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Pancoast tumor picture. Pancoast Tumor: Comprehensive Overview and Expert Insights

What is a Pancoast tumor? How does it differ from other lung cancers? What are the symptoms and treatment options? Get answers to your questions about this rare but serious condition.

Understanding Pancoast Tumors

Pancoast tumors are a unique type of lung cancer that originate in the upper portion of the lung, also known as the lung apex. These cancers were first described by American physician Henry Pancoast in 1932, and are therefore often referred to as “Pancoast tumors” or “superior pulmonary sulcus tumors.” Pancoast tumors account for less than 5% of all lung cancer cases, making them a relatively rare form of this disease.

Anatomy and Spread of Pancoast Tumors

Pancoast tumors are characterized by their location at the top of the lung. Due to this positioning, these cancers can spread and invade surrounding structures, including the:

  • First ribs in the chest (thoracic ribs)
  • Upper part of the back
  • Bundle of nerves that send signals from the spinal cord to the shoulder, arm, and hand (brachial plexus)
  • Blood vessels supplying the arms

This ability to infiltrate nearby anatomical structures sets Pancoast tumors apart from other lung cancers, which typically grow and spread within the lung tissue itself.

Histological Subtypes of Pancoast Tumors

The majority of Pancoast tumors are a type of non-small cell lung cancer, most commonly adenocarcinomas. Adenocarcinomas originate from the mucus-producing gland cells lining the airways. Other less common subtypes include squamous cell carcinoma and small cell lung cancer.

Symptoms of Pancoast Tumors

What are the typical symptoms associated with Pancoast tumors? Due to their location at the lung apex, these cancers can put pressure on or damage the brachial plexus – the bundle of nerves running from the upper chest into the neck and arms. This can lead to a characteristic set of symptoms, including:

  • Severe shoulder or arm pain
  • Muscle weakness or atrophy in the hand and arm
  • Numbness or tingling sensations in the hand and arm
  • Drooping eyelid and constricted pupil on the affected side (Horner’s syndrome)

In addition, Pancoast tumor patients may also experience more general lung cancer symptoms such as cough, shortness of breath, and weight loss.

Diagnosis and Imaging of Pancoast Tumors

How are Pancoast tumors detected and diagnosed? Initial imaging with a chest X-ray may show subtle changes, such as a non-homogenous opacity in the upper lung zone or tracheal deviation. However, in up to 1.7% of cases, the chest X-ray may appear normal despite the presence of a Pancoast tumor. Therefore, if there is a high clinical suspicion, further imaging with a CT scan of the chest is warranted. CT scans can clearly demonstrate the soft tissue mass in the lung apex and assess for invasion of surrounding structures.

Treatment Approaches for Pancoast Tumors

The treatment of Pancoast tumors typically involves a multimodal approach, often combining surgery, radiation therapy, and chemotherapy. The specific treatment plan depends on the stage and extent of the tumor, as well as the patient’s overall health and preferences. In early-stage Pancoast tumors, surgical resection may be the primary treatment, potentially followed by adjuvant (additional) therapies. For more advanced or inoperable tumors, neoadjuvant (pre-surgical) chemotherapy and radiation therapy may be used to try to shrink the tumor prior to surgery. In some cases, definitive chemoradiation therapy without surgery may be the most appropriate approach.

Prognosis and Outcomes

The prognosis for patients with Pancoast tumors can vary widely, depending on factors such as the stage at diagnosis, the tumor’s resectability, and the patient’s response to treatment. In general, early-stage Pancoast tumors that are surgically resectable tend to have a better prognosis, with 5-year survival rates around 30-40%. However, more advanced or inoperable Pancoast tumors have a poorer prognosis, with 5-year survival rates often less than 10%. Continuous advancements in treatment approaches and the use of multimodal therapy have helped to improve outcomes for some patients with Pancoast tumors in recent years.

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BMJ Case Rep. 2012; 2012: bcr2012006285.

Published online 2012 Jun 12. doi: 10.1136/bcr-2012-006285

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A 61-year-old man was referred to our rheumatology unit with a 3-month history of worsening left-sided neck and shoulder pain. His general practitioner (GP) suspected Giant cell arteritis and a temporal artery biopsy was performed which was negative. Shoulder and neck x-rays were also normal. He had a 40-pack-year smoking history and a chest radiograph was organised by his GP. On questioning, he admitted to significant weight loss and hoarseness of voice.

On examination, shoulder movements did not exacerbate his pain and he had a full range of shoulder and upper-limb movements. He had a left Horner’s syndrome, a cyanosed left forearm with feebly palpable left upper-limb pulses. The temporal arteries were non-tender. Chest examination was unremarkable. His erythrocyte sedimentation rate and C-reactive protein level were raised at 30 mm/h and 60 mg/l, respectively. Other blood tests were unremarkable.

A chest radiograph () showed slight right-sided tracheal deviation and subtle non-homogenous left upper-lobe opacity. The history and clinical features along with radiological findings were highly suggestive of a left apical lung lesion. An urgent enhanced CT scan of the thorax ( and ) was arranged and demonstrated a soft-tissue mass (6. 9 cm × 5.4 cm × 7.7 cm) in the left lung apex encasing the left subclavian artery.

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Chest radiograph with slight right tracheal deviation and subtle non-homogenous opacity in left upper zone (black arrows).

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Coronal enhanced CT scan image of the thorax demonstrates a soft-tissue mass (6.9 cm × 5.4 cm × 7.7 cm), in left lung apex encasing the subclavian artery (white arrows).

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Sagittal enhanced CT scan image of the thorax shows encased subclavian artery by a Pancoast tumour (white arrows).

Of the patients presenting with a Pancoast tumour, 1.7% have a normal plain chest radiograph.1 Our case illustrates that when there is a high index of clinical suspicion, CT imaging should be undertaken to exclude a Pancoast tumour even when the plain radiograph changes are subtle.

Shoulder pain has been reported as being the first presenting feature of a Pancoast tumour in 90% of cases. 2 It is of interest that the original description of a Pancoast tumour in 1932 by Henry Pancoast3 was of shoulder pain due to an apical mass.

Competing interests: None.

Patient consent: Obtained.

1. Fletcher F, Johnston RN, Stradling P.
The normal chest radiograph in bronchial carcinoma. BMJ
1976;2:403.1. [PMC free article] [PubMed] [Google Scholar]

2. Yacoub M, Hupert C.
Shoulder pain as an early symptom of Pancoast tumour. J Med Soc N J
1980;77:583–6. [PubMed] [Google Scholar]

3. Pancoast H.
Superior pulmonary sulcus tumour. JAMA
1932;99:1391–6. [Google Scholar]


Articles from BMJ Case Reports are provided here courtesy of BMJ Publishing Group


Pancoast tumours | Lung cancer

Pancoast tumours are cancers that start in the top part of the lung (the apex). 

These cancers were named after an American doctor called Professor Henry Pancoast in 1932.  They are also called superior pulmonary sulcus tumours.

Cancers in the top part of the lung are rare. Fewer than 5 in every 100 cases of lung cancer (5%) are Pancoast tumours.

A Pancoast tumour can spread into one or more structures in the top part of the chest, which include:

  • the first ribs in the chest (thoracic ribs)
  • upper part of the back
  • the bundle of nerves that sends signals from the spinal cord to the shoulder, arm and hand (the brachial plexus)
  • blood vessels that supply blood to the arms

Types of Pancoast tumour

Most Pancoast tumours are a type called non small cell cancer and most commonly adenocarcinomas. These are cancers that start in the mucus making gland cells in the lining of your airways.

Symptoms

Because the cancer is at the top of the lungs, it might put pressure on or damage a group of nerves that runs from the upper chest into your neck and arms. The group of nerves is called the brachial plexus.

Pressure on the brachial plexus can cause several very specific symptoms:

  • severe pain in the shoulder or the shoulder blade (scapula)
  • pain in the arm and weakness of the hand on the affected side
  • Horner syndrome

Horner syndrome is the medical name for a group of symptoms. They include:

  • flushing on one side of the face
  • not sweating in the face
  • the eye on the same side has a smaller (constricted) pupil with a drooping or weak eyelid

Diagnosing Pancoast tumours

Pancoast tumours can be difficult to diagnose. This is because, in the early stages, they often don’t show up easily on x-ray. To help diagnose a Pancoast tumour, you might have a:

  • needle biopsy
  • biopsy through a video assisted thoracoscopy surgery (VATS)
  • biopsy through a small cut in the chest wall (small thoracotomy)
  • scans such as a CT, MRI or PET-CT

The symptoms are unusual, and this might lead your doctor to suspect other conditions before lung cancer.

Treatment

Treatment for a Pancoast tumour depends on the stage of the cancer, it’s exact position in the lung and your general health. The stage means the size of the cancer and whether it has spread to other areas of the body.

Chemoradiotherapy and surgery

If you are fit enough to have surgery, you usually have a combination of chemotherapy and radiotherapy (chemoradiotherapy) first. This helps to shrink the cancer. 

Surgery for Pancoast tumours is often difficult. It needs to be carried out by a team of specialist surgeons at a specialist cancer hospital. The surgery involves removing the top two ribs or sometimes more.

Sometimes the surgeon also needs to remove a major artery behind the collar bone. They replace it with an artificial tube (graft). This keeps a good blood supply to the arm on the affected side. They might carry out the surgery through a cut in the back or the front of the chest.

Chemoradiotherapy and immunotherapy

If you can’t have surgery, you might have chemoradiotherapy (chemotherapy with radiotherapy).

You might then have immunotherapy after chemoradiotherapy. Immunotherapy uses our immune system to fight cancer. It works by helping the immune system recognise and attack cancer cells.

Radiotherapy or supportive care

You usually have radiotherapy if:

  • the cancer can’t be removed with surgery
  • has spread to other areas of the body

This treatment shrinks the cancer and reduces symptoms. You can also have other medicines or treatments to control symptoms.

Targeted treatment

Your doctor will test your cancer cells for certain receptors of particular proteins. The receptors make them sensitive to targeted cancer drugs. If these receptors are present, your doctor might offer you treatment with a targeted cancer drug.

More information and support

You can phone the Cancer Research UK nurses on freephone 0808 800 4040, from 9am to 5pm, Monday to Friday. They can help with questions on cancer.

  • Lung cancer: diagnosis and management

    National Institute for Health and Care Excellence, March 2019 (updated September 2022)

  • Management of lung cancer
    Scottish Intercollegiate Guideline Network, February 2014

  • Diagnosing and treating pancoast tumors
    K Zarogoulidis and others
    Expert Review of Respiratory Medicine, 2016

    Volume 10, Issue 12

  • Pancoast tumour: current therapeutic options

    VD Palumbo and others

    Clinica Terapeutica, 2019

    Volume 170, Issue 4

  • Superior pulmonary sulcus (Pancoast) tumors

    UpToDate website

    Accessed January 2023

  • Cancer: Principles and Practice of Oncology (11th edition)

    VT DeVita, TS Lawrence, SA Rosenberg

    Wolters Kluwer, 2019

  • The information on this page is based on literature searches and specialist checking. We used many references and there are too many to list here. If you need additional references for this information please contact [email protected] with details of the particular risk or cause you are interested in.

Last reviewed: 

03 Jan 2023

Next review due: 

03 Jan 2026