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Biting off more than you can chew: a rare case of hyperparathyroidism jaw tumour syndrome.
Oxf Med Case Reports
January 2025
Consultant Nephrologist-Department of Nephrology and Transplantation, Fiona Stanley Hospital, Perth, WA, Australia.
Hyperparathyroidism Jaw Tumour Syndrome (HPT-JT) is a rare autosomal dominant disorder within the familial hyperparathyroidism group. Individuals with the disorder carry a gene mutation that predisposes them to early-onset primary hyperparathyroidism, ossifying jaw tumours, renal cystic disease, uterine tumours and parathyroid carcinomas. We present a case of a 41-year-old man referred to nephrology clinic with haemoproteinuria who was noted to have the constellation of renal cystic disease, personal and family history of hyperparathyroidism and recent jaw tumour excision.
View Article and Find Full Text PDFEvaluation of Pelvic Pathology of Subfertile Women by Transvaginal Sonography and Correlation with Laparoscopic Findings.
Mymensingh Med J
January 2025
Dr Mariam Akter Sumi, Registrar, Infertility, Mymensingh Medical College Hospital (MMCH), Bangladesh; E-mail:
Damage of fallopian tube, endometriosis, fibroid uterus, adenomysis and polycystic ovary syndrome are the major pelvic pathology that causes subfertility. Although there are many diagnostic tests available, the clinical presentation of each patient can usually be linked to specific and efficient testing strategies. Transvaginal sonographic (TVS) imaging is an effective, easy to use, safe and readily available noninvasive means to evaluate fertility potential.
View Article and Find Full Text PDFHead and neck cancer surveillance: A guide past the five-year mark.
Aust J Gen Pract
December 2024
MB BChir (Cantab), MA (Med) (Cantab), FRCS (Eng), FRACS (OHNS), Consultant Otolaryngologist, Head and Neck Surgeon, Royal Brisbane and Women@s Hospital/Surgical, Treatment and Rehabilitation Service, Brisbane, Qld; Deputy Director of Surgery, Surgical, Treatment@and Rehabilitation Service, Brisbane, Qld; Adjunct Associate Professor, Griffith Institute of Drug Discovery, Griffith University, Brisbane, Qld; Senior Academic Lecturer, School of Clinical Medicine, The@University of Queensland, Brisbane, Qld.
Background: A head and neck cancer patient has completed treatment and five-year surveillance with their oncologists and surgeons and has been discharged back into your care. What is next and what do you not want to miss in this patient?
Objective: This article aims to provide the general practitioner with a practical guide and an up-to-date evidence-based review on how to manage the head and neck cancer survivor.
Discussion: Attentive surveillance encompassing risk stratification and guidance, early detection of recurrence and second malignancies, effective management of chronic symptoms and the provision of psychosocial support are fundamental in providing a holistic and comprehensive care plan for the head and neck cancer survivor.
Using Large Language Models for Efficient Cancer Registry Coding in the Real Hospital Setting: A Feasibility Study.
Pac Symp Biocomput
December 2024
Department of Computer Science, National Yang Ming Chiao Tung University Hsinchu, 300093, Taiwan, ROC, Taiwan.
The primary challenge in reporting cancer cases lies in the labor-intensive and time-consuming process of manually reviewing numerous reports. Current methods predominantly rely on rule-based approaches or custom-supervised learning models, which predict diagnostic codes based on a single pathology report per patient. Although these methods show promising evaluation results, their biased outcomes in controlled settings may hinder adaption to real-world reporting workflows.
View Article and Find Full Text PDFPositive cystic duct margin for low grade dysplasia with intestinal metaplasia after routine laparoscopic cholecystectomy: Case report.
Int J Surg Case Rep
January 2025
General Surgery Junior Resident, General Surgery Department, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Introduction: Incidental neoplastic findings after routine cholecystectomy are becoming more common. However, low-grade dysplasia at the cystic duct resection margin remains rare and lacks established management guidelines.
Case Presentation: A 37-year-old male underwent a routine laparoscopic cholecystectomy.
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