A Case of Pediatric Mixed Epithelial and Stromal Tumor of the Kidney With Atypical Stromal Cells

Mixed epithelial and stromal tumor of the kidney (MESTK) is a rare renal tumor characterized by both cystic and solid components. Although typically benign, its components can undergo malignant transformation, manifesting as a sarcomatous feature. Carcinomatous transformations are exceedingly rare. MESTK predominantly affects perimenopausal women, with male patients being rare and often associated with a history of hormonal therapy. Pediatric MESTK is extremely rare, with few reports. We herein report an eight-year-old child diagnosed with MESTK, exhibiting typical histological findings and featuring a few stromal cells with atypia in a focal area. These atypical cells exhibited bizarre nuclei and were positive for p53, although no mitotic figures were observed, and the Ki-67 labeling index was not elevated compared with the surrounding areas. The follow-up period was relatively short and there was no evidence of recurrence or metastasis. The patient remains under careful observation.

Authors

Institutions

Publication Details

Journal
Cureus
Published
2024-10-16
DOI
https://doi.org/10.7759/cureus.71661
Citations
1
Primary Topic
Renal and related cancers
Type
article
Field-Weighted Citation Impact
0.23
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

A Case of Pediatric Mixed Epithelial and Stromal Tumor of the Kidney With Atypical Stromal Cells

Tomonori Tanaka, Kenichi Kohashi, Chisato Ohe, Yasuyoshi Okamura et al.
1 citations
Cureus
Renal and related cancers
0.23
article

A Case of Pediatric Mixed Epithelial and Stromal Tumor of the Kidney With Atypical Stromal Cells

Tomonori Tanaka, Kenichi Kohashi, Chisato Ohe, Yasuyoshi Okamura, Keiichiro Uehara, Takahiro Tsuchiya, Tomoo Itoh
article en
1 citations

Abstract

Mixed epithelial and stromal tumor of the kidney (MESTK) is a rare renal tumor characterized by both cystic and solid components. Although typically benign, its components can undergo malignant transformation, manifesting as a sarcomatous feature. Carcinomatous transformations are exceedingly rare. MESTK predominantly affects perimenopausal women, with male patients being rare and often associated with a history of hormonal therapy. Pediatric MESTK is extremely rare, with few reports. We herein report an eight-year-old child diagnosed with MESTK, exhibiting typical histological findings and featuring a few stromal cells with atypia in a focal area. These atypical cells exhibited bizarre nuclei and were positive for p53, although no mitotic figures were observed, and the Ki-67 labeling index was not elevated compared with the surrounding areas. The follow-up period was relatively short and there was no evidence of recurrence or metastasis. The patient remains under careful observation.

CureusVol. 16(10)
Kobe University Hospital (JP), Yodogawa Christian Hospital (JP), The University of Osaka (JP)
Good health and well-being
Openalex Percentile: Top 42%
Renal and related cancers
0.23
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

A Case of Pediatric Mixed Epithelial and Stromal Tumor of the Kidney With Atypical Stromal Cells — Tomonori Tanaka, Kenichi Kohashi, et al. · Cureus (2024) | TGRS Research Map | TGRS