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(hypervascular)
2,999 results
  • Pediatric gastroenteropancreatic neuroendocrine tumor: A case report and review of the literature. [Journal Article]
    Medicine (Baltimore) 2019; 98(37):e17154Gaiani F, de'Angelis N, … de'Angelis GL
  • CONCLUSIONS: Duodenal neuroendocrine tumors represent 1% to 3% of all GEP-NETs. They are rare in adults and extremely rare in children. Therefore, the diagnostic and therapeutic approach should be multidisciplinary, including laboratory, endoscopic, and specific imaging tests and strictly follows guidelines, to avoid misdiagnosis and inadequate treatments. Although the prognosis is benign in most cases, they can present with metastases. Therefore, a careful follow-up is extremely important.
  • A Huge Oropharyngeal Pyogenic Granuloma in a Patient Presenting with Dysphagia. [Journal Article]
    Dysphagia 2019Arslan IB, Ozkara SA, … Cukurova I
  • A 39-year-old woman experienced dyspnea and progressive dysphagia for 1 year. Dysphagia appeared for solid foods at the beginning but advanced for liquids. She described 17 kg weight loss in the past 6 months and her current weight was 38 kg [body mass index (BMI) 16 kg/m2]. Dyspnea presented with effort and lying was included after 1 month. There was no disease or surgery except chronic hepatiti…
  • [Giant subcutaneous metastasis originating from vesicular thyroid carcinoma: about a case]. [Case Reports]
    Pan Afr Med J 2018; 31:245Andrianandrasana NOT, Razakanaivo M, … Rafaramino FJ
  • Secondary subcutaneous metastasis originating from vesicular thyroid carcinoma is unusual. It accounts for more than 5.8% of most common sites of metastasis for thyroid carcinoma. We here report the case of a 60-year old woman presenting with slowly evolving giant hypervascular lesion in the subcutaneous tissue of the skull occurred 7 years after right thyroid lobectomy. Anatomopathological exami…
  • Pleomorphic hyalinizing angiectatic tumor of the mesorectum: a rare case and review of literature. [Case Reports]
    Autops Case Rep 2019 Jul-Sep; 9(3):e2019097Balasubiramaniyan V, Muduly D, … Das PK
  • Pleomorphic hyalinizing angiectatic tumor (PHAT) is a rare tumor of uncertain tissue origin. Although it has been classified as a benign tumor under the WHO classification, it is locally aggressive, and multiple recurrences have been reported. PHAT commonly involves the lower extremities; however, various unusual sites of origin have been reported. We present the case of a 30-year-old female with…
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