Results 41 to 50 of about 6,796 (202)

Case Report: T‐Lymphoblastic Leukemia in a Dog With Erythrophagia

Veterinary Clinical Pathology, EarlyView.
ABSTRACT A 2‐year‐old male German Shepherd dog was presented with progressive weight loss, lethargy, and hyporexia. Hematologic analysis revealed a moderate macrocytic normochromic anemia and moderate thrombocytopenia. Additionally, a pronounced leukocytosis was observed, characterized by 33% large lymphoid cells, marked neutrophilia with a significant
Francisca B. Lang, Matheus Y. dos Santos, Vinicius N. Hirata, Felipe A. B. de Sousa, Augusto de Oliveira, Lucas T. de Castro, Rafael A. Fighera, Alexandre Krause   +7 more
wiley   +1 more source

Kikuchi-Fujimoto disease complicated by aseptic meningitis and hemophagocytosis successfully treated with intrathecal dexamethasone [PDF]

, 2020
Kikuchi-Fujimoto disease (KFD) is thought to be a self-limited disease featuring fever and cervical lymphadenopathy; most cases having a favorable outcome. Severe disease and death are occasionally reported.
Cai, J, Wang, Y, Huang, X, Tong, SW, Zhang, L, Deng, C, Chen, X   +6 more
core   +1 more source

In the Midst of a Cytokine Storm—The Hemophagocytic Syndrome (Hemophagocytic Lymphohistiocytosis/Macrophage Activation Syndrome)

Veterinary Clinical Pathology, EarlyView.
ABSTRACT Background Hemophagocytic syndrome (HPS)/hemophagocytic lymphohistiocytosis (HLH) is a life‐threatening hyperinflammatory syndrome characterized by immune dysregulation, cytokine overproduction, hemophagocytosis, cytopenias, and multiorgan dysfunction.
Joanne B. Messick
wiley   +1 more source

Bone marrow hemophagocytosis and immunological abnormalities in a patient with lysinuric protein intolerance

, 1997
Lysinuric protein intolerance (LPI) is an inborn error of amino acid transport characterized by a wide spectrum of clinical and biochemical abnormalities.
Tumer, L, Gursel, T, Kocak, U, Hasanoglu, A   +3 more
core   +1 more source

Febrile Pancytopenia and Hemophagocytosis From Disseminated Histoplasmosis in HIV/AIDS Patients: Two Cases and a Review of Combined Antifungal and Steroid Therapy

Case Reports in Infectious Diseases
Hemophagocytosis is a clinical condition characterized by the engulfment of bone marrow cellular elements, including erythrocytes, leukocytes, platelets, and their precursors, by activated macrophages.
Chinelo Animalu, Nupur Singh, Kenneth Cory Guice, Kase Maner   +3 more
doaj   +1 more source

Síndrome de ativação macrofágica em pacientes com artrite idiopática juvenil Macrophage activation syndrome in patients with juvenile idiopathic arthritis

Revista Brasileira de Reumatologia, 2004
A síndrome de ativação macrofágica (SAM) é uma complicação rara das doenças reumáticas crônicas, particularmente a artrite idiopática juvenil (AIJ) de início sistêmico.
Rogério do Prado, Maria Teresa R. A. Terreri, Cláudio A. Len, Josefina Braga, Maria Odete E. Hilário   +4 more
doaj   +1 more source

Prognostic Value of Skin Lesion Characteristics in Subcutaneous Panniculitis‐Like T‐Cell Lymphoma: A Retrospective Cohort Study Assessing the Applicability of T Category of the TNM Classification for Primary Cutaneous Lymphomas Other Than Mycosis Fungoides and Sézary Syndrome

International Journal of Dermatology, Volume 65, Issue 11, Page 2307-2314, November 2026.
Subcutaneous panniculitis‐like T‐cell lymphoma. Survival outcomes according to the presence of hemophagocytic lymphohistiocytosis (HLH) and T category. Relapse‐free survival was inferior in patients presenting with generalized (T3) skin lesions. Overall survival was poor in patients with HLH. Relapse‐free survival was also reduced in patients with HLH.
Myoung Eun Choi, Joon Min Jung, Soo Hyun Jeon, Chong Hyun Won, Sung Eun Chang, Mi Woo Lee, Woo Jin Lee   +6 more
wiley   +1 more source

Lymph node hemophagocytosis in rickettsial diseases: a pathogenetic role for CD8 T lymphocytes in human monocytic ehrlichiosis (HME)? [PDF]

, 2006
Background Human monocytic ehrlichiosis (HME) and Rocky Mountain spotted fever (RMSF) are caused by Ehrlichia chaffeensis and Rickettsia rickettsii, respectively.
Kerry L Dierberg, J Stephen Dumler, Dierberg Kerry L, Dumler J Stephen   +3 more
core   +2 more sources

Case report: Drug reaction with eosinophilia and systemic symptoms (DRESS)-induced hemophagocytic disorder

Frontiers in Pharmacology, 2022
Hemophagocytic disorders are severe and life-threatening conditions that can be genetic in origin [i.e., primary hemophagocytic lymphohistiocytosis (HLH)] or result from infections (i.e., secondary hemophagocytic lymphohistiocytosis), rheumatologic ...
Eliza I. Pope, Hosanna Au, Hosanna Au, Deborah M. Levy, Deborah M. Levy, Ruud H. J. Verstegen, Ruud H. J. Verstegen, Ruud H. J. Verstegen   +7 more
doaj   +1 more source

Hemophagocytosis in a patient with sickle cell disease [PDF]

Blood, 2016
![Figure][1] A 33-year-old man with history of sickle cell disease who receives regularly scheduled exchange transfusion and transfusions was found to be neutropenic. His absolute neutrophil count (ANC) initially recovered after administration of filgrastim; however, his ANC fell below 1000/
Irene, Thung, H Elizabeth, Broome
openaire   +2 more sources