Which are the symptoms of Scleromyxedema?

See the worst symptoms of affected by Scleromyxedema here

Scleromyxedema is a rare, chronic, and progressive skin disorder that falls under the umbrella of mucinosis, a group of conditions characterized by the abnormal accumulation of a substance called mucin in the skin and other organs. This condition primarily affects adults, with a slight predilection for males over females.

The hallmark symptom of scleromyxedema is the presence of skin changes. These changes typically manifest as a diffuse thickening and hardening of the skin, giving it a waxy appearance. The affected skin may feel tight and be difficult to move, leading to limited joint mobility. The thickening can occur in various areas of the body, but it most commonly affects the face, neck, upper trunk, and extremities.

Another prominent symptom of scleromyxedema is the presence of papules and nodules on the skin. These lesions are usually small, firm, and reddish-brown in color. They can be scattered across the body or concentrated in specific areas. The papules and nodules may be itchy or tender, causing discomfort to the affected individuals.

In addition to skin changes, scleromyxedema can also involve other organs, leading to a range of systemic symptoms. Neurological symptoms are relatively common and can include peripheral neuropathy, which may cause numbness, tingling, or weakness in the extremities. Some individuals may experience difficulty with coordination or balance.

Ocular manifestations are also observed in scleromyxedema, with symptoms such as dry eyes, gritty sensation, and blurred vision. These ocular symptoms can significantly impact visual function and quality of life.

Systemic symptoms may include weight loss, fatigue, muscle weakness, joint pain, and gastrointestinal disturbances. These symptoms can vary in severity and may significantly affect the overall well-being of individuals with scleromyxedema.

It is important to note that scleromyxedema is a rare condition, and its symptoms can overlap with other disorders, making diagnosis challenging. Therefore, it is crucial to consult a healthcare professional for a comprehensive evaluation if any of the aforementioned symptoms are present.

Diseasemaps

The itching is unbearable. Joint and muscle pain comes and goes along with the migraines. Not being able to use wrists to open anything or to grasp.The shrinking of your mouth makes it difficult to eat. After being diagnosed with the disease back in 2012, it's been an emotional rollercoaster! Some days nothing, others, body would be on fire, with the itching being uncontrollable. Every 5 weeks I receive the IVIG treatment. But symptoms it still come and go. Sometimes worse than others.

Posted Aug 14, 2017 by Kelsey 100

Lack of general mobility with many side effects including eating and swallowing, loss of strength, difficulty handling almost anything, getting dressed , impaired hearing due to mucin build up, balance problems, driving is ok but only for short duration, anything over 15-20 mins. can become tedious as pain starts to build from sitting too long. Going to the toilet can be a problem. Relationships have been affected to the point of breakup. Probably the eating disorders would be my first thing to fix. We could go on a lot further but I think people would get the general idea that this disease is one that would be well down the list if you had to pick one and it is said to be incureable although some have got relief from symptoms so much so that they live reasonably well but without treatment life is miserable.

Posted Jan 18, 2019 by Rob 2750

Hard, elephant-like, skin with papules. Rock-hard red nose, swollen in size. Tight mouth which is impossible to open, and a teaspoon being the only feeding utensil to fit. Very painful fingers, wrists and feet.

Posted Jan 26, 2019 by Kay 2500