RBC Morphology & Shapes | Pathology | NEET PG 2022 | Dr. Preeti Sharma

Added:

RBC Size & Color
Spherocytes & Reticulocytes
Three 'D' Cells
Schistocytes & Targets
Echinocytes & Acanthocytes
Rouleaux vs Agglutination
Stomatocytes & Pincer Cells

RBC Size & Color

2:04
Playing Section
  • 1

    Use lymphocyte nucleus as size reference for RBCs.

  • 2

    Assess central pallor to determine color and hemoglobin content.

  • 3

    Microcytic hypochromic picture with pencil cells suggests iron deficiency.

Normal histology and structure of a mature red blood cell, including its biconcave disc shape and lack of organelles.
The process of erythropoiesis and the stages of red blood cell maturation in the bone marrow.
Basic composition of the RBC cell membrane, focusing on key structural proteins like spectrin and ankyrin.
Standard hematological indices from a complete blood count (CBC), such as MCV, MCH, and RDW.
Pathophysiology and clinical presentation of hereditary hemolytic anemias (e.g., Hereditary Spherocytosis, Sickle Cell Anemia).
Differential diagnosis of microangiopathic hemolytic anemias (MAHA) based on the presence of schistocytes (e.g., TTP, HUS, DIC).
Interpretation of peripheral blood smears in correlation with clinical case vignettes for competitive exams like NEET PG.
Advanced diagnostic workups for anemias, including hemoglobin electrophoresis, osmotic fragility testing, and iron studies.
13.7K views449likes33:46@UnacademyLiveNEETPGOriginal Release: 2022-03-05

This comprehensive pathology lesson covers essential red blood cell shapes and morphologies for NEET PG exam preparation, including microcytic and hypochromic cells (smaller than 7 microns with increased central pallor), spherocytes (round, spherical cells without pallor seen in autoimmune hemolytic anemia, hereditary spherocytosis, and G6PD deficiency), reticulocytes (large blue cells indicating immature RBCs), bite cells (degmacytes) and sickle cells (drapanocytes) associated with G6PD deficiency and sickle cell anemia respectively, teardrop cells (dacrocytes) in myelofibrosis, fragmented cells (schistocytes) in microangiopathic hemolytic anemia, target cells (codocytes) in hemoglobin disorders, echinocytes (burst cells) in burns and renal failure, acanthocytes (spur cells) in abetalipoproteinemia, rouleaux formation (stack of coins) in multiple myeloma due to loss of zeta potential, agglutination in cold agglutinin disease, stomatocytes (with central slit) in stomatocytosis, and pincer cells in band 3 defects.