The document provides an introduction to basic pathology including the study of microscopic tissue and cellular changes of disease. It discusses key concepts like cells, tissues, organs and systems. It also describes different pathological lesions and how to describe pathological features both grossly and microscopically.
The document provides an introduction to basic pathology including the study of microscopic tissue and cellular changes of disease. It discusses key concepts like cells, tissues, organs and systems. It also describes different pathological lesions and how to describe pathological features both grossly and microscopically.
Histopathology: study of the microscopic tissue changes of a disease. Cytopathology: study of the microscopic cellular changes of a disease. Importance Bridge between basic science (diagnostic information) and clinical medicine (treatment) Cell: the smallest unit of a living body. Tissue: mass of similar cells arranged to make up a part of an organ and perform a specific function. Each tissues consists of cells and extracellular matrices. Organ: is made up of different tissues (heart). Organs of the body are composed of varying proportions of the four tissues. System: group of organs having similar or related function. Types of tissues: 1. Epithelial tissues (covering surfaces) 2. Muscular tissues (voluntary or involuntary) 3. Nervous tissues (central or peripheral) 4. Connective tissues (fill in-between tissues) Histopathology specimen is obtained from: 1. Biopsy: during life (surgery – endoscopy). 2. Autopsy: after death. 3. Cytology: from (body fluids – fine needle). Different pathological lesions: 1. Congenital lesions (birth defects): present before or at birth (genetic or during development). 2. Inflammatory lesions: reaction to injury Acute (suppurative or non suppurative) Chronic 3. Neoplastic lesions (tumor): abnormal overgrowth Benign Malignant (carcinoma – sarcoma) How describe pathological lesion? Morphology includes gross and microscopic features. 1. Gross pathology: by naked eye Size and weight Ulcer (loss of the surface covering) Nodule (small, rounded, irregular, distinct lump) Cavity (space filled with a content and separated from the surroundings by a wall) 2. Microscopic pathology: by microscope Types of microscopes 1. Light microscopy: use visible light as a source of illumination, examine tissue after staining (H&E) or special stain. 2. Fluorescent microscopy: use laser as a source of illumination, examine tissue stained by fluorescent dyes. 3. Polarized light microscopy: use polarized light as a source of illumination, examine birefringent (doubly-refracting) anisotropic substances. 4. Electron microscopy: use electron beam as a source of illumination, examine cellular organelles with a magnification up to x500000, use glutaraldehyde in fixation. Parts of light microscope: 1. Optical system Ocular lens (eyepieces): topmost element, binocular head 10x 4 Objective lens (attached to nosepiece) 4x, 10x, 40x, 100x (oil) 2. Movable specimen support Stage with knob Stand: Base (lamp) Arm (connect base to binocular head) and has fine and course focus 3. Illumination system Condenser lens with its diaphragm (just below the stage) Lamp Setting of condenser diaphragm for optimum resolution Condenser is used in its highest position. Work with the scanning (4x) and low-power (10x) the condenser diaphragm should be wide open. Work with the high-dry (40x) and oil-immersion objectives (100x), the condenser diaphragm should be closed slowly. Final magnification = ocular magnification objective magnification. Diaphragm should be adjusted for each magnification.
Cleaning of objective lens
When finished using oil-immersion objective, it must be cleaned with lens paper or alcohol.