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http://dx.doi.org/10.4318/tjg.2013.0462 | DOI Listing |
Sci Rep
August 2025
Infectious and Tropical Diseases Research Center, Dezful University of Medical Sciences, Dezful, Iran.
In 2020, colorectal cancer (CRC) had over 1.9 million new cases and around 0.9 million deaths, making it the third most common cancer and the second leading cause of cancer deaths globally.
View Article and Find Full Text PDFLung Cancer
August 2025
Division of Thoracic Surgery, Keio University School of Medicine, Tokyo, Japan.
Introduction: Thymic neuroendocrine tumors (TNETs) are rare malignancies characterized by aggressive clinical behavior and limited therapeutic options. In small cell lung cancer (SCLC), molecular subtypes based on the expression of lineage-defining transcription factors (TFs)-ASCL1, NEUROD1, POU2F3, and YAP1-have been proposed. However, the TF landscape of TNETs remains poorly defined.
View Article and Find Full Text PDFAnn Med Surg (Lond)
July 2025
Department of Pathology, National Academy of Medical Sciences, Bir Hospital, Mahaboudha, Nepal.
Introduction And Importance: Bladder paraganglioma is a rare neuroendocrine tumor, accounting for less than 0.06% of all bladder tumors. Due to its nonspecific symptoms, it is frequently misdiagnosed, leading to delays in appropriate management.
View Article and Find Full Text PDFCancer Cytopathol
September 2025
Department of Pathology, University of California, San Francisco, California, USA.
Background: Current American Society of Clinical Oncology guidelines state that patients with metastatic prostate cancer (MPC) should undergo germline and somatic DNA sequencing. The authors examined the utility of next-generation sequencing (NGS) on fine-needle aspiration (FNA) biopsies in which NGS was performed on cell block (CB) and/or smears.
Methods: A retrospective review was performed of cytology cases with diagnosis of MPC either before and/or after NGS on FNA material.
J Investig Med High Impact Case Rep
August 2025
Faculty of Medicine, Palestine Polytechnic University, Hebron, Palestine.
McCune-Albright syndrome (MAS) is a rare disorder, occurring in 1 in 100 000 to 1 in 1 000 000 live births, caused by post-zygotic somatic mutations in the GNAS gene. This leads to fibrous dysplasia (FD), café-au-lait (CAL) skin pigmentation, and hyperfunctioning endocrinopathies. We present a 32-month-old girl with recurrent vaginal bleeding, bilateral breast enlargement, and multiple irregular CAL spots crossing the midline.
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