Background: Tuberous sclerosis complex is e genetic disorder characterized by lesions affecting the brain, skin, eyes and internal organs - kidneys, heart, liver and lungs. Case Report: The case of a 17-year-old boy with delayed proper diagnosis of tuberous sclerosis complex and multiple lesions in brain, lungs, heart and kidneys has been described. Conclusions: The authors would like to underline the very rare incidence of sclerosis tuberous complex and the need for periodic follow-up imaging of central nervous system, chest (with thorough evaluation of heart and lungs), and abdominal cavity. Moreover, the authors would like to underline a significantl delay in a process of reaching a final diagnosis of the disease.
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