LE1 Pathology Practical Exam Practice Flashcards

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This set of 100 vocabulary flashcards covers the pathology practical exam transcript, including cellular adaptations, necrosis, inflammation, hemodynamics, and genetic disorders.

Last updated 8:44 AM on 8/8/26
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101 Terms

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Hypertrophy (Myocardium)

An adaptive change occurring when hormonal or functional stimuli increase protein synthesis resulting in larger cells.

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Hypertrophy (Uterus)

A physiologic adaptation during pregnancy where elevated estrogen levels stimulate smooth muscle cells to increase in size.

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Physiologic Adaptation

A process where cell size increases but cell number remains the same, such as in the gravid uterus, and is reversible after childbirth.

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Benign Prostatic Hyperplasia (BPH)

A pathologic hyperplasia common in older men, characterized by a firm, nodular, and enlarged prostate.

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Dihydrotestosterone (DHT)

A potent derivative of testosterone that stimulates the proliferation of glandular epithelial and stromal cells in the prostate.

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Fat Necrosis

A type of enzymatic necrosis seen in acute pancreatitis characterized grossly by chalky white deposits and microscopically by ghost-like outlines of fat cells.

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Acute Pancreatitis

A condition presenting with severe abdominal pain where pancreatic lipases cause the destruction of fat cells in the peritoneum.

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Jaundice

Yellow discoloration of the skin and sclera caused by the accumulation of bilirubin.

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Bilirubin

The end product of heme degradation and biliverdin breakdown, transported to the liver for conjugation and excretion.

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Fibrinous Inflammation

Occurs when vascular permeability is severe enough to let fibrinogen escape into the extracellular space, often seen in the pericardium.

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Bread and Butter Appearance

The gross morphologic description of the pericardium in cases of fibrinous inflammation.

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Immune Granuloma

A granuloma formed when persistent antigens like Mycobacterium tuberculosis trigger a T-cell mediated immune response.

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Epithelioid Macrophage

The hallmark cell of granulomatous inflammation, which is an activated macrophage transformed by IFNγIFN-\gamma released by CD4+CD4^+ cells.

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Granulation Tissue

Early healing tissue characterized by the presence of new capillaries, fibroblasts, and inflammatory cells.

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Keloid

A type of abnormal scar that results from excessive collagen deposition and spreads beyond the borders of the initial injury without regressing.

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Hypertrophic Scar

A healing tissue reaction that remains contained within the site of injury and may regress over time.

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Serous Inflammation

Inflammation result from endothelial cell damage, leads to increased vascular permeability and escape of cell-poor fluid into the interstitial space.

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Cardiac Thrombus

A lesion formed on cardiac valves that consists of laminated layers of fibrin and platelets, which may detach and cause cerebral infarction.

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Postmortem Clot

A soft, non-adherent mass formed after death due to clotting factors, showing chicken fat (yellow) and currant jelly (dark red) appearances.

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Antemortem Thrombus

A mass formed before death through the interaction of platelets, vessels, and clotting factors, characterized by the presence of lines of Zahn.

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Fat Embolism

Commonly occurs after long bone fractures, like the femur, when fat droplets enter circulation and lodge in the lungs.

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Psammoma Bodies

Round concentric laminated calcified bodies found in abnormal tissues, representing dystrophic calcification.

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Dystrophic Calcification

Calcification occurring in previously necrotic or diseased tissue in the absence of systemic calcium imbalances.

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Down's Syndrome

A chromosomal disorder involving an extra copy of a gene on chromosome 2121, often presenting with a Simian crease.

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Simian Crease

A straight line running medial to lateral along the whole palm, consistent with Trisomy 2121.

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Klinefelter's Syndrome

A genetic condition in phenotypically male patients with a positive X chromosome test (Barr bodies) and a karyotype like 47,XXY47, XXY.

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Barr Body

A condensed, inactive X chromosome tested in buccal smears to identify Klinefelter's Syndrome in males.

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Translocation

A chromosomal abnormality where one big chromosome and one small chromosome are formed due to the loss and rearrangement of genetic material.

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Gaucher's Disease

A storage disease leading to progressive splenomegaly and the accumulation of glucocerebrosides in enlarged phagocytes.

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Gaucher Cells

Enlarged, distended phagocytes containing accumulated glucocerebrosides.

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Marfan's Syndrome

A genetic disorder that may cause ectopia lentis, joint dislocation, and dissected aneurysms due to lost elastin and high pressure.

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Dissected Aneurysm

A condition where blood is forced into a weakened wall of the aorta through an intimal tear.

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Atrophy

Decrease in cell size and number resulting in a decrease in the size of the organ, often due to loss of endocrine stimulation.

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Metaplasia

A reversible change where one differentiated cell type is replaced by another cell type, such as columnar to squamous.

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Squamous Metaplasia

Commonly occurring in the respiratory tract in response to chronic irritation or smoking.

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Steatosis

Also known as fatty liver or fatty change, characterized by the accumulation of lipids within hepatocytes.

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Caseous Necrosis

A pattern of necrosis typical of tuberculosis, featuring eosinophilic, amorphous debris rimmed by inflammatory cells.

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Tuberculosis

The most common disease associated with caseous necrosis and chronic granulomatous inflammation.

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Amyloid

A pink amorphous protein substance that accumulates in organs like the liver sinusoids.

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Congo Red

The most commonly used special stain to identify amyloid deposits in pathological specimens.

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Chronic Passive Congestion (CPC)

A lung condition resulting from increased hydrostatic pressure, causing thickened fibrotic alveolar septa and congested capillaries.

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Heart Failure Cells

Hemosiderin-laden macrophages located in the alveolar spaces, associated with chronic pulmonary congestion.

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Hemosiderin

A pigment derived from hemoglobin found within macrophages in the lungs during chronic congestion.

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Lipofuscin

Also known as lipochrome or 'wear and tear' pigment, appearing as yellowish-brown granules in the heart and liver.

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Brown Atrophy

A condition of the heart characterized by the prominent accumulation of lipofuscin.

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Acute Appendicitis

Inflammation of the appendix characterized by neutrophils extending through the wall and a serosa covered with exudate.

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Granuloma

An ovoid-shaped lesion composed of epithelioid cells surrounded by a collar of lymphocytes.

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Ulcer

A lesion characterized by a crater-like defect and the absence of a necrotic debris layer in specific healing phases.

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Angiogenesis

The proliferation of new blood vessels, a hallmark histologic feature of granulation tissue.

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Hypercoagulability

A possible cause of thrombosis, such as that seen in hemorrhoids during pregnancy.

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White Infarct

An anemic ischemic necrosis that appears pale and wedge-shaped, typically caused by arterial occlusion in solid organs.

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Hyperemia

The active increase of blood flow to an organ, seen as redness and edema in early acute appendicitis.

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Edward's Syndrome

Also known as Trisomy 1818, with a karyotype of 47,XY,+1847, XY, +18.

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Rocker Bottom Feet

A physical characteristic found in infants with Edward's Syndrome or Patau's Syndrome.

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Moro Reflex Loss

A motor abnormality associated with Down's Syndrome.

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Hypotonia

Decreased muscle tone, which is a common motor feature of Down's Syndrome infants.

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Meiotic Nondisjunction

The most common cause of Trisomy 2121, accounting for 90%90\% of cases.

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Langhans-type Giant Cells

Multinucleated cells formed by the fusion of activated macrophages within a granuloma.

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Chronic Inflammation

A tissue reaction where lymphocytes are the predominant inflammatory cell, often following acute processes or chronic irritation.

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Fibroblasts

Cells responsible for the proliferation of connective tissue and the formation of fibrous scars.

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Aortic Valve Intimal Tear

A lesion in Marfan's Syndrome caused by loss of elastin and hydrostatic pressure.

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Glucocerebrosides

The specific substance that accumulates in Gaucher's Disease.

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Basophilic Calcium Deposits

Microscopic findings in areas of fat necrosis, appearing as bluish mineral accumulations.

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Lipid Vacuoles

Intracellular spaces in hepatocytes that displace the nucleus to the periphery in fatty liver.

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Hepatomegaly

An enlarged liver, which can weigh up to 46kg4-6\,kg in cases of severe steatosis.

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Sinusoids

Spaces in the liver where amyloid deposits are frequently found.

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Alveolar Capillary Congestion

The filling of lung capillaries with blood due to increased pressure, seen in CPC.

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Dusky Blue Color

Gross appearance of an organ undergoing passive hyperemia or congestion due to deoxygenated blood.

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Overlapping Fingers

A clinical manifestation used to identify Edward's Syndrome.

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Epicanthic Folds

A facial profile characteristic of Down's Syndrome infants.

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Protruding Tongue

A common facial feature observed in patients with Trisomy 2121.

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Chronic Passive Hyperemia

A condition where impaired venous outflow leads to blood stasis and deoxygenated blood accumulation.

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Enzymatic Necrosis

A specific mechanism of cell death in the pancreas involving the release of lipases.

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Stratified Squamous Epithelium

The tissue type that replaces ciliated columnar epithelium in respiratory squamous metaplasia.

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Ciliated Columnar Epithelium

The normal cell type of the respiratory tract that undergoes metaplastic change due to smoking.

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Trigone

Area of the bladder where squamous metaplasia is considered physiologic in women.

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Keratinizing Squamous Metaplasia

A pathologic form of metaplasia occurring due to chronic infection or irritation of the urinary bladder.

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Prostate Stromal Cells

Non-glandular cells that proliferate alongside epithelial cells in Benign Prostatic Hyperplasia.

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Estrogen Stimulation

The hormonal cause of physiologic hypertrophy in the myometrium during pregnancy.

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Protein Synthesis

The cellular process that increases to create larger cells during hypertrophy.

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Oblique Palpebral Fissures

Slanted eye openings that are a clinical sign of Down's Syndrome.

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Simian Crease

The palm finding associated with an extra copy of chromosome 2121.

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X-ray: Bulky Femoral Neck

A radiographic finding in Gaucher's Disease where the neck thickens and the depression is lost.

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Ectopia Lentis

Bilateral lens dislocation, a diagnostic feature of Marfan's Syndrome.

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Joint Dislocation

A recurrent clinical finding in Marfan's Syndrome patients due to connective tissue weakness.

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Hematin

A pigment related to heme that is distinct from the bilirubin seen in jaundice.

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Neutrophils

The predominant inflammatory cells that extend through the wall of the appendix in acute appendicitis.

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Zone of Necrotic Debris

The histologic layer of an ulcer containing neutrophils and cell debris.

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Angiogenesis

The process of neovascularization seen in granulation tissue.

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Stasis

Abnormal blood flow that can lead to thrombosis in settings like pregnancy-induced hemorrhoids.

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White Infarct (Pyramidal)

The characteristic triangular shape of ischemic necrosis in the spleen.

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Deoxygenated Blood

The substance that causes the dusky or bluish-red color in passive congestion.

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Trisomy 18

The numerical chromosomal abnormality also known as Edward's Syndrome.

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Meiotic Nondisjunction (90%90\%)

The primary mechanism for the formation of the most common chromosomal disorder, Trisomy 2121.

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Mosaicism (1%1\%)

A less common cause of Down's Syndrome compared to nondisjunction.

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Chronic Granulomatous Inflammation (TB)

The specific inflammation type associated with chronic cough and low-grade afternoon fever.

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Pink Hyaline Materials

Substances seen in arteries that are distinct from the fat necrosis of acute pancreatitis.

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Vitamin A Deficiency

A nutritional cause for the replacement of transitional epithelium with stratified squamous epithelium.

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Hemorrhage

Prominent blood vessel finding on the serosa of an appendix affected by acute inflammation.

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Mononuclear Inflammation

A histologic feature of granulation tissue involving single-nucleus inflammatory cells.