Venkata Subramanian Krishnaraju

Venkata Subramanian Krishnaraju

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Research Focus & Metrics

Academic Career Length

9Years (2018-Present)

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

Representative Publications

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1 May 2022 in Radiology
Verified
Journal Article
Closed access
RKRajender Kumar
Rajender Kumar
SSShrawan Kumar Singh
Shrawan Kumar Singh
BMBhagwant Rai Mittal
Bhagwant Rai Mittal
SVShelvin Kumar Vadi
Shelvin Kumar Vadi
NKNandita Kakkar
Nandita Kakkar
ABAnish Bhattacharya
Anish Bhattacharya
Gallium 68 prostate-specific membrane antigen PET/CT-guided, robotic-assisted, transgluteal prostate biopsy is safe and retrieved specimens adequate for a pathologic diagnosis of cancer in the majo... Background Transrectal US-guided biopsy with or without MRI fusion is performed for diagnosing prostate cancer (PCa) but has limitations. Gallium 68 (68Ga) prostate-specific membrane antigen (PSMA)...

13 October 2023 in Diagnostics
Verified
Journal Article
Open access
PDF file
DJDaya Krishna Jha
Daya Krishna Jha
GPGupta Pankaj
Gupta Pankaj
PNPardhu B. Neelam
Pardhu B. Neelam
RKRajender Kumar
Rajender Kumar
VKVenkata Subramanian Krishnaraju
Venkata Subramanian Krishnaraju
VSVishal Sharma
Vishal Sharma
It is challenging to differentiate between tuberculous peritonitis and peritoneal carcinomatosis due to their insidious nature and intersecting symptoms. Computed tomography (CT) is the modality of choice in evaluating diffuse peritoneal disease. We conducted an ambispective analysis of patients suspected as having tuberculous peritonitis or peritoneal tuberculosis between Jan 2020 to Dec 2021. The study aimed to identify the clinical and radiological features differentiating the two entities. We included 44 cases of tuberculous peritonitis and 45 cases of peritoneal carcinomatosis, with a median age of 31.5 (23.5–40) and 52 (46–61) years, respectively (p ≤ 0.001). Fever, past history of tuberculosis, and loss of weight were significantly associated with tuberculous peritonitis (p ≤ 0.001, p = 0.038 and p = 0.001). Pain in the abdomen and history of malignancy were significantly associated with peritoneal carcinomatosis (p = 0.038 and p ≤ 0.001). Ascites was the most common radiological finding. Loculated ascites, splenomegaly and conglomeration of lymph nodes predicted tuberculous peritonitis significantly (p ≤ 0.001, p = 0.010, p = 0.038). Focal liver lesion(s) and nodular omental involvement were significantly associated with peritoneal carcinomatosis (p = 0.011, p = 0.029). The use of clinical features in conjunction with radiological findings provide better diagnostic yields because of overlapping imaging findings.

12 May 2021 in British Journal of Radiology
Verified
Journal Article
Closed access
VKVenkata Subramanian Krishnaraju
Venkata Subramanian Krishnaraju
HSHarmandeep Singh
Harmandeep Singh
RKRajender Kumar
Rajender Kumar
SSSarika Sharma
Sarika Sharma
BMBhagwant Rai Mittal
Bhagwant Rai Mittal
ABAnish Bhattacharya
Anish Bhattacharya
Localizing the sites of infection in the body is possible in nuclear medicine using a variety of radiopharmaceuticals that target different components of the infective and inflammatory cascade. Gamma(γ)-emitting agents such as [67Ga]gallium citrate were among the first tracers used, followed by development of positron-emitting tracers like 2-deoxy-2-[18F]fluoro-D-glucose (18F-FDG). Though these tracers are quite sensitive, they have limited specificity for infection due to their concentration in sites of non-infective inflammation. White blood cells (WBC) labelled with γ or positron emitters have higher accuracy for differentiating the infective processes from the non-infective conditions that may show positivity with tracers such as 18F-FDG. We present a pictorial review of potential clinical applications of PET/CT using 18F-FDG labelled WBC.

1 May 2018 in Clinical Nuclear Medicine
Verified
Journal Article
Closed access
PDF file
VKVenkata Subramanian Krishnaraju
Venkata Subramanian Krishnaraju
RBRajender Kumar Basher
Rajender Kumar Basher
HSHarmandeep Singh
Harmandeep Singh
SSShrawan Kumar Singh
Shrawan Kumar Singh
ABAmanjit Bal
Amanjit Bal
BMBhagwant Rai Mittal
Bhagwant Rai Mittal
68Ga-labeled prostate-specific membrane antigen is a novel radiotracer for imaging of prostate cancer. We report a hormonally treated patient with prostate carcinoma, presenting with lower urinary tract symptoms and rising prostate-specific antigen levels, who underwent 68Ga-labeled prostate-specific membrane antigen PET/CT for suspected recurrence. No tracer avid lesion was noted in the prostate gland and locoregional area. However, intense tracer avid heterogeneously enhancing soft tissue lesion with cystic areas and coarse calcifications was seen in the anterior mediastinum. PET/CT-guided biopsy from the mediastenal lesion revealed type B2 thymoma.

1 September 2022 in Journal of Gastrointestinal Cancer
Verified
Journal Article
Closed access
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NANishtha Ahuja
Nishtha Ahuja
SMSuvradeep Mitra
Suvradeep Mitra
ABAmanjit Bal
Amanjit Bal
ADAshim Das
Ashim Das
CTCHERRING TANDUP
CHERRING TANDUP
VKVenkata Subramanian Krishnaraju
Venkata Subramanian Krishnaraju

15 March 2021 in Journal of Nuclear Medicine Technology
Verified
Journal Article
Closed access
PDF file
TJTarun Kumar Jain
Tarun Kumar Jain
VKVenkata Subramanian Krishnaraju
Venkata Subramanian Krishnaraju
BMBhagwant Rai Mittal
Bhagwant Rai Mittal
ASAshwani Sood
Ashwani Sood
RKRajender Kumar
Rajender Kumar
SKSunil Kumar
Sunil Kumar
Breast is unusual site for metastasis from malignant tumors though may be the first manifestation of extra-mammary malignancy with primary typically arising from lung, melanoma, ovary and lymphoma. Breast metastasis is extremely rare from thyroid carcinoma and may take years to develop as differentiated thyroid carcinoma are usually indolent, slow growing and metastasize to lymph nodes, lungs and bones. Here is a middle-aged woman (post-subtotal thyroidectomy for multi-nodular goitre 24 years ago) showing discordant FDG and iodine avidity in proven metastatic disease involving lymph nodes, bones, spleen and breast on whole-body radioiodine and FDG-PET/CT due to tumor heterogeneity.