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71 Cards in this Set
- Front
- Back
Histologically in glomerulonephritis (Systemic lupus erythematosus- SLE)
-glomerulus is full of ___& ___ |
-glomerulus is full of full of CELLS & SOLIDS
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Histologically in glomerulonephritis (Systemic lupus erythematosus- SLE)
-glomerular capillary loops are partially obstructed by _____ ______& _______ -______. |
-glomerular capillary loops are partially obstructed by ACTIVATED ENDOTHELIAL & MESANGIAL CELLS
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Histologically in glomerulonephritis (Systemic lupus erythematosus- SLE)
-thicker _____ ______ ______ |
thicker GLOMERURAL BASEMENT MEMBRANE
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Glomerulonephritis- Changes result from??? 2 things
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changes result from: 1.Deposition of immune complexes (antigens/Ab) & 2.Response of intrinsic glomerular cells
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Glomerulonephritis- Symptoms of Lupus nephritis: 5
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-Symptoms of lupus nephritis: 1.Hematuria,
2.Proteinuria, 3.Nephrotic syndrome, 4.Hypertension, 5.Chronic renal failure |
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Diabetic Renal Disease =--
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Diabetic Nephropathy-
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What is the most common cause of renal failure in affluent countries?
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Diabetic Nephropathy!
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Diabetic Nephropathy is increased in type __ Diabetes occurs w/ increasing what?
Decreasing what? What else? |
Diabetic Nephropathy is increased in TYPE--2-Diabetes
Occurs w/ 1.Increasing OBESITY 2.Decreasing EXERCISE 3.(& some GENTIC FACTORS) |
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Early signs of diabetic nephropathy is ??
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Proteinuria
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Diabetic Nephropathy Histologically: thickening of _______ ________ membrane & increase in _______ ______ =__________ __________
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Diabetic Nephropathy Histologically: thickening of MESANGIAL BASEMENT MEMBRANE & increase in MESANGIAL MATRIC
=DIABETIC GLOMERULOSCLEROSIS |
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Diabetic Nephropathy- Proteinuria can be caused by:
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1.Chemical mediators that induce increased deposition of mesangial matrix b/c of high [glucose]
2.Directpodocyte injury 3.Changes in slit pore membrane |
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In Diabetic Renal Diseases:
Diabetics also suffer: |
1. Vascular Disease,
2. Hypertension, 3. Increased Infections in Kidney |
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Anterior Pituitary Disorders:
Benign (don’t’ invade tissues) but have fatal consequences -excessive continuous production of hormone (uncontrolled by feedback mechanisms) - |
-Pituitary adenoma-
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Anterior Pituitary Disorders
-Tumor of corticotrophs secretes excess ____ which stimulates ______ to produce a lot of corticosteroid |
Tumor of corticotrophs secretes excess ATCH which stimulates ADRENALS to produce a lot of Corticosteriod.
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-Tumor of corticotrophs secretes excess ACTH- stimulates adrenals to produce a lot of corticosteroid
- Leads to what disease? |
-Leads to Cushing’s disease
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Anterior Pituitary Disorder:
Tumor of somatotrophs produce excess ____ _______ |
Tumor of somatotrophs produce excess GROWTH HORMONE
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Anterior Pituitary Disorder:
Tumor of somatotrophs produce excess growth hormone: Causes- what in children and adults? |
gigantism in children/
Acromegaly in adults |
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Some pituitary adenomas produce no homrones but grow so large towards the:
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towards the sellaturcica
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Gigantism is what kind of disease? where does it come from? how is it caused?
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Anterior pituitary disease/pituitary adenoma
-somatotroph and excess GH |
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Cushings diseases is caused by what / from where? and why?
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anterior pituitary disease/ pituitary adenoma from corcosteriod= excess ATCH
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Acromegaly is what kind of disease? where does it come from? how is it caused?
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anterior pitutary disease / pituitatry adenoma
caused by excess situmulation of GH from somatotophs. |
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Pituitary adenomas produce no homrones but grow so large towards the:Sellaturica Compress/damage ____ _____ & ______ Leading to _____ ______/_______
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Compress/damageCHIASMA & NERVES : VISION PROBLEMS/BLIDNESS
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Anterior Pituitary Glands
-Pituitary gland can rarely be destroyed by disease blocking its arterial supply Leads to necrosis of cells and failure of hormone output= |
Panhypopituitarism
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Tumor-like nodules arise in thyroid gland
-follicle epithelial cells synthesize/secrete thyroid hormone w/o a significant inactive storage phase is what? |
Thyroid Hyperplasia:
=Nodular hyperplasia |
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Grave's disease is part of what category of diesases?
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Thyroid Hyperplasia it is a Diffuse Hyperplasia
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Patient produces autoantibody (Long-acting thyroid stimulator- LATS)
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Grave’s disease-
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Patient produces autoantibody (Long-acting thyroid stimulator- LATS) -LATS mimicks ___& ______ thyroid to secrete excess hormone
-affects ___ _____ ____= -epithelial cells are larger/active and depleted of stored colloid w/I follicles |
Patient produces autoantibody (Long-acting thyroid stimulator- LATS) -LATS mimicks TSH & STIMULATES thyroid to secrete excess hormone
-affects: ALL THYROID FOLLICLES= -epithelial cells are larger/active and depleted of stored colloid w/I follicles |
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Both patterns of hyperplasia: Nodular and Diffusion produce:
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Thyrotoxicosis
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-Normal thyroid, most follicles are full of stored colloid/epithelium is in ______ storage phase
-only a few are ___ _____ -this is under the control of ____ ____ ____ () secreted by ANTERIOR PITUITARY |
-Normal thyroid, most follicles are full of stored colloid/epithelium is in INACTIVE storage phase
-only a few are RELEASING HORMONE -this is under the control of THYROID STIMULATING HORMONE(TSH) secreted by anterior pituitary |
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TSH is secreted by?
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anterior pituitary
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Disorders of the Parathyroid Gland:
-Parathyroid glands overwork |
Hyperparathyroidism-
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Disorders of the Parathyroid Gland:
HYPERPARATHYRODISM-Parathyroid glands overwork= -Most common cause: |
Most common coause: Benign tumor in 1 of the parathyroid glands- Parathyroid adenoma
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-Hyperparathyroidism
-Most common cause: benign tumor in 1 of the parathyroid glands- Parathyroid adenoma =>Unresponsive to normal feedback mechanisms related to ____ ____ ______ -excess parathormone stimulates excess OCl erosion of bone w/ release of bone____ =________ |
=>Unresponsive to normal feedback mechanisms related to BLOOD CA2+ LEVELS
-Excess parathormone stimulates excess OCl erosion of bone w/ release of BONE CA = HYPERCALCEMIA |
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HYPERCALCEMA from hyperparathyroidism leads to_____ ,x-ray abnormalities, increased risk of ____ _____ = ______ ___________
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-Leads to BONE PAIN, bbone pain, x-ray abnormalities, increased risk of KIDNEY STONES == PRIMARY HYPERARATHYROIDISM
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2ndary response of parathyroid glands to low Ca in patients w/ kidney failure
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Secondary Hyperparathyroidism-
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Secondary Hyperathyrodism-parathyroids become enlarged= _______ _____& secrete excess parathormone
attempts to bring ____ _____ ______ back to normal |
parathyroids become ENLARGE= PARATHYROID HYPERLASIA) &secrete excess parathormone
attempts to bring SERUM CA LEVELS back to normal |
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PARATHYROID HYPERPLASIA=
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ENLARGED PARATHYROID
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Parathyroid glands underwork
-produce little/no hormone -rare and due to surgical removal of all parathyroid glands during total thyroidectomy |
HYPOparathyroidism-
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Hypoparathyroidism-parathyroid glands underwork
-produce ____/___hormone -___ & due to ____ ____ of all parathyroid glands during total ______ |
Hypoparathyroidism-parathyroid glands underwork
-Produce LITTLE/NO hormone -RARE& due to SURGICAL REMOVAL of all parathyroid glands during total THYROIDECTOMY |
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.Disorders of the Adrenal Cortex:
-Destruction of adrenals cause failure of secretion of all adrenal cortical hormones= Hypoadrenalism -Addison’s Disease- weakness, fatigue, skin pigmentation, postural hypotension, hypovolemia, low blood Na |
. Disorders of the Adrenal Cortex:
-Destruction of adrenals cause failure of secretion of all ADRENAL CORTICAL HORMONES=Hypoadrenalism |
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Disorders of Adrenal Cortex:
-Destruction of adrenals cause failure of secretion of all adrenal cortical hormones=________ |
HYPOADRENALISM
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Adrenal cortex disease of hypoadrenalism which causes: weakness, fatigue, skin pigmentation, postural hypotension, hypovolemia, low blood Na????
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-Addison’s Disease-
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Adrenal cortex disorder of excess secretion of 1+ cortical hormones ??
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Hyperadrenalism- (More common adrenal cortex disorder
ex. cushings and conns syndromes |
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Hyperadrenalism- excess secretion of 1+ cortical hormones-
Adrenalcortx secretion of mineralocorticoids? |
Conn’s Syndrome
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Hyperadrenalism- excess secretion of 1+ cortical hormone
-adrenal cortex secretion of glucocorticoids? |
Cushing’s syndrome
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Adrenal cortex disorders
Excess hormone produced by: |
1. Benign tumor (Adrenal cortical adenoma)
2. Malignant tumor (adrenal cortical carcinoma) 3.affects all 3 types of cortical hormone (including androgens)-Diffuse hyperplasia |
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Ectopic ACTH syndrome- is what kind of disorder?
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is an ADRENAL CORTEX DISORDER
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Adrenal Cortex Disorder:
That occurs when a tumor elsewhere in body secretes excessive amts of ACTH which stimulates the zona fasciculate to produce excess glucocorticoids |
Ectopic ACTH syndrome-
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Adrenal Cortex Disorder:
That occurs when a tumor elsewhere in body secretes excessive amts of ACTH which stimulates the zona fasciculate to produce excess glucocorticoids |
Ectopic ACTH syndrome-
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Ectopic ACTH syndrome-is an adrenal cortex disorder that occurs when a tumor elsewhere in body secretes excessive amts of ____ which stimulates the ___ _______ to produce excess ___________-
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Ectopic ACTH syndrome-is an adrenal cortex disorder that occurs when a tumor elsewhere in body secretes excessive amts of ACTH which stimulates the ZONA FASCICULATE to produce excess GLUCOCORTICOIDS
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Ectopic ACTH syndrome-is an adrenal cortex disorder that occurs when a tumor elsewhere in body secretes excessive amts of ____ which stimulates the ___ _______ to produce excess ___________-
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Ectopic ACTH syndrome-is an adrenal cortex disorder that occurs when a tumor elsewhere in body secretes excessive amts of ACTH which stimulates the ZONA FASCICULATE to produce excess GLUCOCORTICOIDS
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Islets of Langerhans contain _____ cells which produce a range of ______
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Islets of Langerhans contain ENDOCRINE cells which produce a range of HORMONES!
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Islets of Langerhans contain _____ cells which produce a range of ______
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Islets of Langerhans contain ENDOCRINE cells which produce a range of HORMONES!
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Disorders of the Endocrine Pancreas:
Disease of insulin metabolism |
Diabetes Mellitus:
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Disorders of the Endocrine Pancreas:
Disease of insulin metabolism |
Diabetes Mellitus:
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Disorders of the Endocrine Pancreas:
Diabetes Mellitus: disease of insulin metabolism -Type that begins in childhood??? |
Type I:
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Disorders of the Endocrine Pancreas:
Diabetes Mellitus: disease of insulin metabolism -Type that begins in childhood??? |
Type I:
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Diabetes Mellitus: disease of insulin metabolism
-Type I: begins in childhood -Results in: loss of _____ ___ in _______ ______(including the ones that secrete ______) -Islet cells destruction is due to: _______ response (via ____ infection) -widespread effects on carb, protein, fat metabolism leads to ______ _____ ______ ______ |
-Type I: begins in childhood
-Results in: loss of ENDOCRINE CELLS in PANCREATIC ISLETS (including the ones that secrete INSULIN) -Islet cells destruction is due to: AUTOIMMUNE RESPONSE (via VIRAL infection) -Widespread effects on: CARB, PROTEIN, FAT METABOLISM leads to COMPLEX METABOLIC STRUCTURAL DISEASES |
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Diabetes Mellitus: disease of insulin metabolism
-Type I: begins in childhood -Results in: loss of _____ ___ in _______ ______(including the ones that secrete ______) -Islet cells destruction is due to: _______ response (via ____ infection) -widespread effects on carb, protein, fat metabolism leads to ______ _____ ______ ______ |
-Type I: begins in childhood
-Results in: loss of ENDOCRINE CELLS in PANCREATIC ISLETS (including the ones that secrete INSULIN) -Islet cells destruction is due to: AUTOIMMUNE RESPONSE (via VIRAL infection) -Widespread effects on: CARB, PROTEIN, FAT METABOLISM leads to COMPLEX METABOLIC STRUCTURAL DISEASES |
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Disorders of the Endocrine Pancreas: Diabetes Mellitus- disease of insulin metabolis: Type that occurs in late adult life??
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Type II:
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Disorders of the Endocrine Pancreas: Diabetes Mellitus- disease of insulin metabolis: Type that occurs in late adult life??
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Type II:
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Disorders of the Endocrine Pancreas: Diabetes type 2:
-Late adult life -________ of target cells to the effect of insulin -NOT _______ of insulin production by ______ _____ |
Diabetes type 2:
-Late adult life -RESISTANCE of target cells to the effect of INSULIN -NOT FAILURE of insulin production by PANCREATIC ISLETS |
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Disorders of the Endocrine Pancreas: Diabetes type 2:
-Late adult life -________ of target cells to the effect of insulin -NOT _______ of insulin production by ______ _____ |
Diabetes type 2:
-Late adult life -RESISTANCE of target cells to the effect of INSULIN -NOT FAILURE of insulin production by PANCREATIC ISLETS |
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Disorders of the Endocrine Pancreas:
-insulin secreting tumor produces Hyperinsulinism w/ hypoglycemic symptoms -rarely produce disease from excessive secretion of 1 of the islet hormones |
Tumors of the Islets of Langerhans:
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Disorders of the Endocrine Pancreas:
-insulin secreting tumor produces Hyperinsulinism w/ hypoglycemic symptoms -rarely produce disease from excessive secretion of 1 of the islet hormones |
Tumors of the Islets of Langerhans:
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Disorders of the Endocrine Pancreas:
Tumors of the Islets of Langerhans: -____secreting tumor produces _______ w/ hypoglycemic symptoms -rarely produce disease from excessive secretion of 1 of the islet hormones |
Tumors of the Islets of Langerhans:
-INSULIN secreting tumor produces HYPERINSULINM w/ HYPOGLYCEMIC symptoms -rarely produce disease from excessive secretion of 1 of the islet hormones |
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Disorders of the Endocrine Pancreas:
Tumors of the Islets of Langerhans: -____secreting tumor produces _______ w/ ______ symptoms -rarely produce disease from excessive secretion of 1 of the _____ ______ |
Tumors of the Islets of Langerhans:
-INSULIN secreting tumor produces HYPERINSULINISM w/ HYPOGLYCEMIC symptoms -rarely produce disease from excessive secretion of 1 of the ISLET HORMONES |
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Tumors of the Diffuse Neuroendocrine System:
-most frequent?? |
-Small Cell (Oat Cell) Carcinoma-
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Tumors of the Diffuse Neuroendocrine System:
-Small Cell (Oat Cell) Carcinoma- most frequent -Highly ______ tumor of neuroendocrine cells of the _____ _______ -Grows ____ & ____/_______ _____ Tissues -Can also spread to ___, ____, ____ ... -Retains the capacity to make/secrete hormone or hormone precursor molecules -->secretes ____ which stimulates _______ secretion of hormones from the _____ _____ |
Small Cell (Oat Cell) Carcinoma- most frequent
-Highly MALIGNANT tumor of neuroendocrine cells of the BRONCHIAL TREE -Grows RAPIDLY & INFILTRATES/DESTORYS NEARLY TISSUES -can also spread to BONE, LIVER & BRAIN -Retains the capacity to make/secrete hormone or hormone precursor molecules -->secretes ACTH which stimulates UNCONTROLLED secretion of hormones from the ADRENAL CORTEX |
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Tumors of the Diffuse Neuroendocrine System:
Most common in alimentary tract (especially in sm. Intestine and appendix) |
Carcinoid Tumor
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Tumors of the Diffuse Neuroendocrine System:
Carcinoid tumor- most common in alimentary tract (especially in sm. Intestine & appendix) -Grows _____ -Secretes 5-hydroxytryptamine -usually has no systemic effect because it passed from the tumor in the gut via the ____ _____ _____to the ______ -it is inactivated in the ____ -_____ &can spread to _____ sites away from the ___ -Carcinoid syndrome- 5-hydroxytryptamine enters blood and produces ________ ______ |
Carcinoid tumor- most common in alimentary tract (especially in sm. Intestine and appendix)
-Grows SLOWLY -Secretes 5-hydroxytryptamine -usually has no systemic effect bc it passed from the tumor in the gut via the HEPATIC PORTAL VEIN to the LIVER -it is inactivated in the LIVER -MALIGNANT & can spread to 2NDARY sites away from the GUT -Carcinoid syndrome- 5-hydroxytryptamine enters blood and produces METABOLIC EFFECTS |