Journal article
GATA3 expression in clear cell adenocarcinoma of the lower urinary tract: a potential diagnostic pitfall
Diagnostic pathology, Vol.17(1), 87
11/01/2022
DOI: 10.1186/s13000-022-01269-6
PMCID: PMC9623977
PMID: 36320040
Abstract
Background: Clear cell adenocarcinoma of the lower urinary tract (CCACLUT) is a rare primary malignant neoplasm with heterogenous morphology. There is a paucity of data in the literature regarding its immunohistochemical profile.
Methods: The immunohistochemical features (extent and intensity) of a multinational cohort of CCACLUT were evaluated with comparison between clear cell adenocarcinoma of the female genital tract (CCACFGT, tissue microarray) and nephrogenic adenoma (NA).
Results: 33 CCACLUT (24 female, 9 male; mean age 59 years) were collected. CCACLUT most commonly arose from the urinary bladder (26/33, 78%), particularly from the trigone (10/33, 30.3%) followed by the urethra (8/33, 22%). All 12 NA cases were located at the urinary bladder, whereas the most common CCACFGT location was the ovary (29/56, 52%). None of the CCACLUT patients had, intestinal metaplasia, NA, or urothelial carcinoma. One patient had concurrent endometriosis of the sigmoid colon. Most frequently observed morphology in CCACLUT was papillary/tubulocystic (9/3; 27.3%), followed by papillary/tubular (6/33; 18.2%) and papillary/solid (5/33; 15.2%). GATA3 expression was significantly higher in CCACLUT (18/33, 54.5%) and NA (6/12, 50%), when compared to CCACFGT cases 6/56, 11.7%)(p = 0.001 and p = 0.022, respectively). The extent of GATA3 was significantly higher in CCACLUT group (19.2 ± 16.6%) than the other groups (9.6 ± 22.5% in NA and 2.6 ± 9% in CCACFGT group) (p = 0.001). 4/33 patients (12.1) had weak, 10/33 patients (30.3%) had moderate, and 4/33 patients (12.1%) had strong GATA3 intensity in CCACLUT group. In NA group, one patient (8.3%, 1/12) had weak, one patient (8.3%, 1/12) had moderate and 4 patients (33.3%, 4/12) had strong GATA3 intensity. Most cases (CCACLUT 29/33, 88%; NA 11/12, 92%; CCACFGT 46/56, 82.1%) had positive Napsin A expression, by which CCACLUT had significantly more cases with Napsin A expression (p = 0.034). p63 was consistently negative in all cases (30/33 (91.9%) CCACLUT; 12/12 (100%) NA; 42/56 (75%) CCACFGT. Ki67 (MIB) proliferation index was significantly higher in CCACLUT group (54.6 ± 21%) when compared to NA group (4.5 ± 2.7%) and CCACFGT group (35.5 ± 25.8%) (p = 0.001).
Conclusion: CCACLUT has consistent GATA3 expression, which may cause challenge in the diagnosis of urothelial carcinoma but can be used to distinguish CCACLUT from CCACFGT.
Details
- Title: Subtitle
- GATA3 expression in clear cell adenocarcinoma of the lower urinary tract: a potential diagnostic pitfall
- Creators
- Mahmut Akgul - Albany, NY, USARobert Humble - Iowa City, IA, USAAbdullah Osme - Cleveland, OH, USAServet Yuce - Istanbul, TurkeyElif N. Kocak - Istanbul, TurkeyParisa Najafzadeh - Los Angeles, CA, USAAnkur Sangoi - Mountain View, CA, USANiharika Pattnaik - SRL Diagnostics, Bhubaneswar, Orissa, IndiaSourav Mishra - Apollo Hospitals, Bhubaneswar, Orissa, IndiaShivani Sharma - DCP, Core Diagnostics, Gurgaon, Haryana, IndiaNada Shaker - Columbus, OH, USASeema Kaushal - Delhi, IndiaManas Baisakh - Apollo Hospitals, Bhubaneswar, Orissa, IndiaAndrea R. Lightle - Albany, NY, USABonnie L. Balzer - Los Angeles, CA, USAGuang-Qian Xiao - Los Angeles, CA, USAGregory T. MacLennan - Cleveland, OH, USAAdeboye O. Osunkoya - Atlanta, GA, USAAnil Parwani - Columbus, OH, USALiang Cheng - Indianapolis, IN, USAAndrew Bellizzi - Iowa City, IA, USASambit K. Mohanty - DCP, Core Diagnostics, Gurgaon, Haryana, India Oncologic Surgical and Molecular Pathology, Advanced Medical Research Institute, Senior Oncologic Surgical and Molecular Pathologist, CORE Diagnostics, 406, Udyog Vihar III, 122001 Gurgaon, Haryana, India
- Resource Type
- Journal article
- Publication Details
- Diagnostic pathology, Vol.17(1), 87
- DOI
- 10.1186/s13000-022-01269-6
- PMID
- 36320040
- PMCID
- PMC9623977
- NLM abbreviation
- Diagn Pathol
- ISSN
- 1746-1596
- eISSN
- 1746-1596
- Publisher
- BioMed Central
- Language
- English
- Date published
- 11/01/2022
- Academic Unit
- Pathology
- Record Identifier
- 9984307657902771
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