Poikiloderma

From WikiMD's Wellness Encyclopedia


Poikiloderma
Synonyms
Pronounce N/A
Specialty N/A
Symptoms Skin atrophy, telangiectasia, hyperpigmentation, hypopigmentation
Complications
Onset
Duration
Types N/A
Causes Genetic disorders, environmental factors
Risks
Diagnosis Clinical examination, biopsy
Differential diagnosis Lupus erythematosus, scleroderma
Prevention N/A
Treatment Sun protection, topical treatments
Medication
Prognosis
Frequency
Deaths N/A


Poikiloderma is a condition characterized by changes in the skin, including atrophy, telangiectasia, and variations in pigmentation such as hyperpigmentation and hypopigmentation. It is often a result of genetic disorders or environmental factors.

Signs and Symptoms[edit | edit source]

Poikiloderma presents with a combination of skin changes:

Causes[edit | edit source]

The causes of poikiloderma can be varied and include:

Diagnosis[edit | edit source]

Diagnosis of poikiloderma is primarily clinical, based on the appearance of the skin. A biopsy may be performed to rule out other conditions and confirm the diagnosis.

Differential Diagnosis[edit | edit source]

Conditions that may present similarly to poikiloderma include:

Treatment[edit | edit source]

Management of poikiloderma focuses on:

See Also[edit | edit source]

References[edit | edit source]


External Links[edit | edit source]

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Contributors: Prab R. Tumpati, MD