Large Granular Lymphocytic Leukemia is a rare disease characterized by unexplained elevation in large granular lymphocytes in the blood.
These cells cause the immune system to create antibodies to one’s own cells and kill them. This results in anemia, low white blood cells and platelets
No prevalence information has been added yet.
Human T-lymphotropic virus type 1 ( HTLV-1 ) is thought to be one of the factors involved in developing T-LGL in some people.
References:
http://en.wikipedia.org/wiki/Human_T-lymphotropic_virus
http://www.moffitt.org/ccjroot/v5n1/article3.html
Many will find this illness when being checked for something else
It is sometimes referred to as “indolent” because it can be slow growing. Less common are more aggressive forms. Patients are prone to infections (mainly skin, respiratory). Fatigue with or without anemia. Large spleen.
Fibromyalgia – widespread joint pain – has been reported as an attendent secondary diagnosis.
We don't have any symptoms yet.
No diagnosis information has been added yet.
Flow Cytometry, Bone Marrow Biopsy
We don't have any tests yet.
Some may never need treatment. Majority will require treatment at some point. The first line of treatment is methotrexate and then cyclosporine. Other treatment options include cytoxan, CAMPATH, fludarabine and pentostatin.
A leading T-LGL expert, Dr. Loughran, published a paper Dec 29, 2010, “How I treat LGL leukemia.”Look near the end to see “Our therapeutic recommendation” and the following flow chart. http://bloodjournal.hematologylibrary.org/content/117/10/2764.full.pdf
We don't have any treatments yet.
No prognosis information has been added yet
We don't have any tips yet.
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