Heerfordt syndrome
Heerfordt syndrome | |
---|---|
Synonyms | Uveoparotid fever |
Pronounce | N/A |
Specialty | N/A |
Symptoms | Fever, parotitis, anterior uveitis, facial nerve palsy |
Complications | Chronic sarcoidosis |
Onset | Typically in adulthood |
Duration | Variable |
Types | N/A |
Causes | Unknown, associated with sarcoidosis |
Risks | Genetic predisposition, autoimmune disease |
Diagnosis | Clinical evaluation, biopsy, imaging studies |
Differential diagnosis | Sjogren's syndrome, mumps, Bell's palsy |
Prevention | N/A |
Treatment | Corticosteroids, immunosuppressive therapy |
Medication | N/A |
Prognosis | Generally good with treatment |
Frequency | Rare |
Deaths | N/A |
Heerfordt Syndrome is a rare disorder characterized by parotid gland enlargement, uveitis, facial nerve palsy, and fever. It is also known as Heerfordt-Waldenstrom syndrome and is a subtype of sarcoidosis, a condition that causes inflammation in various parts of the body.
Symptoms
The symptoms of Heerfordt Syndrome can vary greatly from person to person. The most common symptoms include:
- Fever
- Facial nerve palsy
- Uveitis
- Parotid gland enlargement
Causes
The exact cause of Heerfordt Syndrome is unknown. However, it is believed to be a subtype of sarcoidosis, a condition that causes inflammation in various parts of the body.
Diagnosis
Diagnosis of Heerfordt Syndrome is often challenging due to its rarity and the variety of symptoms. It is typically diagnosed through a combination of clinical examination, imaging studies, and biopsy of affected tissues.
Treatment
Treatment for Heerfordt Syndrome is primarily aimed at managing the symptoms. This may include medications to reduce inflammation and control symptoms, as well as physical therapy to manage facial nerve palsy.
Prognosis
The prognosis for individuals with Heerfordt Syndrome is generally good, with most individuals experiencing a full recovery with appropriate treatment. However, the condition can be chronic and relapsing in some cases.
See Also
References
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