What is Hurthle Cell Thyroid Carcinoma?

Generally, thyroid cancers have been categorized into four types: papillary, follicular, medullary, and anaplastic. These types (papillary, follicular, and medullary) are grouped under differentiated thyroid tumors, meaning they look a lot like normal thyroid tissue. Hurthle cell carcinoma (HCC), a less commonly known thyroid cancer type, used to be considered a form of follicular thyroid cancer as it shared certain similarities, such as how it appears and its metastatic spread – which means how the cancer spreads to other parts of the body. However, in 2017, the World Health Organization decided to classify it as a distinct type of tumor due to its substantial differences with follicular thyroid cancer in both cell structure and molecular makeup. So now, Hurthle cell thyroid cancer is defined as a cancer that originates from follicular thyroid cells, rather than being a variant of follicular cancer itself.

What Causes Hurthle Cell Thyroid Carcinoma?

There’s no direct cause known yet for Hurthle cell thyroid cancer. However, certain things can increase your chances of getting it. For example, if you have been exposed to radiation in the areas of your head, neck, or chest, or if your family has a history of thyroid cancer, you may be more likely to get thyroid cancers.

Risk Factors and Frequency for Hurthle Cell Thyroid Carcinoma

Hurthle cell carcinoma, a type of thyroid cancer, makes up about 5% of all differentiated thyroid cancers. It’s more common in women and is usually diagnosed after the age of 40.

Signs and Symptoms of Hurthle Cell Thyroid Carcinoma

Hurthle cell cancers, a type of thyroid cancer, are usually discovered when patients have thyroid nodules, or when these nodules are spotted unexpectedly during neck scans. In more advanced stages, the cancer may present itself as swollen glands in the neck, known as ‘cervical adenopathy’. In rare cases, the first sign of this disease could be cancer spreading to distant parts of the body, also known as ‘distant metastasis’.

Testing for Hurthle Cell Thyroid Carcinoma

If a health professional identifies suspicious growths or lumps (nodules) in your thyroid gland, they will typically recommend a few tests to check its functionality. These tests include thyroid-stimulating hormone (TSH) and thyroxine (T4) levels. The existence and size of the nodules can be further confirmed through an ultrasound scan.

If your TSH level is low, this could indicate a functional nodule. In this case, a radioiodine imaging scan is typically used to confirm. Functionally hyperthyroid, or “hot”, nodules are rarely cancerous, but they may require treatment to manage an overactive thyroid (hyperthyroidism) or excessive thyroid hormone in the body (thyrotoxicosis).

If the nodules don’t make excessive thyroid hormone (non-thyrotoxic thyroid nodules), a fine-needle aspiration (FNA) and biopsy might be recommended. FNA involves inserting a thin needle into the nodule to collect a sample of cells. This technique can accurately diagnose some types of thyroid cancer, like papillary and anaplastic thyroid cancers.

However, when it comes to follicular and Hurthle cell tumor types, FNA might be insufficient to determine if it’s benign (non-cancerous) or malignant (cancerous). Usually, a larger portion of the thyroid needs to be removed (thyroid lobectomy or thyroidectomy), after which a detailed examination of the removed tissue will be conducted to identify invasive cancer.

In recent times, molecular studies have gained prominence to differentiate between benign and malignant tumors derived from follicular cells. This has helped in avoiding unnecessary aggressive surgeries. These tests include looking for BRAF and RAS mutations, mRNA genomic sequencing, and checking the expression of certain genes through microRNA gene expression modalities.

In some cases, if widespread disease is suspected based on your symptoms, your doctor may recommend other imaging tests like computed tomography (CT) or magnetic resonance imaging (MRI). Laryngoscopic evaluation could be necessary if you are experiencing issues with your voice (dysphonia) or difficulty swallowing (dysphagia).

In patients suspected of having the disease spread to other parts of the body (metastatic disease), a special type of imaging that combines PET and CT scans (PET-CT) might be useful.

Treatment Options for Hurthle Cell Thyroid Carcinoma

Surgery is the primary treatment for a type of cancer called Hurthle cell tumors. Two types of surgery, thyroid lobectomy (partial removal of the thyroid) and total thyroidectomy (complete removal of the thyroid), have been found to have similar results for non-invasive Hurthle cell tumors. If the cancer is invasive, however, a total thyroidectomy is needed.

Radioactive iodine (RAI) is often used as a secondary treatment for cases where the cancer is harder to treat, such as having a larger tumor, spread to the neck lymph nodes, cancerous cells at the edge of the surgically removed tissue, invasion into small blood vessels, or high levels of a protein called thyroglobulin after surgery. However, only around 10% of Hurthle cell carcinoma patients respond to this treatment, making it less effective than for other types of thyroid cancers. This is because most Hurthle cell carcinomas don’t absorb iodine, so a negative RAI scan may not necessarily mean there’s no cancer left. For these high-risk patients, an FDG-PET scan is recommended, which can help detect cancer cells more accurately.

If the cancer is present in the neck (cervical disease) after initial treatment, neck dissection (a surgery to remove lymph nodes) can be considered. If surgery is not possible or advisable, then radiation therapy may be an option.

For patients who have Hurthle cell carcinoma that has spread to other parts of the body (metastatic), the choice of treatment depends on several factors. If the patients have no symptoms and the tumor is growing slowly, it may be possible to just monitor the condition. If the tumor is growing rapidly and absorbs iodine, RAI is preferred. On the other hand, if the tumor does not respond to RAI, certain medications like lenvatinib or sorafenib may be used. However, these medications can have side effects, and lenvatinib is typically preferred over sorafenib.

There’s also data supporting the use of drugs like larotrectinib or entrectinib for tumors with specific genetic changes, and pembrolizumab for tumors with a high number of mutations. Similarly, selpercatinib and pralsetinib may be beneficial for patients with RET fusion, a specific genetic change that can occur in cancers. If no other treatments work, chemotherapy may be used as a last resort, although it hasn’t been shown to help significantly in Hurthle cell carcinoma cases.

Hurthle cell carcinoma is a type of thyroid cancer that shares a lot of similarities with other forms of thyroid cancers, especially follicular thyroid carcinoma. However, there are some key differences.

  • Hurthle cell carcinomas are often bigger in size than follicular thyroid carcinomas.
  • They tend to have more than one tumor (multifocal).
  • There is a higher chance of Hurthle cell carcinomas spreading to other parts of the thyroid (local thyroid invasion), to the lymph nodes (lymph node metastases), and to distant parts of the body (distant metastases).
  • They have unique features when studied under a microscope (histological features), and unlike other types, they show low uptake of radioactive iodine in medical imaging.

Fast-growing thyroid carcinomas should always be checked for anaplastic thyroid carcinoma. This type is more dangerous and needs immediate treatment. This treatment could include chemotherapy and radiation therapy for the neck.

What to expect with Hurthle Cell Thyroid Carcinoma

Hurthle cell carcinomas are types of cancers that are believed to be more severe and spread more easily compared to follicular thyroid carcinomas, which are another type of thyroid cancer. This results in lower overall survival rates according to certain medical reviews.

Factors that contribute to a worse prognosis, or outcome, for Hurthle cell carcinomas include older age, a larger tumor size when first diagnosed, the tumor spreading beyond the thyroid, being female, and having a higher stage, or severity, at the time of diagnosis.

Possible Complications When Diagnosed with Hurthle Cell Thyroid Carcinoma

The complications associated with Hurthle cell carcinomas are similar to those seen in general thyroid growths. These complications occur when the carcinoma starts spreading to nearby areas in the neck such as the voice box, vocal cords, esophagus, windpipe, or area between the lungs, and by putting pressure on critical nerves and blood vessels due to swollen lymph nodes. The cancer might also spread, or metastasize, to the lungs, bones, and occasionally, the brain.

Complications of Hurthle cell carcinomas:

  • Spread to nearby throat structures (voice box, vocal cords, esophagus, windpipe, or area between the lungs).
  • Pressure on crucial nerves and vessels in the neck from swollen lymph nodes.
  • Spreading of cancer to lymph nodes, lungs, and bones.
  • Less commonly, spreading to the brain.

Preventing Hurthle Cell Thyroid Carcinoma

Hurthle cell carcinomas, a type of thyroid cancer, can be more aggressive than other types of thyroid cancers. Currently, there are no standard methods to screen for thyroid tumors recommended for use in people who don’t show any symptoms, according to the United States Preventive Services Task Force. However, individuals with a family history of a specific type of thyroid cancer known as medullary thyroid carcinomas, multiple endocrine neoplasias (a grouping of disorders that affect the body’s endocrine system), a personal history of thyroid cancer, familial adenomatous polyposis syndrome (an inherited condition that causes precancerous polyps to grow in the colon), or those who have been exposed to radiation, are at a high risk of developing thyroid cancer. These high-risk individuals should be made aware of any suspicious signs and symptoms and should remain vigilant. Moreover, they need to understand the importance of getting any unusual thyroid nodules (small lumps of cells) or neck masses checked out promptly.

Frequently asked questions

Hurthle Cell Thyroid Carcinoma is a distinct type of tumor that originates from follicular thyroid cells, rather than being a variant of follicular cancer itself.

Hurthle cell carcinoma makes up about 5% of all differentiated thyroid cancers.

The signs and symptoms of Hurthle Cell Thyroid Carcinoma include: 1. Thyroid nodules: These are abnormal growths or lumps in the thyroid gland. They can be felt as a lump in the neck or may be discovered during routine neck scans. 2. Swollen glands in the neck: In more advanced stages of Hurthle Cell Thyroid Carcinoma, the cancer may cause swollen glands in the neck, known as cervical adenopathy. This can be a sign that the cancer has spread to nearby lymph nodes. 3. Distant metastasis: In rare cases, the first sign of Hurthle Cell Thyroid Carcinoma could be cancer spreading to distant parts of the body. This can cause symptoms such as bone pain, difficulty breathing, or neurological symptoms depending on the location of the metastasis. It is important to note that these signs and symptoms can also be caused by other conditions, so it is essential to consult a healthcare professional for an accurate diagnosis.

There is no direct known cause for Hurthle cell thyroid cancer, but certain factors can increase the chances of getting it, such as exposure to radiation in the head, neck, or chest areas, or having a family history of thyroid cancer.

The doctor needs to rule out the following conditions when diagnosing Hurthle Cell Thyroid Carcinoma: - Benign (non-cancerous) tumors derived from follicular cells - Malignant (cancerous) tumors derived from follicular cells - Widespread disease - Metastatic disease - Anaplastic thyroid carcinoma

The types of tests needed for Hurthle Cell Thyroid Carcinoma include: 1. Thyroid-stimulating hormone (TSH) and thyroxine (T4) levels to check the functionality of the thyroid gland. 2. Ultrasound scan to confirm the existence and size of nodules. 3. Radioiodine imaging scan to confirm functional nodules. 4. Fine-needle aspiration (FNA) and biopsy to collect a sample of cells for diagnosis. 5. Molecular studies to differentiate between benign and malignant tumors, including looking for BRAF and RAS mutations, mRNA genomic sequencing, and checking gene expression through microRNA gene expression modalities. 6. Computed tomography (CT) or magnetic resonance imaging (MRI) for imaging tests if widespread disease is suspected. 7. Laryngoscopic evaluation if there are voice or swallowing issues. 8. PET-CT scan for patients suspected of having metastatic disease. 9. Neck dissection or radiation therapy for cervical disease after initial treatment. 10. Treatment options for metastatic disease include monitoring, radioactive iodine (RAI) if the tumor absorbs iodine, medications like lenvatinib or sorafenib if the tumor does not respond to RAI, drugs like larotrectinib or entrectinib for tumors with specific genetic changes, pembrolizumab for tumors with a high number of mutations, selpercatinib and pralsetinib for RET fusion, and chemotherapy as a last resort.

Hurthle Cell Thyroid Carcinoma is primarily treated with surgery. The two types of surgery commonly used are thyroid lobectomy (partial removal of the thyroid) and total thyroidectomy (complete removal of the thyroid). These surgeries have similar results for non-invasive tumors. However, if the cancer is invasive, a total thyroidectomy is necessary. Radioactive iodine (RAI) is often used as a secondary treatment for more challenging cases, but it is less effective for Hurthle Cell Carcinoma compared to other types of thyroid cancers. Neck dissection and radiation therapy are options if the cancer is present in the neck after initial treatment. For metastatic cases, the choice of treatment depends on various factors, including the tumor's growth rate and its response to RAI. Medications like lenvatinib or sorafenib may be used if RAI is not effective. Other drugs, such as larotrectinib, entrectinib, pembrolizumab, selpercatinib, and pralsetinib, may be beneficial for tumors with specific genetic changes. Chemotherapy is considered a last resort if other treatments are unsuccessful.

The complications or side effects when treating Hurthle Cell Thyroid Carcinoma include: - Spread to nearby throat structures such as the voice box, vocal cords, esophagus, windpipe, or area between the lungs. - Pressure on crucial nerves and vessels in the neck from swollen lymph nodes. - Spreading of cancer to lymph nodes, lungs, and bones. - Less commonly, spreading to the brain.

The prognosis for Hurthle Cell Thyroid Carcinoma is generally worse compared to other types of thyroid cancer. Factors that contribute to a worse prognosis include older age, larger tumor size at diagnosis, tumor spreading beyond the thyroid, being female, and higher stage at the time of diagnosis. Overall survival rates are lower for Hurthle cell carcinomas compared to follicular thyroid carcinomas.

An endocrinologist or an oncologist.

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