imagebank.hematology.orgImageBank | Home | Regular Bank

tag): -- Main Navigation Account Navigation Main Content JavaScript is disabled on your browser Please enable JavaScript or upgrade to a JavaScript-capable browser to use the ASH Image Bank. ASH Home ASH Store ASH Academy Sign In Search Show Main Menu + ABOUT IMAGE BANK FAQ HELP PERMISSIONS COLLECTION Images of peripheral blood and/or bone marrow of blood disorders and normal hematopoiesis. ATLAS Normal and abnormal blood cells REFERENCE CASES Complete cases of common blood disorders (peripheral blood, bone marrow, and diagnostic studies). UPLOAD IMAGES Featured Image AML with NPM1 and FLT3 mutations Authors: Ke Xu, MD Category: AML with mutated NPM1 Published Date: 01 April 2021 AML with myelodysplasia related changes- Bone marrow aspirate Authors: Manisha Goel, MD, MBBS; Girish Venkataraman, MD, MBBS Category: Acute myeloid leukemia with myelodysplasia-related changes Published Date: 23 October 2020 Gaucher's disease: Cytochemical diagnosis Authors: DR. RUPALI PARIKH, BHATIA HOSPITAL, MUMBAI Category: Histiocyte/macrophage – storage disease Published Date: 01 April 2021 Cat Scratch Disease-H&E Low Power Authors: Reva Channah Goldberg; Girish Venkataraman, MD, MBBS; Megan Parilla Category: Cat Scratch Disease Published Date: 05 August 2019 Burkitt Lymphoma Authors: Timothy C Carll, MD; Girish Venkataraman, MD, MBBS Category: Burkitt Lymphoma Published Date: 23 March 2018 Explore Collection View all #00063465 Bare megakaryocyte nuclei (naked nuclei) peripheral blood 1 Mohammad Asees, MSc hematology, PhD CLS Micromeg Bare megakaryocyte nuclei (naked nuclei) p... Mohammad Asees, M... Micromeg #00063482 AML with NPM1 and FLT3 mutations Ke Xu, MD AML with muta AML with NPM1 and FLT3 mutations Ke Xu, MD AML with muta #00063487 Circulating megakaryocyte in peripheral blood smear Dr. Hind Al-Humaidan, MD, FRCPA;Dr. Mohammed Al Sharif, MD Megakary Circulating megakaryocyte in peripheral bl... Dr. Hind Al-Humai... Megakary #00063488 Gaucher's disease: Cytochemical diagnosis DR. RUPALI PARIKH, BHATIA HOSPITAL, MUMBAI Histiocyte/macrophage – storage disease Gaucher's disease: Cytochemical diagnosis DR. RUPALI PARIKH... Histiocyte/macrop... #00063483 Beta-thalassemia major Ke Xu, MD Beta-thalassemia Beta-thalassemia major Ke Xu, MD Beta-thalassemia #00063494 Bone Marrow Necrosis 5 Krunal Shah, DNB B-lymphoblastic leukemia/lymphoma Bone Marrow Necrosis 5 Krunal Shah, DNB B-lymphoblastic l... #00063493 Bone Marrow Necrosis 4 Krunal Shah, DNB B-lymphoblastic leukemia/lymphoma Bone Marrow Necrosis 4 Krunal Shah, DNB B-lymphoblastic l... #00063491 Bone Marrow Necrosis 2 Krunal Shah, DNB B-lymphoblastic leukemia/lymphoma Bone Marrow Necrosis 2 Krunal Shah, DNB B-lymphoblastic l... #00063492 Bone Marrow Necrosis 3 Krunal Shah, DNB B-lymphoblastic leukemia/lymphoma Bone Marrow Necrosis 3 Krunal Shah, DNB B-lymphoblastic l... #00063490 Bone Marrow Necrosis 1 Krunal Shah, DNB B-lymphoblastic leukemia/lymphoma Bone Marrow Necrosis 1 Krunal Shah, DNB B-lymphoblastic l... #00063489 Bi-Clonal CLL Maxwell Roth;Yanhua Wang Flow cytometry Bi-Clonal CLL Maxwell Roth;Yanh... Flow cytometry #00063484 Spontaneous bruising in a middle aged male Prarthna Bhardwaj MBBS, Chandravathi Loke MD Bleeding disorders Spontaneous bruising in a middle aged male Prarthna Bhardwaj... Bleeding disorders View all Category All categories Granulomatous Normal cells Lymph Node Blood cells Normal lymphocyte Normal eosinophil Normal monocyte Normal platelet Bone marrow cells (biopsy and aspirate) Megakaryocytes NK-cell enteropathy Myeloid/lymphoid neoplasms with PDGFRA rearrangement Morphologic variants of normal cells Morphologic variants of platelets/megakaryocytes Micromegakaryocytes Small platelets Grey platelet syndrome Hypogranular platelets Large and giant platelets May-Hegglin Morphologic variants of Red Blood Cells/precursors Normal Red blood cell morphology with resting lymphocyte for comparison Anisocytosis Macrocytosis Microcytosis Color Hypochromia Polychromasia Inclusions Coarse basophilic stippling Heinz body (supravital stain) Hemoglobin C crystals Hemoglobin H inclusions Howell-Jolly bodies nRBC Pappenheimer bodies Reticulocyte (supravital stain) Other Cold agglutinin Leukoerythroblastic picture Rouleaux Poikilocytosis Acanthocytes Blister cells Echinocytes (Burr) Elliptocytosis/ovalocytes Oxidative changes (bite cell) Schistocytes (Helmet, keratocyte) Sickle cells Spherocytes Stomatocytes Target cells Teardrop (dacrocyte) cells Abnormal Rouleax formation Erythroid Precursors Morphologic variants of white blood cells Neutrophil Abnormal neutrophils Alder Reilly Chediak-Higashi Syndrome Hypersegmented neutrophil Hyposegmented neutrophil Leukemic myeloblast with Auer rod May Hegglin anomaly Toxic granulation/Dohle bodies True Pelger Huet Normal neutrophil Normal basophil Normal mast cell Plasma cells Abnormal lymphocytes Reactive lymphocyte Epstein-Barr Virus Pertussis Large granular lymphocyte Histiocyte/macrophage in peripheral blood Paroxysmal Nocturnal Hemoglobinuria Defect_747 test2 test2.1 Test new Miscellaneous Marrow Failure Disorders Bin Thrombosis Miscellaneous Red Cell : Other Disorders Congenital erythrocytosis Megaloblastic Anemia Scurvy Toxins (arsenic) B12 / folate Medications Anemia of chronic disease Congenital Dyserythropoietic Anemias (CDA) Congenital Dyserythropoietic Anemia, type I Congenital Dyserythropoietic Anemia, type II Congenital Dyserythropoietic Anemia, type III Anemia in special populations Newborn Anemias Pregnancy/Post-partum Anemia Bone/metabolic disease Oxalosis Anemia of renal osteodystrophy Red Cell Aplasia Red Cell : Disorders of Iron Metabolism and Heme Synthesis Iron Deficiency and related disorders Acquired Iron Deficiency Hereditary Sideroblastic anemias Reversible Sideroblastic anemias Hereditary/Congenital Sideroblastic Anemia X-linked Sideroblastic anemia Sideroblastic anemia in genetic syndromes XLSA with ataxia Thaimine-responsive Megaloblastic anemia MItochondrial Myopathy, lactic acidosis and Sideroblastic anemia Pearson Marrow-Pancreas Syndrome Acquired/Reversible Sideroblastic Anemias Alcoholism Copper deficiency Drugs/medication Lead poisoning Myelodysplastic Syndromes Pyridoxine deficiency Hemochromatosis Primary hemochromatosis Hereditary conditions affecting the hepcidin/ferroportin axis Ferroportin disease- hereditary hyperferritinemia-cataract syndrome Hemojuvelin Hemochromatosis Hepcidin Hemochromatosis HFE Hemochromatosis in Caucasians Transferrin Receptor 2 Hemochromatosis Secondary hemochromatosis x linked (and other) hereditary sideroblastic anmia Other hereditary conditions Porphyria Cutanea Tarda Porphyria Variegate (type acute intermittent) Hepatoerythropoietic Porphyria Hereditary Coporporphyria (type acute intermittent) Hypogranular eosinophils (eosinophil count will be falsely low) Melanesian Iron Overload Aceruloplasminemia African Iron Overload Congenital Erythropoietic Porphyria Erythropoietic Protoporphyria Conditions of ineffective erythropoiesis Congenital Dyserythropoietic Anemias Alcohol abuse Autoimmune disorders Hemoglobin E/β-Thalassemia Hemoglobin H Disease Hereditary and Acquired Sideroblastic Anemias β-thalassemia Major and Intermedia Multiple blood transfusions Poryphyrias Red Cell : Hemolytic Anemia (HA) Paroxysmal Noctural Hemoglobinuria (PNH) Paroxysmal Nocturnal Hemoglobinuria Non-autoimmune HS/HE and RBC membrane or enzyme Disorders Hereditary HA due to Enzyme Deficiency Autoimmune Hemolytic Anemias Cold-active antibodies Cold agglutinin disease (CAD) Primary CAD Secondary CAD Lymphoproliferative diseases Autoimmune Infectious Mycoplasma Infectious mononucleosis Other viruses Paroxysmal Cold Hemoglobinuria Syphilis Measles, mumps and other viruses Warm-active antibodies Idiopathic autoimmune hemolytic anemia (AIHA) Secondary autoimmune HA (AIHA) Lymphoproliferative disorders Autoimmune and immunodeficiency Malignancy Viral Drug-induced HA Drug adsorption (penicillin) Neoantigen type (quinidine/sti...