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Updated: Oct 29, 2025

Macrophage Differentiation and Polarization into an M2-Like Phenotype using a Human Monocyte-Like THP-1 Leukemia Cell Line
Published on: August 2, 2021
[Macrophagic activation syndrome revealing Hodgkin lymphoma: an individual case]
Ghita Elghouat1, Ilham Karrati1, Raja Nakhli1
1Laboratoire d'hématologie, Centre Hospitalier Universitaire Mohamed-VI, Marrakech, Maroc, Faculté de médecine et de pharmacie, Université Cadi Ayyad, Marrakech, Maroc.
Abstract:
Macrophagic activation syndrome (SAM) or Hemophagocytic lymphohistiocytosis is a clinical-biological entity of non-specific proliferation and activation of macrophages of the reticulohistiocytic system, with phagocytosis of the figurative elements of blood. It is a rare pathology combining non-specific clinical and biological signs and images of hemophagocytosis. It can be primary or acquired secondary to an infection, an autoimmune or neoplastic disease. While T or NK lymphomas are the classic causes of reactive SAM and its association with Hodgkin lymphoma is exceptional. This is a diagnostic and therapeutic emergency given the risk of development towards a fatal multivisceral failure due to an absence of appropriate support. This is a report of a case of SAM revealing a case of Hodgkin lymphoma in a 35-year-old patient.

