CASE SUMMARY

A 60-year-old female presented to the ENT department of our hospital with a complaint of progressive neck swelling of three months’ duration and a shorter duration of dysphagia, neck pain, and mild breathing difficulty. Thyroid function test results were unremarkable. Ultrasound neck done elsewhere showed a large cystic lesion in the thyroid with no increased vascularity on color Doppler.

IMAGING FINDINGS

A CT scan of the neck revealed a large, well-defined, slightly lobulated soft-tissue heterogeneous mass arising from the right lobe, isthmus, and part of the left lobe of the thyroid gland with no micro- or macrocalcifications (Figure 1). The lesion was hypoenhancing, predominantly of low attenuation and well delineated from the peripheral normal enhancing residual thyroid parenchyma (Figures 2, 3). The mass was seen infiltrating the strap muscles and the subcutaneous soft-tissue plane. Inferiorly, the lesion extended retrosternally into the superior mediastinum (Figures 4, 5). Also seen were multiple heterogeneously enhancing level II, III, and IV cervical lymph nodes (Figure 6), with the most significant measuring 3 × 3.7 cm on the left side.

A chest CT scan performed as part of additional workup revealed multiple subcentimetric, soft tissue, nodular densities scattered in bilateral lung fields (Figures 7, 8), with a few showing the feeding-vessel sign. Incidentally noted was cylindrical bronchiectasis with mucus plug impaction in the right middle lobe and lingular left upper lobe segment (Figure 9). No significant mediastinal lymphadenopathy was noted (Figure 10). A contrast-enhanced CT scan of the abdomen for metastasis was unremarkable. In our case, the patient showed progressive dyspnoea and dysphagia on follow-up. An FNAC of the thyroid lesion revealed squamous cell carcinoma.

DIAGNOSIS

Squamous cell carcinoma of thyroid with lymph nodal and pulmonary metastases

DISCUSSION

Thyroid cancer is the most common endocrine malignancy and is the seventh-most common cancer in women. Typically, these malignancies arise from the normal thyroid tissues and are of papillary, follicular, or medullary histology.1 Primary squamous cell carcinoma (SCC) of the thyroid is a sporadic malignant disease because the thyroid lacks squamous cells. The disease is almost always fatal. Fewer than 100 cases have been reported in the literature;2 it represents <1% of all primary carcinomas of the thyroid gland.3,4 Overall survival usually does not exceed 6 months’ post-diagnosis. In our case, there was progressive tracheal compression on short-term follow-up.

Primary SCC usually affects older patients between the 5th and 6th decades and is traditionally associated with a history of goiter. In most cases, the patient presents with a rapidly enlarging neck mass with local infiltration, followed by symptoms of compression of adjacent neck structures, such as dyspnea and hoarseness.3 Metastases from primary SCC are common, especially to cervical lymph nodes (35%), but they may also occur in the lungs, bones, liver, kidney, and heart.4

Although CT is the preferred imaging modality, both CT and magnetic resonance imaging (MRI) scans are useful for assessing and characterizing thyroid swellings. They allow delineation and differentiation of thyroid masses from adjoining neck masses and enable assessment of the adjacent laryngotracheal region to discern displacement, luminal narrowing, and vascular displacement and invasion. Evaluation should also assess calcification, cyst formation, necrosis, hemorrhage, lesion margin definition and extraglandular extension. Computed tomography of the chest, abdomen, and pelvis helps exclude a primary source for secondary SCC of the thyroid gland.5

SCC is of unknown etiology, as the thyroid typically lacks squamous epithelium. There are three theories to explain the pathophysiology. First, the embryonic nest theory postulates the origin of squamous cells from the remnants of thyroglossal duct or the epithelium of the thymus.4,6 Second, the metaplasia theory suggests that these cells present because of environmental stimuli (inflammation and Hashimoto’s thyroiditis).7 Third, the de-differentiation theory indicates that existing papillary, follicular, medullary, and anaplastic thyroid carcinoma de-differentiate into SCC.8

Cho et al performed a systematic review and individual participant data meta-analysis regarding primary SCC of the thyroid. In this meta-analysis of 89 patients, SCC presents at a mean age of 63 years (range 24-90 years) with a two-times female preponderance and anterior neck mass as the most frequent presenting complaint. Fine-needle aspiration cytology (FNAC) could accurately diagnose the cases in less than one-third of patients (as in our case) with more than half remaining nondiagnostic or giving papillary thyroid carcinoma as a false diagnosis. Complete surgical resection of the tumor was the only significant prognostic factor in the multivariate analysis, but the benefit of adjuvant treatment could not be proven. Moreover, the prognosis of these patients was poor (only 20% 3-year survival rate).9

Anaplastic thyroid carcinoma, carcinoma showing thymus-like elements (CASTLE) disease of the thyroid gland and metastasis from adjacent organs are the differentials to be kept in mind while diagnosing squamous cell carcinoma of the thyroid.3

CONCLUSION

Squamous cell carcinoma of the thyroid is an extremely rare, aggressive, and highly lethal neoplasm. Though primary SCTC may coexist with papillary and anaplastic thyroid cancer, pure SCTC, occurring solitarily without other tumors, is extremely rare. Computed tomography plays an important role in detection and characterization of the lesion, extrathyroid invasion, and metastases.

REFERENCES Kuczmarska A, Patel MD, Mehta N. Primary squamous cell carcinoma of the thyroid. J Cancer Biol Res. 2014; 2(2):1051. Shenoy VS, Rao RA, Kamath PM, et al. Primary squamous cell carcinoma of thyroid – a rare malignant goitre. Indian J Surg Oncol. 2016 Dec;7(4):467-469. K, Anastasiadis I, Panteli N, et al. Primary squamous cell carcinoma of the thyroid gland. Journal of Surgical Case Reports. 2014;12:1–3. doi: 10.1093/jscr/rju133. Wygoda A, Rutkowski T, Szcześniak-Kłusek B, et al, Primary squamous-cell thyroid carcinoma – a successful treatment with five-year follow-up. Endokrynol Pol. 2017;68 (5): 592–596. Syed MI, Stewart M, Syed S, Dahill S, et al. Squamous cell carcinoma of the thyroid gland: primary or secondary disease? The Journal of Laryngology & Otology. 2011; 125:3–9. Goldberg HM, Harrey P. Squamous cell cysts of the thyroid with special reference to the etiology of squamous epithelium in the human thyroid. Br J Surg. 1956; 43:565–9. Chaudhary RK, Barnes EL, Myers EN. Squamous cell carcinoma arising in Hashimoto’s thyroiditis. Head Neck. 1994;16: 582–585. Kebapci N, Efe B, Kabukcuoglu S, et al. Diffuse sclerosing variant of papillary thyroid carcinoma with papillary squamous cell carcinoma. J Endocr Invest. 2002; 25:730–734. Cho JK, Woo SH, Park J, et al. Primary squamous cell carcinomas in the thyroid gland: an individual participant data meta-analysis. Cancer Med. 2014;3(5):1396-1403. Back To Top