Mycosis fungoides natural history, complications and prognosis

Revision as of 14:19, 25 January 2016 by Sowminya Arikapudi (talk | contribs)
Jump to navigation Jump to search

Cutaneous T cell lymphoma Microchapters

Home

Patient Information

Overview

Classification

Mycosis fungoides
Sezary syndrome

Pathophysiology

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

Overview

If left untreated, cutaneous T cell lymphoma may progress to develop patches , plaque, and tumors. Depending on the extent of the lymphoma at the time of diagnosis, the prognosis may vary.

Natural history[1]

  • Cutaneous T cell lymphoma is usually initially seen by dermatologists with patients presenting with skin lesions
  • Patients often have a history of several years of eczematous or dermatitic skin lesions before the diagnosis is finally established
  • The skin lesions then progress from the patch stage to the plaque stage to cutaneous tumors

Prognosis[2]

  • Cutaneous T cell lymphoma is usually a slow-growing (indolent) lymphoma
  • The prognosis for people with cutaneous T cell lymphoma is based on the extent of disease and how the person responds to treatment
  • Although more advanced stages of cutaneous T cell lymphoma may not be cured, the lymphoma can still be controlled with treatment

Favorable prognosis

  • Early stage disease
  • Lymphoma is confined to the skin

Unfavorable prognosis

  • More advanced disease
  • Lymphoma has spread to lymph nodes
  • Lymphoma has spread to other organs


References

  1. Mycosis fungoides. Radiopaedia.http://radiopaedia.org/articles/mycosis-fungoides Accessed on January 20, 2016
  2. Cutaneous T cell lymphoma. Canadian Cancer Society. http://www.cancer.ca/en/cancer-information/cancer-type/non-hodgkin-lymphoma/non-hodgkin-lymphoma/types-of-nhl/cutaneous-t-cell-lymphoma/?region=on Accessed on January 19, 2016


Template:WikiDoc Sources