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The effects of everolimus on tuberous sclerosis-associated lesions can be dramatic but may be impermanent

Authors :
Ashley Wachsman
Katherine Haker
Joseph M. Miller
Dechu Puliyanda
Fataneh Majlessipour
Moise Danielpour
Source :
Pediatric Nephrology. 30:173-177
Publication Year :
2014
Publisher :
Springer Science and Business Media LLC, 2014.

Abstract

Tuberous sclerosis complex (TSC) predisposes to the development of benign lesions within multiple organ systems, including the brain, kidneys, heart, lungs, and skin. Disease mortality is due to space-occupying subependymal giant cell astrocytomas and hemorrhage-prone renal angiomyolipomas. The recent use of mTORC1 inhibitors, such as everolimus, has allowed for direct targeting of TSC-associated mass lesions without apparent effect on surrounding tissues. Because of the mechanism of these drugs, there is reason to believe that these effects are not durable and that there may be need for continued long-term maintenance therapy.We present a case of TSC-associated mass lesions that were ill-suited for definitive surgical therapy. The patient was started on everolimus, however due to a complex social situation treatment was discontinued and ultimately resumed many months later. Radiologic studies acquired before and after each period of therapeutic onset/cessation reveal the dramatic but impermanent effects of mTORC1 inhibition.While everolimus provides a non-invasive way to treat TSC-associated lesions, patients may require lifelong therapy. When termination of therapy is considered, the patient should be made aware of the expectation of potentially dramatic increases in lesion size. If consideration is to be given to definitive surgical therapy, it should be pursued while the patient is still on the medication, or at least soon after treatment is halted.

Details

ISSN :
1432198X and 0931041X
Volume :
30
Database :
OpenAIRE
Journal :
Pediatric Nephrology
Accession number :
edsair.doi.dedup.....ac47d873be8ac056d76c44246bacde44
Full Text :
https://doi.org/10.1007/s00467-014-2949-6