BMS 151: Tissue Accumulations & Deposits

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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?

  • 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?

  • 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?

  • 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?

<p>Congo red stain (B)</p> Signup and view all the answers

Which of the following mechanisms is most directly implicated in the pathogenesis of dystrophic calcification?

<p>Local tissue necrosis and subsequent calcium deposition (B)</p> Signup and view all the answers

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?

<p>Anthracosis (D)</p> Signup and view all the answers

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?

<p>Lipofuscin (D)</p> Signup and view all the answers

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?

<p>Prussian blue stain (D)</p> Signup and view all the answers

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?

<p>Uric acid (E)</p> Signup and view all the answers

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?

<p>Hepatocytes with clear, swollen cytoplasm (C)</p> Signup and view all the answers

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?

<p>Catarrhal inflammation (A)</p> Signup and view all the answers

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?

<p>Lung alveoli (B)</p> Signup and view all the answers

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?

<p>Dystrophic calcification (B)</p> Signup and view all the answers

A patient presents with jaundice and is found to have increased levels of bilirubin in the liver. What would this be classified as?

<p>Endogenous pigmentation (C)</p> Signup and view all the answers

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?

<p>Hemosiderin (B)</p> Signup and view all the answers

A patient with renal tubular acidosis has increased tubular calcium concentrations. What type of calcification is she at risk of developing?

<p>Metastatic calcification (A)</p> Signup and view all the answers

Chronic heart failure (brown atrophy) causes what type of tissue accumulation?

<p>Lipofuscin (A)</p> Signup and view all the answers

In necrotizing pancreatitis, foci of fat necrosis may develop in the peripancreatic adipose fat. What type of tissue accumuluation can occur in this scenerio?

<p>Calcium (B)</p> Signup and view all the answers

A patient undergoes a skin biopsy, and the pathologist reports the presence of melanin. Which type of classification of tissue accumulation would melanin be?

<p>Pathological pigmentation (E)</p> Signup and view all the answers

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?

<p>Glycogen (E)</p> Signup and view all the answers

What color does Congo Red stain and what can it be used to detect?

<p>Apple Green and Amyloid (C)</p> Signup and view all the answers

Which of the following best describes the pathogenesis of primary gout?

<p>Genetic factors affecting uric acid metabolism or excretion. (C)</p> Signup and view all the answers

In the context of cellular pathology, what is the clinical significance of identifying Russell bodies?

<p>Specific to Rhinoscleroma (hyalinosis) (B)</p> Signup and view all the answers

Which factor most directly contributes to the development of metastatic calcification?

<p>Elevated levels of calcium or phosphate in the bloodstream. (D)</p> Signup and view all the answers

A patient who has chronic lead poisoning (plumbism) has increased levels of lead. What is this an example of?

<p>Ingestion (D)</p> Signup and view all the answers

Which statement accurately links a pathological condition with its diagnostic histological finding?

<p>Amyloid presents green birefringence with congo red stain. (D)</p> Signup and view all the answers

A patient with hyperparathyroidism develops nephrocalcinosis and calcium deposits in the gastric mucosa. What type of tissue accumulation is this?

<p>Metastatic calcification (C)</p> Signup and view all the answers

What key feature distinguishes localized from systemic amyloidosis concerning their extent of impact on the body?

<p>Localized impacts specific sites, while systemic spreads widely. (A)</p> Signup and view all the answers

What is the role of vascular compression and pressure atrophy in the pathogenesis of amyloidosis-related organ dysfunction?

<p>Reduces blood flow and impairs cellular metabolism, leading to impaired tissue integrity. (C)</p> Signup and view all the answers

What is the underlying process that increases lipofuscin accumulation in tissues and the heart?

<p>Autophagy of cellular components. (D)</p> Signup and view all the answers

What mechanism underlies the development of urate crystals in gout, especially affecting joints?

<p>Supersaturation of synovial fluid, causing crystal deposition. (C)</p> Signup and view all the answers

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?

<p>Reactive amyloidosis (E)</p> Signup and view all the answers

A patient undergoes a tattoo. Which type of classification of tissue accumulation is tattooing?

<p>Pathological pigmentation (B)</p> Signup and view all the answers

What is the main characteristic one might observe histologically in an individual that has gout?

<p>Needle shaped crystals (A)</p> Signup and view all the answers

A 60-year-old man has localized amyloidosis. What type of amyloidosis can he have?

<p>Senile (C)</p> Signup and view all the answers

What is the common site that Na urates deposit at?

<p>A, B, C are correct (A)</p> Signup and view all the answers

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?

<p>Melanoma (D)</p> Signup and view all the answers

Flashcards

Gout

Disturbance in purine metabolism with deposition of sodium urate in tissues, increasing blood and urine levels.

Primary Gout

Familial, with males more affected, due to increased purine breakdown or decreased clearance.

Secondary Gout

Increased cellular destruction, such as in polycythemia rubra vera.

Gout: Common Sites

Skin, kidney, and joints, especially the metatarsophalangeal joint of the big toe.

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Glycogen Accumulation

Disturbance in carbohydrate metabolism, leading to accumulation due to abnormal glycogen metabolism.

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Microscopic View of Glycogen Accumulation

Cells swollen with clear cytoplasmic vacuoles; use PAS stain.

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Mucin Accumulation examples

Catarrhal inflammation and mucoid carcinoma.

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Microscopic View of Mucin Accumulation

Cells distended with mucin (signet-ring cell); cells may rupture, releasing mucin.

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Hyalinosis definition

Presence of glassy, refractile, homogenous, structureless protein material that stains red with eosin.

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Hyalinosis: Examples

Russell's bodies in rhinoscleroma and corpora amylacea in prostatic hyperplasia.

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Definition of Amyloidosis

Extracellular deposition of abnormal fibrillary protein, appearing as homogenous eosinophilic material.

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Localized Amyloidosis

Affects tongue, larynx, and lung.

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1ry Systemic Amyloidosis

Occurs in plasma cell tumors (multiple myeloma).

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2ry Systemic Amyloidosis

Occurs in inflammatory diseases (tuberculosis).

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Heredofamilial Amyloidosis

Family history of amyloidosis.

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Effects of Systemic Amyloidosis

Progressive organ dysfunction due to vascular compression and pressure atrophy.

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Pathological Calcification

Abnormal deposition of calcium salts in tissue other than bone and teeth.

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Dystrophic Calcification

Occurs in nonviable tissue with normal blood calcium levels.

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Metastatic Calcification

Occurs in viable tissue with hypercalcemia.

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Dystrophic Calcification Examples

Fat necrosis, chronic abscess walls, old scars, dead parasites, fibrosed valves, atheroma.

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Causes of Metastatic Calcification

Excess calcium absorption from the intestine, excess mobilization from bone, endocrinal disorders.

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Sites of Metastatic Calcification

Kidney tubules, artery walls, stomach mucosa, lung alveoli.

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Stone formation

Biliary tract, urinary tract and salivary gland.

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Pathological Pigments: Definition

Colored substances that stain the tissue; can be exogenous or endogenous.

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Exogenous Pigments: Routes of Entry

Inhalation (anthracosis), ingestion (lead poisoning), inoculation (tattooing).

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Endogenous Pigments

Melanin, lipochrome (lipofuscin), hemosiderin.

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Localized hyperpigmentation

Nevus and melanoma.

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Generalized Hyperpigmentation

Prolonged exposure to sunlight.

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Localized Hypopigmentation

Vitiligo.

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Generalized Hypopigmentation

Albinism.

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Lipochrome (Lipofuscin)

Yellowish-brown fat-soluble pigment.

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Normal location Lipochrome

Heart, testis, seminal vesicles, corpus luteum, adrenal cortex.

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Causes of Lipochrome Increase

Old age, wasting diseases, cancer cachexia.

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Hemosiderosis

Deposition of hemosiderin (iron-containing brown pigment) detected with Prussian blue stain.

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Localized Hemosiderosis

Due to localized haemorrhage.

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Generalized Hemosiderosis

Primary: inborn error of metabolism. Secondary: repeated blood transfusions, hemolytic anemias.

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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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