By Jason Wasserman MD PhD FRCPC
February 7, 2023
Spindle cell squamous cell carcinoma (SCC) of the larynx is a fast-growing and aggressive type of throat cancer. Another name for this type of cancer is sarcomatoid squamous cell carcinoma.
The tumour starts from specialized squamous cells that cover the inside surface of the larynx. Spindle cell SCC can start anywhere in the larynx although the most common site is the glottis which includes the vocal cords. Less common sites include the supraglottis and subglottis.
Tobacco smoking and high levels of alcohol consumption increase the risk of developing spindle cell SCC of the larynx.
Most spindle cell SCCs of the larynx develop from a pre-cancerous disease called keratinizing squamous dysplasia. Like spindle cell SCC, keratinizing squamous dysplasia is associated with tobacco smoking and high levels of alcohol consumption.
The most common symptom of spindle cell SCC is hoarseness, a change in the quality of the voice which can make the voice sound scratchy or strained.
The diagnosis of spindle cell SCC can only be made after a tissue sample from the tumour is examined under the microscope by a pathologist. In order to obtain this tissue sample, your doctor may perform an examination called an upper endoscopy which uses a camera to look at the parts of the larynx. During this examination, a small sample of tissue can be removed in a procedure called a biopsy.
When examined under the microscope, the tumour is made up of very abnormal-looking spindle cells. The term “spindle cell” means that the cells are long and thin. Pathologists often describe the cells in the tumour as pleomorphic because there is considerable variation in cell size, shape, and colour throughout the tumour. Areas of “better differentiated” SCC (tumour cells that look more like squamous cells) may be seen within the tumour. A precancerous condition called keratinizing squamous dysplasia may also be seen near the inside surface of the larynx on the edge of the tumour. Both features help confirm the diagnosis.
The larynx is divided into three parts: supraglottis, glottis, and subglottis. The term transglottic is used to describe a tumour that involves more than one part. For example, a tumour would be described as transglottic if it involved both the supraglottis and glottis. A transglottic tumour is associated with a worse prognosis and is given a higher pathologic tumour stage (pT). Transglottic extension can only be assessed after the entire tumour has been removed.
Perineural invasion is a term pathologists use to describe tumour cells attached to or inside a nerve. A similar term, intraneural invasion, is used to describe tumour cells inside a nerve. Nerves are like long wires made up of groups of cells called neurons. Nerves are found all over the body and they are responsible for sending information (such as temperature, pressure, and pain) between your body and your brain. Perineural invasion is important because the tumour cells can use the nerve to spread into surrounding organs and tissues. This increases the risk that the tumour will regrow after surgery.
Lymphovascular invasion means that tumour cells were seen inside a blood vessel or lymphatic vessel. Blood vessels are long thin tubes that carry blood around the body. Lymphatic vessels are similar to small blood vessels except that they carry a fluid called lymph instead of blood. The lymphatic vessels connect with small immune organs called lymph nodes that are found throughout the body. Lymphovascular invasion is important because tumour cells can use blood vessels or lymphatic vessels to spread to other parts of the body such as lymph nodes or the lungs.
In pathology, a margin is the edge of a tissue that is cut when removing a tumour from the body. The margins described in a pathology report are very important because they tell you if the entire tumour was removed or if some of the tumour was left behind. The margin status will determine what (if any) additional treatment you may require.
Most pathology reports only describe margins after a surgical procedure called an excision or resection has been performed for the purpose of removing the entire tumour. For this reason, margins are not usually described after a procedure called a biopsy is performed for the purpose of removing only part of the tumour. The number of margins described in a pathology report depends on the types of tissues removed and the location of the tumour. The size of the margin (the amount of normal tissue between the tumour and the cut edge) depends on the type of tumour being removed and the location of the tumour.
Pathologists carefully examine the margins to look for tumour cells at the cut edge of the tissue. If tumour cells are seen at the cut edge of the tissue, the margin will be described as positive. If no tumour cells are seen at the cut edge of the tissue, a margin will be described as negative. Even if all of the margins are negative, some pathology reports will also provide a measurement of the closest tumour cells to the cut edge of the tissue.
A positive (or very close) margin is important because it means that tumour cells may have been left behind in your body when the tumour was surgically removed. For this reason, patients who have a positive margin may be offered another surgery to remove the rest of the tumour or radiation therapy to the area of the body with the positive margin. The decision to offer additional treatment and the type of treatment options offered will depend on a variety of factors including the type of tumour removed and the area of the body involved. For example, additional treatment may not be necessary for a benign (non-cancerous) type of tumour but may be strongly advised for a malignant (cancerous) type of tumour.
Lymph nodes are small immune organs found throughout the body. Tumour cells can spread from a tumour to lymph nodes through small vessels called lymphatics. For this reason, lymph nodes are commonly removed and examined under a microscope to look for tumour cells. The movement of tumour cells from the tumour to another part of the body such as a lymph node is called metastasis.
Tumour cells typically spread first to lymph nodes close to the tumour although lymph nodes far away from the tumour can also be involved. For this reason, the first lymph nodes removed are usually close to the tumour. Lymph nodes further away from the tumour are only typically removed if they are enlarged and there is a high clinical suspicion that there may be tumour cells in the lymph node.
If any lymph nodes were removed from your body, they will be examined under the microscope by a pathologist and the results of this examination will be described in your report. Most reports will include the total number of lymph nodes examined, where in the body the lymph nodes were found, and the number (if any) that contain tumour cells. If tumour cells were seen in a lymph node, the size of the largest group of tumour cells (often described as “focus” or “deposit”) will also be included.
The examination of lymph nodes is important for two reasons. First, this information is used to determine the pathologic nodal stage (pN). Second, finding tumour cells in a lymph node increases the risk that tumour cells will be found in other parts of the body in the future. As a result, your doctor will use this information when deciding if additional treatment such as chemotherapy, radiation therapy, or immunotherapy is required.
A neck dissection is a surgical procedure performed to remove lymph nodes from the neck. The lymph nodes removed usually come from different areas of the neck and each area is called a level. The levels in the neck include 1, 2, 3, 4, and 5. Your pathology report will often describe how many lymph nodes were seen in each level sent for examination. Lymph nodes on the same side as the tumour are called ipsilateral while those on the opposite side of the tumour are called contralateral.
Pathologists often use the term “positive” to describe a lymph node that contains tumour cells. For example, a lymph node that contains tumour cells may be called “positive for malignancy” or “positive for metastatic carcinoma”.
Pathologists often use the term “negative” to describe a lymph node that does not contain any tumour cells. For example, a lymph node that does not contain tumour cells may be called “negative for malignancy” or “negative for metastatic carcinoma”.
All lymph nodes are surrounded by a thin layer of tissue called a capsule. Extranodal extension means that tumour cells within the lymph node have broken through the capsule and have spread into the tissue outside of the lymph node. Extranodal extension is important because it increases the risk that the tumour will regrow in the same location after surgery. For some types of tumours, extranodal extension is also a reason to consider additional treatment such as chemotherapy or radiation therapy.
The pathologic stage for spindle cell SCC of the larynx is based on the TNM staging system, an internationally recognized system originally created by the American Joint Committee on Cancer. This system uses information about the primary tumour (T), lymph nodes (N), and distant metastatic disease (M) to determine the complete pathologic stage (pTNM). Your pathologist will examine the tissue submitted and give each part a number. In general, a higher number means a more advanced disease and a worse prognosis.
There are three different tumour staging systems for spindle cell SCC of the larynx. The system selected depends on where in the larynx the tumour started.
Spindle cell SCC of the larynx is given a nodal stage between 0 and 3 based on the examination of all lymph nodes received. Both N2 and N3 are further divided into sub-stages (for example N2a, N2b, etc).
The following four features are used to determine the nodal stage:
Using these features your pathologist will provide a nodal stage as follows:
Spindle cell SCC of the larynx is given a metastatic stage of 0 or 1 based on the presence of tumour cells at a distant site in the body (for example the lungs). The metastatic stage can only be assigned if tissue from a distant site is sent for pathological examination. Because this tissue is rarely present, the metastatic stage cannot be determined and is listed as MX.