On the basis of Hashimoto's thyroiditis, to form papillary thyroid carcinoma, metastasized and then to de-differentiate into poorly differentiated squamous cell carcinoma

doi:10.21203/rs.3.rs-215643/v1

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On the basis of Hashimoto's thyroiditis, to form papillary thyroid carcinoma, metastasized and then to de-differentiate into poorly differentiated squamous cell carcinoma

https://doi.org/10.21203/rs.3.rs-215643/v1

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Background: Thyroid squamous cell carcinoma is very rare. At present, it is limited to case reports. Since the thyroid follicular epithelium is the non-squamous epithelium, how primary squamous cell carcinoma(SCC) of the thyroid occurs is still a controversial issue. Hashimoto's thyroiditis(HT) is considered to be an independent risk factor for thyroid cancer, under the basis of HT, how tumor cells evolve and develop to papillary thyroid carcinoma(PTC), and particularly to de-differentiate into SCC is elusive.

Patient: We report a 72-year-old female patient who developed multiple subtypes of PTC on a basis of HT, and finally to de-differentiate into SCC within the local foci of lymph node metastasis.

Summary: We found that there was a variety of sub-types of PTC in this patient in the background of HT. SCC was found within local lymph node metastasis. Pathomorphology, immunohistochemistry, and molecular pathology have confirmed that SCC was derived from PTC, and then developed into poorly differentiated SCC and/or anaplastic carcinoma. We also conducted a comprehensive literature review.

Conclusions: Thyroid SCC is derived from PTC and de-differentiated into poor differentiated SCC and/or anaplastic carcinoma, which is the result of the continuous evolution of PTC. It is suggested that the prognosis of the patient is very poor.

Oncology

Papillary thyroid cancer

Thyroid squamous cell carcinoma

Pathomorphology

Molecular pathology

Multidisciplinary

Papillary thyroid carcinoma(PTC) is a relatively well-differentiated malignant tumor of the thyroid gland, accounting for more than 85% of all types of thyroid cancer(1). The relationship between immunity and inflammation has been concerned by scientists for a long time. More and more evidence shows that the thyroid is an autoimmune organ, which can occur in a variety of autoimmune-related inflammatory diseases, such as Hashimoto's thyroiditis (HT), chronic lymphocytic thyroiditis (CLT), and so on(2). When HT occurs, in addition to a large number of interstitial lymphocyte infiltration and the formation of lymphoid follicles, fibrosis and calcification can also be appeared, especially the proliferation of thyroid follicular epithelium, and even form neoplastic hyperplasia. Up to 40% of PTC is accompanied by HT and/or CLT. On the basis of immune inflammation, thyroid cancer, especially PTC could be induced(3-6). However, the association between thyroid cancer and concomitant autoimmune thyroiditis is controversial(4, 7).

In addition to conventional PTC, there are other variants, including papillary microcarcinoma, follicular variant, tall cell variant, cribriform-morular variant, columnar cell variant, hobnail variant, solid/trabecular variant,warthin-like variant, oncocytic variant, et al(8, 9). Most of the PTCs are usually a single histological subtype, and a few cases can also have two or more histological subtypes(1, 10, 11). More than 95% of thyroid malignant tumors are derived from thyroid follicular epithelium, which includes PTC, follicular thyroid cancer (FTC), poorly differentiated thyroid cancer (PDTC), and undifferentiated (anaplastic) thyroid cancer (ATC), among them, PTC accounts for about 85%(12, 13). SCC accounts for only 0.1-1% of thyroid cancer (13, 14). In theory, the thyroid gland has no squamous epithelium, and how primary squamous cell carcinoma of the thyroid occurs is still a controversial issue. At present, some researchers believe that thyroid SCC may come from embryonic residues(15). The literature on thyroid SCC is limited to case reports (14, 16-20). Whether thyroid SCC can become cancerous on the basis of HT, and then form from PTC to squamous metaplasia is worthy of further discussion. Due to the different clinical prognosis and treatment strategies of different types of thyroid cancer, especially thyroid SCC, it is necessary to make an in-depth study of this kind of cases.

Here, we present a special case of PTC with various subtypes in the background of HT and transforming into SCC in local lymph node metastases. A comprehensive literature review was also carried out.

Patient

A 72-year-old female underwent bilateral total thyroidectomy plus left cervical lymph node dissection due to thyroid cancer in the local hospital, one and a half years ago. The pathological diagnosis was PTC on the left side of the thyroid, and was a nodular goiter on the right side of the low thyroid lobe. The patient took levothyroxine sodium tablets 100 micrograms per day after the operation. She denies having a medical history of high blood pressure, diabetes, and other diseases.

Half a year ago, she was found a new mass in the left neck in our hospital. Ultrasounds showed that the mass about 2.5 cm in diameter was on the left side of the neck. PET-CT showed that there was a mass in area II-V of the left neck, which showed necrosis and increased glucose metabolism, and lymph node metastasis was considered. Needle biopsy showed lymph node metastatic SCC in pathology on the left side of the neck lymph node. Ear, nose, and throat (ENT) evaluation with fiberoptic transnasal laryngoscopy was negative for other head and neck primary tumors. Then, a cleaning operation for lymph nodes on the left side was performed.

Pathological examination

Specimen handling: The postoperative specimens were carefully observed to describe the size, color, texture, and other characteristics of the mass. The processes of sampling, dehydration, embedded in paraffin, cut slides, and hematoxylin and eosin (H&E) staining were performed according to the requirements.

Immunohistochemical staining (IHC): We used 18 different related antibodies to conduct an IHC comparative study of primary PTC and SCC in lymph node metastasis. The operation of IHC is by the guidelines of the Dako Omnis machine. All 18 antibodies including clones, manufacturer, and dilutions were showed table 1.

Q-PCR: The BRAF exon 15, KRAS exon 2-4, NRAS exon 2-4, HRAS exon 3, PIK3CA exon 20, and TERT promoter mutation in the primary PTC foci and metastatic SCC foci were detected by the method of fluorescence PCR using the human gene mutation detection kit made from Amoy Dx Biology Co., Ltd. The operation process is based on the manufacturer's instructions.

Morphological examination

Grossing, a piece of gray-red tissue 5×3×2 cm in volume was removed from the left thyroid. The section showed a mass of 2.5 cm in diameter, gray-white colors, and hard in texture. The resected right thyroid gland was 4×2.5×2 cm in volume, with grayish red colors, nodular shape, and medium texture. Besides, more than 20 lymph nodes in the central region of the left neck and 6-8 cervical regions were examined. The lymph nodes are enlarged, ranging from 0.5 to 3 centimeters in diameter. Histologically, on the left side of the thyroid, H&E slides showed hyperplasia of thyroid follicular epithelial under the background of HT（figure 1-A）, and the follicular epithelium in the focal area of HT was transformed into PTC（figure 1-B）. Importantly, in addition to a typical subtype of PTC（figure 1-C）, there were other subtypes of PTC, such as oncocytic variant（figure 1-D）, follicular and solid patterns(figure 1-E). In some focal areas, we also found metaplasia of columnar epithelium into squamous epithelium（figure 1-F）.

Immunohistochemistry staining (IHC)

To further clarify the nature and types of the tumor, we performed immunohistochemistry staining (IHC) on a series of antibodies, including CK19, TPO, TG, CD56, TTF-1, Galectin-3, etc. on formalin-fixed paraffin-embedded (FFPE) tissues. A list of all antibodies is shown in table 1. IHC staining indicated that it was a typical pattern of PTC in which CK19, TTF1, and Galectin-3 were strong positive, and TPO, CD56, and TG were negative showed in figure 2(A-F). IHC also showed that CT, MC, and Syn were negative (not showed).

Imaging and surgical findings

After the first operation, the patient took levothyroxin sodium tables 100ug/day regularly. Fourteen months later, the patient herself found a mass in the anterior region of the left neck, which was gradually enlarged, and the left upper limb occasionally felt numbness and pain, and then came to our hospital for a medical treatment. Physical examination: A mass was palpable in the anterior region of the left neck, about 8 cm in maximum diameter, texture hard, unclear boundary, and poor mobility. Contrast-enhanced CT scanning in the neck diagnosed that the thyroid gland in both sides was absent, and the mass in the left neck supraclavicular region was considered as PCT postoperative recurrence or lymph nodes metastasis (figure 3-A). Systemic PET/CT examination： PET/CT showed that the bilateral lobe of the thyroid was absent after operation, and there was no definite sign of a malignant tumor in the operation area. The tumor in the IV-V area of the left neck showed internal necrosis and increased glucose metabolism in a ring. There were several lymph node metastases showed in the left neck (II-V) region showed in figure 3-B.

After multidisciplinary discussion in our hospital, it was considered that there was a symptom of tumor compression, and due to the effect of radiotherapy and chemotherapy was not obvious, so we choose the operation to reduce the burden of the tumor. It was found during the operation that the boundary among the original operating area and sternocleidomastoid muscle, and local cervical skin was not clear. The space between the lesion and the common carotid artery was disappeared, the trachea was compressed to the right, and the left internal jugular vein was not seen (showed in figure 3-C). Multiple lymph nodes were removed in the left neck II-V regions, it was possible to consider lymph nodes metastasis (showed in figure 3-D）.

Pathological examination of local lymph nodes

Postoperative pathology confirmed that it was metastatic carcinoma of lymph nodes. Interestingly, there were various types of carcinoma in metastatic lesions, including classical papillary carcinoma(figure4-A), tall columnar papillary carcinoma(figure4-B), SCC(figure4-C), and undifferentiated cell carcinoma or thyroid anaplastic cancer (figure4-D). In order to further clarify the characteristics of these tumor cells, we performed IHC on these tumor cells. There was a patchy nesting area of poorly differentiated or undifferentiated carcinoma in local lymph node metastases(figure5-A). The IHC results showed that the tumor cells had the dual characteristics of PTC and SCC, which P40, P63, CK5/6，TTF-1, and CK19 were strongly positive showed in figures 5B-F. These results strongly suggested that the tumor had double characteristics of PTC and SCC.

A comparative study of IHC and molecular pathology in primary PTC and SCC within local lymph node metastasis

For further exploring the biological and origin relationship between primary PTC and SCC in local lymph node metastasis, we made a comparative study by IHC and molecular pathology. Firstly, we compared the expression of PD-L1, TP53, BRAF^V600E,and Ki67 in primary thyroid tumor and local lymph node metastasis by IHC. The results indicated that PD-L1 is negative in the primary tumor (figure 6-A) and a strong positive in metastatic tumors (figure 6-E). TP53 was expressed in both primary and metastatic tumors, but the positive rate in tumor cells was different. The expression rate of TP53 in primary tumors is about 20% (figure 6-B), while in metastatic tumors, the expression rate of TP53 is about 80% (figure 6-F). BRAF^V600E was expressed in both primary and metastatic tumors, and there was no significant difference in the positive rate (figure 6-C and G). In primary tumors, the Ki67 proliferation index is about 5% (figure 6-D), while in metastatic tumors, the Ki67 proliferation index is about 30% (figure 6-H). Then, we detected the mutations of BRAF exon 15, KRAS exon 2-4, NRAS exon 2-4, HRAS exon 3, PIK3CA exon 20, and TERT promoter mutation in primary and metastatic tumors by QPCR to further clarify the relationship between them. The results showed that BRAF exon 15 mutation was found in both primary and metastatic tumors, and no other gene mutations were found (figure 7A-B).

Further treatment and follow-up

After the second operation, she received radiotherapy for two months. The effect of radiotherapy was not good, and the patient finally gave up the treatment, which is still under follow-up.

This is a complicated case which is in the basis of HT, to induce into PTC, and form a variety of subtypes and different stages of PTC. The tall-cell subtype of PTC further metaplasia into squamous cell carcinoma, and de-differentiate into undifferentiated carcinoma.

The association between thyroid autoimmune inflammatory disorders and cancer has attracted much attention for a long time. Changes in autoimmune inflammatory diseases, such as HT and CLT, can be coexisted in about 40% of thyroid cancers, especially PTC. This has to make people associate autoimmune inflammation of the thyroid gland with thyroid cancer. HT is the most common thyroid immune diseases. There is overwhelming evidence to show that HT is closely related to thyroid cancer, especially PCT (2-7, 21-23). Giuseppa G et al found that in a study of 305 cases of PTC divided into two groups, up to 40.2% of the patients coexisted both diffuse HT and PTC in one group, and the results of this study indicated that the coexistence of HT and PTC was very high (4). Several other studies have also shown that HT is closely related to PTC (2, 5, 21, 22). Studies also suggested that HT might be an independent risk factor for thyroid cancer(23). It seems like that the factor of HT may promote the development of thyroid cancer. The case we provided here showed that the atypical hyperplasia and canceration of the focal thyroid follicular epithelium were commonly noted in the background of HT. Our case provides further evidence that there is a close relationship between HT and thyroid cancer. However, the results from another group indicated that HT might decrease the stages of differentiated thyroid cancer, and had a good prognosis with HT(7). Therefore，It is most likely that thyroid autoimmune inflammation has different effects on the occurrence, development, and prognosis of different types and stages of thyroid cancer. The possible mechanism of thyroid cancer caused by thyroid autoimmune inflammation remains to be further studied.

The appearance of different subtypes of PTC in the same tumor is a manifestation of tumor diversity, and its essence is determined by intratumoral heterogeneity(ITH)，and ITH are determined by the diversity of tumor genetic background(24). In our case, there are several different histological subtypes of PTC, such as classical, oncocytic, solid and follicular, and tall cell columnar subtypes. Different subtypes of histological types in the same tumor must have different genetic alterations and biological characteristics, and also have a different response to treatment. These subtypes also represent different differentiation stages and different prognosis of thyroid carcinoma. Therefore, in clinicopathological diagnosis, we need to label each different histological subtype. In addition to different subtypes of PTC, the morphology of thyroid anaplastic cancer can also be seen in this case. Although there are many studies on the relationship between different histological types of thyroid cancer and prognosis, opinions are still controversial(25, 26). It has been debated for a long time whether anaplastic carcinomas arise de novo or derive from the evolution of a preexisting well-differentiated carcinoma through either “anaplastic transformation” or "dedifferentiation” driven by the gaining of genetic abnormalities(8). The existence of poorly differentiated forms with morphological, prognostic, and genetic features intermediate between well-differentiated and anaplastic carcinomas seems to support the hypothesis of a multistep carcinogenic process. In these series, papillary thyroid carcinoma represents the most common histotype associated with anaplastic carcinoma(10).

In addition to different subtypes of PTC, the most notable phenomenon was that squamous cell carcinoma or poor-differentiated anaplastic carcinomas appear in lymph node metastases. What's most interesting was that these poor-differentiated tumor cells express double antigens of PTC and SCC，which P40，P63，CK5/6，TTF1 and CK19 were all strong positive. The results of molecular pathology also showed that BRAF^V600Emutations were found in both PTC in the primary tumor and SCC in lymph node metastasis. These findings indicated that PTC and SCC have a similar genetic background, and strongly suggest that SCC or poor-differentiated anaplastic carcinomas may develop from PTC. So far, we have only seen one case reported regarding BRAF mutation (c.1799 T>A;1801_1812del) in primary SCC of the thyroid(27). As we know that BRAF mutations, especially, BRAF^V600E mutation is the most common molecular genetic change in PTC(28-32). Therefore, we believe that the SCC in the metastatic foci of this case may be evolved from the tall-cell subtype of PTC.

Our understanding of the prognosis of different subtypes of PTC is still insufficient, and the biological characteristics of different subtypes of PTC are still controversial. Allen S.Ho et al. found that the prognosis of well-differentiated PTC (WDPTC), poorly differentiated cancer, and variant cancer is significantly different,and suggesting that treatment should be tailored to specific histologic subtypes (25). Different histological subtypes of PTC have different invasiveness. For example, the tall-cell subtype is more aggressive than the classic type(11). In general, different histopathological types of thyroid cancer will affect the prognosis of their patients. Therefore, a multidisciplinary care plan requires surgical pathologists to be aware of the "so-called" aggressive variants of PTC. It is recommended that the proportion of thyroid cancer of different histological subtypes should be noted in the pathological diagnosis report (11). It is essential to distinguish different subtypes of PTC，because of different histological subtypes, the treatment and prognosis are also different(1, 33, 34). Research indicated that the most invasive variants of PTC are: diffuse sclerosis variant (DSV), tall cell variant (TCV), columnar cell variant (CCV), solid variant (SV), and hobnail variant (HV). These variants are generally closely related to higher recurrence and metastasis rates and have low sensitivity to chemotherapy and radioactive iodine therapy, and the survival rate may also be low(1, 25, 33, 35-41). Finally, we compared the biological characteristics of tumor cells in primary thyroid carcinoma and lymph node metastasis. The results showed that the expression of Ki67 and TP53 in lymph node metastasis was much higher than that in primary lymph node metastasis, indicating that a more malignant tumor cell population appeared in lymph node metastasis, and further revealed the process of tumor progression. It was also found that PD-L1 changed from negative in the primary foci to positive in the lymph node metastasis. The significance of this change needs to be further studied. BRAF^V600E proteins were positive by IHC, and BRAF^V600E were mutated by molecular pathological test, in both primary thyroid carcinoma and lymph node metastasis. It is further suggested that their origins may be the same.

This is a good example that shows a continuous process of developing into PTC based on HT, then transforming into SCC, developing into lymph node metastatic carcinoma, and further dedifferentiating into highly malignant anaplastic carcinoma. In particular, there are some tumor cell subsets with different histological subtypes and biological characteristics, which brings great difficulties to clinical diagnosis and treatment. Although the patient underwent two operations, plus radiotherapy and chemotherapy, the effect of treatments was still not good due to the phenotypic transformation of highly malignant tumor cells. We also recognize once again that primary thyroid SCC are actually derived from the subtype of tall columnar cells of PTC, and can further evolve into undifferentiated carcinoma.

Ethics Statement

This case was reviewed and approved by the Ethics Committee of Affiliated Hospital, Guangdong Medical University（LW2021001）, China. The patient provided her written informed consent to participate in this study.

Declaration of Conflicting Interests

The author(s) declared no potential conflicts of interest for the research, authorship, and/or publication of this article.

Funding

The author(s) received no financial support for the research, authorship, and/or publication of this article.

Author Contributions

J.H. designed the project; J.H. and B.H. wrote the main manuscript text; J.H. and J.W. prepared figures 1-3; J.H., X.R.,H.W. and D.Z. prepared figures 4-6; J.H., B.L. and Y.O. prepared figures 7. All authors reviewed the manuscript.

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Table 1. Antibody clones, manufacturer, and dilutions used in the immunohistochemical study.

Antibody	Gene symbol	Clone	Species	Vendor	Address	Cat#	Dilution
p53	TP53	DO-7	Mouse monoclonal	Ventana	Tucson, AZ	800-2912(G04027)	Prediluted
CD56	NCAM1	MX039	Mouse monoclonal	MXB Biotechnologies	Fuzhou, China	MAB-0743(2007090743C4)	1:150
CK5/6	KRT5/KRT6	MX040	Mouse monoclonal	DAKO	Carpinteria, CA	IR780(20077790)	1:150
CK19	KRT19	A53B/A2.26	Mouse monoclonal	MXB Biotechnologies	Fuzhou, China	MAB-0829(2007300056C3)	1:75
Ki67	MKI67	MIB-1	Mouse monoclonal	DAKO	Carpinteria, CA	IR626(20081075)	Prediluted
P40	TP63	ZR8	Mouse monoclonal	MXB Biotechnologies	Fuzhou, China	RMA-0815(2007300815C4)	1:150
P63	TP63	DAK-P63	Mouse monoclonal	DAKO	Carpinteria, CA	IR662(20081031)	Prediluted
TG	TG	2H11+6E1	Mouse monoclonal	MXB Biotechnologies	Fuzhou, China	MAB-0797(1908150797C2)	Prediluted
TPO	TPO	2G2	Mouse monoclonal	MXB Biotechnologies	Fuzhou, China	MAB-0800(2007300800C3)	1:150
PAX-8	PAX-8	EP298	Rabbit monoclonal	MXB Biotechnologies	Fuzhou, China	RMA-0817(20073000817C2)	Prediluted
b-Cantenin	CTNNB	MX043	Mouse monoclonal	MXB Biotechnologies	Fuzhou, China	MAB-0754(1904080754C2)	Prediluted
TTF-1	TTF-1	MX011	Mouse monoclonal	MXB Biotechnologies	Fuzhou, China	MAB-0599(2007090599C4)	1:150
PD-L1	CD274	SP263	Rabbit monoclonal	Ventana	Tucson, AZ	743-7066(G13629)	Prediluted
BRAF-V600E	BRAF	VE1	Mouse monoclonal	Ventana	Tucson, AZ	790-5095(G01373)	Prediluted
CT	CALCA	SP17	Rabbit monoclonal	MXB Biotechnologies	Fuzhou, China	RMA-0553(181101553C2)	Prediluted
Gal-3	LGALS3	9C4	Mouse monoclonal	MXB Biotechnologies	Fuzhou, China	MAB-0572(1904080572C3)	Prediluted
MC	N/A	HBME-1	Mouse monoclonal	MXB Biotechnologies	Fuzhou, China	MAB-0130(1912050130C4)	1:50
SYN	SYP	MX038	Rabbit monoclonal	MXB Biotechnologies	Fuzhou, China	MAB-0742(2007020742C1)	1:70

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On the basis of Hashimoto's thyroiditis, to form papillary thyroid carcinoma, metastasized and then to de-differentiate into poorly differentiated squamous cell carcinoma

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