Results 91 to 100 of about 21,085 (234)

Safety of Lowering the Platelet Transfusion Threshold Before Central Venous Catheterisation in Patients With Haematological Diseases

European Journal of Haematology, EarlyView.
ABSTRACT Introduction Central venous catheter (CVC) insertion is frequently required in patients with haematological diseases. Despite limited evidence, thrombocytopenia often prompts prophylactic platelet transfusion before catheterisation. Methods We conducted an observational before‐and‐after study including the first non‐tunnelled CVC insertion ...
Mathias Lazarevic Lindblad, Elin Pålsson, Vladimir Lazarevic, Leila Naddi, Ola Borgquist, Lars Nilsson, Maria Adrian, Björn P. Bark, Thomas Kander   +8 more
wiley   +1 more source

Secondary Hemophagocytic Lymphohistiocytosis in Turkish Children

, 2005
: Between January 1998 and January 2005, a total of 18 children 2 weeks–72 months of age were diagnosed as having secondary hemophagocytic lymphohistiocytosis.
Cengiz, Bulent, Gurgey, A, Kara, A, Gumruk, Fatma, Ceyhan, Mehmet, Ceyhan, M, Secmeer, Gulten, Gurgey, Aytemiz, Kuskonmaz, Baris, Cetin, M, Cengiz, B, Cetin, Mualla, Secmeer, G, Tavil, B, Tavil, Betül, Ozen, Hasan, Kushkonmaz, BÜLENT BARIŞ   +16 more
core   +1 more source

ICSH Guidance on Bone Marrow Examination and Reporting

International Journal of Laboratory Hematology, EarlyView.
ABSTRACT Examination of the bone marrow (BM) remains fundamental to the diagnosis, classification, prognostication, and monitoring of hematolymphoid and other disorders affecting blood cell production. Since publication of the International Council for Standardization in Haematology (ICSH) guideline in 2008, advances in diagnostic technologies, disease
Wendy N. Erber, Alexandar Tzankov, Olga Pozdnyakova, Hiromichi Matsushita, Gina Zini, Leonie Saft, on behalf of the International Council for Standardization in Haematology   +6 more
wiley   +1 more source

Comparison of the HemoScreen Point‐Of‐Care Haematology Analyser With Sysmex XN, Beckman Coulter DxH 560 and HORIBA Yumizen H550 in Patients With Abnormal Blood Counts

International Journal of Laboratory Hematology, EarlyView.
ABSTRACT Introduction HemoScreen is a portable point‐of‐care testing (POCT) haematology analyser capable of measuring 20 complete blood count (CBC) parameters, including a 5‐part leukocyte differential, from venous and capillary blood. This study compared selected CBC and white blood cell (WBC) differential parameters obtained using HemoScreen with ...
Katarína Hradská, Martin Pulcer, Michaela Skořupová, Tereza Popková, Michal Kaščák, Jana Mihályová, Ivo Demel, Barbora Dluhošová, Kateřina Benková, Juraj Ďuraš, Soňa Kolářová, Veronika Hanzelková, Simona Pulcerová, Roman Hájek   +13 more
wiley   +1 more source

Secondary Dengue Infection Complicated by Hemophagocytic Lymphohistiocytosis: A Case Report

Case Reports in Infectious Diseases
Hemophagocytic lymphohistiocytosis is a fatal hyperinflammatory disorder in which CD8+ cytotoxic T-cells, natural killer cells, and macrophages destroy hematopoietic cells and vital organs. Viral infections, such as Epstein–Barr virus, are known to cause
Dominique D. Davis, Saffett Guleryuz, Yehuda Galili, Pablo A. Bejarano   +3 more
doaj   +1 more source

Disseminated tuberculosis and hemophagocytic syndrome although TB prophylaxis in patients with inflammatory bowel disease treated with Infliximab

IDCases, 2019
Purpose: We present de case of a 27-year-old woman admitted to ICU after scheduled splenectomy to study her short course of fever, leukopenia and splenic space-occupying lesions and splenomegaly.
Modesto Martínez-Pillado, Marina Varela-Durán, Ismael Said-Criado, Pilar Díaz-Parada, María Rodríguez-Losada, María Mendoza-Pintos   +5 more
doaj   +1 more source

Hemophagocytic lymphohistiocytosis: A diagnostic conundrum

Journal of Pediatric Neurosciences, 2017
Hemophagocytic lymphohistiocytosis (HLH) is a syndrome of excessive immune activation causing widespread inflammation and tissue destruction leading to multi-organ dysfunction and failure. Making the diagnosis of HLH could be quite challenging due to the broad range of presenting symptoms and their lack of specificity.
Grzybowski, Brittany, Vishwanath, Vijay A.   +1 more
openaire   +3 more sources

Pediatric Stevens–Johnson Syndrome and Toxic Epidermal Necrolysis Hospitalizations in the United States

Pediatric Dermatology, EarlyView.
ABSTRACT Stevens–Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are rare life‐threatening mucocutaneous reactions that remain poorly characterized in pediatric populations. Using the Healthcare Cost and Utilization Project (HCUP) Kids' Inpatient Database (KID), the prevalence of SJS/TEN hospitalizations declined from 0.02% in 2016 to 0.009%
Shazli Razi, Priya Agarwal, Gaurav N. Pathak, Christian Kaunzinger, Aaron Morgan, Babar K. Rao   +5 more
wiley   +1 more source

CASE REPORT Familial Hemophagocytic Lymphohistiocytosis in Two Brothers

, 2014
Familial hemophagocytic lymphohistiocytosis is a disorder which presents with fever, pancytopenia, liver dysfunction and also an increase in non-malignant histiocytes with prominent hemophagocytosis in various organs.
Medical Centre, Hematology Unit, Subang Jaya   +2 more
core  

Primary Hemophagocytic Lymphohistiocytosis in a Newborn Child

, 2014
The article presents the data of clinical observation of hemophagocytic lymphohistiocytosis in newborn child, complicated with spontaneous splenic rupture. Issues of diagnosis according to the recommendations of the International society for the study of
T.A. Khalturina, V.P. Kandyba, O.A. Zorya, M.I. Perkhun, V.A. Klimenko, O.V. Piontkovskaya, A.I. Kozhemyaka, A.V. Postnikov   +7 more
core   +1 more source