T-cell leukemia natural history, complications and prognosis: Difference between revisions

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==Overview==
==Overview==
==Natural History==
==Natural History==
* The natural history of adult T-cell leukemia varies between the different subtypes of the disease.  
* The natural history of adult T-cell leukemia varies between the different subtypes of the disease.<ref name="pmid18042693">{{cite journal| author=Matutes E| title=Adult T-cell leukaemia/lymphoma. | journal=J Clin Pathol | year= 2007 | volume= 60 | issue= 12 | pages= 1373-7 | pmid=18042693 | doi=10.1136/jcp.2007.052456 | pmc=PMC2095573 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=18042693  }} </ref>
* Usually patients with '''acute''' adult T-cell leukemia have an aggressive clinical course with a median survival period of less than 12 months. If left untreated, most of the patients with acute adult T-cell leukemia will develop systemic symptoms, lymphadenopathy, and organomegaly within a few weeks of diagnosis.
* Usually patients with '''acute''' adult T-cell leukemia have an aggressive clinical course with a median survival period of less than 12 months. If left untreated, most of the patients with acute adult T-cell leukemia will develop systemic symptoms, lymphadenopathy, and organomegaly within a few weeks of diagnosis.
* Usually patients with '''chronic''' adult T-cell leukemia will have an stable clinical course. If left untreated, most of the patients with chronic adult T-cell leukemia will develop lymphocytosis for months, or even years, before presenting with the typical skin manifestations.  
* Usually patients with '''chronic''' adult T-cell leukemia will have an stable clinical course. If left untreated, most of the patients with chronic adult T-cell leukemia will develop lymphocytosis for months, or even years, before presenting with the typical skin manifestations.  
* Most patients with '''smouldering''' adult T cell leukemia are initially asymptomatic. If left untreated, most of the patients with '''smouldering''' adult T cell leukemia will develop steroid-responsive skin rash and multiple lung infiltrates.  
* Most patients with '''smouldering''' adult T cell leukemia are initially asymptomatic. If left untreated, most of the patients with smouldering adult T cell leukemia will develop steroid-responsive skin rash and multiple lung infiltrates.  
==Complications==
==Complications==
* Common complications of adult T-cell leukemia include:
* Common complications of adult T-cell leukemia include:

Revision as of 19:26, 24 January 2016

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Haytham Allaham, M.D. [2]

Overview

Natural History

  • The natural history of adult T-cell leukemia varies between the different subtypes of the disease.[1]
  • Usually patients with acute adult T-cell leukemia have an aggressive clinical course with a median survival period of less than 12 months. If left untreated, most of the patients with acute adult T-cell leukemia will develop systemic symptoms, lymphadenopathy, and organomegaly within a few weeks of diagnosis.
  • Usually patients with chronic adult T-cell leukemia will have an stable clinical course. If left untreated, most of the patients with chronic adult T-cell leukemia will develop lymphocytosis for months, or even years, before presenting with the typical skin manifestations.
  • Most patients with smouldering adult T cell leukemia are initially asymptomatic. If left untreated, most of the patients with smouldering adult T cell leukemia will develop steroid-responsive skin rash and multiple lung infiltrates.

Complications

  • Common complications of adult T-cell leukemia include:
  • Cardiac arrhythmias (due to hypercalcaemia)
  • Opportunistic infections (due to defective immune system)
  • Bone fractures (due to lytic bone lesions)

Prognosis

References

  1. Matutes E (2007). "Adult T-cell leukaemia/lymphoma". J Clin Pathol. 60 (12): 1373–7. doi:10.1136/jcp.2007.052456. PMC 2095573. PMID 18042693.

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