CASTLE is a rare disease of unknown etiology, accounting for 0.1–0.15% of all thyroid gland cancer. It commonly occurs at around the age of 40 to 50 years and has a slight female predominance. It was first described by Miyauchi et al. in 1985 and named “thymus carcinoma in the thyroid” [2]. In 1991, Chan and Rosai classified this type of tumor into four groups: ectopic hamartomatous thymoma, ectopic cervical thymoma, spindle epithelial tumors with thymic-like differentiation (SETTLE), and carcinoma showing thymus-like elements (CASTLE) [3]. SETTLE and CASTLE show characteristics of malignant tumors, the other two pathologies are considered as benign tumors. SETTLE commonly occurs among the young, while CASTLE is more common at the ages of 50 [4, 5].
The histopathology and immunohistochemistry of the CASTLE tumor show feature similar to thymus carcinoma cancer and possibly due to initial origin in the thymus gland or branchial pouch. The immunohistochemical test shows characteristic CD5-positive staining in most cases and negative staining with thyroid gland markers such as thyroglobulin and calcitonin. Molecular analysis shows p63-positive on most tumors of thymus origin, but negative results are found on cystic carcinoma and poorly differentiated form in the thyroid gland [6].
CASTLE generally shows indolent growth and has a favorable prognosis. Most patients present with a painless, slowly growing mass in the neck. Some patients may also experience hoarseness or difficulty in swallowing due to tumor invasion in neighboring soft tissues and regional lymph nodes. Other symptoms include a dry cough and short of breath [7]. In our patient, after initial total thyroidectomy, the recurrence was associated with slowing growing cervical lymph nodes over 3 years resulting in tracheal compression. It has been reported that CASTLE can rarely metastasize to the brain, liver, and lungs [8].
CASTLE arises in the thyroid gland or the soft tissue in the neck. It is necessary to differentiate CASTLE from the other tumors such as primary or metastatic head and neck squamous cell carcinomas or carcinomas of the thyroid gland because the prognosis and treatment are different. Diagnostic imaging methods include neck ultrasound, CT scan, and MRI. CASTLE tumors on CT scan often show an unclear boundary and no calcification in the lesion. Fine needle aspiration cytology plays an important role in the diagnosis of thyroid cancer. However, cytology cannot differentiate CASTLE from less differentiated thyroid cancer such as squamous carcinoma or undifferentiated thyroid carcinoma [6, 9]. A needle biopsy can obtain a tissue sample with an appropriate size for immunohistochemistry. The IHC analysis of the CASTLE tumor shows a strong positive staining with CD5, p63, and cytokeratin but negative staining with thyroglobulin, TTF1, and calcitonin [7, 10]. Positive staining with CD5 marker helps to differentiate CASTLE from other tumors of the thyroid, respiratory tract, or upper gastrointestinal tract [11]. We found similar results on pathology and IHC analyses in our case: the lesion was positive with CK5, CK7, p63, C-kit, and CD5 but negative with TTF-1, Thyroglobulin, GATA3, ER, CD99, and NKX2.2 (Fig. 3).
Due to the rarity of the disease, there are currently no standard treatment guidelines, but surgery is usually considered the first choice. According to the reports, the rates of extracellular invasion and lymph node metastases are relatively high, at 50–60% and 50% respectively [1, 12, 13]. It has also been reported that patients receiving curative surgery including total thyroidectomy and cervical lymph node dissection had favorable results, with regional recurrence rates of 14%, and 5 years and 10 years survival rates of 90 and 82% respectively [14]. Therefore, complete resection of the tumor, including removal of invaded organs, is essential to reduce rates of local recurrence and improve survival rates. CASTLE is considered a disease that has a good response to radiotherapy [9]. In the case series of Tsutsui H et al. [6], one patient refused surgery and was treated with radiotherapy only; the tumor showed a complete response, and a follow-up for 7 years with CT scans did not show a recurrence. In a series of 10 patients with CASTLE tumor (9 patients with a breaking thyroid tumor) who underwent surgery and adjuvant radiotherapy, only 4 patients had a recurrence, all outside the irradiated areas [10]. It has been suggested that patients with CASTLE should undergo surgery to completely remove tumors followed by adjuvant radiotherapy. Also, some authors have suggested that postoperative radiotherapy should be considered for patients with positive or suspected lymph node involvement. As reported by Roka and Piacentini, surgery appears to be sufficient for patients who do not have lymph node metastases, as any of the patients in their series relapsed [1, 15]. In the study by Tsutsui H et al. [6], 2 patients who had no lymph node metastases and did not receive postoperative radiotherapy, were followed up for 5 years and 10 years respectively without showing recurrence. Sun et al. have shown that it rarely recurred after lymph node removal at initial surgery with negative pathology results [11]. For patients who have a recurrence after the initial treatment, surgery and radiotherapy still play an important role rather than chemotherapy. Some reports have indicated lower rates of local recurrence in the group of patients who had locally invasive tumors and cervical lymph node metastases when treated with radiotherapy [10]. However, in our case, the patient and her family decided not to undergo treatment for the recurrence. At present, after 15 months of follow-up, the patient remains stable, suggesting conservative management is an acceptable approach in selected cases of recurrence when surgery is not feasible.
