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43 Cards in this Set
- Front
- Back
Fibrosis |
The healing process that results after persistent tissue damage. |
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Labile cells |
Renewing cells, that can proliferate rapidly. Ex. epithelium of skin/gut, and bone marrow |
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Stable cells |
Cells that are capable of regeneration, but only do so when necessary Ex. Fibroblasts, endothelial cells, bone, cartilage, liver, kidney, exocrine pancreatic acini |
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Permanent cells |
Cells that cannot proliferate/regenerate after a certain stage in development Ex. Myocardiocytes & neurons |
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Granulation Tissue |
Healing process that includes fibroblasts and connective tissue bridging the gap created by the wound. Also includes angiogenesis, where the blood vessels run perpendicular (toward the surface) to the connective tissue. |
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First Intention Healing |
When the damage is clean cut, with minimal infection and foreign bodies, the healing process is by primary union. 1. Scab formation & neutrophil infiltration 2. Basal layer proliferation & granulation tissue 3. Fibrous union between sides and remodeling |
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Secondary Intention Healing |
Result of a less-than-perfect wound healing. Usually due to delayed healing, due to necrotic debris, foreign material, infection, or excessive granulation tissue. 1. Blood clot & acute inflammation 2. Granulation tissue, scab, and basal layer proliferation 3. Scab is shed & granulation tissue brings sides together. 4. Puckering of healed wound and/or depressed scar. |
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Anisocytosis |
Varying cell size |
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Anisokaryosis |
Varying nuclear size |
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Pleomorphism |
Abnormal cell shape |
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Hamartoma |
Disorganized mature tissue in a normal anatomic location. They are enlargements but typically not malignant. |
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Choristoma |
Normal mature tissue at an abnormal site Ex. Dermoid |
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Benign |
Unlikely to cause harm. Often slow growing and can compress (but not invade) surrounding tissue. Well demarcated with recognizable cell types. |
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Malignant |
Likely to cause harm. Often rapid growth and invasive qualities. Acquire their own blood supply. Poorly demarcated and can contain hemorrhage and necrosis. |
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Carcinoma |
Malignant neoplasm of epithelial origin |
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Sarcoma |
Malignant neoplasm of mesenchymal origin |
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Metastasis |
Spread of neoplasm to secondary sites |
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Round Cell Neoplasm |
Distinct circular cells histologically. Ex. lymphoma, mast cell tumor, plasma cell tumor |
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Epithelial Neoplasm |
Neoplasm arising from organ cells Ex. liver, kidney, pancreas, skin |
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Papilloma |
Exophitic growth from cutaneous or mucocutaneous surface |
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Polyp |
Growth projecting into a lumen. |
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Mesenchymal Neoplasm |
Arises from embryonic mesodermal origin, and consisting of cells that make up supportive tissue. Ex. Bone, muscle, tendon, nerve, fascia, vessels, cartilage |
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Fibroma |
Benign fibrocyte tumor |
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Lipoma |
Benign adipocyte tumor |
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Osteoma |
Benign bone tumor |
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Adenoma |
Benign gland tumor |
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Angioma or Hemangioma |
Benign endothelial tumor |
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Chondroma |
Benign cartilage tumor |
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Melanocytoma or melanoma |
Benign melanocyte tumor |
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Pheochromocytoma |
Benign adrenal medulla tumor |
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Fibrosarcoma |
Malignant fibrocyte tumor |
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Osteosarcoma |
Malignant bone tumor |
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Adenocarcinoma |
Malignant gland tumor |
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Transitional cell carcinoma |
Malignant bladder epithelial tumor |
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Leiomyosarcoma |
Malignant smooth muscle tumor |
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Rhabdomyosarcoma |
Malignant skeletal muscle tumor |
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Liposarcoma |
Malignant adipose tumor |
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Lymphosarcoma |
Malignant lymphocyte tumor |
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Malignant melanoma |
Malignant melanocyte tumor |
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Chondrosarcoma |
Malignant cartilage tumor |
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Hemangiosarcoma |
Malignant endothelial tumor |
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Carcinogenesis |
Initiation - irreversible alteration Promotion - selective outgrowth of initiated cells Progression - development of features of malignancy due to genetic changes |
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Latency |
Time before a tumor is clinically detectable Smallest detectable mass is 1 cm in diameter (10^9 cells) |