Venkateswar Surabhi

Dr. Venkateswar Surabhi


Research Focus & Metrics

Academic Career Length

16Years (2011-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 May 2016 in Radiologic Clinics of North America
Verified
Journal Article
Closed access
VSVenkateswar Surabhi
Venkateswar Surabhi
SCSteven Chua
Steven Chua
RPRajan P. Patel
Rajan P. Patel
NTNaoki Takahashi
Naoki Takahashi
NLNeeraj Lalwani
Neeraj Lalwani
SPSrinivasa R. Prasad
Srinivasa R. Prasad

1 November 2013 in Radiologic Clinics of North America
Verified
Journal Article
Closed access
VSVenkateswar Surabhi
Venkateswar Surabhi
CMChristine O. Menias
Christine O. Menias
VGVerghese George
Verghese George
CSCary Lynn Siegel
Cary Lynn Siegel
SPSrinivasa R. Prasad
Srinivasa R. Prasad

26 July 2015 in International Urogynecology Journal
Verified
Journal Article
Closed access
PDF file
MIMalak Itani
Malak Itani
AKAnia Kielar
Ania Kielar
CMChristine O. Menias
Christine O. Menias
MDManjiri Kiran Dighe
Manjiri Kiran Dighe
VSVenkateswar Surabhi
Venkateswar Surabhi
NLNeeraj Lalwani
Neeraj Lalwani

1 September 2016 in RadioGraphics
Verified
Journal Article
Closed access
VSVenkateswar Surabhi
Venkateswar Surabhi
CMChristine O. Menias
Christine O. Menias
AAAhmed M. Amer
Ahmed M. Amer
MEMohamed Elshikh
Mohamed Elshikh
VKVenkata S. Katabathina
Venkata S. Katabathina
CSCary L. Siegel
Cary L. Siegel
Familiarity with the epidemiology, pathogenesis, imaging features, and treatment of a wide spectrum of anal canal and perianal region tumors and tumorlike conditions can aid radiologic diagnosis and guide appropriate patient treatment. Tumors and tumorlike conditions of the anus and perianal region originate from the anal canal and anal margin or result from direct extension of tumors from adjacent organs. The anatomy of the anal canal is complex, and its different histologic characteristics can lead to diverse pathologic conditions. The anal canal extends from the anorectal junction to the anal verge. The World Health Organization classification of anal canal tumors includes (a) anal intraepithelial neoplasia, the precursor of squamous cell carcinoma (SCC), and (b) invasive tumors. Invasive tumors are further classified on the basis of cell type as epithelial tumors (SCC, adenocarcinoma, mucinous adenocarcinoma, small cell carcinoma, and undifferentiated carcinoma), nonepithelial tumors, carcinoid tumors, melanoma, and secondary tumors (direct spread from rectal, cervical, or prostate carcinoma). The anal margin, or perianal skin, lies outside the anal verge and encompasses a radius of 5 cm from the anal verge. Tumors in the anal margi...

1 September 2015 in American Journal of Roentgenology
Verified
Journal Article
Closed access
VSVenkateswar Surabhi
Venkateswar Surabhi
CMChristine O. Menias
Christine O. Menias
VGVerghese George
Verghese George
EMEduardo Matta
Eduardo Matta
RKRavi K. Kaza
Ravi K. Kaza
JHJoseph Hasapes
Joseph Hasapes
OBJECTIVE. Congenital anomalies of the kidneys and urinary tract (CAKUT) encompass a spectrum of anomalies that result from genetic, epigenetic, environmental, and molecular signal aberrations at key stages of urinary tract development. CAKUT can be seen incidentally on cross-sectional imaging of the abdomen or can be a cause for adult-onset chronic kidney disease, posing new challenges for nephrologists, urologists, and radiologists. CONCLUSION. Awareness of CAKUT and familiarity with their imaging findings permit optimal patient management and thorough workup to prevent hypertension and progression from CAKUT to renal failure. The purpose of this article is to review the cross-sectional imaging findings of CAKUT that may present in adulthood.

21 September 2020 in Journal of Personalized Medicine
Verified
Journal Article
Open access
PDF file
Charissa KimCharissa Kim
Charissa Kim
NCNatasha Cigarroa
Natasha Cigarroa
VSVenkateswar Surabhi
Venkateswar Surabhi
Balaji GaneshanBalaji Ganeshan
Balaji Ganeshan
APAnil K. Pillai
Anil K. Pillai
Rapidly progressive hepatocellular carcinoma (RPHCC) is a subset of hepatocellular carcinoma that demonstrates accelerated growth, and the radiographic features of RPHCC versus non-RPHCC have not been determined. The purpose of this retrospective study was to use baseline radiologic features and texture analysis for the accurate detection of RPHCC and subsequent improvement of clinical outcomes. We conducted a qualitative visual analysis and texture analysis, which selectively extracted and enhanced imaging features of different sizes and intensity variation including mean gray-level intensity (mean), standard deviation (SD), entropy, mean of the positive pixels (MPP), skewness, and kurtosis at each spatial scaling factor (SSF) value of RPHCC and non-RPHCC tumors in a computed tomography (CT) cohort of n = 11 RPHCC and n = 11 non-RPHCC and a magnetic resonance imaging (MRI) cohort of n = 13 RPHCC and n = 10 non-RPHCC. There was a statistically significant difference across visual CT irregular margins p = 0.030 and CT texture features in SSF between RPHCC and non-RPHCC for SSF-6, coarse-texture scale, mean p = 0.023, SD p = 0.053, MPP p = 0.023. A composite score of mean SSF-6 binarized + SD SSF-6 binarized + MPP SSF-6 binarized + irregular margins was significantly different between RPHCC and non-RPHCC (p = 0.001). A composite score ≥3 identified RPHCC with a sensitivity of 81.8% and specificity of 81.8% (AUC = 0.884, p = 0.002). CT coarse-texture-scale features in combination with visually detected irregular margins were able to statistically differentiate between RPHCC and non-RPHCC. By developing an image-based, non-invasive diagnostic criterion, we created a composite score that can identify RPHCC patients at their early stages when they are still eligible for transplantation, improving the clinical course of patient care.