Hydatid cyst of the thyroid gland with tracheal fistula: A case report and review of the literature

  • Authors:
    • Tiemin Jiang
    • Qiang Guo
    • Bo Ran
    • Ruiqing Zhang
    • Tuerganaili Aji
    • Yingmei Shao
  • View Affiliations

  • Published online on: May 28, 2019     https://doi.org/10.3892/etm.2019.7620
  • Pages: 573-579
  • Copyright: © Jiang et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

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Abstract

Hydatid disease, also known as echinococcal disease, is a zoonotic disease caused by Echinococcus infection. Hydatid cysts of the thyroid are rare. The present case study reports on a patient with hydatid cyst in the thyroid with tracheal fistula. A 54‑year‑old male patient without any history of exposure to farm animals was hospitalized due to fever and productive cough with occasional hydatid daughter cyst. The patient was diagnosed with a hydatid cyst of the thyroid gland with tracheal fistula by relevant examination. An operation was performed to remove the hydatid cyst and to repair the fistula. The patient took oral albendazole after surgery to prevent hydatid recurrence. Operative recovery was uneventful and the patient resumed his normal activities. Prompt diagnosis and an appropriate surgical treatment prevented a potentially fatal outcome. Furthermore, the characteristics of thyroid cystic echinococcosis, and its diagnosis and treatment in the present case and other cases reported in the literature were summarized and reviewed. Although the thyroid gland is rarely affected, hydatid cyst disease should be considered as a differential diagnosis of cystic lesions of the thyroid gland in patients living in regions where hydatid cyst disease is endemic.

Introduction

Echinococcosis caused by Echinococcus granulosus is a common type of zoonosis in farming and grazing areas and is distributed worldwide (1). The major organ affected is the liver, but extrahepatic disease is also possible. Only few cases of thyroid cystic hydatid disease have been reported worldwide. However, the possibility of cystic hydatid disease cannot be ignored in those areas with a high incidence of hydatid disease.

Echinococcosis in rare sites, including the thyroid, is mostly misdiagnosed, predominantly due to its rarity. It is at times diagnosed as cystic echinococcosis during surgery and even treated on the basis of the incorrect diagnosis. For echinococcosis in rare locations, including thyroid cystic echinococcosis, various countries and regions have implemented different treatment modalities, such as total thyroidectomy, partial thyroidectomy and fine needle aspiration cytology (FNAC) (2,3).

The present study presents a case of hydatid cyst-tracheal fistula in the thyroid. Furthermore, the literature on cystic echinococcosis of the thyroid gland was reviewed to summarize the characteristics of thyroid cystic echinococcosis, and compare its diagnosis and treatment among studies.

Case report

A 54-year-old male patient without any history of exposure to farm animals presenting with a gradual swelling on the left side of the lower part of the neck over a period of two years was admitted to the First Affiliated Hospital of Xinjiang Medical University in November 2013. The swelling was first noticed ~20 years previously. Furthermore, the patient presented with fever and productive cough with occasional hydatid daughter cyst for 2 months. Difficulty in breathing appeared twice and the symptoms were alleviated after oxygen therapy and intramuscular injection of dexamethasone. During physical examination, a non-tender, soft and fluctuant mass was palpable on the left lateral side of the neck. The size of the mass was measured as 7×4 cm. The computed tomography (CT) scan of the abdomen and pelvis indicated no evidence of hydatid cyst. Bronchoscopy examination revealed an ulcer just 2 cm below the glottis and this ulcer was 8 mm in diameter. The hydatid immunology test was positive. CT (Fig. 1A) and magnetic resonance imaging (MRI; Fig. 1B) revealed hydatid on the two sides of the thyroid.

The patient received surgery for excision of the internal capsule. During surgery, the hydatid cyst was removed, while the surrounding area was protected. A fistula of 1 cm in diameter was identified between the trachea and cyst (Fig. 2), and the fistula was repaired. Two drainage tubes were placed in the operation area. The post-operative pathological diagnosis was echinococcosis granulosa of the thyroid (Fig. 3). The fistula orifice between the hydatid residual cavity and the trachea was still visible on CT at 5 days after the surgery (Fig. 4). Inflammation in the lung was also still visible. A small amount of gas (~50 cm3) appeared in the drainage bag of the operated area when the patient coughed. The gas volume was generally low. Due to the low quantity of the gas, the tube was pulled out on the fifth day after the operation. The fistula had disappeared in the review CT scan at 5 days after the surgery. The patient continued to receive albendazole therapy (15 mg/kg/day) for 1 year post-operatively. No recurrence was observed in the thyroid during the 54-month post-operative follow-up period.

Discussion

Hydatid disease is a parasitic infection with worldwide prevalence (4). A hydatid cyst of Echinococcus granulosus may develop in any part of the body (58). Although it mostly tends to form cysts in the liver (75%) or lung (15%), other organs of the body, including the brain, heart, bones, muscle, kidney and pancreas, may also be affected (811). While thyroid involvement of echinococcosis is rare, thyroid hydatid with tracheal fistula is even rarer.

A high circulatory flow rate in the thyroid gland may have an important role in the development of the thyroid hydatid cyst (6,8,9). It remains elusive how the relatively high thyroid blood flow is paralleled with a disproportionately low incidence of thyroid cyst disease, but one theory indicates that the relatively small caliber of the thyroid arteries together with their position at a right angle to the carotids is an anatomical arrangement that is thought to offer the thyroid gland a certain measure of protection against the invading parasite (4).

Patients with thyroid hydatid cyst are at times asymptomatic. A few hydatid patients present with symptoms including hoarseness and dyspnea, which are caused by the compression of surrounding tissues during the growth of the hydatid. When the patients present with symptoms of cough and expectoration, hydatid-bronchial fistula should be considered. If the patient has coughed-up discharge of cystic fluid and even daughter cyst of hydatid, hydatid-tracheal fistula may be diagnosed.

Ultrasound, CT and MRI are of great value in the diagnosis of thyroid primary disease. Thyroid hydatid should be distinguished from thyroid cyst. The imaging findings of thyroid hydatid and thyroid cyst are similar. Through analyzing the patient's epidemiological history (such as history of exposure to farm animals or history of living in an area with high prevalence) and history of hepatic hydatid disease, and considering the immunological results, thyroid hydatid may be diagnosed.

At present, the management of choice for hydatid disease is early detection. Surgical intervention includes the excision of the cyst and a part of the involved adjacent thyroid gland (4). It is preferred to not excise the thyroid or excise the thyroid as little as possible, as this avoids post-operative hypothyroidism. Surgery should be performed carefully to prevent extrusion of the hydatid fluid or sac into the trachea. At present, surgical treatment is the first choice for treating hydatid disease. However, drug treatment prior to and after surgery may improve the cure rate and reduce the recurrence rate of the disease (12).

A literature search was performed in the PubMed, Medline and Google Scholar databases by using key words, including ‘Thyroid’, ‘Echinococcosis’, ‘Hydatid cyst’ and ‘Hydatid disease’, in different combinations. Studies were limited to those in English and Chinese language. The abstracts were retrieved and reviewed for pre-selection, followed by retrieval of the full articles. A total of 18 articles (4,7,1328) with detailed descriptions were identified, and 21 cases were reported in them. Table I presents the detailed data of these studies. Based on the specific data in these studies, the diagnosis and treatment thyroid cystic echinococcosis was summarized and analyzed.

Table I.

Detailed characteristics of all published cases of hydatid cyst of thyroid gland from 2010.

Table I.

Detailed characteristics of all published cases of hydatid cyst of thyroid gland from 2010.

Authors (year)CountryAge (years)SexSignsCyst in other organsTreatment methodPunctureOperationDrug treatmentRecurrencePost-operative complications(Refs.)
Xiong and Li (2017)China27FPhysical findings (such as a mass)NoSurgeryNoPartial thyroidectomyNoNot mentionedNot mentioned(13)
Rauhofer et al, (2003)Australian14FPhysical findings (such as a mass)NoSurgery+medical therapyNoEnucleation of cystPostoperative albendazole for 3 monthsNoNo(14)
Akbulut et al, (2015)Turkey26FPainYesSurgeryNoTotal thyroidectomyNoNoNot mentioned
57FHoarsenessYesMedical therapy+surgeryNoTotal thyroidectomyPreoperative albendazole for 2 weeksNoHypocalcemia(15)
Eken et al, (2016)Turkey65FDyspneaYesSurgery+medical therapyNoTotal thyroidectomyPostoperative albendazole for 3 weeksNoNo(16)
Moghimi et al, (2009)Iran35FEnlarged massesNoSurgeryNoTotal thyroidectomyNoNoNo(17)
Oksuz et al, (2013)Turkey23MHoarsenessNoSurgery+medical therapyNoPartial thyroidectomyPostoperative albendazole for 2 monthsNoNo(18)
Ozaydin et al, (2009)Turkey25MEnlarged massesNoSurgery+medical therapyYesPartial thyroidectomyPostoperative albendazole for 6 monthsNoNo(7)
Yilmaz et al, (2013)Turkey18MEnlarged massesYesSurgery+medical therapyNoPartial thyroidectomyPreoperative albendazole 400 mg/day, postoperative albendazole for 2 monthsNoNo(4)
21MEnlarged massesNoSurgery+medical therapyNoTotal thyroidectomyPostoperative albendazole for 6 weeksNoNo
25FPainNoSurgery+medical therapyNoTotal thyroidectomyPostoperative albendazole for 6 weeksNoNo
Capoglu et al, (2002)Turkey40FEnlarged massesNoSurgeryNoTotal thyroidectomyNoNot mentionedNo(19)
Jain et al, (2005)India55FHoarseness and dyspneaNoSurgery+medical therapyNoEnucleation of cystMebendazole (no mention of dosage and course of treatment)NoNo(20)
Zulfikaroglu et al, (2008)Turkey50FEnlarged massesNoSurgeryNoPartial thyroidectomyNoNoNo(21)
Dey et al, (2014)India30FEnlarged massesNot mentionedSurgery+medical therapyNot mentionedFNACPostoperative albendazole 400 mg/day for 28 daysNoNo(22)
Bartin et al, (2014)Turkey32FHoarsenessNoSurgery+medical therapyNoTotal thyroidectomyAlbendazole for 2 months (400 mg/day)NoNo(23)
Avcut et al, (2010)Turkey48MEnlarged massesNoMedical therapy+SurgeryNot mentionedPAIRPreoperative albendazole (10 mg/kg) for 1 week+ anti-allergy treatment for 15 minutes before surgery+postoperative albendazole (10 mg/kg) for 2 weeksNoNo(24)
Azendour et al, (2011)Morocco23FEnlarged massesNoSurgery+medical therapyNoTotal thyroidectomyPostoperative albendazole for 2 months (400 mg/day)NoNo(25)
Erkilic et al, (2004)Turkey9MEnlarged massesNoSurgeryNoPartial thyroidectomyNot mentionedNoNot mentioned(26)
Gokce et al, (2003)Turkey33MEnlarged massesNoSurgery+medical therapyPre-operative fine needle aspirationTotal thyroidectomyPostoperative albendazole for 6 months (400 mg/day)NoNo(27)
Dissanayake et al, (2016)USA44FEnlarged massesNoSurgery+medical therapyYesNot mentionedAlbendazole (no mention of mentioned dosage and course of treatment)Not mentionedNo(28)

[i] F, female; M, male; PAIR, puncture-aspiration of cyst contents-injection of hypertonic saline solution-reaspiration.

Of the 18 studies from 7 countries, 11 studies from Turkey reported on 14 patients, 2 studies from India reported on 2 cases and the remaining articles were from the USA, Morocco, Iran, Australia and China, with each study reporting on one case. The studies comprised a total of 21 patients (14 women and 7 men). The age at onset was 9–65 years with the median age of 30 years.

The major complaints of the patients with thyroid cystic echinococcosis were progressive enlarged neck mass, neck pain, hoarseness and difficulty in breathing. Most of the patients (14/21) presented with enlarged masses on the neck and had no specific symptoms. A total of 4 patients complained of hoarseness and 2 of neck pain, and 2 patients had dyspnea. Two patients presented with thyroid cystic lesions revealed through physical examination. The hydatid lesion itself appeared to cause no specific symptoms and the abovementioned complaints were mainly caused by compression of the increased hydatid lesions.

Pre-operative diagnosis is important for thyroid hydatid disease. The diagnostic methods include review of the patient history, physical examination, imaging examination, serological examination and FNAC diagnosis (29). The imaging diagnosis is considered to be the most important one (24,30,31). The imaging diagnosis usually includes ultrasound, CT and MRI. Ultrasonography is effective in detecting the cystic lesions and is important for the pre-operative diagnosis (32). CT scan and MRI are usually complementary diagnostic tools. For multiple hydatid cysts, particularly in patients with a history of hydatid disease, the diagnosis is straightforward; however, for a less experienced clinician, it is difficult to identify a primary thyroid monocystic echinococcosis from a single cyst. The most common misdiagnoses are simple thyroid cysts. By ultrasound, the round and non-echo lesions, visible floating small light spots in the dark area and the ‘sand bag syndrome’ may be observed (33). The cystic wall is smooth and complete and exhibits a double-layer sign (34). Regarding the differential diagnosis, ultrasound is superior to CT and MRI (35). In addition, the patient's epidemiological history and information on whether hydatid disease is present in the liver are helpful for making a definite diagnosis. CT examination is able to accurately display the narrowing and displacement when the hydatid lesions involve the blood vessels and trachea (36), and may clearly display the association of the hydatid lesions with surrounding tissues (37), which is of significance in guiding pre-operative preparation and surgical planning. However, bronchial fistula is characterized by the presence of a shadow of gas density in the hydatid cavity. For larger fistula, CT and MRI may indicate the size and location of the fistula. Bronchoscopy may directly display the fistula and the location of the fistula in lesions generally presents as the most prominent site of the trachea.

FNAC is generally accepted in the clinical treatment of the single thyroid nodules (38). Although no study has reported any allergic reactions after FNAC, this technique is not recommended, as it may cause the diffusion of the cystic fluids or allergic reactions. Therefore, FNAC should be avoided when differential diagnosis of thyroid hydatid cysts is needed.

The immunological method is also an important modality for the diagnosis of echinococcosis, particularly as a differential diagnosis (39). The traditional Casoni intradermal test has a high false-positive rate and is overly sensitive. Immune disturbances seriously affect the follow-up after treatment and have been removed from the World Health Organization (WHO)'s Hydatid Disease Diagnosis and Treatment Guidelines (2001 edition) (3). In addition, the test strip and ELISA methods also have important roles in the screening for echinococcosis.

Among all cases analyzed, thyroid hydatid was a condition primary to the thyroid. Examination of patients (15/21) revealed that only the thyroid gland contained cystic hydatid and that no organs had any hydatid lesions. In general, the liver is the most susceptible and the first site of infection for echinococcosis (40). Among the 21 cases, only two were combined with hepatic cystic echinococcosis. One case was combined with hydatid in multiple sites, including the liver, lung and abdomen. One patient had lung hydatid 10 years previously, which was removed by surgery. One patient had hepatic hydatid 2 years previously, which was treated by surgery. In another case, there was no mention of whether any other organs exhibited any hydatid cysts.

Of the 21 cases, one patient received puncture treatment twice prior to surgery. Three patients underwent FNAC pathological examination in order to clarify the pre-operative diagnosis. One case from Turkey reported in 2010 (24) received puncture-aspiration of cyst contents-injection of hypertonic saline solution-reaspiration (PAIR) treatment. In this case, two daughter cysts of the hydatid lesions were punctured, 35% of cyst fluid was aspirated and 20% hypertonic saline was injected into the cavity for 10 min. The patient was subjected to post-operative albendazole treatment for 2 weeks and reported no complications during the treatment. During the 4-month follow-up, a ‘pseudotumor appearance’ without any fluid component or daughter vesicles was noted. In the case of the present study, surgical treatment was preferred, as PAIR technology may rather be suitable for monocystic hydatid cyst. For multiple hydatid cysts, hypertonic saline cannot completely destroy the capsule wall of the daughter cyst as well as inactivate the hydatid sac. However, spillage of the cyst fluids may also occur, which may even increase the risk of allergic reactions. Therefore, puncture treatment of the hydatid cysts is not recommended at our medical center. Among the reviewed literature, three studies (19,20,22) also indicated that the hydatid puncture is considered to be associated with a high risk and is not recommended. Therefore, the safety and efficacy of PAIR remains controversial and requires further investigation.

Surgical treatment remains the preferred method for the treatment of thyroid hydatid cysts (41). Most of the patients underwent partial or complete thyroidectomy. The cases reviewed comprised 17 cases of thyroidectomy, including 9 cases of total thyroidectomy, 6 cases of ipsilateral partial thyroidectomy and 2 cases of hydatid cyst removal. One of the patients presented with hypocalcemia directly after total thyroidectomy and during the post-operative 4-year follow-up (42). The case reported in the present study only received excision of the hydatid and repair of the fistula orifice connected with the bronchus. Based on previous experience, for the excision of the thyroid gland, regardless of whether it is a total or an ipsilateral excision, the removal of the normal thyroid tissue may be unnecessary and easily causes other associated complications, including peripheral nerve or parathyroid damage. Even if no other complications occur, total resection of the thyroid may require lifelong treatment with thyroid hormones. In summary, the surgical removal of hydatid cysts followed by post-operative albendazole treatment is a safe and effective method.

A total of 5 patients with total thyroidectomy and 2 with ipsilateral thyroidectomy did not take any anti-hydatid drugs after the surgery, whereas the remaining 13 patients took anti-hydatid drugs after the surgery. In the reviewed studies, most patients were advised to take oral albendazole. Only one case from India reported in 2005 (20) was treated with oral mebendazole. Among the studies, a large difference in the duration of drug intake was noted; for instance, the duration of albendazole treatment was as short as 2 weeks in one case (15) and the maximum time was 6 months (27). The specific duration of taking the drug was not specified in two of the studies. The dose of albendazole was 400 mg/day in 4 of the studies (22,23,25,27) and 10 mg/kg/day based on the weight of the patient in one study (24).

At present, the preferred drugs for the treatment of echinococcosis are benzimidazole drugs, of which the representative drugs are mebendazole and albendazole (43,44). The treatment effect of albendazole has been demonstrated to be significantly better than that of mebendazole (3,12), and it has now replaced mebendazole and become one of the drugs of choice recommended by the WHO (2,3). Albendazole is metabolized into albendazole and sulfoxide in the liver and exerts an anti-helminthic effect; it significantly inhibits the parasite's absorption of glucose, resulting in the exhaustion of glucose or inhibition of the fumarate reductase system. This mechanism impedes the formation of ATP, making parasites unable to survive and reproduce. As echinococcosis has a high recurrence rate (45) and each patient has a different extent of disease, the post-operative drug therapy for hydatidosis patients should be individualized based on the activity of the hydatid lesions and the specific circumstances of the patients. Even if a non-curative surgery is performed and the activity of the hydatid lesions is not high or even in a state of solid necrosis, the time for taking the drug may be reduced. For single-capsule, multi-ascendant and internal capsule collapse types, 3–12 months of post-operative drug therapy is recommended (45). It is more clinically significant to determine the dose according to the weight of the patient. Based on our experience, the total daily dose is 10–15 mg/kg, half of which should be administered each morning and evening. An individual study also reported the administration of pre-operative prophylactic oral albendazole (24), and according to expert consensus, pre-operative treatment for 3–7 days is also recommended.

Despite significant advances in diagnostic research, as well as medical and surgical treatment, echinococcosis remains a challenging disease with high morbidity. Hydatid cyst in the thyroid is rare. The diagnosis of hydatid cyst in the thyroid should be considered in epidemic regions of hydatid disease. The diagnosis and treatment of thyroid cystic hydatid vary considerably among different regions, particularly the choice of surgical procedure and the duration and dosage of therapeutic drugs. At present, there is no uniform standard of treatment. In conclusion, the diagnosis and treatment of hydatid cyst in the thyroid reported in recent years were reviewed. The present study may enhance the understanding and awareness of hydatid cyst in the thyroid and provide a reference for clinicians.

Acknowledgements

Not applicable.

Funding

The present study was supported by the National Science Foundation of China (grant nos. 81560098 and 81660108) and Natural Science Foundation of Xinjiang Province (grant no. 2016D01C274).

Availability of data and materials

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

Authors' contributions

TJ, BR, RZ and QG collected the data. TJ wrote the manuscript. YS and TA conceived and designed the present study, and revised the manuscript. All authors read and approved the final version of the manuscript.

Ethics approval and consent to participate

The present study was approved by the ethics review board of the First Affiliated Hospital of Xinjiang Medical University (Xinjiang, China).

Patient consent for publication

Informed consent was obtained from the patient.

Competing interests

The authors declare that they have no competing interests.

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July-2019
Volume 18 Issue 1

Print ISSN: 1792-0981
Online ISSN:1792-1015

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Spandidos Publications style
Jiang T, Guo Q, Ran B, Zhang R, Aji T and Shao Y: Hydatid cyst of the thyroid gland with tracheal fistula: A case report and review of the literature. Exp Ther Med 18: 573-579, 2019
APA
Jiang, T., Guo, Q., Ran, B., Zhang, R., Aji, T., & Shao, Y. (2019). Hydatid cyst of the thyroid gland with tracheal fistula: A case report and review of the literature. Experimental and Therapeutic Medicine, 18, 573-579. https://doi.org/10.3892/etm.2019.7620
MLA
Jiang, T., Guo, Q., Ran, B., Zhang, R., Aji, T., Shao, Y."Hydatid cyst of the thyroid gland with tracheal fistula: A case report and review of the literature". Experimental and Therapeutic Medicine 18.1 (2019): 573-579.
Chicago
Jiang, T., Guo, Q., Ran, B., Zhang, R., Aji, T., Shao, Y."Hydatid cyst of the thyroid gland with tracheal fistula: A case report and review of the literature". Experimental and Therapeutic Medicine 18, no. 1 (2019): 573-579. https://doi.org/10.3892/etm.2019.7620