Results 81 to 90 of about 163,193 (205)

Combined nutritional anemia coexisting with microcytic anemia

, 2013
Objective: Iron deficiency is a leading cause of microcytic anemia for children. On the other hand, B12 deficiency, which is a relatively rare event than iron deficiency, coexists with macrocytic anemia.
Saygi, Semra, Demirbilek, HÜSEYİN, Soker, Murat, Aliosmanoglu, Cigdem, Yildirim, Aysen Turedi   +4 more
core   +1 more source

Neuropathy caused by B12 deficiency in a patient with ileal tuberculosis: A case report

Journal of Medical Case Reports, 2008
Introduction Vitamin B12 deficiency can result in macrocytic anemia. Neurologic abnormalities of B12 deficiency include sensory deficits, loss of deep tendon reflexes, movement disorders, neuropsychiatric changes and seizures.
Toosi Taraneh, Shahi Farhad, Afshari Ali, Roushan Nader, Kermanshahi Marjan   +4 more
doaj   +1 more source

Acute Fulminant Systemic Granulocytic Vasculitis Involving Arteries and Veins in Vacuoles, E1 Enzyme, X‐Linked, Autoinflammatory, Somatic (VEXAS) Syndrome: An Autopsy Case Report

Pathology International, Volume 76, Issue 9, September 2026.
We report an autopsy case of VEXAS syndrome presenting with aggressive clinical course. Pathologically, the disease manifested as systemic granulocytic vasculitis affecting both arteries and veins, characterized by the presence of histiocytoid myeloid cells associated with low‐risk MDS.
Kayo Ueda, Masakazu Fujimoto, Yumi Shiroishi, Masafumi Ito, Masahiko Osawa, Mayumi Inaba   +5 more
wiley   +1 more source

A stepwise diagnostic approach for undiagnosed Anemia in children: A model for low-middle income country

, 2023
Background: Reaching a precise diagnosis in rare inherited anemia is extremely difficult and challenging, especially in areas with limited use of genetic studies, which makes undiagnosed anemia a unique clinical entity in tertiary hematology centers.
Ragab I. A., Aly N. H., Elalfy M. S., Iolascon A., Andolfo I., Elhabashy S. A., Russo R., Mowafy N. M.   +7 more
core   +1 more source

Large granular lymphocyte leukemia serum and corresponding hematological parameters reveal unique cytokine and sphingolipid biomarkers and associations with STAT3 mutations

Cancer Medicine, 2020
Large granular lymphocyte (LGL) leukemia is a rare hematological disorder with expansion of the T‐cell or natural killer (NK) cell lineage. Signal transducer and activator of transcription 3 (STAT3) exhibits somatic activating mutations in 30%‐40% of LGL
Kristine C. Olson, Katharine B. Moosic, Marieke K. Jones, Paige M. K. Larkin, Thomas L. Olson, Mariella F. Toro, Todd E. Fox, David J. Feith, Thomas P. Loughran Jr   +8 more
doaj   +1 more source

Optimizing diagnostic thresholds of total vitamin B12 (B12) for identifying cobalamin deficiency in adults with macrocytic anemia

Objectives: Identifying individuals with vitamin B12 (B12) deficiency is challenging due to poor harmonization across total B12 assays. To establish clinically meaningful thresh olds for the Roche assay, we characterized B12 concentra tions ...
Zuccotti, Gianvicenzo, Cesana, Bruno Mario, Montagnana, Martina, Campigotto E., Zuccotti G., Tosi, Martina, Plebani, Mario, Ferraro, Simona, Tosi M., Cesana B. M., Musso, Giulia, Lalli L., Lalli, Luca, Pelloso M., Plebani M., Campigotto, Edoardo, Musso G., Montagnana M., Ferraro S., Pelloso, Michela   +19 more
core   +1 more source

Recognizing missed opportunities to diagnose and treat iron deficiency anemia: A study based on prevalence of anemia among children in a teaching hospital

Journal of Family Medicine and Primary Care, 2019
Background: In developing world, anemia is a significant cause of mortality and morbidity in children under 5 years of age. Iron deficiency anemia (IDA) is a very important causative factor for childhood anemia.
Dipshikha Maiti, Suchi Acharya, Surupa Basu   +2 more
doaj   +1 more source

Rud′s syndrome

Indian Dermatology Online Journal, 2014
Rud′s syndrome is a rare autosomal recessive hereditary disorder characterized by congenital ichthyosis, epilepsy, dwarfism, sexual infantilism, polyneuritis, and macrocytic anemia.
K Pavani, B. S. N. Reddy, B Amar Singh
doaj   +1 more source

Peripheral Blood and Bone Marrow Changes in Chronic Renal Failure (Investigation of 50 Cases) [PDF]

Acta Medica Iranica, 1973
Anemia and morphological features of the hemopoietic system in 50 Iranian patients suffering from chronic uremia was investigated. The results were compared with the results observed by others; our findings in most instances are nearly in accordance but ...
Seyed Nasroiah Sayar, Mohsen Naficy   +1 more
doaj   +1 more source

Onset of X-linked sideroblastic anemia in the fourth decade

Haematologica, 2004
We report the case of a 40-year female who manifested late onset, pyridoxine-refractory X-linked sideroblastic anemia, heterozygous for the first described frameshift ALAS2 mutation, CD506-507 (-C).
E Cortesao, J Vidan, J Pereira, P Goncalves, ML Ribeiro, G Tamagnini   +5 more
doaj