The disease is acquired, meaning it’s not an inherited condition or present at the time of birth. Typically, the syndrome begins in childhood or young adulthood, and usually, the facial atrophy occurs on the left side of the face.
Parry-Romberg syndrome may be referred to by other names as well, such as:
Progressive hemifacial atrophy (PHA)Progressive facial hemiatrophyIdiopathic hemifacial atrophyRomberg’s syndrome
In certain circumstances, the disease may progress to both sides of the face. It may even affect an arm, the midsection, or a leg.
The first descriptions of PRS were provided by physicians Caleb Parry in 1825 and Moritz Romberg in 1846. Often, PRS is linked to a form of the autoimmune disease scleroderma called linear scleroderma, or “en coupe de sabre” (ECDS). In linear scleroderma, a localized area of the skin and the tissues beneath it contain abnormalities similar to those found in PRS. At the present time, the cause of the syndrome isn’t well understood and may vary between one person and another.
Symptoms
The signs and symptoms of PRS can range from mild to severe. The characteristic symptoms of PRS are atrophy (wasting away) of the skin and soft tissues. Additionally, muscle, cartilage, and bone may be affected. Because PRS is a progressive disease, all symptoms worsen over time until reaching a period of stability.
Causes
The cause of PRS is unknown, but a number of theories have emerged over the years as to possible factors that contribute to the disease. Such ideas include:
Trauma (some cases of PRS seemed to have originated from trauma to the face or neck) Autoimmunity (immune response that mistakenly attacks healthy cells) Bacterial infections like Lyme disease (caused by tick bites) Viral infections like herpes Dysfunction of the nervous system Encephalitis, or inflammation of the brain Vasculitis, or blood vessel abnormalities Scleroderma (group of diseases that cause hardening and tightening of skin and connective tissue) Benign (noncancerous) tumors
One cause may not apply to all people with PRS. Factors that contribute to the development of the condition in one individual may be entirely different in another person. Currently, more research is needed to help pinpoint an underlying source of this condition.
Diagnosis
To diagnose PRS, your physician or medical team will look for the distinguishing characteristics of the condition. Generally, the onset of PRS occurs in children between the ages of 5 and 15 years of age. The doctor will take a detailed medical history and perform a comprehensive physical examination.
During the physical exam, the physician will check for reduced facial skin integrity and a loss of fat, muscle, and bone. The doctor may decide further testing is needed, such as a CT (computed tomography) scan or MRI (magnetic resonance imaging), to confirm a diagnosis of PRS.
In some cases, a biopsy (removing a sample of tissue for further examination) of the affected skin may be recommended when a patient has a diagnosis of linear scleroderma as well.
Treatment
To date, there’s no one-size-fits-all approach to treating PRS. Treatment is aimed at providing symptom relief, controlling seizures when they’re present, and stopping the further advancement of the disease, states a literature review in the American Journal of Neuroradiology.
Several medical specialists may be involved in care, including dermatologists (skin specialists), eye doctors, surgeons, and neurologists (nervous system specialists). Treatment follows no established guidelines, and most research has involved small numbers of people or case reports.
Because the cause of PRS is often unclear, there are reports in medical literature of many treatments being tried, although none yet has proven helpful, including:
Immunosuppressive therapies like corticosteroidsImmunomodulators, including a combination of methotrexate and prednisonePlasmapheresis (filtering of blood plasma)Anticonvulsant drugs to reduce seizures when applicableAntimalarials (drugs to fight malaria)Vitamin D
PRS is considered self-limiting, meaning there’s a progressive period of deterioration until it reaches a period of stabilization. Once the condition has stabilized, surgical intervention and cosmetic treatments may be necessary to improve facial function and appearance. These treatments may include:
Pulsed dye lasers Dermal fat grafts Autologous fat grafts where fat is removed from your own body Muscle flap grafts Silicone injections or implants Bone grafts Cartilage grafts Hyaluronic acid injections to fill in areas beneath the skin
Prognosis
Although PRS is a self-limiting condition, the severity of the symptoms can vary significantly from one person to the next. Furthermore, the period of time it takes the disease to reach a period of stability also differs considerably among individuals.
GARD suggests it may take a person between two and 20 years to reach a point of stability. Additionally, those who develop PRS later in life may experience a less severe form of the condition due to having a fully developed nervous system and craniofacial structures.
It is possible for patients with PRS to relapse after treatment, according to a study in a 2014 issue of the Orphanet Journal of Rare Diseases.
A Word From Verywell
There is still a lot of information yet to discover about PRS, and a diagnosis of the condition can have negative ramifications on a person’s mental health and social life. Due to the rarity of the syndrome, individuals may feel as if they are alone. Therefore, it’s important to find a doctor whom you can trust and communicate your questions and concerns to.
If you’re looking to connect with others with this disease, organizations like The Romberg’s Connection and the International Scleroderma Network offer support to patients and families and may be able to point you toward additional resources as well.
