Study of Skin Tumors in Tuberous Sclerosis



Status:Recruiting
Conditions:Cancer, Neurology
Therapuetic Areas:Neurology, Oncology
Healthy:No
Age Range:18 - 90
Updated:4/6/2019
Start Date:January 26, 2000
Contact:Tania R Machado
Email:tania.machado@nih.gov
Phone:(301) 496-3632

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Cutaneous Tumorigenesis in Patients With Tuberous Sclerosis

Tuberous sclerosis is a rare, hereditary disease in which patients develop multiple tumors.
Although not cancerous, the tumors can affect various organs, including the heart, lungs,
kidneys, skin, and central nervous system, with serious medical consequences. The severity of
disease varies greatly among patients, from barely detectable to fatal. This study will
investigate what causes skin tumors to develop in patients with this disease.

Patients with tuberous sclerosis 18 years and older may enroll in this study. Participants
will undergo a medical history and thorough skin examination by a dermatologist. Those with
skin tumors will be asked to undergo biopsy (tissue removal) of up to eight lesions, under a
local anesthetic, for research purposes. The biopsies will all be done the same day. The
tissue samples will be used for: examination of genetic changes, measurement of certain
proteins and other substances, and growing in culture to study the genetics of tuberous
sclerosis.

Patients with tuberous sclerosis develop benign cutaneous tumors that are typically multiple
in number and location. These tumors include facial angiofibromas, forehead plaques, shagreen
patches, periungual fibromas, and gingival fibromas. The tumors are permanent, slow growing,
and often disfiguring. The purpose of this study is to elucidate the molecular basis for
these tumors. Specifically, we plan to identify the genetically altered cells in these
hamartomatous lesions, and to quantify factors (e.g. cytokines) produced by these cells which
induce the growth of these tumors. To accomplish this, we plan to obtain samples of these
cutaneous tumors, to test tumor DNA for loss of heterozygosity, and to measure RNA and
protein expression levels.

- INCLUSION CRITERIA:

Patients will be those already diagnosed with TSC (definite, probable, or possible) based
on clinical criteria and/or genetic testing, and ranging in age from 18 to 90 years old.

The clinical features of TSC considered of major significance are: facial angiofibromas or
forehead plaque, nontraumatic periungual fibromas, three or more hypomelanotic macules,
shagreen patch, multiple retinal nodular hamartomas, cortical tuber, subependymal nodule,
subependymal giant cell astrocytoma, cardiac rhabdomyoma, lymphangioleiomyomatosis, and
renal angiomyolipoma.

The minor features of TSC are: multiple randomly distributed pits in dental enamel,
hamartomatous rectal polyps, bone cysts, cerebral white matter radial migration lines,
gingival fibromas, nonrenal hamartoma, retinal achromic patch, confetti skin lesions, and
multiple renal cysts (5). Definite TSC is diagnosed by the presence of two major features
or one major feature plus two minor features. Probable TSC is diagnosed by the presence of
one major feature and one minor feature. Possible TSC is diagnosed by the presence of
either one major feature or two or more minor features. Patients will not be preselected
for skin lesions, but about 80% of patients with TSC are expected to have skin lesions.

EXCLUSION CRITERIA:

Inability to give informed consent.

Tendency to keloid formation.

Allergy to anesthetics.

Bleeding abnormality.
We found this trial at
1
site
9000 Rockville Pike
Bethesda, Maryland 20892
Phone: 301-496-3632
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mi
from
Bethesda, MD
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