ICD-10 Diagnosis Code L57.4

Cutis laxa senilis

Diagnosis Code L57.4

ICD-10: L57.4
Short Description: Cutis laxa senilis
Long Description: Cutis laxa senilis
This is the 2017 version of the ICD-10-CM diagnosis code L57.4

Code Classification
  • Diseases of the skin and subcutaneous tissue
    • Radiation-related disorders of the skin and subcutaneous tissue (L55-L59)
      • Skin changes due to chronic expsr to nonionizing radiation (L57)

Information for Medical Professionals

Diagnostic Related Groups
The diagnosis code L57.4 is grouped in the following Diagnostic Related Group(s) (MS-DRG v33.0)


Convert to ICD-9 Additional informationCallout TooltipGeneral Equivalence Map
The ICD-10 and ICD-9 GEMs are used to facilitate linking between the diagnosis codes in ICD-9-CM and the new ICD-10-CM code set. The GEMs are the raw material from which providers, health information vendors and payers can derive specific applied mappings to meet their needs.

  • Atrophy of skin caused by drug
  • Cutis laxa
  • Cutis laxa following hypersensitivity reaction
  • Cutis laxa following urticaria-angioedema
  • Cutis laxa senilis
  • Cutis laxa with complement deficiency
  • Cutis laxa, acquired type
  • Cutis laxa, acquired type
  • Cutis laxa, acquired type
  • Drug-induced cutis laxa
  • Elastosis senilis
  • Post-inflammatory cutis laxa
  • Redundant skin
  • Senile dermatosis

Index of Diseases and Injuries
References found for the code L57.4 in the Index of Diseases and Injuries:

Information for Patients

Connective Tissue Disorders

Connective tissue is the material inside your body that supports many of its parts. It is the "cellular glue" that gives your tissues their shape and helps keep them strong. It also helps some of your tissues do their work. Cartilage and fat are examples of connective tissue.

There are over 200 disorders that impact connective tissue. Some, like cellulitis, are the result of an infection. Injuries can cause connective tissue disorders, such as scars. Others, such as Ehlers-Danlos syndrome, Marfan syndrome, and osteogenesis imperfecta, are genetic. Still others, like scleroderma, have no known cause. Each disorder has its own symptoms and needs different treatment.

  • Dupuytrens contracture

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