Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.1016/j.medcli.2009.06.027 | DOI Listing |
Publication Analysis
Top Keywords
Similar Publications
Recurrence of fusocellular subtype GIST with SDHB mutation: A case of SDHB-loss and therapeutic challenges.
J Surg Oncol
September 2024
General Surgery Deparment, Hospital Felicio Rocho, Belo Horizonte, Brazil.
Gastrointestinal stromal tumors (GISTs) are sarcomas affecting the stomach and small intestine, with a rare subtype characterized by succinate dehydrogenase B (SDHB)-loss posing significant diagnostic and therapeutic challenges. A 62-year-old man with weight loss and abdominal pain was diagnosed with a gastric GIST showing SDHB-loss. Initial treatment with Imatinib reduced the tumor size, but surgery revealed no residual tumor.
View Article and Find Full Text PDFLow-Grade Myofibroblastic Sarcoma of the Oral and Maxillofacial Region: An International Clinicopathologic Study of 13 Cases and Literature Review.
Head Neck Pathol
September 2023
Department of Oral Diagnosis, Oral Pathology Area, Piracicaba Dental School, State University of Campinas, Piracicaba, SP, Brazil.
Article Synopsis
- Low-grade myofibroblastic sarcoma (LGMS) is a rare tumor typically found in the oral cavity and head/neck region, characterized by myofibroblast cells and a high chance of returning locally but low risk of spreading to distant sites.
- The study analyzed 13 cases of LGMS from various countries, revealing that most patients are young females, often presenting with nodular lesions in the maxilla, and exhibiting specific microscopic and immunohistochemical features that confirm the diagnosis.
- Complete surgical removal of the tumor is recommended for treatment, but additional long-term studies are needed to better understand recurrence rates and metastasis potential.
Embryonal Rhabdomyosarcoma of the Tongue in Adults.
Life (Basel)
May 2023
Department of Oral and Maxillofacial Surgery, Instituto de Investigación Sanitaria Gregorio Marañon (liSGM), Gregorio Marañon General University Hospital, 28007 Madrid, Spain.
(1) Background: Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma in the first two decades of life. One third of cases appear in the head and neck, with 60% of these being embryonal type. RMS is extremely rare in adults, comprising only 1% of adult malignancies, and of those, only 3.
View Article and Find Full Text PDFGingival metastasis of angiosarcoma of the breast as a first manifestation of spreading disease: Case report and review of the literature.
Spec Care Dentist
March 2024
Department of Stomatology, A.C.Camargo Cancer Center, São Paulo, Brazil.
Background: Angiosarcoma is an aggressive malignant neoplasm of vascular origin. Oral metastases of angiosarcoma are rare and have a non-specific clinical presentation, thus the diagnosis may be challenging.
Case Report: Herein we report a case of a 34-year-old female patient after treatment of a high-grade angiosarcoma of the breast, who presented an asymptomatic bleeding purplish nodule in the maxillary interdental papilla between the first and second premolar.
Atrial Fusocellular Sarcoma: An Uncommon Presentation.
CASE (Phila)
March 2023
Cardiology Department, Fundación Cardioinfantil-LaCardio, Bogotá, Colombia.
• Cardiac tumors are rare but not uncommon. • There is no definitive treatment available for spindle cell sarcoma. • TTE (or TEE) is usually the initial imaging modality for these tumors.
View Article and Find Full Text PDFWant 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!