L90.8 - Other atrophic disorders of skin
ICD-10: | L90.8 |
Short Description: | Other atrophic disorders of skin |
Long Description: | Other atrophic disorders of skin |
Status: | Valid for Submission |
Version: | ICD-10-CM 2023 |
Code Classification: |
L90.8 is a billable ICD-10 code used to specify a medical diagnosis of other atrophic disorders of skin. The code is valid during the fiscal year 2023 from October 01, 2022 through September 30, 2023 for the submission of HIPAA-covered transactions.
Approximate Synonyms
The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:
- Anetoderma
- Anetoderma following varicella
- Anetoderma secondary to syphilis
- Atrophia cutis senilis
- Atrophic condition of skin
- Atrophic spots of skin
- Atrophoderma neuriticum
- Atrophy of skin due to drug
- Atrophy of skin due to drug
- Atrophy of skin due to systemic corticosteroid
- Atrophy of skin due to topical corticosteroid
- Congenital skin contracture
- Cutaneous atrophy due to corticosteroids
- Diffuse and macular atrophic dermatosis of Stevanovic
- Drug-induced anetoderma
- Drug-induced pseudoxanthoma elasticum
- Elastoderma
- Follicular atrophoderma
- Follicular atrophoderma with palmoplantar hyperkeratosis
- Gower's panatrophy
- Hereditary anetoderma
- Idiopathic mid-dermal elastolysis
- Intrinsic aging of skin
- Laminopathy with premature aging
- Lethal tight skin contracture syndrome
- Linear atrophoderma of Moulin
- Local panatrophy
- Local panatrophy
- Local panatrophy
- Nephrogenic systemic fibrosis
- Nevus atrophicus
- Noninflammatory dermal elastolysis
- Panatrophy
- Perifollicular elastolysis
- Perifollicular macular atrophy
- Primary anetoderma
- Pseudoxanthoma elasticum
- Renal insufficiency
- Rombo syndrome
- Scleroderma-like secondary cutaneous sclerosis
- Sclerotic panatrophy
- Secondary anetoderma
- Senile degenerative atrophy of skin
- Senile dermatosis
- Senile dermatosis
- Severe systemic illness tissue wasting
- Severe systemic illness-induced cutaneous atrophy
- Skin disease attributable to corticosteroid therapy
- Stellate pseudoscar
- Stellate pseudoscar due to corticosteroid
Clinical Information
- Anetoderma-. benign dermatosis caused by a loss of dermal elastic tissue resulting in localized sac-like areas of flaccid skin. it can be either primary (idiopathic) or secondary to other skin conditions, penicillamine use, or premature birth.
- Pseudoxanthoma Elasticum-. an inherited disorder of connective tissue with extensive degeneration and calcification of elastic tissue primarily in the skin, eye, and vasculature. at least two forms exist, autosomal recessive and autosomal dominant. this disorder is caused by mutations of one of the atp-binding cassette transporters. patients are predisposed to myocardial infarction and gastrointestinal hemorrhage.
- Acute Kidney Injury-. abrupt reduction in kidney function. acute kidney injury encompasses the entire spectrum of the syndrome including acute kidney failure; acute kidney tubular necrosis; and other less severe conditions.
- Renal Insufficiency-. conditions in which the kidneys perform below the normal level in the ability to remove wastes, concentrate urine, and maintain electrolyte balance; blood pressure; and calcium metabolism. renal insufficiency can be classified by the degree of kidney damage (as measured by the level of proteinuria) and reduction in glomerular filtration rate.
- Renal Insufficiency, Chronic-. conditions in which the kidneys perform below the normal level for more than three months. chronic kidney insufficiency is classified by five stages according to the decline in glomerular filtration rate and the degree of kidney damage (as measured by the level of proteinuria). the most severe form is the end-stage renal disease (chronic kidney failure). (kidney foundation: kidney disease outcome quality initiative, 2002)
- Anetoderma-. a dermatologic condition characterized by focal loss of elastic tissue. clinically it presents with atrophic depressions or saccular outpouchings of the skin.
- ABCC6 wt Allele|ABC34|ARA|ATP-Binding Cassette, Sub-Family C (CFTR/MRP), Member 6 wt Allele|ATP-Binding Cassette, Subfamily C, Member 6 Gene|EST349056|GACI2|MLP1|MOAT-E|MOATE|MRP6|PXE|PXE1|Pseudoxanthoma Elasticum Gene|URG7-. human abcc6 wild-type allele is located in the vicinity of 16p13.1 and is approximately 75 kb in length. this allele, which encodes multidrug resistance-associated protein 6, plays a role in the active transport of drugs across the plasma membrane. mutation of the gene is associated with pseudoxanthoma elasticum and generalized arterial calcification of infancy type 2.
- Pseudoxanthoma Elasticum-. a rare, progressive, autosomal recessive inherited disorder caused by mutations in the abcc6 gene. it is characterized by calcification and fragmentation of the elastic fibers of the skin, retina, and cardiovascular system. signs and symptoms include skin plaques and bumps, thickened skin, retinal hemorrhage and obstruction of the blood vessels.
Index to Diseases and Injuries References
The Index to Diseases and Injuries is an alphabetical listing of medical terms, with each term mapped to one or more ICD-10 code(s). The following references for this diagnosis code are found in the injuries and diseases index:
- - Anetoderma (maculosum) (of) - L90.8
- - Atrophia - See Also: Atrophy;
- - cutis senilis - L90.8
- - senilis - R54
- - dermatological - L90.8
- - Atrophoderma, atrophodermia (of) - L90.9
- - maculatum - L90.8
- - et striatum - L90.8
- - neuriticum - L90.8
- - senile - L90.8
- - maculatum - L90.8
- - Atrophy, atrophic (of)
- - macular (dermatological) - L90.8
- - skin (patches) (spots) - L90.9
- - degenerative (senile) - L90.8
- - senile - L90.8
- - Dermopathy
- - nephrogenic fibrosing - L90.8
- - Disorder (of) - See Also: Disease;
- - skin - L98.9
- - atrophic - L90.9
- - specified NEC - L90.8
- - atrophic - L90.9
- - skin - L98.9
- - Glossy skin - L90.8
Convert to ICD-9 Code
Source ICD-10 Code | Target ICD-9 Code | |
---|---|---|
L90.8 | 701.8 - Skin hypertro/atroph NEC | |
Approximate Flag - The approximate mapping means there is not an exact match between the ICD-10 and ICD-9 codes and the mapped code is not a precise representation of the original code. |
Patient Education
Skin Conditions
Your skin is your body's largest organ. It covers and protects your body. Your skin:
- Holds body fluids in, preventing dehydration
- Keeps harmful microbes out, preventing infections
- Helps you feel things like heat, cold, and pain
- Keeps your body temperature even
- Makes vitamin D when the sun shines on it
Anything that irritates, clogs, or inflames your skin can cause symptoms such as redness, swelling, burning, and itching. Allergies, irritants, your genetic makeup, and certain diseases and immune system problems can cause rashes, hives, and other skin conditions. Many skin problems, such as acne, also affect your appearance.
NIH: National Institute of Arthritis and Musculoskeletal and Skin Diseases
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Code History
- FY 2023 - No Change, effective from 10/1/2022 through 9/30/2023
- FY 2022 - No Change, effective from 10/1/2021 through 9/30/2022
- FY 2021 - No Change, effective from 10/1/2020 through 9/30/2021
- FY 2020 - No Change, effective from 10/1/2019 through 9/30/2020
- FY 2019 - No Change, effective from 10/1/2018 through 9/30/2019
- FY 2018 - No Change, effective from 10/1/2017 through 9/30/2018
- FY 2017 - No Change, effective from 10/1/2016 through 9/30/2017
- FY 2016 - New Code, effective from 10/1/2015 through 9/30/2016 (First year ICD-10-CM implemented into the HIPAA code set)