Hemolytic-uremic syndrome history and symptoms: Difference between revisions
No edit summary |
m (Categories) |
||
| Line 2: | Line 2: | ||
{{HUS}} | {{HUS}} | ||
{{CMG}} | {{CMG}} | ||
==Overview== | ==Overview== | ||
==History and Symptoms== | ==History and Symptoms== | ||
The classic childhood case of HUS occurs after bloody [[diarrhea]] caused by [[Escherichia coli O157:H7|''E. coli'' O157:H7]], a strain of ''[[E. coli]]'' that expresses [[verotoxin]] (also called [[Shiga toxin]]). The toxin enters the bloodstream, attaches to [[kidney|renal]] [[endothelium]] and initiates an [[inflammation|inflammatory]] reaction leading to [[acute renal failure]] (ARF) and [[disseminated intravascular coagulation]] (DIC). The [[fibrin]] mesh destroys [[red blood cell]]s and captures [[thrombocytes]], leading to a decrease of both on [[complete blood count]]. The usual age of onset is between 2 and adolescence. | The classic childhood case of HUS occurs after bloody [[diarrhea]] caused by [[Escherichia coli O157:H7|''E. coli'' O157:H7]], a strain of ''[[E. coli]]'' that expresses [[verotoxin]] (also called [[Shiga toxin]]). The toxin enters the bloodstream, attaches to [[kidney|renal]] [[endothelium]] and initiates an [[inflammation|inflammatory]] reaction leading to [[acute renal failure]] (ARF) and [[disseminated intravascular coagulation]] (DIC). The [[fibrin]] mesh destroys [[red blood cell]]s and captures [[thrombocytes]], leading to a decrease of both on [[complete blood count]]. The usual age of onset is between 2 and adolescence. | ||
| Line 33: | Line 35: | ||
:*Skin rash that looks like fine red spots ([[petechiae]]) | :*Skin rash that looks like fine red spots ([[petechiae]]) | ||
:*Yellow skin ([[jaundice]]) | :*Yellow skin ([[jaundice]]) | ||
==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} | ||
{{WH}} | {{WH}} | ||
{{WS}} | {{WS}} | ||
[[Category:Nephrology]] | [[Category:Nephrology]] | ||
[[Category:Hematology]] | [[Category:Hematology]] | ||
Revision as of 17:13, 17 June 2016
|
Hemolytic-uremic syndrome Microchapters |
|
Differentiating Hemolytic-uremic syndrome from other Diseases |
|---|
|
Diagnosis |
|
Treatment |
|
Case Studies |
|
Hemolytic-uremic syndrome history and symptoms On the Web |
|
American Roentgen Ray Society Images of Hemolytic-uremic syndrome history and symptoms |
|
Risk calculators and risk factors for Hemolytic-uremic syndrome history and symptoms |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
History and Symptoms
The classic childhood case of HUS occurs after bloody diarrhea caused by E. coli O157:H7, a strain of E. coli that expresses verotoxin (also called Shiga toxin). The toxin enters the bloodstream, attaches to renal endothelium and initiates an inflammatory reaction leading to acute renal failure (ARF) and disseminated intravascular coagulation (DIC). The fibrin mesh destroys red blood cells and captures thrombocytes, leading to a decrease of both on complete blood count. The usual age of onset is between 2 and adolescence.
HUS occurs after 2-7% of all E. coli O157:H7 infections.
Adult HUS has similar symptoms and pathology but is an uncommon outcome of the following: HIV; antiphospholipid syndrome (associated with Lupus erythematosus and generalized hypercoagulability); post partum renal failure; malignant hypertension; scleroderma; and cancer chemotherapy (mitomycin, cyclosporine, cisplatin and bleomycin).
A third category is referred to as familial HUS. It represents 5-10% of HUS cases and is largely due to mutations in the complement proteins factor H, membrane cofactor protein and factor I leading to uncontrolled complement system activation. Recurrent thromboses result in a high mortality rate.
- HUS often begins with vomiting and diarrhea, which may be bloody. Within a week, the person may become weak and irritable. Persons with this condition may urinate less than normal. Urine output may almost stop.
- Red blood cell destruction leads to symptoms of anemia.
- Early symptoms:
- Later symptoms: