Somatic Symptom and Related Disorders | Symptoms & Causes
Common symptoms of somatic symptom and related disorders
General symptoms
- fatigue
- dry mouth
- hot or cold sweats
- dizziness, headaches
- trouble concentrating
- trouble with memory, etc.
Symptoms from the stomach and gastrointestinal tract
- stomach pain or bloating
- feeling “full” after only a few bites
- frequent burping
- burning sensation in the chest or upper abdomen
- nausea
- vomiting
- loose stools or diarrhea
Symptoms from the heart and lungs
- palpitations
- chest pain
- difficulty breathing/shortness of breath
Symptoms from the musculoskeletal system
- arm or leg pain
- muscle aches and pains
- joint pains, back pain
- pain when moving
Symptoms from the neurologic motor system
- weakness or paralysis
- abnormal movements (i.e., tremors, stiff/rigid movements, episodes of abnormal generalized limb shaking)
- abnormal limb postures
- abnormalities with gait/walking
Symptoms from the neurologic sensory system
- altered
- reduced, or absent vision or hearing
- reduced or absent speech volume; altered speech articulation
- skin numbness
- sensation of a lump in the throat
- episodes of unresponsiveness resembling fainting or coma
Adapted from American Psychiatric Association, DSM-5, 2013.
How do the somatic symptoms happen?
The brain is a powerful organ. In addition to being responsible for processing our thoughts, feelings, and behaviors, the brain manages all of the body’s functions, from sensations like pain, touch, and temperature to movements of our limbs, our heartbeat, bowel and bladder function, and more. Think of the brain as a control tower that sends and receives messages, or “signals,” from the entire body, carried by the nerves.
When the mind-body connection works well, the brain filters out unimportant signals without us even knowing. However, children and adolescents with SSDs tend to have hypersensitive signals and become aware of body signals that are normally filtered out by the brain. The brain and parts of the body where there is no disease may also start signaling to each other more frequently. For instance, some children with SSDs have many signals in the brain’s pain centers, which can make pain feel worse and may even show up on brain scans.
During childhood, SSDs are equally common in boys and girls, but in adolescence and adulthood, they are more common in females. Up to half of children and adolescents with an SSD also experience depression and anxiety.
Somatic Symptom and Related Disorders | Diagnosis & Treatments
How do we diagnose SSDs?
When an SSD is being considered, a pediatrician and a mental health clinician should evaluate the child or adolescent from physical, psychological, social, and developmental angles, both separately and in relation to each other. Having an SSD does not exclude the possibility of a physical illness, and vice versa. Both can and often coexist in the same child, so evaluation from multiple perspectives is key.
In evaluating for SSDs, clinicians will consider whether a child’s symptoms are more frequent and intense than the passing somatic symptoms we all experience, whether the child is having excessive and persistent thoughts and anxiety about existing physical symptoms, and whether the symptoms interfere with daily life, including school, home life and/or peer relationships
Medical evaluation
Medical evaluation is based on symptoms and guided by any previous tests the child or adolescent may have had. Many youth with SSDs have been subjected to a variety of medical tests already, so any medical work-up is balanced with the need to avoid unnecessary and potentially harmful tests and procedures.
Generally, in children and adolescents with SSDs, the physical examination will find that the symptoms change in different contexts, may not be consistent with any medical findings, or may be more severe than what would be expected from the medical findings.
Psychological evaluation
If an SSD is suspected, a psychiatric consultation can help the child’s care team understand what may be contributing to the child’s distress and which treatments are likely to be most effective. Through careful interviews with the child and family, the team will seek to get a picture of:
- the nature of the physical symptoms
- the history of any past episodes of symptoms
- how the child is functioning emotionally, socially, and academically
- how the child and family are currently coping with the symptoms
- family life in general
The psychiatric clinician will also evaluate the child for mood and anxiety disorders. These disorders often accompany SSDs and can themselves cause physical symptoms that tend to go away when the mood/anxiety disorder is treated.
How Boston Children’s Hospital approaches SSDs
Having a condition that is “invisible” or being told your symptoms are “just in your mind” only adds to the stress of having an SSD. Our specialists understand this and will pull together a diverse team to address the mind and the body at the same time. For many families, it’s a relief to get validation that the symptoms are real and to know that others are going/have gone through the same thing.
SSDs are often temporary, and many children and adolescents fully recover. The most effective treatment involves a team of different specialists — medical doctors, psychologists, psychiatrists, physical therapists, and nurses — working together to address the mind and the body at the same time.
Types of treatment for SSDs
These are the approaches that research has shown to be most helpful:
Cognitive-behavioral therapy
Cognitive behavioral therapy (CBT) helps patients redirect themselves away from negative thoughts and beliefs that make SSDs harder to cope with and can even worsen symptoms.
Imagine the nervous system as a dimmer switch. When the setting is low, the nervous system is calm and symptoms are few and mild; when the setting is high, the nervous system is more activated and symptoms escalate. The setting can be influenced by many factors, including:
- how much the child thinks about their symptoms
- how people around the child react to their symptoms
- the child’s past experiences with the symptoms
- the child’s worry about what is wrong
- the child’s ability to distract themselves from the symptoms
Through CBT techniques like relaxation training and biofeedback, children and adolescents get psychological support and learn strategies to gain more control over their stressful emotions and body sensations, keeping the dimmer switch on a “low” setting.
Families often participate in CBT as well, to help reinforce their child’s new coping strategies and support their recovery.
Exercise and physical rehabilitation
Many youth with SSD experience a deterioration of their physical fitness. Some have previously been very active, and it may be hard to accept that their abilities have changed. Along with the psychological support of CBT, physical rehabilitation gets youth moving, an essential part of their “toolbox” of wellness strategies. Working with a physical therapist or occupational therapist will gradually increase their energy, endurance, and ability, one step at a time.
Medication
As physicians continue to monitor the child’s health, they might suggest medications to help with the SSD. Medication can be used to reduce the physical symptoms and discomfort, as well as to treat anxiety, sleep problems, or mood disorders like depression that can make the physical symptoms worse.
CBT and physical rehabilitation — the two mainstays of treatment — require hard work. The more motivated youth and families are to engage in these forms of treatment, the more they will benefit from them.
In some instances SSDs can become chronic and disabling, particularly when they are unrecognized for a long time. When an SSD is severe and debilitating, a more intensive multidisciplinary treatment program like a partial hospitalization or inpatient care may be recommended to support the child’s physical and psychological recovery.
Prognosis
Most children and adolescents with SSDs benefit from this multi-team treatment. Studies show that some are cured and many will feel significantly better. Follow-up care can generally be handled by their pediatrician.
Symptoms may wax and wane in times of change or stress, but being aware of this possibility can help prevent new episodes or help with quick recovery if they occur again.