PATHOLOGY Flashcards

memorization (134 cards)

1
Q

The study of the structural, biochemical, and functional changes in cells, tissues, and organs; study of suffering

A

Pathology

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2
Q

Father of modern Pathology:

A

Rudolf Ludwig Carl Virchow

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3
Q

Term for diseases of unknown origin:

A

Idiopathic

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4
Q

Origin of the disease/causative agent

A

Etiology

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5
Q

Refers to the sequence of events that follow the exposure of cells or tissues to an injurious agent

A

Pathogenesis

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6
Q

Refers to the structural alterations in cells or tissues that are either characteristic of a disease or diagnostic of an etiologic process

A

Morphologic changes

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7
Q

The END RESULT of genetic, biochemical and structural changes in cells and are functional abnormalities which leads to the clinical manifestations of disease, as well as its progress

A

Clinical manifestations

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8
Q

Difference of signs and symptoms:

A

Signs - OBJECTIVE evidence of the disease; physical observations

Symptoms - SUBJECTIVE evidence of the disease; experienced by the patient

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9
Q

The sum total of changes in the living tissues, in response yo an injurious agent

A

Inflammation

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10
Q

Five cardinal signs of inflammation:

A
  1. Rubor - Redness - increase rate of blood flow
  2. Tumor - Swelling - increase capillary permeability
  3. Calor - Heat - transfer of internal heat
  4. Dolor - Pain - pressure upon sensory nerve
  5. Function laesa - Loss of function - Pain interference
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11
Q

Classification of Inflammation according to severity or duration:

A
  1. Acute inflammation
  2. Chronic inflammation
  3. Subchronic inflammation
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12
Q

Inflammation of sudden onset, characterized with 5 cardinal signs

A

Acute inflammation

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13
Q

Predominant cells in Acute Inflammation:

A

Neutrophils

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14
Q

Inflammation that involves persistence of injurious agent for weeks or years characterized by proliferation:

A

Chronic inflammation

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15
Q

predominant cells in Chronic Inflammation:

A

Mononuclear cells (plasma cells, lymphocytes, macrophages, monocytes)

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16
Q

Inflammation that represents integrade between acute and chronic inflammation

A

Subchronic inflammation

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17
Q

Classification of inflammation according to type of exudate:

A
  1. Serous inflammation
  2. Hemorrhagic inflammation
  3. Fibrinous inflammation
  4. Purulent inflammation
  5. Catarrhal inflammation
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18
Q

Characterized by extensive outpouring of WATERY, LOW PROTEIN-FLUID derived from either the blood serum or secretions from serosal mesothelial cells (example: blister)

A

Serous inflammation

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19
Q

Characterized by the admixture of BLOOD and elements of exudates

A

Hemorrhagic inflammation

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20
Q

Characterized by exudation of large amounts of FIBRINOGEN and precipitation of fibrin masses

A

Fibrinous inflammation

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21
Q

Characterized by the production of large amount of PUS or purulent exudates:

A

Purulent inflammation

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22
Q

Characterized by HYPERSECRECTION OF MUCOSA with degenerative changes in the epithelium

A

Catarrhal inflammation

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23
Q

Defined as a DISRUPTION of the normal anatomical structure and function of the SKIN or other tissues in the body;

A

WOUND

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24
Q

Injuries where the SKIN IS BROKEN exposing underlying tissues to the environment

A

OPEN WOUNDS

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25
Types of OPEN WOUNDS:
1. Puncture 2. Incision 3. Laceration 4. Abrasion 5. Avulsion 6. Amputation mnemonic: "OPEN ang mall" - "PILAAA" bago pumasok
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Open wound caused by sharp object that deeply penetrates the skin:
Puncture wound
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Open wound caused by sharp-edged object:
Incision
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Torn or jagged wounds caused by tearing of the skin via external force:
Laceration
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Open wound caused by FRICTION AGAINST A ROUGH SURFACE:
Abrasion
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Partial or complete tearing away of the skin causing the separation of the skin from tissue
Avulsion
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Complete detachment of limb
Amputation
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Injuries where the SKIN REMAINS INTACT, but there is damage to underlying tissues; these wounds may not be immediately visible, making them potentially more dangerous if not diagnosed:
Closed wounds
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types of closed wounds:
1. Blister 2. Hematoma 3. Contusions 4. Crush-injuries 5. Seroma mnemonic: "CLOSED" ang mall - BaHa, kaya Closed, sayang may Class Suspension pa naman
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Fluid-filled sac that forms between the upper layers of the skin, usually as a result of friction, burns, or other types of trauma:
Blister
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Blood-filled area that develops under the skin/tissue
Hematoma
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Blunt trauma due to damaged small blood vessels
Contusions
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Due to squeezing between two surfaces of the body
Crush-injuries
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Fluid-filled area that develops under the skin/tissue
Seroma
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THREE ABNORMALITIES IN CELL GROWTH:
1. Retrogressive changes 2. Progressive changes 3. Degenerative changes
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Abnormal cell growth where organs or tissues are smaller than normal:
Retrogressive changes
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Abnormal cell growth where organs or tissues are larger than normal
Progressive changes
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Abnormal cell growth where organs or tissues have problems in cellular growth patterns
Degenerative changes
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Types of RETROGRESSIVE CHANGES:
1. Aplasia 2. Agenesia 3. Atresia 4. Atrophy 5. Hypoplasia
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Retrogressive change characterized by incomplete or defective development of a tissue or organ
Aplasia
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Retrogressive change characterized by complete non-appearance of an organ
Agenesia
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Retrogressive change characterized by failure of an organ to form an opening
Atresia
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Retrogressive change characterized by acquired decrease in size of a normally developed or mature tissue or organ. It can be PHYSIOLOGIC or PATHOLOGIC
Atrophy
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Retrogressive change characterized by failure of an organ to reach or achieve its full mature or adult size due to incomplete development
Hypoplasia
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Types of PROGRESSIVE CHANGES:
1. Hypertrophy 2. Hyperplasia
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Increase in size of tissues or organs due to INCREASE IN THE SIZE of individual cells:
Hypertrophy
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Usually observed in the skeletal muscles, heart, kidney, endocrine organs and smooth muscles of hollow viscera due to increased work load and endocrine. Examples include - Uterine hypertrophy during pregnancy - Bulging muscles of bodybuilders
Physiologic hypertrophy
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Due to edema fluid and connective tissue proliferation, Examples include: - Enlargement of the heart in response to pressure overload
Pathologic hypertrophy
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Involves one of the paired organs when the other opposite organ has been removed or suffered from functional insufficiency
Compensatory hypertrophy
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Increase in size of an organ or tissue due to INCREASE IN THE NUMBER of cells resulting from growth of new cells:
Hyperplasia
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Due to the action of hormones or growth factors occurs when there is a need to increase functional capacity of hormone sensitive organs occurring as natural phenomenon. Example include: - ENLARGMENT OF FEMALE BREAST AT PUBERTY AND DURING PREGNANCY
Physiologic hyperplasia
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Caused by excessive or inappropriate actions of hormones or growth factors acting on target cells. Examples include: - Endometrial hyperplasia which is a common cause of abnormal uterine bleeding - Benign prostatic hypeplasia - Viral infections, such as papillomaviruses
Pathological hyperplasia
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Examples of DEGENERATIVE CHANGES:
1. Dysplasia 2. Anaplasia 3. Metaplasia 4. Neoplasia mnemonic: "DAMN"
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Regressive alteration in adult cells manifested by variation in size, shape and orientation, associated with chronic inflammation and protracted irritation
Dysplasia
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Marked regressive change in adult cells toward more primitive or embryonic cell types, utilized as a criterion toward malignancy/ example: Carcinoma
Anaplasia
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Reversible change involving the transformation in one type of adult cell to another
Metaplasia
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Continuous abnormal proliferation of cells without control; represents a pathologic overgrowth of the tissue:
Neoplasia
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IRREVERSIBLE degenerative changes:
Neoplasia Anaplasia
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REVERSIBLE degenerative changes:
Metaplasia Dysplasia
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Represents a pathologic condition or overgrowth of tissue and is usually autonomous in nature; means "new growth" and a new growth is called neoplasmas
Neoplasia
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TWO PARTS OF TUMOR:
1. Parenchyma 2. Stroma
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Part of tumor that refers to the active elements of the tumor
Parenchyma
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Part of the tumor that refers to the connective tissue framework with lymphatic and vascular channels
Stroma
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Classification of TUMOR according to CAPACITY TO PRODUCE DEATH
Benign Malignant
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Encapsulated' grow slowly' non-spreading' minima; mitotic activity; resemble parent tissue; DO NOT PRODUCE DEATH
BENIGN TUMOR
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Benign tumors arising from GLANDS
Adenoma Mnemonic: PE 'GA' = Glands-Adenoma
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Benign tumors arising from EPITHELIAL SURFACES:
Papilloma mnemonic: 'PE' GA = Papilloma-Epithelial surfaces
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Increase number of cells; invades tissue; lymphatic spread; metastasis; with nuclear structures; WILL PRODUCE DEATH
Malignant tumor
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Malignant tumors of EPITHELIAL tissue origin:
CARCINOMA mnemonic: 'CE' SC = Carcinoma-Epithelial tissue
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Malignant tumors of CONNECTIVE tissue of origin
SARCOMA mnemonic: CE 'SC' = Sarcoma-Connective tissue
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Classification of TUMOR according to HISTOLOGIC CHARACTERISTICS
1. Medullary tumors 2. Scirrhous tumors
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There are more cells than connective tissues; it is SOFT and VERY MALIGNANT
Medullary tumors
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There are more connective tissues than cells; it is characterized as STONY and HARD
Scirrhous tumors
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Suffix used for Benign Tumors:
-oma
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Suffix used for Malignant Tumors of Mesenchymal/Connective tissue:
-sarcoma
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Suffix used for Malignant Tumors of Epithelial Tissue:
-carcinoma examples: Glands and Ducts - AdenoCARCINOMA Finger-like (warty) projections - Papillary CARCINOMA
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Grading of Tumors:
Differentiated Cells: Resembles NORMAL CELLS Undifferentiated Cells: Resembles YOUNGER CELLS
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BRODERS CLASSIFICATION Grade I Differentiated cells: Undifferentiated cells: Remarks:
BRODERS CLASSIFICATION Grade I Differentiated cells: 76-100% Undifferentiated cells: 0-25% Remarks: Well-differentiated
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BRODERS CLASSIFICATION Grade II Differentiated cells: Undifferentiated cells: Remarks:
BRODERS CLASSIFICATION Grade II Differentiated cells: 51-75% Undifferentiated cells: 26-50% Remarks: Moderately-differentiated
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BRODERS CLASSIFICATION Grade III Differentiated cells: Undifferentiated cells: Remarks:
BRODERS CLASSIFICATION Grade III Differentiated cells: 26-50% Undifferentiated cells: 51-75% Remarks: Poorly-differentiated
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BRODERS CLASSIFICATION Grade IV Differentiated cells: Undifferentiated cells: Remarks:
BRODERS CLASSIFICATION Grade IV Differentiated cells: 0-25% Undifferentiated cells: 76-100% Remarks: Anaplastic/Pleomorphic
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Value of grading: Guide for treatment LOWER GRADES: HIGHER GRADES:
Value of grading: Guide for treatment LOWER GRADES: SURGERY HIGHER GRADES: FOR RADIATION/CHEMOTHERAPY
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General Rule in BRODER'S CLASSIFICATION:
- Well-differentiated tumors are LESS MALIGNANT - Higher grades have generally poorer diagnosis
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STAGING OF TUMORS Primary tumors:
STAGING OF TUMORS Primary tumors: - T = T1, T2, T3, T4: with INCREASING size of primary lesion
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STAGING OF TUMROS Regional Lymph Nodes Involvement:
STAGING OF TUMROS Regional Lymph Nodes Involvement: - N = N0, N1, N2, N3: Indicates PROGRESSIVELY advancing nodal disease
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STAGING OF TUMROS Metastasis:
STAGING OF TUMROS Metastasis: - M = M0, M1, M2: Whether there are distant METASTASIS (transfer of abnormal cell from one organ to another)
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TWO TYOES OF CELL DEATH:
1. Cellular Death 2. Somatic Death
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Refers to the death of individual cells and can encompass various mechanisms
Cellular Death
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Refers to the death of the entire organism, which ultimately results in the death of all the cells in the body
Somatic Death
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Types of CELLULAR DEATH:
1. Apoptosis 2. Necrobiosis 3. Necrosis
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the PROGRAMMED cell death; often PHYSIOLOGIC, means of elimination of unwanted cells; maybe PATHOLOGIC often some forms of cell injury, especially DNA damage; Morphological identified by NUCLEAR CONDENSATION
APOPTOSIS
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The PHYSIOLOGIC cell death
NECROBIOSIS
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The PATHOLOGIC cell death
NECROSIS
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Basic morphologic changes/Hallmark changes seen in necrosis Nuclear changes:
1. Pyknosis 2. Karyorrhexis 3. Karyolysis
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Reduction in size and condensation of the nucleus:
Pyknosis
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Segmentation and fragmentation of the nucleus:
Karyorrhexis
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Dissolution of the nucleus:
Karyolysis
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Large and granular (cloudy swelling), more acidophilic, dense and opaque, cell boundary is lost, granular coagulation and fragmentation
Cytoplasmic changes
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Types of necrosis according to location or extent:
1. Focal necrosis 2. Massive necrosis
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Necrosis that involves a SPECIFIC organ or a particular structure:
Focal necrosis
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Necrosis that involves the WHOLE or GREATER part of the organ
Massive necrosis
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Types of necrosis according to morphologic changes:
1. Coagulative necrosis 2. Liquefactive necrosis 3. Fat necrosis 4. Caseous necrosis 5. Gangrenous necrosis
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Most common type of necrosis; characterized by TOMBSTONE FORMATION; usually encountered when the ARTERIAL SUPPLY IS CUT OFF anemic or ischemic infarction; also seen in myocardial infarction
COAGULATIVE NECROSIS
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Caused by RAPID TOTAL ENZYMATIC DISSOLUTION of the cells with complete destruction of the entire cell; Seen in BACTERIAL INFECTIONS which lead to the formation of pus, probably due to the release of proteolytic enzymes; most commonly encountered in the BRAIN causing HYPOXIC DEATH OF CNS
LIQUEFACTIVE NECROSIS
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Involves the peculiar destruction of tissue particularly found in PANCREATIC DEGENERATION resulting to the release of lipase; morphologically, the tissue is characterized by presence of a dull, opaque circumscribed, flat area with CHALKY WHITE PRECIPITATE
FAT NECROSIS
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SOFT, FRIABLE CHEESE appearance in its gross state; highly associated with TUBERCULOSIS, also in syphilis, tularemia, and lymphagranuloma inguinale
CASEOUS NECROSIS
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Refers to the MASSIVE DEATH OR NECROSIS OF TISSUE caused by combination of ischemia and superimposed bacterial infection
GANGRENOUS NECROSIS
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DRY gangrene is caused by:
Arterial occlusion (ex. Hands)
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WET gangrene is caused by:
Venous occlusion (ex. Foot -DM)
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Primary changes of death (somatic death):
1. NERVOUS FAILURE - loss of coordination of various functions, chiefly loss of reflexes 2. CIRCULATORY FAILURE - occur when cardiac function ceases, absence of pulse and heartbeat 3. RESPIRATORY FAILURE - absence of oxygen and accumulation of carbon dioxide with loss of oxidative process needed for life mnemonic: NCR
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Secondary changes of death (somatic death):
1. Algor mortis 2. Rigor mortis 3. Livor mortis 4. Post-mortem clot 5. Desiccation 6. Putrefaction 7. Autolysis
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FIRST DEMONSTRABLE CHANGE observed, characterized by COOLING OF THE BODY, occurRing at definite rate of about 7F/hour and usually important in establishing APPROXIMATE TIME OF DEATH
ALGOR MORTIS
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Refers to the RIGIDITY OR STIFFENING of the muscle occurring about 6-12 HOURS after death and persisting for 3-4 DAYS. Change is first seen in the MUSCLES OF THE HEAD AND NECK, later spreading towards the lower extremities, and subsequently disappearing in the same sequence
RIGOR MORTIS
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PURPLISH DISCOLORATION of the body due to STASIS and eventual SETTLING DOWN of blood into blood vessels
LIVOR MORTIS
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Difference between LIVOR MORTIS and ECCHYMOSIS Application of pressure: Oozing blood upon incision: Location:
Difference between LIVOR MORTIS and ECCHYMOSIS Application of pressure LM: discoloration DISAPPEARS UPON PRESSURE and reappears upon release ECCHYMOSIS: No changes Oozing blood upon incision: LM: POSITIVE (+) ECCHYMOSIS: NEGATIVE (-) Location: LM: BLOOD VESSELS ECCHYMOSIS: TISSUE
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Occurs slowly, IMMEDIATELY AFTER DEATH, and may sometimes complicate the determination of the cause of death, particularly regarding the differentiation between post-mortem clots or thrombi
POST-MORTEM CLOT
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Immediately after death; "Chicken Fat" appearance "Currant Jelly" shaped blood vessels "Rubbery" consistency
POST-MORTEM CLOT
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Before death; Friable Tangled, irregular fashion Detachable, do not have a rubbery consistency
ANTE-MORTEM CLOT
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DRYING and WRINKLING OF THE CORNEA and anterior chamber of eye due to absorption of the aqueous humor
DESICCATION
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This is characterized by production of FOUL-SMELLING GASES due to the invasion of the tissue by multiplying saprophytic organisms
PUTREFACTION
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SELF-DIGESTION of cells
AUTOLYSIS
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All are signs of someone who has COVID-19, EXCEPT: A. Loss of test B. Productive cough C. Fever D. Positive SARC-COV-2 antigen
A. Loss of taste - Symptom, not sign
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Rubor: Redness; Calor: A. Swelling B. Pain C. Heat D. Loss of function
C. Heat
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Which of the following wounds is caused by friction against a rough surface? A. Laceration B. Contusion C. Hematoma D. Abrasion
D. Abrasion
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Which among the choices below is a closed wound? A. Abrasion B. Laceration C. Hematoma D. Amputation
C. Hematoma
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What progressive change is characterized by an increase in size of tissues or organs due to increase in the size of individual cells? A. Hyperplasia B. Hypoplasia C. Hypertrophy D. Neoplasia
C. Hypertrophy
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Which of the following is an IRREVERSEIBLE change of tissue? A. Metaplasia B. Dysplasia C. Anaplasia D. Neoplasia
D. Neoplasia - 1st choice! C. Anaplasia is also irreversible but the first choice must be Neoplasia Neoplasia - 1st choice Anaplasia - 2nd choice
132
What is the malignant tumor of epithelial tissue origin, which have less tendency to produce supporting tissue/stroma? A. Sarcoma B. Carcinoma C. Adenoma D. Papilloma
B. Carcinoma
133
What is the physiologic cell death? A. Necrosis B. Apoptosis C. Necrosis and Apoptosis D. Somatic death
B. Apoptosis #1 NECROBIOSIS note: Apoptosis is OFTEN PHYSIOLOGIC, means of elimination of unwanted cells; MAYBE PATHOLOGIC often some forms of cell injury, especially DNA damage' It is morphological identified by NUCLEAR CONDENSATION.
134
Somatic death refers to the death or complete cessation of metabolic and functional activities of the organism or the body as a whole. What are the primary changes of death? A. Nervous and circulatory failure B. Respiratory failure C. Nervous, Circulatory and Respiratory failure D. AOTA
D. AOTA (all of the above)