icd 9 cm code for scleroderma

What is the ICD-9-CM code for systemic sclerosis?

Systemic sclerosis ICD-9-CM 710.1 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 710.1 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).

What is the ICD 10 code for scleroderma?

Systemic sclerosis [scleroderma] M34- 1 circumscribed scleroderma (#N#ICD-10-CM Diagnosis Code L94.0#N#Localized scleroderma [morphea]#N#2016 2017 2018 2019 2020 2021... 2 neonatal scleroderma (#N#ICD-10-CM Diagnosis Code P83.88#N#Other specified conditions of integument specific to newborn#N#2018... More ...

What is the ICD-9 code for diagnosis?

ICD-9-CM 710.1 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 710.1 should only be used for claims with a date of service on or before September 30, 2015.

What is scleroderma (systemic sclerosis)?

Scleroderma, also known as systemic sclerosis, is a chronic systemic autoimmune disease characterised by hardening (sclero) of the skin (derma). In the more severe form, it also affects internal organs.

What is the ICD-10 code for scleroderma?

ICD-10 code M34 for Systemic sclerosis [scleroderma] is a medical classification as listed by WHO under the range - Diseases of the musculoskeletal system and connective tissue .

Can scleroderma be cured?

There is no treatment that can cure or stop the overproduction of collagen that is characteristic of scleroderma. But a variety of treatments can help control symptoms and prevent complications.

What is scleroderma caused by?

Scleroderma is caused by the immune system attacking the connective tissue under the skin and around internal organs and blood vessels. This causes scarring and thickening of the tissue in these areas.

Can scleroderma be fatal?

This form of scleroderma can occur at any age but is most common in women of childbearing age. It occurs in around 30 persons per million population per year and there are an estimated 125,000 active cases in the United States and perhaps 2.5 million worldwide. It is the most fatal of all the rheumatologic diseases.

What were your first signs of scleroderma?

Early symptoms may include swelling and itchiness. Affected skin can become lighter or darker in color and may look shiny because of the tightness. Some people also experience small red spots, called telangiectasia, on their hands and face.

What is the life expectancy of someone with scleroderma?

In general, patients with limited scleroderma have a normal life expectancy. Some have problems with their GI tract, especially heartburn; severe Raynaud's and musculoskeletal pain; and a small subset can develop pulmonary hypertension that can be life-threatening.

What is scleroderma diagnosis?

It is a clinical diagnosis that requires a thorough exam and history by the doctor. The doctor will start by asking questions about symptoms and previous medical history. He or she will also do a physical exam and may order a biopsy to look at a small sample of the affected skin under a microscope.

Who is at risk for scleroderma?

Middle age, female sex, positive family history and exposure to silica are risk factors for scleroderma. Infectious agents, alcohol and cigarette smoking are not risk factors for scleroderma development.

What is the best treatment for scleroderma?

Treating SclerodermaGetting pain relief through nonsteroidal, anti-inflammatory medications or corticosteroids.Easing skin itchiness with skin lotions and moisturizers.Slowing skin thickening and minimizing damage to the internal organs with medication that suppresses the immune system.More items...

Is scleroderma worse than lupus?

Patients with systemic sclerosis (SSc) have worse health-related quality of life than patients with other systemic rheumatic diseases such as rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE), a Korean study found.

What is the difference between lupus and scleroderma?

Lupus, for instance, can have symptoms that include fatigue and fever. Symptoms of scleroderma can include heartburn. When you notice the first symptoms—generally some form of skin rash that doesn't go away or that worsens over time—you may seek treatment from a primary care doctor or dermatologist.

Why is scleroderma so painful?

Some people with Scleroderma develop a painful condition called trigeminal neuralgia. This is caused by inflammation of the nerves that provide sensation to the face. The nerve inflammation causes pain. The intensity of pain isn't constant.

What is the code for cutaneous scleroderma?

Sometimes called systemic sclerosis, the subcategories (all classified to code 710.1) include the following: • Diffuse cutaneous systemic sclerosis — affects skin of the fingers, hands, arms, legs, face, neck, and trunk.

What is the name of the scleroderma that is white with a purple border?

Two subcategories of localized scleroderma (both included in code 701.0) are as follows: • Morphea — oval-shaped, thick patches appear on the skin, which are white in the middle with a purple border. This form of scleroderma most likely occurs on the torso but may also appear on the arms, legs, or forehead.

Where does scleroderma occur?

This form of scleroderma most likely occurs on the torso but may also appear on the arms, legs, or forehead. • Linear scleroderma — results in bands or streaks of hardened skin on one or both of the arms or legs or on the forehead. Systemic scleroderma (710.1) affects not only the skin but also blood vessels and major organs.

Is scleroderma contagious?

The condition, which is not contagious, infectious, or cancerous, may range in seriousness from mild to life threatening. There is currently no cure for scleroderma, and the autoimmune disorder may be fatal if left untreated. Signs and Symptoms.

Can scleroderma be treated with blood tests?

Blood tests may be ordered to check for elevated blood levels of certain antibodies. The physician may also choose to perform a skin biopsy. Although there is no known cure and treatment will not stop the overproduction of collagen, medications will treat symptoms and complications of sc leroderma.

What is systemic scleroderma?

Systemic sclerosis [scleroderma] M34- 1 A chronic disorder, possibly autoimmune, marked by excessive production of collagen which results in hardening and thickening of body tissues. The two types of systemic scleroderma, limited cutaneous and diffuse cutaneous are classified with focus on the extent of affected skin. A relationship exists between the extent of skin area affected and degree of internal organ/system involvement. Systemic scleroderma can manifest itself in pulmonary fibrosis, raynaud's syndrome, digestive system telangiectasias, renal hypertension and/or pulmonary hypertension. 2 A chronic multi-system disorder of connective tissue. It is characterized by sclerosis in the skin, the lungs, the heart, the gastrointestinal tract, the kidneys, and the musculoskeletal system. Other important features include diseased small blood vessels and autoantibodies. The disorder is named for its most prominent feature (hard skin), and classified into subsets by the extent of skin thickening: limited scleroderma and diffuse scleroderma. 3 A disease that is marked by hardening and thickening of skin, connective tissue that surrounds other tissues and organs, and blood vessels. 4 A rare, chronic disease characterized by excessive deposits of collagen in the skin or other organs 5 Systemic disorder of the connective tissue; manifested by hardening and thickening of the skin, by abnormalities involving the microvasculature and larger vessels, and by fibrotic degenerative changes in various body organs including the heart, lungs, kidneys, and gastrointestinal tract.

What is a type 1 exclude note?

A type 1 excludes note is for used for when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition. A chronic disorder, possibly autoimmune, marked by excessive production of collagen which results in hardening and thickening of body tissues.

What is collagen disease?

A rare, chronic disease characterized by excessive deposits of collagen in the skin or other organs. Systemic disorder of the connective tissue; manifested by hardening and thickening of the skin, by abnormalities involving the microvasculature and larger vessels, and by fibrotic degenerative changes in various body organs including the heart, ...

What is the name of the disorder that is marked by hardening and thickening of skin?

The disorder is named for its most prominent feature (hard skin), and classified into subsets by the extent of skin thickening: limited scleroderma and diffuse scleroderma. A disease that is marked by hardening and thickening of skin, connective tissue that surrounds other tissues and organs, and blood vessels.

What is connective tissue disorder?

A chronic multi-system disorder of connective tissue. It is characterized by sclerosis in the skin, the lungs, the heart, the gastrointestinal tract, the kidneys, and the musculoskeletal system. Other important features include diseased small blood vessels and autoantibodies.

What is the ICd code for scleroderma?

The ICD code L940 is used to code Scleroderma. Scleroderma, also known as systemic sclerosis, is a chronic systemic autoimmune disease characterised by hardening (sclero) of the skin (derma). In the more severe form, it also affects internal organs. Specialty:

What is the approximate match between ICd9 and ICd10?

This is the official approximate match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that while there is no exact mapping between this ICD10 code L94.0 and a single ICD9 code, 701.0 is an approximate match for comparison and conversion purposes.