Cutaneous T-cell lymphoma (CTCL) is a type of cancer that, as its name suggests, begins in a type of white blood cell, that is, T lymphocytes. According to the American Cancer Society, B lymphocytes also They can be affected by this pathology, although the primary and most common presentation is the one already mentioned.
Cutaneous lymphoma presents, in most cases, under a disorder called mycosis fungoides. Of course, we are facing an atypical pathology that is difficult to approach, since its causes and clinical manifestations are still not entirely clear. Here we present, then, everything you need to know about the disorder.
What is cutaneous lymphoma?
As we have said before, cutaneous lymphoma is an atypical type of cancer that has its origin in lymphocytes (white blood cells). According to the National Cancer Institute (NIH), under normal conditions, the bone marrow produces the precursors of these cells that will differentiate to produce antibodies and fight infections.
In this general term for skin cancers, the protective cells develop abnormalities that cause them to attack the skin. The misdirected attack causes a series of different types of skin lesions, which can be found in two different clinical pictures: mycosis fungoides and Sézary syndrome (a more aggressive form).
It should be noted that this entire clinical cluster is encompassed within the group of non-Hodgkin’s lymphomas, that is, a group of diseases of the lymphatic system that includes all lymphomas, except Hodgkin’s. The latter is a much more studied and well-known pathology.
How is it distributed in the world?
There are epidemiological studies that put the global situation of this group of diseases into perspective. Some essential data are the following:
The overall incidence of cutaneous lymphoma is 0.36 cases per 100,000 inhabitants per year.
80% of cutaneous lymphomas come from the clonal proliferation of T lymphocytes, with a very heterogeneous clinical and biological behavior.
We have little more information to provide worldwide, because as these bibliographic sources report, we are facing a pathology that has been a source of debate in the medical literature. It still poses detection problems in a good number of cases.
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