Favorable outcome in children with Beckwith-Wiedeman syndrome and intraabdominal malignant tumors

W. Glaze Vaughan, David W. Sanders, Jay L. Grosfeld, Donald A. Plumley, Frederick Rescorla, L. R. Scherer, Karen W. West, Philip P. Breitfeld

Research output: Contribution to journalArticle

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Abstract

Children with Beckwith-Wiedemann syndrome (BWS) have an increased risk of developing Wilms' tumors, hepatoblastomas, and adrenal tumors. This study evaluates disease-free survival in children with BWS and intraabdominal tumors. Sixteen tumors occurred in 13 children with BWS (8 boys, 5 girls). Diagnoses included Wilms' tumor (10) (2 bilateral, 20%), hepatoblastoma (2), bladder rhabdomyosarcoma (1), and adrenal cortical tumor (1). In the 10 children with Wilms' tumor, the average age at diagnosis was 3.5 years (range, 7 months to 5 years). Nine of 10 had initial tumor resection, chemotherapy, and radiation therapy (when indicated). One child with bilateral disease had tumor biopsy, chemotherapy, and partial nephrectomy. Tumors were classified as stage I (5), stage II (2), stage IV (1) and stage V (2), all with favorable histology. Disease-free survival rate was 100% with median follow-up of 9 years (range, 4 to 22 years). One patient had a left adrenal tumor detected during screening sonography 11 years after Wilms' tumor resection. Two infants with advanced-stage hepatoblastoma responded to chemotherapy, allowing subsequent complete hepatic resection. Both tumors had unfavorable histology. Both completed postoperative chemotherapy and have no evidence of disease (NED) with normal alpha-fetoprotein levels at 21 and 12 months, respectively, after tumor detection. One patient with stage III (group 3) bladder rhabdomyosarcoma underwent partial cystectomy following chemoradiation and is alive (NED) after 20 months. Children with BWS should be screened at regular intervals (every 3 to 6 months) for renal, adrenal, and hepatic tumors. The exact duration of screening is not yet determined. Despite an increased risk of tumor occurrence, this study suggests that children with BWS have an improved survival rate (100%). All 13 children are currently alive with NED. BWS may be a favorable biological characteristic for survival.

Original languageEnglish
Pages (from-to)1042-1045
Number of pages4
JournalJournal of Pediatric Surgery
Volume30
Issue number7
StatePublished - Jul 1995

Fingerprint

Beckwith-Wiedemann Syndrome
Wilms Tumor
Neoplasms
Hepatoblastoma
Drug Therapy
Glandular and Epithelial Neoplasms
Disease-Free Survival
Histology
Urinary Bladder
Survival Rate
Rhabdomyosarcoma
Cystectomy
Liver
alpha-Fetoproteins
Nephrectomy
Ultrasonography
Radiotherapy
Kidney
Biopsy
Survival

Keywords

  • Beckwith-Wiedemann syndrome
  • cytogenetics
  • pediatric
  • solid tumors

ASJC Scopus subject areas

  • Surgery
  • Pediatrics, Perinatology, and Child Health

Cite this

Vaughan, W. G., Sanders, D. W., Grosfeld, J. L., Plumley, D. A., Rescorla, F., Scherer, L. R., ... Breitfeld, P. P. (1995). Favorable outcome in children with Beckwith-Wiedeman syndrome and intraabdominal malignant tumors. Journal of Pediatric Surgery, 30(7), 1042-1045.

Favorable outcome in children with Beckwith-Wiedeman syndrome and intraabdominal malignant tumors. / Vaughan, W. Glaze; Sanders, David W.; Grosfeld, Jay L.; Plumley, Donald A.; Rescorla, Frederick; Scherer, L. R.; West, Karen W.; Breitfeld, Philip P.

In: Journal of Pediatric Surgery, Vol. 30, No. 7, 07.1995, p. 1042-1045.

Research output: Contribution to journalArticle

Vaughan, WG, Sanders, DW, Grosfeld, JL, Plumley, DA, Rescorla, F, Scherer, LR, West, KW & Breitfeld, PP 1995, 'Favorable outcome in children with Beckwith-Wiedeman syndrome and intraabdominal malignant tumors', Journal of Pediatric Surgery, vol. 30, no. 7, pp. 1042-1045.
Vaughan WG, Sanders DW, Grosfeld JL, Plumley DA, Rescorla F, Scherer LR et al. Favorable outcome in children with Beckwith-Wiedeman syndrome and intraabdominal malignant tumors. Journal of Pediatric Surgery. 1995 Jul;30(7):1042-1045.
Vaughan, W. Glaze ; Sanders, David W. ; Grosfeld, Jay L. ; Plumley, Donald A. ; Rescorla, Frederick ; Scherer, L. R. ; West, Karen W. ; Breitfeld, Philip P. / Favorable outcome in children with Beckwith-Wiedeman syndrome and intraabdominal malignant tumors. In: Journal of Pediatric Surgery. 1995 ; Vol. 30, No. 7. pp. 1042-1045.
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abstract = "Children with Beckwith-Wiedemann syndrome (BWS) have an increased risk of developing Wilms' tumors, hepatoblastomas, and adrenal tumors. This study evaluates disease-free survival in children with BWS and intraabdominal tumors. Sixteen tumors occurred in 13 children with BWS (8 boys, 5 girls). Diagnoses included Wilms' tumor (10) (2 bilateral, 20{\%}), hepatoblastoma (2), bladder rhabdomyosarcoma (1), and adrenal cortical tumor (1). In the 10 children with Wilms' tumor, the average age at diagnosis was 3.5 years (range, 7 months to 5 years). Nine of 10 had initial tumor resection, chemotherapy, and radiation therapy (when indicated). One child with bilateral disease had tumor biopsy, chemotherapy, and partial nephrectomy. Tumors were classified as stage I (5), stage II (2), stage IV (1) and stage V (2), all with favorable histology. Disease-free survival rate was 100{\%} with median follow-up of 9 years (range, 4 to 22 years). One patient had a left adrenal tumor detected during screening sonography 11 years after Wilms' tumor resection. Two infants with advanced-stage hepatoblastoma responded to chemotherapy, allowing subsequent complete hepatic resection. Both tumors had unfavorable histology. Both completed postoperative chemotherapy and have no evidence of disease (NED) with normal alpha-fetoprotein levels at 21 and 12 months, respectively, after tumor detection. One patient with stage III (group 3) bladder rhabdomyosarcoma underwent partial cystectomy following chemoradiation and is alive (NED) after 20 months. Children with BWS should be screened at regular intervals (every 3 to 6 months) for renal, adrenal, and hepatic tumors. The exact duration of screening is not yet determined. Despite an increased risk of tumor occurrence, this study suggests that children with BWS have an improved survival rate (100{\%}). All 13 children are currently alive with NED. BWS may be a favorable biological characteristic for survival.",
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