Download full-text PDF |
Source |
|---|---|
| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3645111 | PMC |
| http://dx.doi.org/10.1136/bcr-2013-008953 | DOI Listing |
Publication Analysis
Top Keywords
Similar Publications
Pituitary Gigantism in an Adolescent Girl With Postsurgical Residual Disease Treated With Lanreotide.
JCEM Case Rep
January 2025
Department of Pediatrics, Children's Nebraska and University of Nebraska Medical Center, Omaha, NE 68104, USA.
Pituitary gigantism (PG) is a rare endocrine disorder that may present with multiple pituitary hormone abnormalities in pediatric patients. A hallmark presentation is accelerated growth due to growth hormone (GH) excess. Current treatment modalities include surgery, radiation, and medical therapy.
View Article and Find Full Text PDFRevolutionizing Limb Preservation: A Case Report on Recurrent Fungating Giant Cell Tumor with Encased Radial Artery in the Distal Radius.
J Orthop Case Rep
December 2024
Department of Orthopaedics, All India Institute of Medical Sciences, New Delhi, India.
Introduction: Giant cell tumor (GCT) of the bone, although benign, poses significant challenges due to its locally aggressive nature and high recurrence rates post-surgical intervention. Among skeletal GCTs, those affecting the distal radius present unique difficulties, especially when fungating masses encase vital structures such as blood vessels.
Case Report: We present a case of a 28-year-old male with a recurring GCT of the distal radius, where limb-preserving surgery was successfully performed despite encasement of the radial artery.
The Management of a Giant Convexity en Plaque Anaplastic Meningioma with Gerstmann Syndrome: A Case Report of Surgical Outcomes in a 76-Year-Old Male.
Diagnostics (Basel)
November 2024
Department of Neurosurgery "Carol Davila", University of Medicine and Pharmacy, 050474 Bucharest, Romania.
Article Synopsis
- * Surgical intervention involved near-total tumor resection, and histological analysis confirmed the diagnosis of anaplastic meningioma (WHO Grade III) with severe features such as necrosis and brain invasion.
- * Post-surgery, the patient showed marked improvement in neurological functions, suggesting that surgical removal can potentially reverse deficits associated with Gerstmann syndrome, with no recurrence reported in a two-month follow-up.
A giant parathyroid adenoma: a case report.
J Med Case Rep
November 2024
Department of Endocrinology and Medicine, The National Hospital of the Faroe Islands, Torshavn, Faroe Islands.
Article Synopsis
- Primary hyperparathyroidism is an endocrine disorder that can cause high calcium levels, often found without symptoms in patients.
- A 47-year-old male case study highlights the mild presentation of significant hormonal issues, where fasting may have contributed to kidney stone development despite no major symptoms initially.
- After surgery to remove a large parathyroid adenoma, the patient faced additional complications but ultimately achieved biochemical remission, demonstrating the importance of vigilant monitoring in similar cases.
Management of large Trigeminal Schwannoma: long-term oncologic and functional outcome from a multicentric retrospective cohort.
Acta Neurochir (Wien)
November 2024
Department of Neurosurgery, Aix Marseille Univ, APHM, UH North, Chemin des Bourrely, 13015, Marseille, France.
Objective: Trigeminal schwannoma (TS), though a rare and benign tumor, becomes a significant surgical challenge due to its intricate location. This study aims to detail the long-term functional outcomes and tumor control post-surgical resection.
Method: We analyzed a multicentric retrospective cohort of 39 patients operated on for a TS in five tertiary centers between January 1993 and July 2022.
Want AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!