Metanephric Adenoma-Epithelial Wilms Tumor Overlap Lesions: An Analysis of BRAF Status.


Journal

The American journal of surgical pathology
ISSN: 1532-0979
Titre abrégé: Am J Surg Pathol
Pays: United States
ID NLM: 7707904

Informations de publication

Date de publication:
09 2019
Historique:
pubmed: 14 6 2019
medline: 10 4 2020
entrez: 14 6 2019
Statut: ppublish

Résumé

Metanephric adenoma (MA) has historically been considered to represent a differentiated form of epithelial Wilms tumor (WT), based in part upon cases that morphologically overlap these 2 neoplasms. More recently, BRAF V600E mutations have been demonstrated in the majority of MAs but not in unselected or even epithelial-predominant WTs, suggesting 2 genetically distinct entities. However, no prior study has examined BRAF status in neoplasms with overlapping histologic features of epithelial WT and MA. We studied a cohort of 11 such overlapping lesions, 2 of which we considered morphologically to be otherwise typical MAs with unusually prominent mitotic activity and 9 of which we classified as epithelial WTs with areas resembling MA. Both mitotically active MAs demonstrated the BRAF V600E mutation. While the majority (5/9) of epithelial WTs with areas resembling MA were negative for BRAF V600E mutation, 4 such cases were positive. Two BRAF V600E mutation-positive WTs occurred in children. One case in a 6-year-old male was morphologically similar to the BRAF V600E mutation-positive adult cases and subsequently metastasized to the lungs; remarkably, the metastases then completely resolved on Braf targeted therapy. A second occurred in a 3-year-old girl whose posttherapy nephrectomy specimen's tumor was encapsulated and mitotically active like a typical WT, but also had more differentiated areas resembling MA. Immunohistochemistry for Braf V600E paralleled the molecular findings, demonstrating immunoreactivity in both the WT and MA-like areas of all 4 of these neoplasms. In summary, we demonstrate that BRAF V600E mutations are not entirely restricted to typical MA, as they may be seen in MAs showing mitotic activity along with a subset of epithelial-predominant WTs in adults and children that have foci which overlap morphologically with MA.

Identifiants

pubmed: 31192863
doi: 10.1097/PAS.0000000000001240
doi:

Substances chimiques

BRAF protein, human EC 2.7.11.1
Proto-Oncogene Proteins B-raf EC 2.7.11.1

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1157-1169

Auteurs

Sara E Wobker (SE)

Departments of Pathology and Laboratory Medicine.
Urology, University of North Carolina, Chapel Hill, NC.

Andres Matoso (A)

Departments of Pathology.

Christine A Pratilas (CA)

Oncology, Johns Hopkins University School of Medicine, Baltimore, MD.

Shamlal Mangray (S)

Department of Pathology, Nationwide Children's Hospital, Columbus, OH.

Gang Zheng (G)

Departments of Pathology.

Ming-Tseh Lin (MT)

Departments of Pathology.

Marija Debeljak (M)

Departments of Pathology.

Jonathan I Epstein (JI)

Departments of Pathology.
Oncology, Johns Hopkins University School of Medicine, Baltimore, MD.

Pedram Argani (P)

Departments of Pathology.
Oncology, Johns Hopkins University School of Medicine, Baltimore, MD.

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Classifications MeSH