icd 10 code for dsap

by Lilyan Wolf DVM 5 min read

ICD-10-CM Code for Disseminated superficial actinic porokeratosis (DSAP) L56. 5.

Is porokeratosis the same as DSAP?

Disseminated superficial actinic porokeratosis, or DSAP, is an inherited keratinisation disorder that causes discrete dry patches on the arms and legs. DSAP is a special type of inherited 'sunspot". The name porokeratosis means scaly pore and is a misnomer as porokeratosis is not related to pores.

What is DSAP skin condition?

Disseminated superficial actinic porokeratosis (DSAP) is a skin condition that causes dry, scaly patches.[8488] Symptoms include a large number of small, brownish patches with a distinctive border, found most commonly on sun-exposed areas of the skin (particularly the lower arms and legs).[8488][8489] DSAP usually ...

Is DSAP an autoimmune disease?

Disseminated superficial actinic porokeratosis (DSAP) is an inherited skin disease characterized by many uniformly small, annular, anhidrotic, keratotic lesions developing during the third or fourth decade of life on sun-exposed areas of skin [1].

What is porokeratosis?

Porokeratosis is a clonal disorder of keratinization characterized by one or more atrophic patches surrounded by a clinically and histologically distinctive hyperkeratotic ridgelike border called the cornoid lamella.

What is the difference between actinic keratosis and DSAP?

It is sometimes confused with actinic keratosis which is also caused by sun exposure (See Patient Information Leaflet on Actinic Keratoses); however, actinic keratosis is more likely to arise on the face and hands. DSAP is twice as likely to develop in women compared with men and is more common in lighter skin type.

What causes disseminated superficial actinic Porokeratosis?

Disseminated superficial actinic porokeratosis (DSAP) is an uncommon skin condition that leads to reddish brown scaly spots. The spots are mostly seem on the arms and legs, but sometimes will show up on other sun-damaged skin. It is due to an abnormal sun sensitivity leading to pre-cancerous skin cells.

How do you treat DSAP?

Often misdiagnosed as chronic UV-damage or actinic keratoses, patients are treated for years with different therapeutic options with little success. Current treatment options include imiquimod, ingenol mebutate, cryosurgery, photodynamic therapy and topical or systemic therapy with retinoids.

Does DSAP ever go away?

DSAP may be asymptomatic or pruritic, and lesions tend to worsen and multiply when exposed to sunlight or UV light; conversely, these lesions may fade in winter.

Who gets DSAP?

Disseminated superficial actinic porokeratosis (DSAP) is an inherited skin condition that may occur in 50% of children who are born to an affected parent. When one child of a parent with DSAP inherits the condition, it's a good idea to tell any brothers and sisters to also check their skin.

What is the ICD 10 code for porokeratosis?

ICD-10-CM Code for Disseminated superficial actinic porokeratosis (DSAP) L56. 5.

Is porokeratosis malignant?

Porokeratosis is considered a premalignant condition, as all its variants have a potential for malignant transformation. The most common cancer is squamous cell carcinoma followed by basal cell carcinoma.

Why do you get porokeratosis?

This patch grows in size, and the bumps may become raised with a ring around the outside of each spot. The exact cause of porokeratosis is not known, but genetic factors and having a weak immune system may put you at a greater risk for the condition. Sunlight, UV rays, and other radiation worsen the condition.

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This Billing and Coding Article provides billing and coding guidance for Local Coverage Determination (LCD) L34938, Removal of Benign Skin Lesions.

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