<p> Cell Index Microorganisms  Anaplasma phagocytophilum  Babesia species  Bacteria  Brugia malayi  Histoplasma capsulatum  Loa loa  Plasmodium falciparum  Plasmodium malariae  Plasmodium ovale  Plasmodium vivax  Trypanosoma brucei gambiense/rhodesiense  Trypanosoma cruzi  Wuchereria bancrofti  Yeast </p><p>Platelets  Fibrin thread  Megakaryoblast  Megakaryocyte  Micromegakaryoblast  Micromegakaryocyte  Platelet  Platelet clumps  Platelet on RBC  Platelet satellitism  Platelet, abnormal granular  Platelet, abnormal shaped  Platelet, agranular  Platelet, budding  Platelet, giant  Platelet, hypogranular  Platelet on RBC </p><p>Red Blood Cells  Acanthocyte (Spur cell)  Agglutinated RBC  Basophilic stippling  Burr cell (Echinocyte)  Cabot ring  Elliptocyte  Helmet cell  Hemoglobin C crystal  Hemoglobin SC crystal  Howell-Jolly body  Hypochromic RBC  Macrocyte  Macrocyte, oval  Microcyte  Microcyte, hypochromic  Nucleated RBC  Ovalocyte  Pappenheimer body  Phagocytized RBC  Polychromatic RBC  Reticulocyte  Rouleaux  Schistocyte  Sickle cell (Drepanocyte)  Spherocyte  Stomatocyte  Target cell (Codocyte)  Teardrop cell (Dacryocyte) </p><p>Smear Examination - Low power  Scanning - Agglutinated RBCs  Scanning - Fibrin thread  Scanning - Giant, hypogranular platelets  Scanning - Hypogranular cells  Scanning - Immature cell  Scanning - Leukocytosis  Scanning - Leukopenia  Scanning - Normal profile  Scanning - Nucleated RBCs  Scanning - Parasite  Scanning - Platelet clumps  Scanning - Pseudo-Pelger-Huët neutrophils  Scanning - Rouleaux  Scanning - Schistocytes, Spherocytes, Nucleated RBCs  Scanning - Sickle cells  Scanning - Smear edge  Scanning - Spherocytes  Scanning - Thrombocytosis </p><p>White Blood Cells  Aüer rod  Band  Band, eosinophilic  Band, toxic granulation  Basophil  Basophil, immature  Blast  Burkitt lymphoma cell  Degenerating cell  Döhle body  Eosinophil  Faggot cell  Hairy cell  Lymphoblast  Lymphocyte  Lymphocyte, intracellular granule  Lymphocyte, reactive  Lymphoma cell  Lymphoma cell, clefted nucleus  Metamyelocyte  Metamyelocyte, eosinophilic  Metamyelocyte, hypogranular  Mitotic figure  Monoblast  Monocyte  Myeloblast  Myelocyte  Myelocyte, eosinophilic  Myleocyte, hypogranular  Neutrophil  Neutrophil, vacuolated  Plasma blast  Plasma cell  Plasma cell, atypical  Plasmacytoid lymphocyte  Platelet, giant  Polymorphonuclear leukocyte  Polymorphonuclear leukocyte with granule  Polymorphonuclear leukocyte, hypersegmented  Polymorphonuclear leukocyte, hypogranular  Primary granule  Prolymphocyte  Promonocyte  Promyelocyte  Promyelocyte, abnormal  Pseudo-Pelger-Huët neutrophil  Pseudo-Pelger-Huët neutrophil, hypogranular  Pseudo-Pelger-Huët neutrophil, unilobed  Sézary cell  Smudge cell  Toxic granulation </p><p>Diagnosis & Anomaly  Abetalipoproteinemia  Acute erythroid leukemia  Acute lymphoblastic leukemia (ALL), B-cell  Acute lymphoblastic leukemia (ALL), T-cell  Acute megakaryocytic leukemia  Acute monocytic leukemia (AMoL), 5a  Acute monocytic leukemia (AMoL), 5b  Acute myeloid leukemia (AML)  Acute myeloid leukemia (AML), M0  Acute myeloid leukemia (AML), M1  Acute myeloid leukemia (AML), M2  Acute myeloid leukemia (AML), M3  Acute myeloid leukemia (AML), M4  Acute myeloid leukemia (AML), M5a  Acute myeloid leukemia (AML), M5b  Acute myeloid leukemia (AML), M6  Acute myeloid leukemia (AML), M7  Acute myeloid leukemia (AML), therapy related  Acute myeloid leukemia series: Patient in diagnostic phase  Acute myeloid leukemia series: Patient in remission  Acute myeloid leukemia series: Patient on granulocyte-colony-stimulating factor (G-CSF)  Acute myeloid leukemia series: Patient post induction chemotherapy  Acute myelomonocytic leukemia (AMML)  Acute promyelocytic leukemia (APL)  Acute promyelocytic leukemia (APL), micro granular variant  Agglutination  Alcoholism  Artifact  Artifact, platelet  Autoimmune hemolytic anemia (AIHA)  Babesiosis  Bacterial infections  Basophilic leukemia  Biphenotypic leukemia  Burkitt lymphoma  Burns  Chédiak-Higashi anomaly  Chronic idiopathic myelofibrosis (CIMF)  Chronic lymphocytic leukemia/Small lymphocyte lymphoma (CLL/SLL)  Chronic myeloid leukemia (CML) : Blastic phase  Chronic myeloid leukemia (CML), atypical  Chronic myeloid leukemia (CML): Accelerated phase  Chronic myeloid leukemia (CML): Chronic phase  Chronic myelomonocytic leukemia (CMML/CMMoL)  Disseminated intravascular coagulation (DIC)  Essential thrombocythemia (ET)  Granulocyte-colony-stimulating factor (G-CSF) effects  Hairy cell leukemia (HCL)  Hemoglobin SC disease  Hemoglobinopathies  Hemolytic anemia  Hemolytic-Uremic syndrome (HUS)  Heriditary spherocytosis (HS)  Histoplasmosis  Human granulocytotropic anaplasmosis (HGA)  Infectious mononucleosis  Iron deficiency anemia  Lead poisoning  Leukemoid reaction  Liver disease  Macrocytic anemia  May-Hegglin anomaly  Microangiopathic hemolytic anemia (MAHA)  Microcytic hypochromic anemia; Iron deficiency anemia  Microcytic hypochromic anemia; Thalassemia  Multiple myeloma  Myelodysplastic syndrome (MDS)  Myelofibrosis (MF)  Myeloproliferative disorder (MPD)  Myeloproliferative disorder (MPD); Atypical chronic myeloid leukemia (CML)  Myeloproliferative disorder (MPD); Chronic idiopathic myelofibrosis (CIMF)  Myeloproliferative disorder (MPD); Chronic myeloid leukemia (CML): Accelerated phase  Myeloproliferative disorder (MPD); Chronic myeloid leukemia (CML): Blastic phase  Myeloproliferative disorder (MPD); Chronic myeloid leukemia (CML): Chronic phase  Myeloproliferative disorder (MPD); Essential thrombocythemia (ET)  Non-Hodgkin lymphoma (NHL)  Normal  Parasitemia  Plasma cell leukemia  Platelet satellitosis  Postsplenectomy  Prolymphocytic leukemia (PLL)  Renal failure  Reticulocytosis  Septicemia  Sickle cell anemia  Thalassemia  Thrombocytopenia  Thrombotic thrombocytopenic purpura (TTP)  Viral infections  Yeast infection </p>