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Questions and Answers
Which alteration in purine metabolism leads to the deposition of sodium urate crystals in tissues, characteristic of gout?
Which alteration in purine metabolism leads to the deposition of sodium urate crystals in tissues, characteristic of gout?
- Increased activity of adenosine deaminase
- Enhanced renal excretion of uric acid
- Disturbance in purine metabolism (correct)
- Decreased synthesis of purines
- Inhibition of xanthine oxidase
A patient with a history of chronic alcohol abuse presents with an enlarged liver and elevated liver enzymes. A liver biopsy reveals intracellular accumulation of a clear, PAS-positive substance. Which of the following is the most likely diagnosis?
A patient with a history of chronic alcohol abuse presents with an enlarged liver and elevated liver enzymes. A liver biopsy reveals intracellular accumulation of a clear, PAS-positive substance. Which of the following is the most likely diagnosis?
- Alpha-1 antitrypsin deficiency
- Hyalinosis
- Amyloidosis
- Glycogen storage disease (correct)
- Mucin accumulation
A researcher is studying a biopsy sample from a patient with suspected hyalinosis. Which of the following microscopic characteristics would be most consistent with this condition?
A researcher is studying a biopsy sample from a patient with suspected hyalinosis. Which of the following microscopic characteristics would be most consistent with this condition?
- Intracellular accumulation of lipid-laden macrophages
- Amorphous, glassy, eosinophilic material (correct)
- Fibrotic tissue with abundant collagen deposition
- Granular deposits that stain positively with Prussian blue
- Presence of birefringent crystals under polarized light
A patient with a history of chronic inflammatory disease develops kidney failure. A renal biopsy shows extracellular deposition of an amorphous, eosinophilic substance. Which of the following stains would be most appropriate to confirm a diagnosis of amyloidosis?
A patient with a history of chronic inflammatory disease develops kidney failure. A renal biopsy shows extracellular deposition of an amorphous, eosinophilic substance. Which of the following stains would be most appropriate to confirm a diagnosis of amyloidosis?
Which of the following mechanisms is most directly implicated in the pathogenesis of dystrophic calcification?
Which of the following mechanisms is most directly implicated in the pathogenesis of dystrophic calcification?
A coal miner who has worked for 30 years presents with shortness of breath and a chronic cough. A lung biopsy reveals black pigment accumulation in the lung parenchyma. Which of the following best describes the type of pigmentation observed?
A coal miner who has worked for 30 years presents with shortness of breath and a chronic cough. A lung biopsy reveals black pigment accumulation in the lung parenchyma. Which of the following best describes the type of pigmentation observed?
An elderly patient presents with brown atrophy of the heart. Microscopic examination reveals a yellowish-brown, fat-soluble pigment within cardiomyocytes. Which of the following pigments is most likely responsible for this finding?
An elderly patient presents with brown atrophy of the heart. Microscopic examination reveals a yellowish-brown, fat-soluble pigment within cardiomyocytes. Which of the following pigments is most likely responsible for this finding?
A patient with hemochromatosis undergoes a liver biopsy. Histological examination reveals an accumulation of iron within hepatocytes. Which special stain would best highlight the presence of this pigment?
A patient with hemochromatosis undergoes a liver biopsy. Histological examination reveals an accumulation of iron within hepatocytes. Which special stain would best highlight the presence of this pigment?
A patient presents with painful swelling of the metatarsophalangeal joint of the big toe. Analysis of synovial fluid reveals needle-shaped crystals that are negatively birefringent under polarized light. Which of the following substances is most likely deposited in the joint?
A patient presents with painful swelling of the metatarsophalangeal joint of the big toe. Analysis of synovial fluid reveals needle-shaped crystals that are negatively birefringent under polarized light. Which of the following substances is most likely deposited in the joint?
A 5-year-old child is diagnosed with a glycogen storage disease. Which of the following microscopic findings in a liver biopsy would be most suggestive of this diagnosis?
A 5-year-old child is diagnosed with a glycogen storage disease. Which of the following microscopic findings in a liver biopsy would be most suggestive of this diagnosis?
A pathologist examines a breast biopsy and identifies signet-ring cells. Further analysis reveals that these cells contain an accumulation of mucin. In which of the following conditions would the accumulation of mucin be most likely the predominant abnormality in the histological analysis?
A pathologist examines a breast biopsy and identifies signet-ring cells. Further analysis reveals that these cells contain an accumulation of mucin. In which of the following conditions would the accumulation of mucin be most likely the predominant abnormality in the histological analysis?
A patient with a history of chronic renal failure develops secondary hyperparathyroidism. Which of the following sites is most likely to exhibit metastatic calcification in this patient?
A patient with a history of chronic renal failure develops secondary hyperparathyroidism. Which of the following sites is most likely to exhibit metastatic calcification in this patient?
A patient undergoes a tissue biopsy, and the pathologist reports the presence of psammoma bodies. Which type of tissue accumulation is most likely represented by psammoma bodies?
A patient undergoes a tissue biopsy, and the pathologist reports the presence of psammoma bodies. Which type of tissue accumulation is most likely represented by psammoma bodies?
A patient presents with jaundice and is found to have increased levels of bilirubin in the liver. What would this be classified as?
A patient presents with jaundice and is found to have increased levels of bilirubin in the liver. What would this be classified as?
A woman who had repeated blood transfusions due to Thalassemia over many years develops liver damage. Which type of pigment accumulation is most likely present in her liver?
A woman who had repeated blood transfusions due to Thalassemia over many years develops liver damage. Which type of pigment accumulation is most likely present in her liver?
A patient with renal tubular acidosis has increased tubular calcium concentrations. What type of calcification is she at risk of developing?
A patient with renal tubular acidosis has increased tubular calcium concentrations. What type of calcification is she at risk of developing?
Chronic heart failure (brown atrophy) causes what type of tissue accumulation?
Chronic heart failure (brown atrophy) causes what type of tissue accumulation?
In necrotizing pancreatitis, foci of fat necrosis may develop in the peripancreatic adipose fat. What type of tissue accumuluation can occur in this scenerio?
In necrotizing pancreatitis, foci of fat necrosis may develop in the peripancreatic adipose fat. What type of tissue accumuluation can occur in this scenerio?
A patient undergoes a skin biopsy, and the pathologist reports the presence of melanin. Which type of classification of tissue accumulation would melanin be?
A patient undergoes a skin biopsy, and the pathologist reports the presence of melanin. Which type of classification of tissue accumulation would melanin be?
A patient undergoes a biopsy, and the pathologist stains the tissue with Periodic Acid-Schiff (PAS). Which of the following might the pathologist be testing for?
A patient undergoes a biopsy, and the pathologist stains the tissue with Periodic Acid-Schiff (PAS). Which of the following might the pathologist be testing for?
What color does Congo Red stain and what can it be used to detect?
What color does Congo Red stain and what can it be used to detect?
Which of the following best describes the pathogenesis of primary gout?
Which of the following best describes the pathogenesis of primary gout?
In the context of cellular pathology, what is the clinical significance of identifying Russell bodies?
In the context of cellular pathology, what is the clinical significance of identifying Russell bodies?
Which factor most directly contributes to the development of metastatic calcification?
Which factor most directly contributes to the development of metastatic calcification?
A patient who has chronic lead poisoning (plumbism) has increased levels of lead. What is this an example of?
A patient who has chronic lead poisoning (plumbism) has increased levels of lead. What is this an example of?
Which statement accurately links a pathological condition with its diagnostic histological finding?
Which statement accurately links a pathological condition with its diagnostic histological finding?
A patient with hyperparathyroidism develops nephrocalcinosis and calcium deposits in the gastric mucosa. What type of tissue accumulation is this?
A patient with hyperparathyroidism develops nephrocalcinosis and calcium deposits in the gastric mucosa. What type of tissue accumulation is this?
What key feature distinguishes localized from systemic amyloidosis concerning their extent of impact on the body?
What key feature distinguishes localized from systemic amyloidosis concerning their extent of impact on the body?
What is the role of vascular compression and pressure atrophy in the pathogenesis of amyloidosis-related organ dysfunction?
What is the role of vascular compression and pressure atrophy in the pathogenesis of amyloidosis-related organ dysfunction?
What is the underlying process that increases lipofuscin accumulation in tissues and the heart?
What is the underlying process that increases lipofuscin accumulation in tissues and the heart?
What mechanism underlies the development of urate crystals in gout, especially affecting joints?
What mechanism underlies the development of urate crystals in gout, especially affecting joints?
A patient with a history of tuberculosis (TB) undergoes a tissue biopsy, and pathologist reports the presence of 2ry amyloidosis. What best describes type of infection?
A patient with a history of tuberculosis (TB) undergoes a tissue biopsy, and pathologist reports the presence of 2ry amyloidosis. What best describes type of infection?
A patient undergoes a tattoo. Which type of classification of tissue accumulation is tattooing?
A patient undergoes a tattoo. Which type of classification of tissue accumulation is tattooing?
What is the main characteristic one might observe histologically in an individual that has gout?
What is the main characteristic one might observe histologically in an individual that has gout?
A 60-year-old man has localized amyloidosis. What type of amyloidosis can he have?
A 60-year-old man has localized amyloidosis. What type of amyloidosis can he have?
What is the common site that Na urates deposit at?
What is the common site that Na urates deposit at?
An individual who has had significant sun exposure can develop hyperpigmentaiton of the skin due to localized deposits of melanin. Which of the following is NOT a skin condition that can be caused by melanin deposits?
An individual who has had significant sun exposure can develop hyperpigmentaiton of the skin due to localized deposits of melanin. Which of the following is NOT a skin condition that can be caused by melanin deposits?
Flashcards
Gout
Gout
Disturbance in purine metabolism with deposition of sodium urate in tissues, increasing blood and urine levels.
Primary Gout
Primary Gout
Familial, with males more affected, due to increased purine breakdown or decreased clearance.
Secondary Gout
Secondary Gout
Increased cellular destruction, such as in polycythemia rubra vera.
Gout: Common Sites
Gout: Common Sites
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Glycogen Accumulation
Glycogen Accumulation
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Microscopic View of Glycogen Accumulation
Microscopic View of Glycogen Accumulation
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Mucin Accumulation examples
Mucin Accumulation examples
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Microscopic View of Mucin Accumulation
Microscopic View of Mucin Accumulation
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Hyalinosis definition
Hyalinosis definition
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Hyalinosis: Examples
Hyalinosis: Examples
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Definition of Amyloidosis
Definition of Amyloidosis
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Localized Amyloidosis
Localized Amyloidosis
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1ry Systemic Amyloidosis
1ry Systemic Amyloidosis
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2ry Systemic Amyloidosis
2ry Systemic Amyloidosis
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Heredofamilial Amyloidosis
Heredofamilial Amyloidosis
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Effects of Systemic Amyloidosis
Effects of Systemic Amyloidosis
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Pathological Calcification
Pathological Calcification
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Dystrophic Calcification
Dystrophic Calcification
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Metastatic Calcification
Metastatic Calcification
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Dystrophic Calcification Examples
Dystrophic Calcification Examples
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Causes of Metastatic Calcification
Causes of Metastatic Calcification
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Sites of Metastatic Calcification
Sites of Metastatic Calcification
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Stone formation
Stone formation
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Pathological Pigments: Definition
Pathological Pigments: Definition
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Exogenous Pigments: Routes of Entry
Exogenous Pigments: Routes of Entry
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Endogenous Pigments
Endogenous Pigments
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Localized hyperpigmentation
Localized hyperpigmentation
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Generalized Hyperpigmentation
Generalized Hyperpigmentation
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Localized Hypopigmentation
Localized Hypopigmentation
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Generalized Hypopigmentation
Generalized Hypopigmentation
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Lipochrome (Lipofuscin)
Lipochrome (Lipofuscin)
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Normal location Lipochrome
Normal location Lipochrome
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Causes of Lipochrome Increase
Causes of Lipochrome Increase
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Hemosiderosis
Hemosiderosis
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Localized Hemosiderosis
Localized Hemosiderosis
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Generalized Hemosiderosis
Generalized Hemosiderosis
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Study Notes
- BMS 151 covers the pathology of cellular and tissue response to injury as part 3 of the course.
Case Scenario
- An 84-year-old man with a small, dark brown heart shows light brown paranuclear pigment under microscopic examination
- Possible causes include hemosiderin from iron overload, lipochrome from tissue breakdown, glycogen from a storage disease, cholesterol from atherosclerosis, and calcium deposition following necrosis
Tissue Accumulations (Deposits)
- Intra- and extracellular accumulations and deposition covers, Gout, Carbohydrate & Glycoprotein, Hyalinosis, Amyloidosis, Pathological calcification & Pathological pigmentation
Gout
- A disturbance in purine metabolism results in sodium urate deposition in tissues and increased levels in blood and urine
- Primary causes are familial, more common in males, and due to increased purine breakdown or decreased clearance
- Secondary causes include increased cellular destruction as seen in Polycythaemia rubra vera
- Sodium urates are deposited in the skin, kidneys, and joints, often affecting the metatarsophalyngeal joint of the big toe
Carbohydrates & Glycoproteins
- Glycogen accumulation occurs in glycogen storage diseases due to abnormal glycogen metabolism
- Microscopically, cells are swollen with clear cytoplasmic vacuoles, which stain positive with PAS (Periodic Acid Schiff stain)
- Mucin accumulation examples include:
- Catarrhal inflammation
- Mucoid carcinoma
- Microscopically, cells are distended with mucin, forming signet-ring cells which may rupture and release mucin
Hyalinosis (Hyaline Deposition)
- Defined by the presence of glassy, refractile, homogenous, structureless protein material that stains red with eosin
- Examples: Russell's bodies in Rhinoscleroma and Corpora amylacia in prostatic hyperplasia
Amyloidosis
- Characterized as extracellular deposition of abnormal fibrillary protein that appears as homogenous eosinophilic material
- Localized forms of amyloidosis include nodular deposits (affecting tongue, larynx, lung), senile (cardiac or cerebral, linked to Alzheimer's), and endocrine amyloidosis in endocrine tumors
- Systemic forms are generalized:
- 1ry amyloidosis occurs in plasma cell tumors, such as multiple myeloma
- 2ry amyloidosis, or reactive amyloidosis, occurs in inflammatory diseases like tuberculosis (TB)
- Heredofamilial amyloidosis is another systemic type
- Amyloidosis leads to progressive organ dysfunction due to vascular compression and pressure atrophy
- Diagnosis involves tissue biopsy, which shows esinophilic staining with Hx & E stain, orange-red staining with Congo red, and apple-green birefringence under polarized light after Congo red staining
Pathological Calcification
- Abnormal deposition of calcium salts in tissue other than bone and teeth
- It appears chalky white and hard to the naked eye
- Under a microscope it appears dark blue
- Dystrophic calcification occurs in nonviable tissue with normal blood calcium levels
- Metastatic calcification occurs in viable tissue with hypercalcemia
- Causes are excess absorption of calcium and excess mobilization of calcium from bone
- Stone formation is the third type of calcification
- Sites include:
- Kidney tubules (nephrocalinosis)
- Walls of arteries
- Mucosa of the stomach
- Lung alveoli
- Stone formation involves the precipitation of calcium salts in ducts of the biliary tract, urinary tract, and salivary gland
Pathological Pigmentation
- Pigments are colored substances that stain the tissue
- Exogenous pigments enter the body through:
- Inhalation (anthracosis from carbon particles)
- Ingestion (chronic lead poisoning/plumbism)
- Inoculation (tattooing)
- Endogenous pigments include:
- Melanin
- Lipochrome (lipofuscin)
- Hemosiderin
Melanin
- Hyperpigmentation can be localized (e.g., nevus, melanoma) or generalized (prolonged sun exposure)
- Hypopigmentation can be localized (Vitiligo) or generalized (Albinism)
Lipochrome (Lipofuscin)
- Yellowish-brown, fat-soluble pigment normally present in the heart, testis, seminal vesicles, corpus luteum, and adrenal cortex
- Increases due to tissue breakdown, releasing phospholipids that are phagocytosed by neighboring cells, leading to intracellular accumulation
- Causes include:
- Old age (brown atrophy of the heart)
- Wasting diseases
- Cancer cachexia
Hemosiderin
- Deposition of hemosiderin, an iron-containing brown pigment, that stains blue with Prussian blue
- Localized hemosiderosis occurs due to localized hemorrhage
- Generalized hemosiderosis can be:
- Primary (due to inborn errors of metabolism)
- Secondary (due to repeated blood transfusions or hemolytic anemias)
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