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Abstract
SYSTEMIC ALK-NEGATIVE ANAPLASTIC LARGE CELL LYMPHOMA: A CASE REPORT OF AN ASYMPTOMATIC PATIENT FROM SYRIA
Lujain Hamdan*, Souliman Diab, Zuheir Al-Shehabi and Michael Georgeos
ABSTRACT
Anaplastic large cell lymphomas (ALCLs) are uncommon malignancies; they include a group of CD30-positive Non-Hodgkin T-cell lymphomas that share similar morphologic and immunophenotypic features. The World Health Organization identifies 3 entities: primary cutaneous ALCL, anaplastic lymphoma kinase (ALK)-positive ALCL, and ALK-negative ALCL. ALK-negative ALCL is known for its aggressive behaviour and poor prognosis. It usually affects males at a median age of 55-60 years old. The majority of patients are presented with B symptoms and stage III–IV of the disease. Medical literature has reported very few cases of systemic ALK-negative ALCL. Here we demonstrate a unique case of a 47-year-old male, with no systemic symptoms, diagnosed with a stage IV, CD30+, ALK-negative ALCL presented with several tender, enlarged, inguinal lymph nodes and extranodal involvement in the skin, lung, liver and the bone marrow.
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