Human T-lymphotropic virus (HTLV-1) is a retrovirus infecting CD4+ lymphocytes. This virus has a distinct geographical distribution (
1). It is prevalent in Japan, the Caribbean basin, certain regions of South America and Africa and in immigrants from these countries to other regions. (
2). In Iran, the main highly endemic regions for HTLV-1 are the Northeastern regions, particularly Mashhad and Neyshabur (
3).
Adult T‐cell leukemia (ATL) is a rare mature T‐cell neoplasm of post‐thymic lymphocytes etiologically linked to HTLV‐I. The disease manifests with leukemia in greater than two thirds of patients, while the remaining patients have a lymphomatous form. The clinical course is aggressive with a median survival of less than 12 months in the acute and lymphoma forms (
4).
Clinical form, age, performance status, elevation of lactate dehydrogenase (LDH), β2‐microglobulin, level of CD25, serum neuron‐specific enolase, the presence of hypercalcemia and a high proliferative rate are the main prognostic factors of ATL (
5,
6).
Serum levels of minerals may change during chronic infections. This also occurs in malignancies. Patients infected with ATL have all these conditions simultaneously. Therefore, the current study aimed to explore serum mineral levels of five patients with ATL referred to Imam Reza hospital, Mashhad, Iran.