Steatocystoma Multiplex

Overview

A disorder characterized by multiple, wide spread cutaneous cysts that often become inflamed and rupture. It is caused by the same mutations in the gene coding for KRT-17 that are causative mutations for Pachyonychia congenita, Type 2. Natal teeth involvement is sometimes associated with steatocystoma multiplex.

This information is general and should not be treated as medical advice. Always speak directly with a qualified healthcare professional before making decisions about treatment, diagnosis, procedures, medicines or care.

Quick facts about Steatocystoma Multiplex

Topic type

Condition

Category

Dermatology

MeSH classification

C16.131.831.350.856.500|C16.320.850.250.856.500|C17.800.529.594.500|C17.800.804.350.856.500|C17.800.827.250.856.500

Preparing for an appointment about Steatocystoma Multiplex

If you are speaking with a healthcare professional about Steatocystoma Multiplex, it can help to prepare a few details in advance.

• Write down your symptoms and when they started.
• Bring details of any medicines, supplements or previous treatments.
• Ask what tests or assessments may be needed.
• Ask what treatment or management options may be suitable.
• Ask when you should seek urgent medical help or follow-up care.

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