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Case Report Open Access

Familial genetic tuberous sclerosis complex associated with bilateral giant renal angiomyolipoma: A case report

  • Authors:
    • Lina Wang
    • Dawei Ni
    • Lin Zhong
    • Jianbo Wang
  • View Affiliations / Copyright

    Affiliations: Department of Urology, The First Affiliated Hospital of Dalian Medical University, Dalian, Liaoning 116011, P.R. China, Department of Pathology, The First Affiliated Hospital of Dalian Medical University, Dalian, Liaoning 116011, P.R. China
    Copyright: © Wang et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 7099-7106
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    Published online on: October 10, 2017
       https://doi.org/10.3892/ol.2017.7165
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Abstract

Tuberous sclerosis complex (TSC) is an autosomal dominant disease involving multiple organs, but there are a limited number of reports on family TSC. In the present report, a case of a 52‑year‑old female with a familial genetic TSC, associated with bilateral giant renal angiomyolipoma, was described. The mother, second elder brother and daughter of the patient all exhibited TSC, but the clinical manifestations, and therapeutic prognosis between the family members were not the same. The present case report aimed at identifying an effective diagnostic method and treatment through additional study of familial genetic TSC, in order to prolong and improve the quality of life for patients with TSC. According to the present case and relevant literature reviews, it is suggested that fetal gene detection during pregnancy could prevent the passing of this disease onto further generations. Furthermore, early application of drug treatment may control the development of the disease in diagnosed patients. The combination of classical treatments with a small dose of mammalian target of rapamycin inhibitors is the typical recommendation, which may control the development of the disease more effectively and decrease adverse side‑effects.
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Copy and paste a formatted citation
Spandidos Publications style
Wang L, Ni D, Zhong L and Wang J: Familial genetic tuberous sclerosis complex associated with bilateral giant renal angiomyolipoma: A case report. Oncol Lett 14: 7099-7106, 2017.
APA
Wang, L., Ni, D., Zhong, L., & Wang, J. (2017). Familial genetic tuberous sclerosis complex associated with bilateral giant renal angiomyolipoma: A case report. Oncology Letters, 14, 7099-7106. https://doi.org/10.3892/ol.2017.7165
MLA
Wang, L., Ni, D., Zhong, L., Wang, J."Familial genetic tuberous sclerosis complex associated with bilateral giant renal angiomyolipoma: A case report". Oncology Letters 14.6 (2017): 7099-7106.
Chicago
Wang, L., Ni, D., Zhong, L., Wang, J."Familial genetic tuberous sclerosis complex associated with bilateral giant renal angiomyolipoma: A case report". Oncology Letters 14, no. 6 (2017): 7099-7106. https://doi.org/10.3892/ol.2017.7165
Copy and paste a formatted citation
x
Spandidos Publications style
Wang L, Ni D, Zhong L and Wang J: Familial genetic tuberous sclerosis complex associated with bilateral giant renal angiomyolipoma: A case report. Oncol Lett 14: 7099-7106, 2017.
APA
Wang, L., Ni, D., Zhong, L., & Wang, J. (2017). Familial genetic tuberous sclerosis complex associated with bilateral giant renal angiomyolipoma: A case report. Oncology Letters, 14, 7099-7106. https://doi.org/10.3892/ol.2017.7165
MLA
Wang, L., Ni, D., Zhong, L., Wang, J."Familial genetic tuberous sclerosis complex associated with bilateral giant renal angiomyolipoma: A case report". Oncology Letters 14.6 (2017): 7099-7106.
Chicago
Wang, L., Ni, D., Zhong, L., Wang, J."Familial genetic tuberous sclerosis complex associated with bilateral giant renal angiomyolipoma: A case report". Oncology Letters 14, no. 6 (2017): 7099-7106. https://doi.org/10.3892/ol.2017.7165
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