The DOI matches its Crossref record; 23 of the 23 references it cites were found in a registry or an index.
RENAL LESION GROWTH IN CHILDREN WITH TUBEROUS SCLEROSIS COMPLEX
Abstract
PURPOSE: Renal lesions, including angiomyolipoma, renal cysts (simple and polycystic kidney disease) and renal cell carcinoma, develop in patients with tuberous sclerosis complex. While there is limited information that these lesions may grow in adults with tuberous sclerosis complex, the incidence, characterization and growth rate in children have not been reported. Also, the age at which these lesions first appear, thus providing insight into their natural history, is unknown. We present our data from a longitudinal renal surveillance study of children with tuberous sclerosis complex. MATERIALS AND METHODS: Since 1985 children with tuberous sclerosis complex at our hospital have undergone periodic renal imaging by ultrasonography or computerized tomography to monitor renal lesions. A total of 35 girls and 25 boys 1 to 18 years old have undergone at least 2 or more annual renal ultrasounds. RESULTS: On initial evaluation 33 of 60 children (55%) (mean age 6.9 years) had an identifiable renal lesion, which increased to 48 of 60 (80%) at followup (mean age 10.5 years). Angiomyolipoma was the most frequent lesion (75%) followed by simple renal cysts (17%). Angiomyolipomas increased in size and/or number in 10 of 18 boys (56%) and 18 of 27 girls (66%). The largest growth rate in 1 year was from 0 to 4 cm. and from 5 to 9 cm. in diameter. The youngest patient demonstrated lesions at age 2 years. The average age at which a normal ultrasound became abnormal was 7.2 years. While a total of 27 patients had a normal ultrasound on entering the study, lesions had developed in 15 at followup (11 with angiomyolipomas, 4 with cysts). Five patients had cysts that had disappeared at followup. A 7-year-old boy had a 9 cm. renal cell carcinoma removed. One patient has renal lesions characteristic of autosomal dominant polycystic kidney disease. CONCLUSIONS: Renal involvement in patients with tuberous sclerosis complex begins in infancy, and angiomyolipoma is the most common lesion (75%). Angiomyolipomas are more likely to grow than remain stable, although the rate of growth varies. Simple renal cysts may appear or disappear with time but angiomyolipomas do not disappear. An initially normal renal ultrasound does not rule out future development of lesions. Periodic surveillance is indicated in children with tuberous sclerosis complex.
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Citations
Cites
Identification of the Tuberous Sclerosis Gene TSC1 on Chromosome 9q34
Slegtenhorst, M. V., Hoogt, R. D., Hermans, C., Nellist, M., Janssen, B., Verhoef, S., Lindhout, D., Ouweland, A. V. D., Halley, D., Young, J., et al. (1997) · Science · doi:10.1126/science.277.5327.805 · Cited by 1,648
Identification and characterization of the tuberous sclerosis gene on chromosome 16
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EVIDENCE THAT THE GENE FOR TUBEROUS SCLEROSIS IS ON CHROMOSOME 9
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The Natural History of Renal Angiomyolipoma
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Loss of heterozygosity on chromosome 16p13.3 in hamartomas from tuberous sclerosis patients
Green, A. J., Smith, M., & Yates, J. R. W. (1994) · Nature Genetics · doi:10.1038/ng0294-193 · Cited by 364
Allelic loss is frequent in tuberous sclerosis kidney lesions but rare in brain lesions.
Henske, E. P., Scheithauer, B. W., Short, M. P., Wollmann, R. L., Nahmias, J. A., Hornigold, N., van Slegtenhorst, M., Welsh, C., & Kwiatkowski, D. J. (1996) · PubMed Central · Cited by 322
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Two loci for Tuberous Sclerosis: one on 9q34 and one on 16p13
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Melanocyte-marker-HMB-45 is regularly expressed in angiomyolipoma of the kidney
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Cited by
The Tuberous Sclerosis Complex
Crino, P. B., Nathanson, K. L., & Henske, E. P. (2006) · New England Journal of Medicine · doi:10.1056/nejmra055323 · Cited by 1,793
European Respiratory Society guidelines for the diagnosis and management of lymphangioleiomyomatosis
Johnson, S. R., Cordier, J. F., Lazor, R., Cottin, V., Costabel, U., Harari, S., Reynaud-Gaubert, M., Boehler, A., Brauner, M., Popper, H., et al. (2010) · European Respiratory Journal · doi:10.1183/09031936.00076209 · Cited by 590
Perivascular epithelioid cell neoplasms: pathology and pathogenesis
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The tuberous sclerosis complex
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Metadata
- Authors
- EWALT, D. H., SHEFFIELD, E., SPARAGANA, S. P., DELGADO, M. R., & ROACH, E. S.
- Venue
- Journal of Urology
- Published
- 1998-07
- Volume
- 160
- Issue
- 1
- Pages
- 141-145
- ISSN
- 0022-5347 (ISSN-L)
- 1527-3792
- OpenAlex
- W2072011119
- Cited by
- 344
- References
- 23
- FWCI
- 4.22
- Type
- journal article
- Language
- en
- Open access
- closed
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- EWALT, D. H., SHEFFIELD, E., SPARAGANA, S. P., DELGADO, M. R., & ROACH, E. S. (1998). RENAL LESION GROWTH IN CHILDREN WITH TUBEROUS SCLEROSIS COMPLEX. Journal of Urology. https://doi.org/10.1016/s0022-5347(01)63072-6
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