Neurobrucellosis with Acquired Hemophagocytic Lymphohistiocytosis in a Two-Year-Old Bolivian Male
JL Razer, CM Miraglia - American Society for Clinical Laboratory …, 2016 - clsjournal.ascls.org
Hemophagocytic lymphohistiocytosis (HLH) is a rare hyper-inflammatory syndrome that may
be inherited or acquired. HLH may be a complication of infectious disease, including …
be inherited or acquired. HLH may be a complication of infectious disease, including …
Secondary hemophagocytic lymphohistocytosis in a child with brucellosis
E Pekpak, BS Cetin - Journal of Pediatric Hematology/Oncology, 2017 - journals.lww.com
Hemophagocytic lymphohistocytosis (HLH) is a potentially fatal hyperinflammatory
syndrome that is characterized by proliferation of histiocytes and hemophagocytosis in …
syndrome that is characterized by proliferation of histiocytes and hemophagocytosis in …
Brucellosis as a cause of hemophagocytic syndrome
Hemophagocytic lymphohistiocytosis (HLH) is a rare syndrome of excessive inflammation
and tissue destruction due to abnormal immune activation and inflammation. HLH can occur …
and tissue destruction due to abnormal immune activation and inflammation. HLH can occur …
Hemophagocytic lymphohistiocytosis associated with brucellosis
M Guo, L Zhang, K Chen, D Huang, C Feng… - … and Infectious Disease, 2024 - Elsevier
Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening immune disorder
categorized as familial HLH or secondary HLH. Our case report describes a 63-year-old …
categorized as familial HLH or secondary HLH. Our case report describes a 63-year-old …
[PDF][PDF] Brucellosis-induced hemophagocytic lymphohistiocytosis
J Al Noumani, I Al Busaidi, M Al Hajri, MK Al Hajri - Cureus, 2021 - cureus.com
Hemophagocytic lymphohistiocytosis (HLH) is a fatal syndrome, which can be primary or
triggered by a systemic disease or an infection. The commonly reported infectious causes of …
triggered by a systemic disease or an infection. The commonly reported infectious causes of …
Successful resolution of Hemophagocytic lymphohistiocytosis associated to brucellosis in the adult.
Hemophagocyticlymphohistocytosis (HLH) is a proliferation of histiocytes with
importanthemophagocytosisoccurring in different organs such as the spleen and the bone …
importanthemophagocytosisoccurring in different organs such as the spleen and the bone …
Secondary hemophagocytic lymphohistiocytosis in children with brucellosis: report of three cases
Y Yaman, S Gözmen, AK Özkaya, Y Oymak… - The Journal of Infection …, 2015 - jidc.org
Brucellosis is a systemic zoonotic infectious disease that may cause fever, fatigue, sweating,
arthritis, hepatosplenomegaly, cytopenia, and lymphadenopathy. It continues to be an …
arthritis, hepatosplenomegaly, cytopenia, and lymphadenopathy. It continues to be an …
[PDF][PDF] Hemofagositik Sendrom Sebebi Olarak Bruselloz
S AYDIN, Ö GÜNAL, MH TAŞKIN, A ATİLLA… - Mikrobiyol …, 2015 - researchgate.net
Hemophagocytic lymphohistiocytosis (HLH) is a rare syndrome of excessive inflammation
and tissue destruction due to abnormal immune activation and inflammation. HLH can occur …
and tissue destruction due to abnormal immune activation and inflammation. HLH can occur …
A rare hematological manifestation of brucellosis: reactive hemophagocytic syndrome
E Erduran, M Makuloglu, M Mutlu - Journal of Microbiology, Immunology …, 2010 - Elsevier
Hemophagocytic syndrome (HS) may be primary, or secondary, to malignancy, or to
metabolic, collagen vascular, and infectious diseases such as brucellosis, miliary …
metabolic, collagen vascular, and infectious diseases such as brucellosis, miliary …
[HTML][HTML] Secondary Hemophagocytic Lymphohistiocytosis in a Child with Brucellosis
A Karimi, A Solgi, Z Pourmoghaddas… - Archives of Pediatric …, 2020 - brieflands.com
: Brucellosis, with multi-organ involvement, is recognized as a zoonotic infection in Iran. This
infection has multiple signs and symptoms. On the other hand, hemophagocytic …
infection has multiple signs and symptoms. On the other hand, hemophagocytic …