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Nasopharynx cancer

Nasopharynx cancer
File:Lymphoepithelioma met to LN 6.jpg
Metastatic nasopharyngeal carcinoma in a lymph node
Classification and external resources
Specialty Oncology
ICD-10 C11
ICD-9 147
OMIM 161550
DiseasesDB 8814
eMedicine ped/1553
NCI Nasopharynx cancer
Patient UK Nasopharynx cancer
MeSH D009303

Nasopharynx cancer or nasopharyngeal carcinoma (NPC) is the most common cancer originating in the nasopharynx, the uppermost region of the pharynx ("throat"), behind the nose where the nasal passages and auditory tubes join the remainder of the upper respiratory tract. NPC occurs in children and adults. NPC differs significantly from other cancers of the head and neck in its occurrence, causes, clinical behavior, and treatment. It is vastly more common in certain regions of East Asia and Africa than elsewhere, with viral, dietary and genetic factors implicated in its causation. It is most common in males. It is a squamous cell carcinoma or an undifferentiated type. Squamous epithelial cells are a flat type of cell found in the skin and the membranes that line some body cavities. Differentiation means how different the cancer cells are from normal cells. Undifferentiated is a word used to describe cells that do not have their mature features or functions.

Signs and symptoms

Swelling of the lymph nodes in the neck is the initial presentation in many people, and the diagnosis of NPC is often made by lymph node biopsy. Signs and symptoms related to the primary tumor include trismus, pain, otitis media, nasal regurgitation due to paresis (loss of or impaired movement) of the soft palate, hearing loss and cranial nerve palsy (paralysis). Larger growths may produce nasal obstruction or bleeding and a "nasal twang". Metastatic spread may result in bone pain or organ dysfunction. Rarely, a paraneoplastic syndrome of osteoarthropathy (diseases of joints and bones) may occur with widespread disease.


Nasopharyngeal carcinoma (NPC) is caused by a combination of factors: viral, environmental influences, and heredity.[1] The viral influence is associated with infection with Epstein-Barr virus (EBV).[2][3] The Epstein-Barr virus is one of the most common viruses. 95 percent of all people in the U.S. are exposed to this virus by the time they are 30–40 years old. The World Health Organization does not have set preventative measures for this virus because it is so easily spread and is worldwide. Very rarely does Epstein-Barr virus lead to cancer, which suggests a variety of influencing factors. Other likely etiological factors include genetic susceptibility, consumption of food (in particular salted fish)[4] containing carcinogenic volatile nitrosamines.[5]

The association between Epstein-Barr virus and nasopharyngeal carcinoma is unequivocal in World Health Organization (WHO) types II and III tumors but less well-established for WHO type I (WHO-I) NPC, where preliminary evaluation has suggested that human papillomavirus HPV may be associated.[6] EBV DNA was detectable in the blood plasma samples of 96% of patients with non-keratinizing NPC, compared with only 7% in controls.[3] The detection of nuclear antigen associated with Epstein-Barr virus (EBNA) and viral DNA in NPC type 2 and 3, has revealed that EBV can infect epithelial cells and is associated with their transformation. The etiology of NPC (particularly the endemic form) seems to follow a multi-step process, in which EBV, ethnic background, and environmental carcinogens all seem to play an important role. More importantly, EBV DNA levels appear to correlate with treatment response and may predict disease recurrence, suggesting that they may be an independent indicator of prognosis. The mechanism by which EBV alters nasopharyngeal cells is being elucidated[7] to provide a rational therapeutic target.[7]



Nasopharyngeal carcinoma, commonly known as nasopharyngeal cancer, is classified as a malignant neoplasm, or cancer, arising from the mucosal epithelium of the nasopharynx, most often within the lateral nasopharyngeal recess or fossa of Rosenmüller (a recess behind the entrance of the eustachian tube opening). The World Health Organization classifies nasopharyngeal carcinoma in three types. Type 1 (I) is keratinizing squamous cell carcinoma. Type 2a (II) is non-keratinizing squamous cell carcinoma. Type 2b (III) is undifferentiated carcinoma.[8] Type 2b (III) nonkeratinizing undifferentiated form also known as lymphoepithelioma is most common, and is most strongly associated with Epstein-Barr virus infection of the cancerous cells.[9]


File:PET-CT scan of nasopharyngeal cancer.jpg
FDG-PET/CT scan of a patient with nasopharyngeal cancer. Transverse slice demonstrating FDG-positive primary site

Staging of nasophayngeal carcinoma is based on clinical and radiologic examination. Most patients present with Stage III or IV disease.

Stage I is a small tumor confined to nasopharynx.

Stage II is a tumor extending in the local area, or that with any evidence of limited neck (nodal) disease.

Stage III is a large tumor with or without neck disease, or a tumor with bilateral neck disease.

Stage IV is a large tumor involving intracranial or infratemporal regions, an extensive neck disease, and/or any distant metastasis. [10]


Nasopharyngeal carcinoma can be treated by surgery, by chemotherapy, or by radiotherapy.[11] The expression of EBV latent proteins within undifferentiated nasopharyngeal carcinoma can be potentially exploited for immune-based therapies.[12]


Nasopharynx cancer as of 2010 resulted in 65,000 deaths globally up from 45,000 in 1990.[13]

NPC is uncommon in the United States and most other nations, representing less than 1 case per 100,000 in most populations.[2] but is extremely common in southern regions of China,[14] particularly in Guangdong, accounting for 18% of all cancers in China.[5] It is sometimes referred to as Cantonese cancer because it occurs in about 25 cases per 100,000 people in this region, 25 times higher than the rest of the world.[5] It is also quite common in Taiwan.[5] This could be due to the South East Asian diet which typically includes consumption of salted vegetables, fish and meat.[5] While NPC is seen primarily in middle-aged persons in Asia, a high proportion of African cases appear in children. The cause of increased risk for NPC in these endemic regions is not clear.[9] In low-risk populations, such as in the United States, a bimodal peak is observed. The first peak occurs in late adolescence/early adulthood (ages 15–24 years), followed by a second peak later in life (ages 65–79 years).

See also


  1. Zhang F, Zhang J. (1999). "Clinical hereditary characteristics in nasopharyngeal carcinoma through Ye-Liang's family cluster". Chinese Medical Journal 112 (2): 185–7. PMID 11593591. 
  2. 2.0 2.1 "Initiative for Vaccine Research (IVR): Viral cancers". World Health Organization. Retrieved 2 October 2012. 
  3. 3.0 3.1 Lo KW, Chung GT, To KF. Deciphering the molecular genetic basis of NPC through molecular, cytogenetic, and epigenetic approaches. Semin Cancer Biol. 2012 Apr;22(2):79–86. doi: 10.1016/j.semcancer.2011.12.011. PMID 22245473
  4. Yu, M. C.; Ho, J. H.; Lai, S. H.; Henderson, B. E. (1986). "Cantonese-style salted fish as a cause of nasopharyngeal carcinoma: Report of a case-control study in Hong Kong". Cancer Research 46 (2): 956–961. PMID 3940655. 
  5. 5.0 5.1 5.2 5.3 5.4 Chang E T, Adami H (2006). "The Enigmatic Epidemiology of Nasopharyngeal Carcinoma". Cancer Epidemiol Biomarkers Prev 15 (10): 1765–1777. PMID 17035381. doi:10.1158/1055-9965.EPI-06-0353. 
  6. Lo EJ, Bell D, Woo JS, et al. Human papillomavirus and WHO type I nasopharyngeal carcinoma. Laryngoscope. 2010 Oct;120(10):1990–7. doi: 10.1002/lary.21089. PMID 20824783
  7. 7.0 7.1 Lo AK, Lo KW, Ko CW et al. Inhibition of the LKB1-AMPK Pathway by the Epstein-Barr Virus-encoded LMP1 Promotes Proliferation and Transformation of Human Nasopharyngeal Epithelial Cells. J Pathol. 2013 Apr 17. doi: 10.1002/path.4201. PMID 23592276
  8. Cummings Otolaryngology. 5th ed. (2010). Chapter 99. pg 1344
  9. 9.0 9.1 Richard Cote, Saul Suster, Lawrence Weiss, Noel Weidner (Editor) (2002). Modern Surgical Pathology (2 Volume Set). London: W B Saunders. ISBN 0-7216-7253-1. 
  10. AJCC Cancer Staging Manual. 7th ed. New York, NY: Springer, 2010, pp 41–56.
  11. Brennan, Bernadette (June 26, 2006). "Nasopharyngeal carcinoma" (PDF). Orphanet Journal of Rare Diseases 1:23: 1–5. doi:10.1186/1750-1172-1-23. 
  12. Khanna, Rajiv; Denis Moss and Maher Gandhi (1 March 2005). "Technology Insight: applications of emerging immunotherapeutic strategies for Epstein-Barr virus-associated malignancies". Nature Reviews Clinical Oncology 2: 138–149. doi:10.1038/ncponc0107. 
  13. Lozano, R (Dec 15, 2012). "Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: a systematic analysis for the Global Burden of Disease Study 2010.". Lancet 380 (9859): 2095–128. PMID 23245604. doi:10.1016/S0140-6736(12)61728-0. 
  14. Fang W, Li X, Jiang Q, (2008). "Transcriptional patterns, biomarkers and pathways characterizing nasopharyngeal carcinoma of Southern China". J Transl Med 6: 32. PMC 2443113. PMID 18570662. doi:10.1186/1479-5876-6-32. 

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