Abstract
We describe a 20-year-old man diagnosed with a myelodysplastic syndrome (MDS), admitted to our hospital due to pancytopenia and fever of undetermined origin after myelosuppression with chemotherapy. Disseminated aspergillosis (DIA) was suspected when he developed skin and lung involvement. A rapidly growing mass was detected on the left neck area, during hospitalization. A thyroid ultrasound reported a cm oval heterogeneous structure, suggestive of an abscess versus a hematoma. Fine needle aspiration of the thyroid revealed invasion of aspergillosis. Fungal thyroiditis is a rare occurrence. Thyroid fungal infection is difficult to diagnose; for this reason it is rarely diagnosed antemortem. To our knowledge, this is the 10th case reported in the literature in an adult where the diagnosis of fungal invasion to the thyroid was able to be corroborated antemortem by fine needle aspiration biopsy.
1. Introduction
Thyroiditis by fungal organisms is infrequent. Most cases have been reported on immunocompromised patients, such as those with organ transplant, leukemias, receiving certain types of chemotherapy, subjects with human immunodeficiency virus, and others types of immunosuppression. This uncommon site of infections could be explained by the unique features of the thyroid gland [1], that includes protective mechanisms, such as rich blood supply, separation of the neck by fascial planes, high iodine content, and a fibrous capsule [2]. Among the different types of fungal thyroiditis, Aspergillus spp. are the predominant causative fungus for thyroiditis and asymptomatic thyroid infiltration [2–4]. Aspergillus thyroiditis (AT) has primarily been a postmortem diagnosis on immunocompromised patients with diagnosed disseminated invasive Aspergillosis (DIA) [5, 6]. Reports of antemortem diagnosis are rare, and for this reason in the literature it is difficult to find reports of surviving patients. Here, we report a case describing AT, in an immunocompromised young adult male with a rapidly growing thyroid mass; diagnosis was able to be performed antemortem by FNA cytology. We also review the epidemiology, clinical manifestations, diagnosis, and outcome of the different AT cases reported in the medical literature published during the years 1980–2012 through a search of the PubMed database.
2. Case
A 20-year-old man was admitted to our hospital on July 2012. He was diagnosed as having an MDS one month before; by that moment he had received two courses of chemotherapy consisting of azacitidine. Admission to the hospital was due to pancytopenia and fever of undetermined origin.
During hospitalization, initial chest X-ray revealed a right perihilar rounded confluent pulmonary opacity, and a subsequent noncontrast-enhanced tomography confirmed the infiltrating nodular lesion measuring . With these findings and the skin lesions (Figure 1), DIA was suspected. Intravenous liposomal amphotericin B (5 mg/Kg daily) was initiated. One week after hospitalization, a rapidly painless growing mass was detected on the left neck area by the patient. Physical examination revealed a diffusely enlarged nontender palpable mass in the left thyroid lobe. Laboratory data showed normal thyroid function tests (Table 1). A thyroid ultrasound (Figure 2) revealed a cm oval heterogeneous structure, suggestive of an abscess versus a hematoma.
Microscopy of the thyroid, after fine needle aspiration, revealed infectious thyroiditis with suppurative inflammation and abundant debris. Septate fungal hyphae with branching at acute angles were identified (Figure 3). These findings were consistent with a fungal thyroiditis caused by Aspergillus spp. A culture of the aspirated fluid showed no growth. At this moment the patient was switched from previous antifungal to voriconazole (4 mg/Kg IV q 12 hr).
Two weeks after the initiation of voriconazole, he developed wheezing and dyspnea. His respiratory function deteriorated rapidly, needing an endotracheal intubation, and he was further transferred to the intensive care unit, where he finally died.
3. Discussion
Fungal pathogens are increasingly encountered on immunocompromised patients. Fungal thyroiditis is a rare occurrence. In the last decade, more than 500 cases of different infectious thyroiditis have been reported, but few cases were fungal, most likely due to the unique features of the thyroid gland, that includes protective mechanisms, such as rich blood supply, separation of the neck by fascial planes, high iodine content, and a fibrous capsule [2]. Although several fungi may infect the thyroid gland [2, 4, 14–18], thyroid fungal infection occurs rarely and is clinically overt in a minority of patients.
In a review of 41 fungal thyroiditis cases published between 1970 and 2005, Goldani et al. [19] found that Aspergillus species (spp.) were the most commonly reported cause of fungal thyroid infection. Candida spp. were the second most common cause; other fungal etiologies reported include Cryptococcus neoformans, Coccidioides immitis, Histoplasma capsulatum, and Pseudallescheria boydii, while P. jiroveci is the most common cause of fungal thyroiditis in patients with AIDS, reflecting the high incidence of pneumocystosis in these patients [20]. This observation could suggest that Aspergillus spp. have an increased propensity relative to other fungus to infiltrate the thyroid gland or that Aspergillus spp. are more likely to cause enough destruction of thyroid tissue to cause symptomatic disease.
We performed a review of the literature of the cases reported with Aspergillus thyroiditis in patients over 18 years of age in the medical literature published during 1980–2012 through a search of the PubMed database [4, 7–13, 21–34]. Here, we only report those cases where the diagnosis was able to be corroborated antemortem by fine needle aspiration (FNA) cytology (Table 2).
The infection by Aspergillus spp. is difficult to diagnose; since more than 50% of patients do not exhibit clinical or laboratory manifestations of thyroid dysfunction [5]. Thyroid involvement by Aspergillus was found at autopsy as part of disseminated aspergillosis in 11 (46%) of 24 patients without clinical manifestations and laboratory evidence of thyroid dysfunction. Nineteen (79%) of the 24 patients with AT died, most likely due to the underlying immunosuppression associated with disseminated fungal infection and the delay in diagnosis and treatment. Although involvement of the thyroid gland has been detected at autopsy in patients with disseminated fungal disease, there are few reports that have detected the infection by fine needle aspiration (FNA) cytology antemortem (Table 2). To our knowledge, this is the 10th case reported where FNA biopsy plays a major role in diagnosing this entity.
Finally, Aspergillus thyroiditis is difficult to diagnose without biopsy, but should be considered in the differential diagnosis of any thyroid nodule, mass, or abscess, particularly in patients with conditions causing immunodeficiency. Besides, the survival of patients with invasive aspergillosis depends on the early diagnosis and prompt initiation of therapeutic measures. In conclusion, we report a case describing Aspergillus thyroiditis, in a immunocompromised young adult male with a rapidly growing thyroid mass; diagnosis was able to be performed antemortem by FNA cytology.