John N. Eble
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Research Interests
John N. Eble has a total of 67 co-authors. Here are the top co-authors by number of shared publications:
Liang Cheng
Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, IN, USA; Department of Urology, Indiana University School of Medicine, Indianapolis, IN, USA
8 shared publicationsShaobo Zhang
Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, IN, USA
7 shared publicationsGuido Martignoni
Department of Diagnostic and Public Health, Section of Pathology, University of Verona, Verona, Italy
4 shared publications- Liang Cheng
Department of Pathology and Laboratory Medicine, Department of Surgery (Urology), Brown University Warren Alpert Medical School, the Legorreta Cancer Center at Brown University, and Brown University Health, Providence, RI
4 shared publications - Guido Martignoni
University of Verona
3 shared publications Matteo Brunelli
Department of Diagnostic and Public Health, Section of Pathology, University of Verona, Verona, Italy
3 shared publications
Latest Publications
- 1 October 2021
- Published by Elsevier in Laboratory Investigation
- Vol. 34 (10) , 1921-1934
EWSR1-PATZ1 fusion renal cell carcinoma: a recurrent gene fusion characterizing thyroid-like follicular renal cell carcinoma
- 1 October 2021
- Published by Elsevier in Laboratory Investigation
- Vol. 34 (10) , 1921-1934
EWSR1-PATZ1 fusion renal cell carcinoma: a recurrent gene fusion characterizing thyroid-like follicular renal cell carcinoma
- 18 September 2019
- Published by Elsevier in Laboratory Investigation
- Vol. 33 (6) , 1157-1164
Recurrent KRAS mutations in papillary renal neoplasm with reverse polarity
- 18 September 2019
- Published by Elsevier in Laboratory Investigation
- Vol. 33 (6) , 1157-1164
Recurrent KRAS mutations in papillary renal neoplasm with reverse polarity
- 1 December 2016
- Published by Elsevier in Human Pathology
- Vol. 58, 41-46
Pathological features and clinical associations of 58 small incidental angiomyolipomas of the kidney
- 1 December 2016
- Published by Elsevier in Human Pathology
- Vol. 58, 41-46
Pathological features and clinical associations of 58 small incidental angiomyolipomas of the kidney
- 1 December 2016
- Published by Wolters Kluwer Health in American Journal of Surgical Pathology
- Vol. 40 (12) , 1693-1701
Renomedullary Interstitial Cell Tumors
Renomedullary interstitial cell tumors are common incidental findings in kidney specimens. Despite their frequency, little is known about their morphology and pathogenesis. Kidneys from 402 unselected autopsies were sectioned at 1 to 2 mm intervals, and all lesions were examined histologically. A total of 421 renomedullary interstitial cell tumors were present in 150 patients (37%), ranging from 1 to 23 tumors per patient (mean=3). There was no statistically significant difference in age, sex, hypertension, heart weight, tobacco smoking, diabetes mellitus, and renal function between patients with renomedullary interstitial cell tumors and those without. Almost half the patients with renomedullary interstitial cell tumors (41%) had bilateral tumors, and they were older than patients with unilateral tumors (P=0.0007). The tumors ranged in size from 0.5 to 6 mm (mean 1.7 mm). The lesions varied in cellularity: fibrous stroma was found in older patients, whereas cellular and hypocellular stroma predominated in younger patients (P=0.001 and PP=0.02 and PPPP=0.003) but not to hypertension (P=0.11). On the basis of our findings, renomedullary interstitial cell tumors appear to originate as a proliferation of renomedullary interstitial cells between medullary tubules. As their size increases, cellularity decreases, ropey eosinophilic material is deposited, and tubules disappear.
- 1 December 2016
- Published by Wolters Kluwer Health in American Journal of Surgical Pathology
- Vol. 40 (12) , 1693-1701
Renomedullary Interstitial Cell Tumors
Renomedullary interstitial cell tumors are common incidental findings in kidney specimens. Despite their frequency, little is known about their morphology and pathogenesis. Kidneys from 402 unselected autopsies were sectioned at 1 to 2 mm intervals, and all lesions were examined histologically. A total of 421 renomedullary interstitial cell tumors were present in 150 patients (37%), ranging from 1 to 23 tumors per patient (mean=3). There was no statistically significant difference in age, sex, hypertension, heart weight, tobacco smoking, diabetes mellitus, and renal function between patients with renomedullary interstitial cell tumors and those without. Almost half the patients with renomedullary interstitial cell tumors (41%) had bilateral tumors, and they were older than patients with unilateral tumors (P=0.0007). The tumors ranged in size from 0.5 to 6 mm (mean 1.7 mm). The lesions varied in cellularity: fibrous stroma was found in older patients, whereas cellular and hypocellular stroma predominated in younger patients (P=0.001 and PP=0.02 and PPPP=0.003) but not to hypertension (P=0.11). On the basis of our findings, renomedullary interstitial cell tumors appear to originate as a proliferation of renomedullary interstitial cells between medullary tubules. As their size increases, cellularity decreases, ropey eosinophilic material is deposited, and tubules disappear.
- 28 December 2012
- Published by Springer Nature
- p. 129-180
Clonality Analysis and Tumor of Unknown Primary: Applications in Modern Oncology and Surgical Pathology
- 28 December 2012
- Published by Springer Nature
- p. 129-180
Clonality Analysis and Tumor of Unknown Primary: Applications in Modern Oncology and Surgical Pathology