Guillain-Barré syndrome history and symptoms
|
Guillain-Barré syndrome Microchapters |
|
Diagnosis |
|---|
|
Treatment |
|
Case Studies |
|
Guillain-Barré syndrome history and symptoms On the Web |
|
American Roentgen Ray Society Images of Guillain-Barré syndrome history and symptoms |
|
Risk calculators and risk factors for Guillain-Barré syndrome history and symptoms |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editors-In-Chief: Priyamvada Singh, MBBS [2]
Overview
Guillain-Barré syndrome (GBS) is an acute, autoimmune, polyradiculoneuropathy affecting the peripheral nervous system, usually triggered by an acute infectious process. It is included in the wider group of peripheral neuropathies. There are several types of GBS, but unless otherwise stated, GBS refers to the most common form, acute inflammatory demyelinating polyneuropathy (AIDP). It is frequently severe and usually exhibits as an ascending paralysis noted by weakness in the legs that spreads to the upper limbs and the face along with complete loss of deep tendon reflexes. However, death may occur if severe pulmonary complications and dysautonomia are present.
History and symptoms
History
- Patients with Guillain-Barre syndrome may present with a history of antecedence benign infection of gut or respiratory tract 2-4 weeks prior to the development of symptoms.
- The mean time to the clinical function nadir is 12 days, with 98% of patients reaching a nadir by 4 weeks. This is followed by a plateau phase characterized by persistent, unchanging symptoms. The plateau phase may last for days before initiation of gradual symptoms improvement.
Symptoms
- The first neurological symptoms in many patient may be tingling or numbness sensation of the fingers.
- These symptoms may be followed by development of flaccid paralysis of lower extremities followed by involvement of trunk, upper limb and other parts of the body.
- The progression of symptoms may take hours to days. Depending on the type of GBS involvement of sensory, repiratory and autonomic system may occur.
The disease is characterized by weakness which affects the lower limbs first, and rapidly progresses in an ascending fashion. Patients generally notice weakness in their legs, manifesting as "rubbery legs" or legs that tend to buckle, with or without dysthesias (numbness or tingling). As the weakness progresses upward, usually over periods of hours to days, the arms and facial muscles also become affected. Frequently, the lower cranial nerves may be affected, leading to bulbar weakness, (oropharyngeal dysphagia, that is difficulty with swallowing, drooling, and/or maintaining an open airway) and respiratory difficulties. Most patients require hospitalization and about 30% require ventilatory assistance. Facial weakness is also commonly a feature, but eye movement abnormalities are not commonly seen in ascending GBS, but are a prominent feature in the Miller-Fisher variant (see below.)
Sensory loss, if present, usually takes the form of loss of proprioception (position sense) and areflexia (complete loss of deep tendon reflexes), an important feature of GBS. Loss of pain and temperature sensation is usually mild. In fact, pain is a common symptom in GBS, presenting as deep aching pain usually in the weakened muscles, which patients compare to the pain from overexercising. These pains are self-limited and should be treated with standard analgesics. Bladder dysfunction may occur in severe cases but should be transient. If severe, spinal cord disease should be suspected.
Fever should not be present, and if it is, another cause should be suspected.
In severe cases of GBS, loss of autonomic function is common, manifesting as wide fluctuations in blood pressure, orthostatic hypotension, and cardiac arrhythmias.
Symptoms of Guillain-Barré can get worse very quickly. It may take only a few hours to reach the most severe symptoms, but weakness increasing over several days is also common.
Muscle weakness or the loss of muscle function (paralysis) affects both sides of the body. In most cases, the muscle weakness starts in the legs and then spreads to the arms. This is called ascending paralysis.
Patients may notice tingling, foot or hand pain, and clumsiness. If the inflammation affects the nerves to the diaphragm, and there is weakness in those muscles, the person may need breathing assistance.
Typical symptoms include:
- Loss of reflexes in the arms and legs
- Muscle weakness or loss of muscle function (paralysis)
- Numbness, decreased sensation
- Sensation changes
- Tenderness or muscle pain (may be a cramp-like pain)
- Uncoordinated movement
Additional symptoms may include:
- Blurred vision
- Clumsiness and falling
- Difficulty moving face muscles
- Muscle contractions
- Palpitations (sensation of feeling heartbeat)
Emergency symptoms (seek immediate medical help):
- Breathing temporarily stops
- Can't take a deep breath
- Difficulty breathing
- Difficulty swallowing
- Drooling
- Fainting
- Feeling light-headed when standing