Sidart Pradeep

ORCID: 0000-0003-4271-5912
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Vascular Tumors and Angiosarcomas
  • Gastric Cancer Management and Outcomes
  • Pancreatic and Hepatic Oncology Research
  • Metastasis and carcinoma case studies
  • Neuroendocrine Tumor Research Advances
  • Pharmaceutical studies and practices
  • Neonatal Health and Biochemistry
  • Neuroblastoma Research and Treatments
  • Neonatal Respiratory Health Research
  • Cancer Diagnosis and Treatment
  • Vascular Malformations and Hemangiomas
  • Cardiac tumors and thrombi

Texas Christian University
2023

Baylor Scott & White All Saints Medical Center
2023

CHRISTUS Transplant Institute
2023

Baylor Medical Center at Garland
2023

NHS Blood and Transplant
2023

The University of Texas Health Science Center at San Antonio
2021

Invasive lobular carcinoma (ILC) is the second most common subclass of breast cancer and adds to malignancy burden in women. Studies focused on metastatic patterns ILC have reported bone, gynecologic organs, peritoneum, gastrointestinal tract as potential sites metastasis. Metastatic spread stomach has been reported, but generally remains an infrequent finding. Due vague symptomatology visual limitations endoscopic examination, lesions can often mimic a primary gastric malignancy. Metastasis...

10.7759/cureus.40371 article EN Cureus 2023-06-13

An insulinoma is a rare neuroendocrine tumor characterized by inappropriate secretion of insulin with resultant hypoglycemia and concomitant symptoms. Symptoms include diaphoresis, tremor, palpitations, tachycardia, visual disturbances, weakness, confusion, syncope, seizures, even coma. Enteropancreatic neoplasms are in general but among them, insulinomas the more common tumors though they still have very low incidence. They can be benign or malignant, however, latter exceptionally rare. In...

10.7759/cureus.43469 article EN Cureus 2023-08-14

Primary hepatic angiosarcoma (PHA) is an exceedingly rare and aggressive neoplasm of mesenchymal origin. PHA makes a very small portion primary liver tumors conveys poor prognosis. Symptomatology can be vague often mimics hepatocellular carcinoma upon presentation. Diagnosis requires careful immunohistopathologic confirmation. We present case in patient with abdominal pain suspected underlying cryptogenic cirrhosis.

10.7759/cureus.43529 article EN Cureus 2023-08-15
Coming Soon ...