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==Natural History==
==Natural History==
==Complications==
==Complications==
Major complications include
*Severe complications are much more common in severe and moderate haemophiliacs. Complications may be both directly from the disease or from its treatment:
*[[Hemarthrosis]]: Bleeding into the joints leads to hemophilic arthropathy. Hemorrhage most often occurs in the synovial joints. In descending order, the knee, ankle, elbow, shoulder, and hip are involved.
**Deep internal bleeding, e.g. deep-muscle bleeding, leading to swelling, numbness or pain of a limb.
*[[Hemorrhage]]
**Joint damage from haemarthrosis (haemophilic arthropathy), potentially with severe pain, disfigurement, and even destruction of the joint and development of debilitatingarthritis.
*[[Gastrointestinal bleeding]]
**Transfusion transmitted infection from blood transfusions that are given as treatment.
*[[Menorrhagia]]
**Adverse reactions to clotting factor treatment, including the development of an immune inhibitor which renders factor replacement less effective.
* The clinical and radiologic features of patients with classic hemophilia and Christmas disease are virtually identical.  
**Intracranial haemorrhage is a serious medical emergency caused by the buildup of pressure inside the skull. It can cause disorientation, nausea, loss of consciousness,brain damage, and death.
* Repetitive bleeding into the musculoskeletal system is the most common complication of both conditions.  
**Haemophilic arthropathy is characterized by chronic proliferative synovitis and cartilage destruction. If an intra-articular bleed is not drained early, it may cause apoptosis of chondrocytes and affect the synthesis of proteoglycans. The hypertrophied and fragile synovial lining while attempting to eliminate excessive blood may be more likely to easily re bleed, leading to a vicious cycle of hemarthrosis-synovitis-hemarthrosis. In addition, iron deposition in the synovium may induce an inflammatory response activating the immune system and stimulating angiogenesis, resulting in cartilage and bone destruction.
* Bleeding into muscles causes joint contractures
* Bleeding into bone and adjacent soft tissues results in osseous and soft-tissue pseudotumors.


==Prognosis==
==Prognosis==

Revision as of 02:23, 26 August 2015

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Natural History

Complications

  • Severe complications are much more common in severe and moderate haemophiliacs. Complications may be both directly from the disease or from its treatment:
    • Deep internal bleeding, e.g. deep-muscle bleeding, leading to swelling, numbness or pain of a limb.
    • Joint damage from haemarthrosis (haemophilic arthropathy), potentially with severe pain, disfigurement, and even destruction of the joint and development of debilitatingarthritis.
    • Transfusion transmitted infection from blood transfusions that are given as treatment.
    • Adverse reactions to clotting factor treatment, including the development of an immune inhibitor which renders factor replacement less effective.
    • Intracranial haemorrhage is a serious medical emergency caused by the buildup of pressure inside the skull. It can cause disorientation, nausea, loss of consciousness,brain damage, and death.
    • Haemophilic arthropathy is characterized by chronic proliferative synovitis and cartilage destruction. If an intra-articular bleed is not drained early, it may cause apoptosis of chondrocytes and affect the synthesis of proteoglycans. The hypertrophied and fragile synovial lining while attempting to eliminate excessive blood may be more likely to easily re bleed, leading to a vicious cycle of hemarthrosis-synovitis-hemarthrosis. In addition, iron deposition in the synovium may induce an inflammatory response activating the immune system and stimulating angiogenesis, resulting in cartilage and bone destruction.

Prognosis

References

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