Red Blood Cell Morphology Abnormalities Explained

Added:

RBC Changes Overview
Size Disorders
Color Disorders
Shape Abnormalities
Sickle Cells
Burr & Spur
Teardrop Cells
Clumping & Dot

RBC Changes Overview

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Playing Section
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    Introduces key blood smear diagnostic categories: size, color, shape, distribution.

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    These abnormalities help identify and diagnose various hematological diseases.

Normal red blood cell anatomy and physiology, including the structure and function of hemoglobin and the erythropoiesis process.
Understanding of standard hematological indices from a Complete Blood Count (CBC), specifically MCV, MCH, MCHC, and RDW.
The standard appearance of a normal peripheral blood smear, particularly the typical biconcave disc shape, size, and normal central pallor of RBCs.
Basic laboratory techniques, including how a blood smear is prepared and stained using Romanowsky stains (like Wright-Giemsa).
Clinical correlation of specific abnormal shapes (e.g., schistocytes, sickle cells, target cells, spherocytes) with their corresponding hematologic diseases.
Diagnostic workup and classification of anemias (microcytic, normocytic, and macrocytic) using morphological clues.
Identification and clinical significance of red blood cell inclusions, such as Howell-Jolly bodies, Heinz bodies, Pappenheimer bodies, and basophilic stippling.
Understanding the role of manual blood smear review in confirming automated hematology analyzer flags and maintaining laboratory quality control.
170.6K views2.6Klikes15:24@MedLecturesMadeEasyOriginal Release: 2015-10-16

Red blood cell morphological abnormalities include changes in size (macrocytosis with MCV >100 indicating B12/folate deficiency, microcytosis with MCV <80 indicating iron deficiency/thalassemia/lead poisoning), color (hypochromasia with central pallor >1/3 diameter indicating low hemoglobin, polychromasia showing immature reticulocytes), and shape (target cells in liver disease/thalassemia, spherocytes in hereditary spherocytosis/autoimmune hemolysis, schistocytes in microangiopathic hemolytic anemia, sickle cells in sickle cell anemia from HbS polymerization, echinocytes in renal disease, acanthocytes in liver disease, teardrop cells in myelophthisis), as well as distribution abnormalities like rouleaux formation and agglutination, which help diagnose various hematological conditions.