6. Abnormal accumulation of substances in the cell Flashcards

1
Q

What are the 4 Mechanisms of Abnormal Accumulation of Substances in cells?

{Morphogenesis of Intracellular & Stromal Degeneration)

A
  1. Infiltration = Pathologically INCREASED Reabsorption of Cells / Abnormal Factors in ECM
  2. Decomposition = Disintegration of Membranous Structures of Cells
  3. Pathological Synthesis = Synthesis of Amyloid / Alcoholic Hyaline / Glycogen in Henle’s Loop (DM)
  4. Transformation INTO other Chemical Substances instead of Normal
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2
Q

What is Hyaline?

A

Acellular, Proteinaceous Substances

Appears Glassy + Pink = Stained w/ Hematoxylin & Eosin (HE)

E.g Hyaline Cartilage = Transparent, Glossy Articular Joint Cartilage

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3
Q

What are Hyaline Casts?

A

Acellular Casts

Made up of Protein Matrix

Presence of OCCASIONAL Cast = Normal

Presence INCREASES = Renal Disease

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4
Q

What is Hyaline-Drop Degeneration / Dystrophy?

A

Occurs in = Kidney / Liver + Myocardium

Characterised by Aggregation of Small Protein INTO Cytoplasm of Cells

Organs affected DON’T have Specific Macro Changes

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5
Q

What Causes Hyaline-Drop Degeneration / Dystrophy?

A
  • a-1-antitrypsin deficiency = CAUSES Protein Accumulation in Hepatocyte Cytoplasm
  • Alcoholic Hepatitis
  • Viral Hepatitis
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6
Q

What Happens in Hyaline-Drop Degeneration?

A

Hyaline seen as Eosinophilic Deposits

IN Cytoplasm of Epithelial Cells of Proximal Renal Tubules

Occurs in Diseases w/ Proteinuria = Glomerulonephritis Kidney Amyloidosis / Diabetic Nephropathy

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7
Q

What are the 3 Specific Intracellular Protein Accumulations?

A
  1. Mallory Bodies = Protein Accumulation in Hepatocytes
  2. Russell Bodies = Protein Accumulation in Plasma Cells
  3. Lewy Bodies = Protein Accumulation in Nerve Cells
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8
Q

1| What are Mallory Bodies?

A

Cytoplasm of Hepatocytes shows eosinophilic deposits of intermediate filaments of CYTOKERATIN.

In Alcoholic + Viral Hepatitis; a-1-antitrypsin deficiency

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9
Q

2| What are Russell Bodies?

A

Pink Hyaline Inclusions

IN Cytoplasm of Plasma Cells

Represent Synthesised Igs

Seen in Chronic Infections

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10
Q

3| What are Lewy Bodies?

A

a. Brainstem LBs = Brainstem Nuclei + Diencephalon; SPHERICAL INTRANEURONAL CYTOPLASMIC Inclusions w/ Hyaline Eosinophilic CORES / Concentric LAMELLAR BANDS / NARROW PALE HALOS
b. Cortical LBs = Cerebral Limbic Cortex + Amygdala

Occurs in Lewy Body Dementia + Parkinson’s Disease

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11
Q

What are the 3 Groups of Intracellular Carbohydrate Degeneration?

AND Their Staining?

A
  1. Polysaccharides = Glycogen; Best Carmine’s + PAS Reaction (Dark Pink)
  2. Mucopolysaccharides; Best Carmine’s + PAS Reaction (Red)
  3. Glycoproteides = Mucin / Mucoids; Haile Staining (Blue)
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12
Q

What are Glycogen Accumulations?

A

EXCESSIVE Intracellular Deposits of Glycogen

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13
Q

Which Patient’s have Glycogen Accumulations?

A

Those with Abnormal Glucose / Glycogen Metabolism

E.g = Diabetes Mellitus

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14
Q

What are the Morphological Features of Glycogen Accumulation?

{Testing for Glycogen Accumulation}

A
  1. Formalin Fixative = Water Sol. CAUSES Dissolution of Glycogen FROM Cells
  2. HE Staining + Formalin Fixation = Glycogen (Clear Vacuoles in Cytoplasm)
  3. PAS Reaction w/ PAS Control AFTER Alcohol Fixation = PAS Reaction (Red); PAS Control w/ Amylase (Redness Disappears)
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15
Q

How do we see Glycogen Accumulation in Diabetes Mellitus?

A

Red Granules in:

(i) Epithelial Cells of Loop of Henle
(ii) Lumen of Kidney Canals
(iii) Cytoplasm & Nuclei of Hepatocytes

Armani-Ebstein Cells = GA in Epithelial Cells of Kidney Tubules

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