Sarcoidosis is a rare inflammatory condition that develops when a group of cells in the immune system form patches of swollen tissue. These are called granulomas.

While most people see an improvement in a few months or years, sarcoidosis can also be a life-threatening illness. Therefore, it is essential to know this disease’s symptoms and risk factors.

Sarcoidosis is a rare disease that develops when groups of immune cells form small patches of tissue in the body’s organs. It is uncommon and affects about 1.2 million people around the world. 

Furthermore, it can affect many body parts, including the eyes, skin, lungs, heart, and nervous system.

The disease usually develops as an autoimmune response by the body. While there is no direct cause, experts have traced its genetic origin. It could also have an environmental component that can cause the immune system to go into overdrive. 

It usually starts in the lungs or lymph nodes and then shows signs and symptoms around the body.

The symptoms of this condition vary widely depending on the severity and organs of affectation. For example, those whose lungs are affected have symptoms consistent with lung damage. 

It could also affect the kidneys, heart, and skin, causing symptoms like tachycardia, erythema, and severe fever. These are usually why people go to the hospital to know what’s wrong with them.

More often than not, sarcoidosis affects the skin. This is a primary symptom of the disease. This is called Lofgren syndrome. 

It is a classic triad of fever, erythema nodosum, and bilateral hilar adenopathy (enlargement of the pulmonary lymph nodes). In addition, swollen and painful joints around the body cause discomfort. Red, raised, and tender bumps are also common.

When sarcoidosis strikes the lungs, it is often quite severe. Therefore, the patient experiences wheezing, coughing, shortness of breath, and chest pain. 

Those who present with pulmonary symptoms are classified as having pulmonary sarcoidosis. In severe cases, the lungs become inflamed, which eventually results in fibrosis. Therefore, it is important to treat it as soon as possible.

Sarcoidosis can affect the heart and kidneys at various stages. Therefore, it is important to monitor the function of these organs, as they can increase the severity. 

Cardiac sarcoidosis can cause arrhythmia and even death through heart failure. On the other hand, renal sarcoidosis usually presents with high calcium levels in the blood, causing kidney stones.

As mentioned earlier, sarcoidosis has varying risk factors. These include advanced age, environmental issues, work factors, family history, genetics, race, and ethnicity. 

Therefore, people with a higher risk factor need to be careful about developing the disease. While the severity can be different, it is best to never have it at all. Some risk factors are beyond one’s control, but you can monitor others.

One’s place of residence is a considerable risk factor for the disease. For those who live in places infested with mold, pollutants, or other substances, this may cause constant inflammatory reactions in the body. 

Furthermore, people who work in places like factories with insecticides are prone to lung infections, which can trigger inflammation and lead to sarcoidosis.

Age is a considerable risk factor for sarcoidosis. As most people know, an increase in age means an increase in disease susceptibility, so older people are prone to this disease. 

Most significantly, those over the age of 55 have a higher chance of developing the disease. In addition, it may be more difficult to treat older people with this condition.

People with family members who have sarcoidosis have a higher chance of developing this condition. This is because scientists have found a genetic link that can cause people from a particular bloodline to be more susceptible. 

Race, ethnicity, and descent can also play a huge role. For example, Scandinavian people have a higher chance than black people.

Those who suspect sarcoidosis need to go to the hospital for treatment. Doctors will run several tests, including a CT scan, lung function test, and blood test, to confirm the presence of the condition. 

Most people with sarcoidosis do not require treatment. The condition usually disappears on its own after a few months or years. However, doctors typically prescribe corticosteroids as a primary form of therapy.

Most of the time, the condition is not life-threatening. Therefore, with proper management and medical care, there is a meager chance of death or severe damage. 

Symptoms also improve with time as the body tries to heal itself. About 60% of granulomas that cause sarcoidosis cases will disappear over two to five years, and the patient will recover. Relapse is also unlikely.