lungs either following a pulmonary vein rupture and migration of the cysts 4 or by a direct contact with hydatid cysts originating from the lung. 5

Renal involvement is also rare (2–3%) and it is usually associated to a disseminated disease, they are most commonly asymptomatic, like the case of our patient. The diagnosis was made by an abdominal CT which has a sensitivity of 98% to diagnose hydatid disease. 6

Psoas cysts is also uncommon, our patient presented with two psoas cysts, a finding never been described before in literature.

The patient has also presented with a 30-mm gluteal subcutaneous cyst, this involvement was described in rare cases in literature and usually the patient will have a painless palpable mass history of at least 3 months, and it is usually larger than 3 cm, which is the case in our patient. 7 Subcutaneous cysts tend to involve trunk and limb roots, possibly due to the rich vascularization and relatively less muscle activity in these areas. 8

Another intriguing finding in this case report is the discovery of an aspergilloma, on a lung cavity. Pulmonary aspergilloma occurs as a colonizer of pre-existing pulmonary cavity of any etiology such as sequelae tuberculosis, cavitary neoplasia or operated hydatid cyst and it is a saprophytic infection. 9 Aspergilloma has rarely been described in operated hydatid cyst cavities in immunocompetent patients. 10 For this patient, the aspergilloma was discovered two years after the lung surgery. A very similar case of a 56-year-old patient, who presented with an aspergilloma of the upper right lobe following cystectomy, have been described by M. El Hammoumi et al. 10

Despite the existence of multiple cysts, our patient is doing well with good tolerance and he is asymptomatic.

Conclusion

Multiple hydatidosis is a rare condition which can endanger the vital and functional prognosis. Imaging is essential for the diagnosis and finds its place for the assessment of extension and detection of asymptomatic localization to ensure early treatment. Prevention remains the best treatment for hydatid cyst.

Author contributions

NF, AM and AM actively involved in data collection and processing. RK and MJ were involved in manuscript preparation. HB, AB, SJ, SCH, NR, and FM were involved in manuscript reviewing. All authors have read and approved the manuscript.

Consent

Written informed consent was received from the patient.

Funding Statement

The author(s) declared that no grants were involved in supporting this work.

[version 1; peer review: 1 approved with reservations

Data availability

All data underlying the results are available as part of the article and no additional source data are required.

References

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F1000Res. 2023 Apr 20. doi: 10.5256/f1000research.141537.r170271

Reviewer response for version 1

Mohamed Ali Chaouch 1

Thank you very much for the opportunity to review this paper. The subject is relevant and rare. However, some points of the manuscript should be re-addressed.

1. Background:

  • Add some reference for the different informations provided. The first reference is mentioned in the discussion section. 

  • Switch "human disease" by "an anthropozoonosis" because hydatid cyst is not an only-human infection. 

  • Add a sentence highlighting the interest of medical treatment in case of multiple hydatid cyst in addition to the surgical management.

  • Add the aim of reporting this case to the end of the background.

2. Case presentation:

  • Precisely which protocol of medical treatment was used?

  • Mention if the patient presented any immune deficiency.

3. Discussion:

  • Some citations were historical. Avoid citing articles published more than 20 years ago.

  • Add the citation of the uncommon location for the psoas muscle.

  • Add the citation of the different radiological signs suggesting the hydatid cyst origin of the lesions like the daugher cyst sign that is present in the kidney cyst in your case.

  • Add some details concerning the management of these multiple cysts, like the importance of medical treatment and a radical surgery, avoiding conservative surgery, to reduce the reccurence rate. 

Are enough details provided of any physical examination and diagnostic tests, treatment given and outcomes?

Yes

Is the case presented with sufficient detail to be useful for other practitioners?

Yes

Is sufficient discussion included of the importance of the findings and their relevance to future understanding of disease processes, diagnosis or treatment?

Yes

Is the background of the case’s history and progression described in sufficient detail?

Partly

Reviewer Expertise:

I am a visceral and digestive surgeon in a pandemic country of hydatid cyst.

I confirm that I have read this submission and believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard, however I have significant reservations, as outlined above.

References

  • 1. : A case report of primary multiple hydatid cysts of psoas muscle: An exceptional location. IDCases .2022;30: 10.1016/j.idcr.2022.e01637 10.1016/j.idcr.2022.e01637 [DOI] [PMC free article] [PubMed] [Google Scholar]
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F1000Res. 2023 Mar 14. doi: 10.5256/f1000research.141537.r164950

Reviewer response for version 1

Faisal Ahmed 1

General:

  • I strongly encourage the authors to have a manuscript reviewed by a fluent English speaker and writer to improve its language contents before resubmission.

Abstract:

  • Please add a piece of important information regarding postoperative therapy and the outcome.

Keywords:

  • Please add a case report in your keywords.

Background:

  • It is inappropriate to have a background without a single reference. Please note that all statements must be supported by references.

Case report:

  • This section should be structured according to the subsections included in the CARE Checklist of information to include when writing a case report. All the following subheadings should appear in this section, unless not applicable: Patient Information, Clinical Findings, Timeline of current episode, Diagnostic assessment, Diagnosis, Therapeutic interventions, and Follow-up and outcome of interventions.

  • Please start with the primary concerns and symptoms of the patient. Then, medical, family, and psycho-social history including relevant genetic information, and finally, Relevant past interventions with outcomes.

  • Significant History of contamination such as animal contact, water, etc., should be mentioned.

  • Diagnostic testing such as CT scans, laboratory findings, etc., should be mentioned.

  • Please add all details regarding surgical intervention.

  • The follow-up period for your patient should be mentioned with details such as patient status, radiologic image result, recurrence, and recommended medications.

Discussion:

  • For individual cases, it is advisable to describe how the case is rare/unusual and the educational/scientific merit of its publication, followed by an overview of the topic and a comparison of your case with similar cases described in the literature.

  • There are some sentences that need citations. Please note that all statements must be supported by references.

  • "The conjunction of cysts in these locations simultaneously has not been described in the literature."

    I suggest revising this sentence to "rarely reported in the literature" There are a few mentioned cases such as Cai et al. (2019 1 ), Sachar et al. (2014 2 ) and Dasbaksi et al. (2015 3 ).

  • Please discuss the factors below and compared them with your case:
    • A: Potential risk factors and predisposing factors of cystic echinococcosis.
    • B: Radiologic and laboratory tests.
    • C: Therapeutic options.
    • D: Recommended medication on follow-up and the duration.
    • E: Recurrence, and mortality.
    • F: The correlation between aspergilloma and echinococcosis infection.

References:

  • I see you include old historical papers in references (1,4,5,7, and 9). It is not wrong; however, you fail to include recent articles in your review. Recent similar papers must be reviewed and compared to your case.

  • There are some references not mentioned in your manuscript such as references 3 and 4 (all references must be numbered consecutively).

Figures:

  • Figures 1 and 2: You can combine multiple images in a single panel. Please ensure you label the panel appropriately (A, B, C, etc.) in the image legend, and use the panel indicator to explain or describe the content of the image panel.

Figure 2:

  • The photo of the kidney cyst should be reduced to one photo.

  • Please add a photo of peritoneal and muscle cysts.

Figure ligands:

  • Your ligands are so tall. Please reduce the legends to clearly describe the abnormalities.

Table 1.

  • "Bilobed" please mention the exact size.

  •  "Parieto colic gutter" please use the usual medical term.

  • The treatment column did not provide any information and I suggest deleting it from the table and mentioning the details in your therapeutic intervention section.

Are enough details provided of any physical examination and diagnostic tests, treatment given and outcomes?

Partly

Is the case presented with sufficient detail to be useful for other practitioners?

Yes

Is sufficient discussion included of the importance of the findings and their relevance to future understanding of disease processes, diagnosis or treatment?

Partly

Is the background of the case’s history and progression described in sufficient detail?

Yes

Reviewer Expertise:

the discussion and case report sections need more revision.

I confirm that I have read this submission and believe that I have an appropriate level of expertise to state that I do not consider it to be of an acceptable scientific standard, for reasons outlined above.

References

  • 1. : Case Report: Rare Presentation of Multivisceral Echinococcosis. Am J Trop Med Hyg .2019;100(5) : 10.4269/ajtmh.18-0673 1204-1207 10.4269/ajtmh.18-0673 [DOI] [PMC free article] [PubMed] [Google Scholar]
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Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Data Availability Statement

    All data underlying the results are available as part of the article and no additional source data are required.


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