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pathology of gastro intestinal tract

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**Esophagitis:** Esophagitis is the inflammation of the esophagus, the muscular tube that connects the throat to the stomach. It can be caused by various factors and can lead to discomfort and pain in the chest and difficulty swallowing. Some common causes of esophagitis include: 1. **Gastroesophageal Reflux Disease (GERD):** GERD is the most common cause of esophagitis. It occurs when stomach acid and other stomach contents flow back into the esophagus, irritating and inflaming the esophageal lining. 2. **Infections:** Esophagitis can be caused by infections, such as candida (yeast) or herpes simplex virus (HSV), particularly in individuals with weakened immune systems. 3. **Eosinophilic Esophagitis (EoE):** EoE is an allergic inflammatory condition of the esophagus. It occurs when a type of white blood cell called eosinophils accumulates in the esophageal lining, triggered by food allergies or other immune responses. 4. **Chemical Irritants:** Swallowing toxic substances

pathology of kidneys

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Polycystic kidney disease (PKD) is a genetic disorder characterized by the development of multiple fluid-filled sacs (cysts) in the kidneys. These cysts can grow larger over time, causing the kidneys to enlarge and lose their normal function. PKD can lead to kidney failure if not managed appropriately. There are two main types of polycystic kidney disease: **1. Autosomal Dominant Polycystic Kidney Disease (ADPKD):**    - ADPKD is the most common type of polycystic kidney disease and is typically diagnosed in adulthood.    - It is caused by mutations in the PKD1 or PKD2 genes, which encode for proteins involved in kidney cell function and maintenance.    - ADPKD affects both kidneys and can lead to gradual loss of kidney function over many years. **2. Autosomal Recessive Polycystic Kidney Disease (ARPKD):**    - ARPKD is a rare form of polycystic kidney disease that is usually diagnosed in infancy or early childhood.    - It is caused by mutations in the PKHD1 gene, leadi

brochitis and COPD

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Bronchitis is a respiratory condition characterized by inflammation and irritation of the bronchial tubes, which are the airways that carry air to and from the lungs. It can be classified into two main types: acute bronchitis and chronic bronchitis. **1. Acute Bronchitis:**    - Acute bronchitis is a common condition and is usually caused by viral infections, such as the flu (influenza) or the common cold (rhinovirus).    - It can also be caused by bacterial infections, though less frequently.    - Acute bronchitis is typically self-limiting, and symptoms often improve within a few weeks without specific medical treatment.    - Symptoms of acute bronchitis include:       - Cough (initially dry and irritating, which may later produce mucus or phlegm)       - Sore throat       - Runny or stuffy nose       - Mild fever       - Fatigue       - Shortness of breath or wheezing in some cases **2. Chronic Bronchitis:**    - Chronic bronchitis is a more serious and long-term form

pathology of respiratory system

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Respiratory diseases can be classified into various categories based on their underlying pathology, which refers to the specific changes and abnormalities in the respiratory system that cause the disease. Here are some common classifications of respiratory diseases according to their pathology: **1. Obstructive Lung Diseases:**    - Obstructive lung diseases are characterized by airway narrowing or obstruction, which makes it difficult for air to flow in and out of the lungs. This leads to increased effort in breathing and reduced airflow. Examples of obstructive lung diseases include:       - Chronic Obstructive Pulmonary Disease (COPD): Includes chronic bronchitis and emphysema.       - Asthma: A chronic inflammatory disorder that causes recurrent episodes of wheezing, shortness of breath, chest tightness, and cough. Drugs used in the treatment of an asthmatic attack can be classified into two main categories: quick-relief (rescue) medications and long-term control (ma

subacute bacterial endocarditis

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Subacute bacterial endocarditis (SBE) is a type of infectious endocarditis, which is an infection of the inner lining of the heart (endocardium) and heart valves. SBE is characterized by a slower, more insidious onset compared to acute bacterial endocarditis. It is typically caused by certain bacteria that are less virulent and more likely to be present in the bloodstream due to a low-grade infection elsewhere in the body. If left untreated, SBE can lead to severe complications and damage to the heart valves. Here are the key aspects of subacute bacterial endocarditis: **1. Causative Organisms:**    - SBE is primarily caused by bacteria from the viridans group, including Streptococcus viridans, as well as other less virulent bacteria such as Staphylococcus epidermidis.    - These bacteria are part of the normal flora found in the mouth, throat, and gastrointestinal tract. **2. Predisposing Factors:**    - Certain conditions or medical procedures can increase the risk of d

rheumatic heart disease

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Rheumatic heart disease (RHD) is a condition that results from rheumatic fever, an inflammatory disease caused by an immune response to a group A Streptococcus infection, typically strep throat. RHD primarily affects the heart valves, leading to damage and dysfunction. The pathology of RHD involves several stages, each contributing to the progression of the disease. Let's explore the key pathological aspects of rheumatic heart disease: **1. Initial Group A Streptococcus Infection:**    - The pathology of rheumatic heart disease begins with an infection caused by group A Streptococcus bacteria. This bacterium can cause a range of illnesses, including strep throat and scarlet fever.    - In some individuals, the immune system mounts an abnormal response to the bacterial infection, leading to the development of rheumatic fever. **2. Rheumatic Fever:**    - Rheumatic fever is an autoimmune response triggered by the group A Streptococcus infection.    - During this phase,

platlates physiology pathology

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Platelets are essential blood cells that play a critical role in hemostasis, which is the process of blood clot formation to stop bleeding. Disorders of platelets can lead to abnormal bleeding or clotting tendencies. Some common platelet disorders include: **1. Thrombocytopenia:**    - Thrombocytopenia is a condition characterized by a low platelet count in the blood.    - Causes may include decreased platelet production in the bone marrow, increased destruction of platelets, or sequestration of platelets in the spleen.    - Symptoms can range from mild bruising to severe bleeding, especially in the skin and mucous membranes.    - Thrombocytopenia can be caused by various factors, including autoimmune disorders, viral infections, certain medications, and bone marrow disorders. **2. Immune Thrombocytopenic Purpura (ITP):**    - ITP is an autoimmune disorder in which the body's immune system mistakenly attacks and destroys platelets.    - It leads to a decreased plate

WBC pathology

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Lymphoid neoplasms, also known as lymphomas, are a diverse group of cancers that originate from the cells of the lymphatic system. The lymphatic system is a vital part of the immune system and includes lymph nodes, lymphatic vessels, the spleen, thymus, and bone marrow. Lymphomas are classified into two main categories based on the type of lymphocytes involved: Hodgkin lymphoma (HL) and non-Hodgkin lymphoma (NHL). Let's explore these lymphoid neoplasms in more detail: **1. Hodgkin Lymphoma (HL):**    - Hodgkin lymphoma is a relatively rare type of lymphoma, accounting for about 10% of all lymphoid neoplasms.    - It is characterized by the presence of Reed-Sternberg cells, large abnormal cells, in the lymph nodes or other lymphoid tissues.    - HL usually starts in a single lymph node or a group of adjacent lymph nodes before spreading to other areas of the lymphatic system.    - The two main subtypes of HL are classical Hodgkin lymphoma (cHL) and nodular lymphocyte-

thalassemia , anemia pathology

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Anemia is a condition characterized by a decrease in the number of red blood cells or a decrease in the amount of hemoglobin in the blood. It can result from various underlying causes, leading to different classifications based on etiology. The common classifications of anemia include: 1. Microcytic anemia: In microcytic anemia, the red blood cells are smaller than normal. The main causes of microcytic anemia are iron deficiency, thalassemia, and some cases of anemia of chronic disease. 2. Normocytic anemia: In normocytic anemia, the red blood cells have a normal size, but their number or hemoglobin content is reduced. Normocytic anemia can result from various factors, including acute blood loss, chronic diseases, kidney disease, and some hemolytic anemias. 3. Macrocytic anemia: In macrocytic anemia, the red blood cells are larger than normal. The primary causes of macrocytic anemia are vitamin B12 deficiency and folate deficiency. Based on etiology, anemia can be furthe