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Symptoms » Sepsis » Glossary
 

Glossary for Sepsis

Medical terms related to Sepsis or mentioned in this section include:

  • Abnormal blood test symptoms: Abnormal results from diagnostic blood tests.
  • Bacteremia: A condition where bacteria is present in the blood.
  • Bacterial diseases: Diseases caused by a bacterial infection
  • Birth Injury: An injury to the mother caused by childbirth
  • Blood symptoms: Symptoms affecting the blood and its blood cells.
  • Body symptoms: Symptoms affecting the entire body features.
  • Brain conditions: Medical conditions that affect the brain
  • Campylobacter fetus infection: Campylobacter fetus is a food borne bacterial infection which may vary in severity from mild to severe. The bacteria are opportunistic and mainly affect debilitated patients but can also occur in healthy patients. Abortion due to blood infection in the fetus can occur in pregnant women who become infected. The infection is less likely to cause gastrointestinal symptoms such as diarrhea than other Campylobacter infections but is prone to causing infection in other parts of the body such as the appendix, abdominal cavity, central nervous system (meningitis), gallbladder, urinary tract and blood stream. Cattle and sheep are the main source of this bacteria.
  • Caroli Disease: A rare disorder where the bile ducts inside the liver become enlarged resulting in infection, irritation and gallstone formation.
  • Cholangitis: bile duct inflammation (cholangitis)
  • Colchicine toxicity: The toxic reaction of the body to the substance, possibly via allergic reaction or overdose.
  • Congenital megalo-ureter: A birth defect where the ureter is abnormally dilated due to a structural obstruction of the end portion of the ureter.
  • Congenital microvillous atrophy: A birth disorder involving a defect in the cells lining the intestines which results in watery diarrhea from birth which can be life threatening if not treated.
  • Corticobasal Degeneration: A rare progressive neurological disorder where parts of the brain deteriorate.
  • Cronkhite-Canada Syndrome: A rare non-inherited disorder characterized by numerous growths in the mucous lining of the intestine and stomach, hair loss, dark pigmented skin spots and loss of fingernails.
  • Deal-Barratt-Dillon syndrome: A very rare syndrome characterized mainly by scaly skin, jaundice, diarrhea and Fanconi syndrome (bone marrow fails to make sufficient new blood cells).
  • Edwardsiella tarda infection: A type of bacterial infection. The bacterium (Edwardsiella tarda) infects freshwater-dwelling animals and transmission occurs through consuming infected animals or contact with contaminated water. Symptoms are determined by the location of the infection. Healthy people are often able to fight of the infection but those with an underlying illness or poor immune systems may be more susceptible.
  • Eikenella corrodens infection: A type of anaerobic bacterial infection. The bacterium (Eikenella corrodens) is normally found in tooth plaque and can cause infection in various parts of the body. It tends to occur in patients with head and neck cancers or diabetics and drug users who lick their needles. Symptoms will depend on the location of the infection.
  • Epidermalolysis bullosa: A group of skin disorders characterized by fragile skin which can blister upon little or no trauma to the skin. There are a number of different subtypes with some being inherited and some acquired. The hands and feet are often the main parts of the body affected.
  • Epidermolysis bullosa, simplex: A group of skin disorders characterized by fragile skin which can blister upon little or no trauma to the skin. There are a number of different subtypes with some being inherited and some acquired. The hands and feet are often the main parts of the body affected.
  • Epidermolytic epidermolysis bullosa: A group of skin disorders characterized by fragile skin which can blister upon little or no trauma to the skin. There are a number of different subtypes with some being inherited and some acquired. The hands and feet are often the main parts of the body affected.
  • Fanconi-ichthyosis-dysmorphism: A very rare syndrome characterized by scaly skin (ichthyosis), anemia, muscle anomalies and various other abnormalities. All six reported cases died within 6 months.
  • Febrile Ulceronecrotic Mucha-Habermann disease: A very rare skin disease characterized by bleeding skin ulcers and fever. There is no obvious cause of the condition. The skin ulcers spread and can cover most of the body. Sepsis and death is more likely in adults.
  • Fever: Raised body temperature usually with other symptoms.
  • Flavimonas oryzihabitans: A very rare bacterial infection that is most likely to occur in immunocompromised patients or through the use of catheters. Flavimonas oryzihabitans was previous known as Pseudomonas oryzihabitans.
  • Francisella tularenis infection: Francisella tularenis is a type of bacteria that can cause infection involving the skin, respiratory and gastrointestinal systems. The nature and severity of symptoms varies depending on the location of the infection. The bacteria primarily causes localized tissue necrosis. The pathogen is considered a possible biological weapon.
  • Gas gangrene: Infection of deep tissues with anaerobic bacteria due to introduction of bacteria through a penetrating injury such as a battlefield or surgical wound; the bacterial kill the surrounding tissues and release gas within the tissues.
  • Group B Streptococcal Infections: "Strep" bacteria that may affect newborns and the immune-compromised; compare strep A.
  • HIV/AIDS: HIV is a sexually transmitted virus and AIDS is the progressive immune failure that HIV causes.
  • Head symptoms: Symptoms affecting the head or brain
  • Hematochromatosis: Hemochromatosis is the abnormal accumulation of iron in parenchymal organs, leading to organ toxicity. It is the most common inherited liver disease in whites and the most common autosomal recessive genetic disorder.
  • Hemophilus influenzae B: Bacterial respiratory infection with dangerous complications.
  • Histoplasmosis: Lung infection from fungus Histoplasma capsulatum
  • Infection: Infections as a symptom.
  • Inflammatory symptoms: Symptoms related to inflammation.
  • Listeriosis: Bacterial food poisoning
  • Melioidosis: Bacterial infection from soil or water.
  • Necrotizing enterocolitis: A rare disease that is tends to occur in premature infants and involves inflammation and destruction of gastrointestinal tissue. It usually occurs within weeks of birth - often after the start of milk feeding. The condition can be extremely serious and even fatal.
  • Nerve symptoms: Symptoms affecting the nerves
  • Noma: A gangrenous mouth infection that spreads to include the face.
  • Obstructive biliary disease: A disease process that causes obstruction or blockage in one of the bile ducts which are vessels that carry bile from the liver to the digestive system or gallbladder. Diseases that can cause such obstructions includes tumors, gallstones, parasites, bile duct inflammation, trauma to the bile duct and biliary strictures.
  • Pancreatic abscess: A localized pus-filled cavity (abscess) in the pancreas which usually occurs after pancreatitis. Death can occur if the abscess is not drained.
  • Pyomyositis: A painful muscle inflammation due to bacterial or fungal infection.
  • SCID: Major failure of the immune system, usually genetic.
  • Sepsis Syndrome: A life-threatening condition that results from infection that has spread throughout the body.
  • Sepsis in pregnancy: Sepsis in pregnancy refers to infection in pregnancy, resulting in circulating microorganisms in the blood that is usually characterised by fevers, tachycardia and general malaise.
  • Septicemia: A systemic inflammatory response to an infection.
  • Sickle Cell Anemia: Sickle cell anemia is an inherited blood disorder characterized by red blood cells which are crescent-shaped rather than the normal doughnut shape. These abnormally shaped red blood cells are unable to function normally and tend to undergo premature destruction which leads to anemia. If the genetic defect which causes the condition is inherited from both parents the condition can be quite severe whereas if it is inherited from only one parent, often there are no symptoms. The abnormally shaped red blood cells can cause problems when they clump together and block blood vessels.
  • Simpson-Golabi-Behmel syndrome, type 2: A rare genetic disorder characterized by hydrops fetalis and various other severe abnormalities. The condition usually results in death within two months of birth.
  • Skin symptoms: Symptoms affecting the skin.
  • Streptococcal Infections: Various "strep" bacterial infections.
  • Subphrenic abscess: A pus-filled cavity in the subphrenic region which is the area below the diaphragm but above the colon and liver. The infection can occur as a complication of abdominal surgery, acute pancreatitis and trauma.
  • Toxic epidermal necrolysis: A skin condition causing widespread blisters to erupt over greater than 30% of the body.
  • Urinary tract infection: Infection of the urinary tract
  • Waterhouse-Friederichsen syndrome: A rare syndrome that occurs as complication of septicemia (often due to meningococcal or pneumococcal infection) and involves blood coagulation in blood vessels, adrenal gland hemorrhages and ultimately kidney failure.

Conditions listing medical symptoms: Sepsis:

The following list of conditions have 'Sepsis' or similar listed as a symptom in our database. This computer-generated list may be inaccurate or incomplete. Always seek prompt professional medical advice about the cause of any symptom.

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Conditions listing medical complications: Sepsis:

The following list of medical conditions have 'Sepsis' or similar listed as a medical complication in our database.

 

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