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Showing posts with the label Pathology

BONE MARROW EXAMINATION

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  BONE MARROW EXAMINATION It is the only method of correctly diagnosing diseases of blood. Sites of bone marrow aspiration: The following sites are selected for bone marrow aspiration: Sternum Iliac crest and upper end of tibia in children. Requirements: A special bone marrow needle (salah or klima needle) along with stilette Local anesthesia (Lignocaine) 2 to 5 ml syringe Glass slides Absolute methanol Formal ethanol Procedure: The site of puncture is usually sternum. Sterilize the selected site with soap water, iodine and finally with alcohol. The Site is anesthetized locally using lignocaine. Skin and subcutaneous tissues are punctured using sterilized bone biopsy and needly. When needle reaches periosteum, guarded needle is pushed further about 5 mm. Now the needle is fixed tightly in position. Now the needle is further pushed with boring motion into the cavity of bone. The stilette is removed and well fitted 2-5 ml syringe is used About 0.3 ml of bone marrow contents are sucke...

Bleeding Time and Clotting Time

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Introduction: For the investigation of a case of bleeding disorder,clinical history is very important. An accurate clinical and family history will often give an important time-saving clue to the nature of underlying bleeding disorder. ô€‚„ Appearance of purpuric spots or bruises over minimally injured surface suggests an abnormality of the vascular wall. ô€‚„ Continuous bleeding from mucous membranes, cuts, wounds, deeper haematomas or bleeding into the joints will suggest a defect in the blood coagulation system. ô€‚„ Excessive bleeding following delivery, or retention of dead foetus, or oozing following extensive surgery, suggest the possibility of fibrinogen depletion or presence of circulating anticoagulant agents. ô€‚„ History should also be taken about the ingestion of antiplatelet drugs such as aspirin. Two of the commonly used screening tests, bleeding time and whole blood clotting time, are discussed below. BLEEDING TIME  (BT) Bleeding time is duration of bleeding from a standard...

ROUTINE STAINING (H & E)

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ROUTINE STAINING (H & E) Routine staining is done with haematoxylin and eosin (H&E). Haematoxylin This is a natural dye which is obtained from log-wood tree, Haematoxylon campechianum.  This tree is nowadays commercially grown in Jamaica and Mexico.  The natural extract from the stem of this tree is haematoxylin which is an inactive product.  This product is oxidised to an active ingredient which is haematein.  This process of oxidation is known as ripening which can be done naturally in sunlight, or chemically by addition of oxidant like sodium iodate, KMnO4 or mercuric oxide. A mordant is added to it (e.g. potash alum) which helps in attaching the stain particles to the tissue. Procedure for Staining: Sections are first deparaffinised (removal of wax) by placing the slide in a jar of xylene for 10-15 minutes.  As haematoxylin is a water-based dye, the sections before staining are rehydrated which is done by passing the sections in a series of descendin...

ERYTHROCYTE SEDIMENTATION RATE (ESR)

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ERYTHROCYTE SEDIMENTATION RATE (ESR) ESR is used as an index for presence of an active disease which could be due to many causes. Principle When well mixed anticoagulated blood is placed in a vertical tube, the erythrocytes tend to fall towards the bottom of the tube/pipette till they form a packed column in the lower part of the tube in a given time. Mechanism of ESR Fall of RBCs depends upon following factors: i. Rouleaux formation ii. Concentration of fibrinogen in plasma iii. Concentration of α and β globulins iv. Length of the tube v. Ratio of red cells to plasma vi. Bore of the tube vii. Position of the tube i) Rouleaux formation The erythrocytes sediment in the tube/pipette because their density is greater than that of plasma. When a number of erythrocytes aggregate in the form of rouleaux and settle down, their area is much less than that of the sum of the area of constituent corpuscles. The rouleaux formation is very important factor which increases the ESR. ii) Concentration...

Histopathology Technique - Part 2 (Tissue processor)

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Tissue Processing:       Nowadays all the process of fixation, dehydration, clearing, and impregnation are carried out in a special equipment which is known as automated tissue processor. It can be a open (hydraulic) system or a closed (Vacuum) type. In the open type, the tissue processor has 12 - 16 glass jars for formalin, ascending grades of alcohol, xylene and thermostatically- controlled two paraffin wax baths to keep paraffin wax in molten state. Tissue moves automatically by hydraulic mechanism from one jar to another after fixed time schedule and the whole process takes 16-22 hours. In closed type of tissue processor, tissue cassettes are placed in a single container while different processing fluids are moved in and out sequentially according to electronically programmed cycle. The closed or vacuum  processor has the advantage that there is no hazard of contamination of the laboratory by toxic fumes unlike in open system. In addition, heat and ...

Examination of CSF: Cerebro Spinal Fluid

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Examination of CSF: Cerebro Spinal  Fluid   Function of CSF: Cerebro Spinal Fluid is formed by choroid plexus of ventricles of brain. It protects the brain and spinal cord from external pressure injuries. It also provides nutrients thus acting as a nutrient medium. It is involved in the excreting waste product of metabolism of nervous tissues. Features of CSF: Color: CSF is clear, colorless fluid. Volume: Total volume in adult is 100-150 ml. Specific Gravity: 1.006-1.008. Reaction: Alkaline in reaction. Collection of specimen: CSF is collected by puncturing the space between 3rd and 4th lumber vertebrae. It is called lumber puncture. Specimen collection may be done by expert doctor under sterilized conditions. About 3-5 ml of CSF can be collected in 3 tubes (5 ml each). It is sent immediately to the laboratory for tests. Physical Examination : Normally CSF is crystal clear. Color of CSF is changed in the diseases. Presence ...

Histopathology Techniques - Part 1

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Histopathology Techniques:     Histology is the technique of examination of normal tissues at microscopic level.     Histopathology is examination of tissues for presence or absence of changes in the structure due to disease processes.     Both are done by examine thin sections of tissues which are colored differently by different dyes and stains.     . Selected part of tissue (<4mm) thin is placed in steel or plastic capsules or cassettes and is subjected to the following sequential processing (Tissue processing) Fixation Dehydration Clearing Impregnation Embedding and Blocking Section cutting Routine staining 1. Fixation:     Any tissue removed from the body starts decomposing immediately because of loss of blood supply and oxygen, accumulation of products of metabolism, action of autolytic enzymes and putrefaction by bacteria.     Process of decomposition is prevented by fixation.     Fixation is the method of ...

Examination of Semen

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Examination of Semen:     -Semen is formed by testes present only in male.     -Semen consists of spermatozoa and seminal plasma.     -Semen examination is done in patient of sterility.     -The cause of male sterility may be defective spermatozoa or number number of spermatozoa is quite less.     -Semen examination is also done in person who are operated upon vasectomy, to check that spermatozoa are present in the semen. Collection of Semen: Patient should be asked not to pass semen for about 2-5 days before test. Patient is asked to discharge semen using his hand (masturbstion). Specimen of semen may be collected in clean and dry tube. Specimen should reach laboratory for examination with 15 minutes. Note the date, time of collection, and time of receiving specimen. Examine semen only after liquefication (30-60 minutes). Physical Examination: Volume:    - Measure the volume of semen in graduated cylinder.    - Norma...

Balantidum Coli

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     Balantidum Coli     - Lives in small intestine of human, pigs, and monkeys.      Morphology:     - Parasite exist in 2 phases:     a. Trophozoite     b. Cyst     A.  Trophozoite     - Oval in shape.     - Anterior end is narrow, with groove leading to mouth.     - Posterior ends is broad, with excretory opening.     - Cell is covered with (short - cilia).     - Cilia that line the mouth part is (large - cilia).     - Macro nucleus is kidney shaped.     - Micro nucleus is small, and round shaped.     B.Cyst:     - Spherical / oval in shape.     - Surrounded by thick and transparent double layered wall.     - Macro nucleus, Micro nucleus, and Vacuoles are present in the cyst.     Life Cycle:     - B.Coli passes its life cycle in one host only.     - Pig is the na...