Hypertrichosis
Chapter 12:Diseases of the skin and subcutaneous tissue
ICD-10 L68 is a used to indicate a diagnosis of hypertrichosis.
Hypertrichosis is a condition characterized by excessive hair growth in areas of the body where hair is normally minimal or absent. This condition can be classified into two main types: congenital hypertrichosis, which is present at birth, and acquired hypertrichosis, which develops later in life due to various factors such as hormonal changes, medications, or underlying health conditions. The clinical significance of hypertrichosis lies in its potential psychological impact on affected individuals, as it can lead to social stigma, anxiety, and decreased quality of life. Accurate diagnosis and coding are essential for appropriate treatment and management of the condition.
Standard ICD-10-CM documentation requirements apply
Various clinical presentations within this specialty area
Follow specialty-specific billing guidelines
Standard ICD-10-CM documentation requirements apply
Various clinical presentations within this specialty area
Follow specialty-specific billing guidelines
L68 includes various forms of hypertrichosis, such as congenital hypertrichosis, acquired hypertrichosis, and localized hypertrichosis, which may arise from different etiologies.
L68 codes should be used when documenting cases of hypertrichosis, particularly when the condition is diagnosed or when treatment is initiated, ensuring that the specific type is noted.
Documentation for L68 should include a detailed clinical assessment of the patient's hair growth patterns, any relevant medical history, and the identification of potential underlying causes or contributing factors.
