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Extranodal NK-T-cell lymphoma natural history, complications and prognosis

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ramyar Ghandriz MD[2] Sowminya Arikapudi, M.B,B.S. [3]

Overview

Overview

If left untreated, patients with extranodal NK-T-cell lymphoma, nasal type may progress to develop proptosis and hard palate perforation. Common complications of extranodal NK-T-cell lymphoma include hepatosplenomegaly and pancytopenia. Depending on the extent of the tumor at the time of diagnosis, the prognosis may vary. Prognosis is generally regarded as poor.

Natural History

Natural History

  • Extranodal NK-T-cell lymphoma almost always shows an extranodal presentation.[1][2]
  • Some cases may be accompanied by secondary lymph node involvement although rare instances of primary lymph node disease in the absence of extranodal involvement has been reported.
  • Extension to adjacent tissues such as the nasopharynx, paranasal sinuses, orbit, oral cavity, palate, and oropharynx are possible.
  • Retro-orbital involvement causes proptosis and impairment of extraocular movement.
  • Occasionally local extension from the nasal cavity causes destruction of the hard palate with the characteristic midline perforation, previously referred to as “lethal midline granuloma”.
  • At presentation, the disease is often localized to the upper aerodigestive tract.
  • Disseminated disease may have involvement of the lymph nodes, bone marrow and peripheral blood.
Complications

Complications

  • Extranodal NK-T-cell lymphoma, nasal type, often develop hemophagocytic syndrome. (uncontrolled activation of certain parts of the immune system)[3]
  • Hemophagocytic syndrome results in
Prognosis

Prognosis

  • The prognosis for people with extranodal NK-T-cell lymphoma is often poor and the risk for relapse is high.[3]
  • People with extranodal NK-T-cell lymphoma confined to the nose or nasal passages have a better prognosis than those people with more widespread disease.
  • The International Prognostic Index (IPI) predicts outcome in nasal NK-T-cell lymphoma.[4]
  • Patients with International Prognostic Index of 1 or less were shown to have a better overall survival.
  • In a recent retrospective analysis of 172 patients with extranodal NK-T-cell lymphoma, nasal type 4 prognostic factors were identified :
  • Nonnasal type
  • Stage
  • Performance status
  • Number of extranodal sites
  • In a Korean prognostic model, four prognostic groups have been identified depending on :
References

References

  1. Extranodal NK-/T-cell lymphoma, nasal type. Surveillance, Epidemiology, and End Results Program. http://seer.cancer.gov/seertools/hemelymph/51f6cf56e3e27c3994bd530f/. Accessed on February 04, 2016
  2. Extranodal Natural-Killer/T-Cell Lymphoma, Nasal Type. Hindawi Publishing Corporation. http://www.hindawi.com/journals/ah/2010/627401/. Accessed on February 19, 2016
  3. 3.0 3.1 Extranodal NK/T-cell lymphoma, nasal type. Canadian Cancer Society. http://www.cancer.ca/en/cancer-information/cancer-type/non-hodgkin-lymphoma/non-hodgkin-lymphoma/types-of-nhl/extranodal-nk-t-cell-lymphoma-nasal-type/?region=on. Accessed on February 04, 2016
  4. Extranodal Natural-Killer/T-Cell Lymphoma, Nasal Type. Hindawi. http://www.hindawi.com/journals/ah/2010/627401/. Accessed on February 04, 2016


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