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Case for diagnosis. Steatocystoma multiplex.
Alexandre Moretti de Lima1, Sheila Pereira da Rocha, Carolina Mayana de Ávila Batista
1Hospital Regional da Asa Norte, SES, Brasília, DF, Brazil. morettilima@yahoo.com.br
Anais Brasileiros De Dermatologia
|March 26, 2011
Summary
Steatocystoma multiplex is a rare genetic disorder causing multiple skin cysts. This case report details a 23-year-old male patient’s typical disease progression.
Area of Science:
- Dermatology
- Genetics
- Rare Diseases
Background:
- Steatocystoma multiplex is an autosomal dominant genetic condition.
- It presents as multiple, asymptomatic dermal cysts of varying sizes.
Observation:
- A case of a 23-year-old male patient with steatocystoma multiplex is presented.
- The patient exhibited a typical clinical presentation and disease progression.
Findings:
- The case aligns with the known characteristics of steatocystoma multiplex.
- Detailed observation of clinical and evolutionary aspects was documented.
Implications:
- This case contributes to the understanding of steatocystoma multiplex in young adults.
- It highlights the importance of recognizing typical presentations of rare genetic skin disorders.
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