Pathogenesis of Hemophagocytic Lymphohistiocytosis/Macrophage Activation Syndrome: A Case Report and Review of the Literature.
Chiara GioiaMarino ParoliRaffaella IzzoLorenzo Di SanzoElisabetta RossiPasquale PignatelliDaniele AccapezzatoPublished in: International journal of molecular sciences (2024)
Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening condition characterized by the uncontrolled activation of cytotoxic T lymphocytes, NK cells, and macrophages, resulting in an overproduction of pro-inflammatory cytokines. A primary and a secondary form are distinguished depending on whether or not it is associated with hematologic, infectious, or immune-mediated disease. Clinical manifestations include fever, splenomegaly, neurological changes, coagulopathy, hepatic dysfunction, cytopenia, hypertriglyceridemia, hyperferritinemia, and hemophagocytosis. In adults, therapy, although aggressive, is often unsuccessful. We report the case of a 41-year-old man with no apparent history of previous disease and an acute onset characterized by fever, fatigue, and weight loss. The man was from Burkina Faso and had made trips to his home country in the previous five months. On admission, leukopenia, thrombocytopenia, increased creatinine and transaminases, LDH, and CRP with a normal ESR were found. The patient also presented with hypertriglyceridemia and hyperferritinemia. An infectious or autoimmune etiology was ruled out. A total body CT scan showed bilateral pleural effusion and hilar mesenterial, abdominal, and paratracheal lymphadenopathy. Lymphoproliferative disease with HLH complication was therefore suspected. High doses of glucocorticoids were then administered. A cytologic analysis of the pleural effusion showed anaplastic lymphoma cells and bone marrow aspirate showed hemophagocytosis. An Epstein-Barr Virus (EBV) DNA load of more than 90000 copies/mL was found. Bone marrow biopsy showed a marrow localization of peripheral T lymphoma. The course was rapidly progressive until the patient died. HLH is a rare but usually fatal complication in adults of hematologic, autoimmune, and malignant diseases. Very early diagnosis and treatment are critical but not always sufficient to save patients.
Keyphrases
- epstein barr virus
- diffuse large b cell lymphoma
- bone marrow
- case report
- weight loss
- multiple sclerosis
- mesenchymal stem cells
- computed tomography
- nk cells
- end stage renal disease
- liver failure
- newly diagnosed
- emergency department
- stem cells
- drug induced
- bariatric surgery
- induced apoptosis
- fine needle aspiration
- healthcare
- type diabetes
- pulmonary embolism
- magnetic resonance imaging
- prognostic factors
- peritoneal dialysis
- patient reported outcomes
- depressive symptoms
- image quality
- roux en y gastric bypass
- cell therapy
- contrast enhanced
- ultrasound guided
- endoplasmic reticulum stress
- physical activity
- cerebral ischemia
- signaling pathway
- blood brain barrier
- replacement therapy
- pi k akt
- sleep quality