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WAGR, Sex Reversal, Bilateral Gonadoblastomas, and Intralobar Nephrogenic Rests: Uncertainties of Pre-Biopsy Chemotherapy in a High Risk Syndrome for Nephroblastoma.
Craver, Randall; Stark, Matthew; Moss, Stephanie; Long, Sarah; Prasad, Pinki; C Roth, Christopher.
Afiliação
  • Craver R; Departments of Pathology, Children's Hospital of New Orleans and Louisiana State University Health Science Centers, New Orleans, LA, USA.
  • Stark M; Departments of Pathology, Children's Hospital of New Orleans and Louisiana State University Health Science Centers, New Orleans, LA, USA.
  • Moss S; Departments of Pathology, Children's Hospital of New Orleans and Louisiana State University Health Science Centers, New Orleans, LA, USA.
  • Long S; Department of Radiology, Tulane University Medical School, New Orleans, LA, USA.
  • Prasad P; Hematology and Oncology Section, Department of Pediatrics, Children's Hospital of New Orleans and Louisiana State University Health Sciences Center, New Orleans, LA, USA.
  • C Roth C; Department of Urology, Louisiana State University Health Sciences Center, New Orleans, LA, USA.
Fetal Pediatr Pathol ; 42(1): 63-71, 2023 Feb.
Article em En | MEDLINE | ID: mdl-35199613
Background: WT1 deletions are associated with nephroblastomas, WT mutations are associated with 46, XY sex reversal. It is unclear why only a few WT1 deletions are associated with sex reversal. Case report. This 46, XY female had a 15.2 MB interstitial deletion of 11p14.1p11.2, which included WT1 and FSHB. No pathogenic abnormalities were identified in 156 other genes associated with disorders of sexual development. Bilateral gonadoblastomas were incidentally diagnosed at 17 months of age at the time of prophylactic gonadectomies. She was treated without biopsy for bilateral nephroblastomas radiologically identified at 18 months of age. Bilateral partial nephrectomies contained treated intralobular nephrogenic rests. Conclusion: It is unclear why WT1 deletions are less associated with 46, XY sex reversal than WT1 mutations. Treating suspected nephroblastomas without biopsy, even in patients with syndromes associated with bilateral nephroblastomas, may still lead to diagnostic and therapeutic uncertainties.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Gonadoblastoma / Tumor de Wilms / Neoplasias Renais Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Female / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Gonadoblastoma / Tumor de Wilms / Neoplasias Renais Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Female / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article