(Source: Fibrocartilaginous Embolism; Genetic and Rare Diseases Information Center (GARD) of National Center for Advancing Translational Sciences (NCATS), USA.)
The risk factors for Fibrocartilaginous Embolism may include:
It is important to note that having a risk factor does not mean that one will get the condition. A risk factor increases one’s chances of getting a condition compared to an individual without the risk factors. Some risk factors are more important than others.
Also, not having a risk factor does not mean that an individual will not get the condition. It is always important to discuss the effect of risk factors with your healthcare provider.
(Source: Fibrocartilaginous Embolism; Genetic and Rare Diseases Information Center (GARD) of National Center for Advancing Translational Sciences (NCATS), USA.)
The signs and symptoms of Fibrocartilaginous Embolism may include:
In the majority of cases, FCE develops after a minor or even unnoticed "triggering event" such as a minor head or neck injury or heavy lifting. The amount of time between the "trigger" and the onset of symptoms varies from minutes to days, with the average onset of symptoms being 2-4 days after the triggering incident.
(Source: Fibrocartilaginous Embolism; Genetic and Rare Diseases Information Center (GARD) of National Center for Advancing Translational Sciences (NCATS), USA.)
A diagnosis of Fibrocartilaginous Embolism is generally suspected based on the presence of characteristic signs and symptoms. Other conditions that cause similar features can be ruled out using the following tests:
(Source: Fibrocartilaginous Embolism; Genetic and Rare Diseases Information Center (GARD) of National Center for Advancing Translational Sciences (NCATS), USA.)
Many clinical conditions may have similar signs and symptoms. Your healthcare provider may perform additional tests to rule out other clinical conditions to arrive at a definitive diagnosis.
The complications of Fibrocartilaginous Embolism may include:
Complications may occur with or without treatment, and in some cases, due to treatment also.
There is no specific treatment for Fibrocartilaginous Embolism, and treatment methods are geared toward symptom management and preventing complications. The treatment options may include:
Regular medical screening at periodic intervals with tests and physical examinations are recommended.
(Source: Fibrocartilaginous Embolism; Genetic and Rare Diseases Information Center (GARD) of National Center for Advancing Translational Sciences (NCATS), USA.)
The following DoveMed website link is a useful resource for additional information:
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