Pancoast tumor

Other names: Pulmonary sulcus tumor, superior sulcus tumor, Pancoast syndrome[1]
Chest radiograph showing a Pancoast tumor (labeled as P, non-small cell lung carcinoma, right lung), from a 47-year-old female smoker.
Specialty| Oncology
Symptoms| One sided shoulder pain, arm numbness, large pupil, dropping of the upper eyelid, shinkage of muscles in the hand[1]
Causes| Lung cancer, infection abscess[1]
Diagnostic method| Medical imaging, tissue biopsy[1]
Treatment| Chemotherapy, radiation therapy, surgery[1]
Frequency| 4% of lung cancers[1]

A Pancoast tumor is a cancer that begins in the upper part of the lung.[2] It often spreads to nearby tissues such as the ribs and vertebrae.[2] Symptoms on the affected side may include shoulder pain, arm numbness, large pupil, dropping of the upper eyelid, and shinkage of muscles in the hand.[1] Later in the course of the disease shortness of breath may occur.[1]

More than 95% of Pancoast tumors are non-small cell lung cancers, with most of the rest being small cell lung cancer.[1] Uncommonly it may occur as a result of thyroid cancer, lymphoma, or metastasis.[1] An upper lung abscess may also cause similar symptoms.[1] The underlying mechanism involves compression or invasion of structures in the area.[1] Diagnosis is by medical imaging and tissue biopsy.[1]

Treatment generally involves chemotherapy, radiation therapy, and surgery.[1] Pancoast tumors represent about 4% of lung cancers.[1] It was first described in 1838 by Edward Hare and is named after Henry Pancoast, an American radiologist, who described the condition in 1924.[3]

## Contents

* 1 Signs and symptoms
* 2 Diagnosis
* 3 Treatment
* 4 References
* 5 External links

## Signs and symptoms[edit | edit source]

Aside from cancer general symptoms such as malaise, fever, weight loss and fatigue, Pancoast tumor can include a complete Horner's syndrome in severe cases: miosis (constriction of the pupils), anhidrosis (lack of sweating), ptosis (drooping of the eyelid), and pseudoenophathalmos (because of the ptosis). In progressive cases, the brachial plexus is also affected, causing pain and weakness in the muscles of the arm and hand with a symptomatology typical of thoracic outlet syndrome. The tumor can also compress the recurrent laryngeal nerve and from this a hoarse voice and "bovine" (non-explosive) cough may occur.

In superior vena cava syndrome, obstruction of the superior vena cava by a tumor (mass effect) causes facial swelling cyanosis and dilatation of the veins of the head and neck.

A Pancoast tumor is an apical tumor that is typically found in conjunction with a smoking history. The clinical signs and symptoms can be confused with neurovascular compromise at the level of the superior thoracic aperture. The patient's smoking history, rapid onset of clinical signs and symptoms, and pleuritic pain can suggest an apical tumor. A Pancoast tumor can give rise to both Pancoast syndrome and Horner's syndrome. When the brachial plexus roots are involved, it will produce Pancoast syndrome; involvement of sympathetic fibers as they exit the cord at T1 and ascend to the superior cervical ganglion will produce Horner's syndrome.

## Diagnosis[edit | edit source]

CT scan showing a Pancoast tumor (labeled as P, non-small cell lung carcinoma, right lung), from a 47-year-old female smoker

Diagnosis of Pancoast tumor is usually made after evaluating clinical symptoms and imaging. Chest X-ray is a good screening test even though Chest CT scan can provide a better resolution and extent to which internal organs are being compressed.[citation needed]

## Treatment[edit | edit source]

The treatment of a Pancoast lung cancer may differ from that of other types of non-small cell lung cancer. Its position and close proximity to vital structures (such as nerves and spine) may make surgery difficult. As a result, and depending on the stage of the cancer, treatment may involve radiation and chemotherapy given prior to surgery (neoadjuvant treatment). Surgery may consist of the removal of the upper lobe of a lung together with its associated structures (subclavian artery, vein, branches of the brachial plexus, ribs and vertebral bodies), as well as mediastinal lymphadenectomy. Surgical access may be via thoracotomy from the back[4] or the front of the chest[5] and modifications.[6] Nonsurgical treatment may consist of radiation therapy alone or clinical trials of new combinations of treatment.[7]

## References[edit | edit source]

1. ↑ 1.00 1.01 1.02 1.03 1.04 1.05 1.06 1.07 1.08 1.09 1.10 1.11 1.12 1.13 1.14 Villgran, VD; Chakraborty, RK; Cherian, SV (January 2020). "Pancoast Syndrome". PMID 29489146. `{{cite journal}}`: Cite journal requires `|journal=` (help)
2. ↑ 2.0 2.1 "https://www.cancer.gov/publications/dictionaries/cancer-terms/def/pancoast-tumor". www.cancer.gov. 2 February 2011. Archived from the original on 10 January 2021. Retrieved 11 February 2021. `{{cite web}}`: External link in ``|title=`` (help)
3. ↑ "Pancoast's syndrome". www.whonamedit.com. Archived from the original on 8 July 2020. Retrieved 11 February 2021.
4. ↑ Paulson DL, Shaw RR (May 1960). "Results of bronchoplastic procedures for bronchogenic carcinoma". Ann. Surg. 151 (5): 729–40. doi:10.1097/00000658-196005000-00013. PMC 1613696. PMID 14431029.
5. ↑ Dartevelle PG, Chapelier AR, Macchiarini P, et al. (June 1993). "Anterior transcervical-thoracic approach for radical resection of lung tumors invading the thoracic inlet". J. Thorac. Cardiovasc. Surg. 105 (6): 1025–34. doi:10.1016/S0022-5223(19)33774-2. PMID 8080467.
6. ↑ Nazari S (August 1996). "Transcervical approach (Dartevelle technique) for resection of lung tumors invading the thoracic inlet, sparing the clavicle". J. Thorac. Cardiovasc. Surg. 112 (2): 558–60. doi:10.1016/s0022-5223(96)70296-9. PMID 8751536.
Grunenwald D, Spaggiari L (February 1997). "Transmanubrial osteomuscular sparing approach for apical chest tumors". Ann. Thorac. Surg. 63 (2): 563–6. doi:10.1016/S0003-4975(96)01023-5. PMID 9033349.
Anterior Access for radical resection of Pancoast tumors on YouTube
7. ↑ "Non-Small Cell Lung Cancer Treatment (PDQ®)–Patient Version - National Cancer Institute". www.cancer.gov. 2020-05-22. Archived from the original on 2019-10-31. Retrieved 2020-06-10.

## External links[edit | edit source]

Classification|

* ICD-10: C34.1
* ICD-9-CM: 162.3
* MeSH: D010178
* DiseasesDB: 31266

|

External resources|

* eMedicine: med/3418

* Pancoast Tumor at eMedicine

* v
* t
* e

Cancer involving the respiratory tract

Upper RT|

Nasal cavity

Esthesioneuroblastoma

Nasopharynx

Nasopharyngeal carcinoma
Nasopharyngeal angiofibroma

Larynx

Laryngeal cancer
Laryngeal papillomatosis

Lower RT|

| Trachea|

* Tracheal tumor

|

Lung|

| Non-small-cell lung carcinoma|

* Squamous-cell carcinoma
* Adenocarcinoma (Mucinous cystadenocarcinoma)
* Large-cell lung carcinoma
* Rhabdoid carcinoma
* Sarcomatoid carcinoma
* Carcinoid
* Salivary gland–like carcinoma
* Adenosquamous carcinoma
* Papillary adenocarcinoma
* Giant-cell carcinoma

|

Small-cell carcinoma|

* Combined small-cell carcinoma

Non-carcinoma|

* Sarcoma
* Lymphoma
* Immature teratoma
* Melanoma

By location|

* Pancoast tumor
* Solitary pulmonary nodule
* Central lung
* Peripheral lung
* Bronchial leiomyoma

Pleura|

* Mesothelioma
* Malignant solitary fibrous tumor

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