J4 ›› 2013, Vol. 12 ›› Issue (9): 54-55.

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Clinical Diagnosis Therapy of Tuberous Sclerosis Combined with Bilateral Multifocal Renal Angiomyolipomas

  

  1. Affiliated Hospital of Dali University, Dali, Yunnan 671000, China
  • Received:2013-05-15 Revised:2013-06-13 Online:2013-09-15 Published:2013-09-15

Abstract:

Objective: To investigate the clinical therapy of tuberous sclerosis combined with bilateral multifocal renal
angiomyolipomas. Methods: Clinical document of one case of tuberous sclerosis combined with bilateral multifocal renal angiomyolipomas, as well as related literatures were reviewed to explore the clinical therapy to the disease. Results: The case reported was clearly diagnosed and properly conducted surgical excision, the surgery went was smooth, the effect of postoperative was satisfied. Conclusion: Tuberous sclerosis combined with bilateral multifocal renal angiomyolipomas is an autosomal dominant genetic disease with typical symptoms of facial angiofibroma, torso skin depigmentation of the skin spots, ependymal nodules under the brain, retinal hamartoma combined with bilateral renal angiomyolipoma. Nephrectomy, partial nephrectomy, excision of tumor and arterial embolism became the normal therapeutic methods.

Key words: tuberous sclerosis, renal angiomyolipomas, diagnosis and therapy

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