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Generally, diseases outlined within the ICD-10 codes L80-L81 within Chapter XII: Diseases of the skin and subcutaneous tissue should be included in this category. Disturbances of human pigmentation, either loss or reduction, may be related to loss of melanocytes or the inability of melanocytes to produce melanin or transport melanosomes correctly.
Idiopathic guttate hypomelanosis: No treatment Postinflammatory hypopigmentation: Treat the underlying inflammatory disease to restore pigmentation Pityriasis versicolor: A topical ointment, such as selenium sulfide 2.5% or imidazoles. Can also use oral medications, such as oral imidazoles or triazoles. Vitiligo
Periorbital hyperpigmentation, also known as hereditary dark circles, is characterized by darker skin around the eyes caused by the presence of additional melanin.It is an extremely common hereditary human characteristic and is frequently found on individuals with dark skin.
Idiopathic guttate hypomelanosis is characterised by multiple small whitish flat spots. [1] They are typically irregular, well defined and frequently appear on the arms, legs, and faces of older people. [1] It occurs in up to 80% of people over 70 years old. [2] Females may notice it at a younger age than males. [3]
Skin pigmentation is a frequent disorder that has a number of potential causes. Genetics, sun exposure, and some drugs are the three main factors that contribute to skin pigmentation.
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BCEM, also referred to as conjunctival hypermelanosis, complexion-associated melanosis, or racial melanosis, is a non-cancerous lesion of the conjunctiva that is more commonly found in dark-skinned individuals (over 90% of lesions are found in black persons and around 5% in white persons). [1]
Melanosis is a form of hyperpigmentation associated with increased melanin. [1] It can also refer to: Melanism; Ocular melanosis; Smoker's melanosis; Oral melanosis;