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Questions and Answers
Håfa estådos I hau faisen i patología?
Håfa estådos I hau faisen i patología?
Kåo hiyong patología I eksamen?
Kåo hiyong patología I eksamen?
Kåo hiyong I estådos manmaupay?
Kåo hiyong I estådos manmaupay?
Håfa i hinasso I patología mas ma’å’pu?
Håfa i hinasso I patología mas ma’å’pu?
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Kåo hiyong i taotao kuånto i patología I eksamen?
Kåo hiyong i taotao kuånto i patología I eksamen?
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Kåo hiyong i duhundun para i patología?
Kåo hiyong i duhundun para i patología?
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Kåo hiyong i hinasso ni ha fina'chong i patología?
Kåo hiyong i hinasso ni ha fina'chong i patología?
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Study Notes
Examen Final PATO - Notes
- Síndrome de Ehlers-Danlos (SED): Characterized by autosomal dominant transmission in most cases.
- Autosomal Recessive Transmission: Anemia of sickle cells (drepanocytic anemia) displays this pattern.
- Necrosis Fibrinoide of Blood Vessel Walls: Associated with immunoglobulins and complement deposition.
- Disseminated Intravascular Coagulation (DIC): Involves systemic thrombin activation.
- Atherosclerotic Plaque Localization: Most frequently found in the abdominal aorta.
- Necrosis Fibrinoide: A significant manifestation of Type III hypersensitivity.
- Granuloma in Granulation Tissue: Characterized by a band of fibrinoid necrosis around a granuloma.
- DiGeorge Syndrome: A thymus development disorder.
- Saddle Emboli: Often preceded by deep vein thrombosis.
- Thyroid Autoimmunity: Characterized by lymphocytes in all stages of maturation, including Hurthle cells.
- Antigen-Presenting Cells: Lymphocytes B are prominent in germinal centers of lymph nodes and spleen.
- Tissue Factor: Synthesized by vascular endothelium in hemostasis.
- Anergy: A prolonged, irreversible functional inactivation of dendritic cells.
- Mast Cell Mediators: Include phospholipase A-2, platelet-activating factor (PAF), prostaglandins, and histamine.
- Marfan Syndrome Characteristics: Not caused by a collagen coding alteration.
- Hyperacute Rejection: Mediated by pre-existing antibodies against donor antigens.
- Duchenne Muscular Dystrophy: A sex-linked recessive disorder.
- Amyloid Detection: Congo red staining for birefringence under polarized light is definitive.
- Generalized Edema Causes, Except: Lymphatic obstruction.
- Psoriasis Mechanism: Type IV hypersensitivity..
- Turner Syndrome (45,X): Diagnosed through karyotyping.
- Large Subcutaneous Hematoma: Called an ecchymosis.
- Blood Vessel Wall Necrosis: A characteristic of type III hypersensitivity.
- Autoantibody Targets in Pernicious Anemia: Parietal cells of the stomach.
- Type III Hypersensitivity: Characterized by immune complex deposition.
- Type I Hypersensitivity: Characterized by an immediate response.
- Antinuclear Antibodies (ANAs): Not specific to anti-phospholipids.
- Goodpasture's Syndrome Pathogenesis: Not a type III hypersensitivity manifestation.
- Peri-Orbital Edema: Suggests renal involvement.
- Amyloidosis: Characteristic of plasma cell neoplasms in multiple myeloma.
- Vascular Congestion with Hemosiderin-laden Macrophages: A sign of vascular congestion.
- Primary Lymphoid Organs: Bone marrow and thymus.
- Thrombosis Predisposition: Stasis is a major factor.
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Description
Este examen final abarca conceptos claves sobre síndromes médicos y mecanismos de coagulación. Se exploran temas como el Síndrome de Ehlers-Danlos, la transmisión autosómica recesiva y la coagulación intravascular diseminada. Además, se discuten condiciones como la necrosis fibrinoide y la autoinmunidad tiroidea.