Abstract
Tuberous sclerosis complex (TSC) is an autosomal dominant syndrome due to a mutation in the TSC2 or TSC1 gene. The disease is known to have variable expressivity involving the neurological, cardiovascular, renal, pulmonary, and integumentary systems (Kennedy et al., 2017). We present a case report, and associated literature review, of a toddler with a posterior scalp lesion which was identified as a soft tissue fibroma upon histopathology. Unlike angiofibromas, soft tissue fibromas in the head and neck are not common in patients with TSC. This soft tissue tumor may be considered as one of the major criteria in the diagnosis of TSC.
| Original language | English (US) |
|---|---|
| Article number | 100127 |
| Journal | Oral and Maxillofacial Surgery Cases |
| Volume | 5 |
| Issue number | 4 |
| DOIs | |
| State | Published - Dec 2019 |
| Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2019 The Authors
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Posterior scalp
- Soft tissue fibroma
- Tuberous sclerosis complex
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