Angioimmunoblastic T-cell lymphoma associated with leukocytosis and lymphocytosis; a case report and systematic review
نویسندگان
چکیده
Angioimmunoblastic T-cell lymphoma associated with leukocytosis and lymphocytosis; a case report systematic review
منابع مشابه
CD56+ angioimmunoblastic T-cell lymphoma with evans syndrome : a case report and review of the literature.
A 67-year-old man was diagnosed with CD56(+) angioimmunoblastic T cell lymphoma (AITL), which was associated with autoimmune thrombocytopenic purpura (ATP) and autoimmune hemolytic anemia (AIHA) (Evans syndrome). The ATP was refractory to Helicobacter pylori eradication therapy and steroid. Complete remission (CR) of both AITL and AIHA was achieved with THP-COP chemotherapy (pirarubicin, cyclop...
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Oral cavity T-cell lymphoma occurs rarely. This case report describes a patient with such a tumor. The case was a 75 years old man presented with a painless swelling on his hard palate mucosa. He had suffered from nose- bleeding and nasal obstruction. Pathology revealed the presence of a T-cell lymphoma tumor in the palate. Though rare, the signs and symptoms of the case suggest that T-cell lym...
متن کامل[Angioimmunoblastic T-cell lymphoma: a case report and review of the literature].
Angioimmunoblastic T-cell lymphoma (AITL) is a rare, aggressive form of peripheral T-cell lymphoma that is characterized by lymphadenopathy, night sweats, fever, weight loss, and autoimmune phenomena. Cutaneous manifestations are present in up to 50% of cases. AITL comprises 1-2% of all nonHodgkin’s lymphomas. It typically presents in the seventh decade, however cases have been reported in adul...
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Angioimmunoblastic T cell lymphoma (AITL) is a rare but distinct type of T cell lymphoma with an aggressive course and high mortality. Most patients are diagnosed late in the disease and usually present with generalized lymphadenopathy. A minority have skin lesions at the time of diagnosis, more commonly in the form of nonspecific maculopapular rash with or without pruritus. We report a rare ca...
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Primary cutaneous CD30+ T cell lymphoma is rare lymphoma originally in and confined to the skin. These lymphomas usually present as a large solitary and often ulcerated nodule. Its prognosis is a good and has a good response to radiotherapy. We report a 34- year- old man who had primary cutaneous CD30+T cell lymphoma on his face, which presented as an ulcerated nodule.
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ژورنال
عنوان ژورنال: Iranian Journal of Blood and Cancer
سال: 2023
ISSN: ['2008-4595', '2008-4609']
DOI: https://doi.org/10.58209/ijbc.15.1.36