Results 51 to 60 of about 17,830 (205)

Origins of T‐cell‐mediated autoimmunity in acquired aplastic anaemia

British Journal of Haematology, Volume 206, Issue 4, Page 1035-1053, April 2025.
Acquired aplastic anaemia (AA) is an autoimmune bone marrow failure disease caused by a cytotoxic T‐cell–mediated attack on haematopoietic stem and progenitor cells (HSPCs). Despite significant progress in understanding T‐cell repertoire alterations in AA, the identification of specific pathogenic T cells remains elusive.
Aura Enache, Shannon A. Carty, Daria V. Babushok   +2 more
wiley   +1 more source

Subdural Hematoma in Grave’s Disease Induced Thrombocytopenia. [PDF]

, 2013
Subdural hematoma (SDH) usually occurs secondary to trauma, in bleeding disorders it may occur spontaneously. It is a rare complication of immune thrombocytopenia.
Chandek, S, Diwan, S, Kakani, A, Kumar, S, Nitey, PO   +4 more
core   +1 more source

Thrombotic thrombocytopenic purpura [PDF]

, 2015
Thrombotic thrombocytopenic purpura (TTP) is a disease with a high rate of mortality if a proper treatment is not instated. Plasmapheresis with plasmatic exchange is the treatment of choice. Diagnosis is performed demonstrating microangiopathic hemolytic
Gómez Almaguer, David, Tellez Hinojosa, Carlos Alberto, Vázquez Mellado, Alberto   +2 more
core   +1 more source

A New Diagnostic Approach for Myelodysplastic Neoplasms Using a Combination of Scores Based on Flow Cytometry and Automated Hematology Sysmex XN Analyzers

International Journal of Laboratory Hematology, Volume 47, Issue 2, Page 236-245, April 2025.
ABSTRACT Introduction The first‐step in diagnosis of myelodysplastic neoplasms (MDS) is essentially based on bone marrow cytomorphology. However, cytomorphology of MDS is often a difficult exercise, subject to inter‐operator variability. Our study aims to evaluate whether the combination of two dysplasia scores, the extended Ogata score and the MDS‐CBC
Ludovic Firrera, Benjamin Podvin, Julien Herlem, Marion Magierowicz, Alexandre Willaume, Vincent Thibaud, Agnès Charpentier   +6 more
wiley   +1 more source

Eltrombopag for the treatment of immune thrombocytopenia: The aegean region of Turkey experience [PDF]

, 2015
Objective: Immune thrombocytopenia (ITP) is an immune-mediated disease characterized by transient or persistent decrease of the platelet count to less than 100x109/L. Although it is included in a benign disease group, bleeding complications may be mortal.
Alacacıoğlu, İ., Arslan, Ö., Bilgir, O., Bolaman, Z., Büyükkeçeci, F., Ceylan, C., Gökgöz, Z., Görgün, G., Kabukçu, Sibel, Kadıköylü, G., Kahraman, S., Keskin, A., Kiper, H.D., Payzın, B., Saydam, G., Sevindik, Ö.G., Tombuloğlu, M., Vural, F., Çağlıyan, G.A., Özcan, M.A., Özdemirkıran, F., Şahin, F.   +21 more
core   +3 more sources

Occurrence of immune thrombocytopenic purpura in a patient with essential thrombocythemia: How the immune system can overcome a neoplastic clone

Clinical Case Reports, 2020
Our case highlights the possible coexistence of essential thrombocythemia (ET) and idiopathic thrombocytopenic purpura (ITP), two pathological entities with opposite clinical and laboratory manifestations.
Antonio Carruale, Francesco Longu, Francesca Mura, Giovanni Caocci, Giorgio La Nasa, Claudio Fozza   +5 more
doaj   +1 more source

A case of human parvo virus B 19 infection with erythroid hypoplasia and Idiopathic thrombocytopenic purpura in an immunocompetent child: a case report [PDF]

, 2016
Human parvo virus B19 (B19V) is a small (5.5kb) single stranded DNA (deoxy ribo nucleic acid) virus with known tropism and cytotoxicity for erythroid progenitors.
D., Swaroopa Reddy, Patti, Ganesh, Y. S., Raju   +2 more
core   +2 more sources

Childhood Idiopathic Thrombocytopenic Purpura: A Retrospective Analysis Of Clinical Features And Response To Treatment

مجلة كلية الطب, 2006
Background : A retrospective study was done in the Pediatric ward /AL-Kadhimiyia Teaching Hospital on cases diagnosed as idiopathic thrombocytopenic Purpura admitted since the first of January1992 – the end of December 2004.
Sawsan S. Abbas
doaj  

CAUSES OF DEVELOPMENT OF ACUTE AND CHRONIC THROMBOCYTOPENIA IN CHILDREN OF IRKUTSK REGION

Acta Biomedica Scientifica, 2018
Background. Immune thrombocytopenia in children is not a rare disease. Currently, this diagnosis is found in 2 times more often than 5-10 years ago. Acute immune thrombocytopenia is increasingly taking on a chronic course. Aims.
N. N. Martynovich, O. P. Tolmacheva, V. A. Khyshova   +2 more
doaj   +1 more source