[Tumors of the submaxillary gland].

Ann Otolaryngol Chir Cervicofac

Service ORL, UCL, Clinique Universitaire St-Luc, Bruxelles, Belgique.

Published: May 1991

The tumors of the submaxillary gland are rare. The authors are reviewing 23 cases gathered from three Departments over ten years. The tumors of the submaxillary gland are malignant in as many as 50% of all cases! When the lesion is benign, pleiomorphic adenoma is the most frequent possibility. The authors emphasize the necessity of early and complete surgical treatment, requiring at least total submaxillectomy in case of benign tumor. Cervical mode dissection will be considered if the tumor is malignant.

Download full-text PDF

Source

Publication Analysis

Top Keywords

tumors submaxillary
8
submaxillary gland
8
[tumors submaxillary
4
submaxillary gland]
4
gland] tumors
4
gland rare
4
rare authors
4
authors reviewing
4
reviewing cases
4
cases gathered
4

Similar Publications

Developing Method for Minor Acidic -Glycan Analysis in Mucin and Cancer Cell Samples.

J Proteome Res

October 2024

Faculty of Pharmacy, Kindai University, 3-4-1 Kowakae, Higashi-osaka, Higashi, Osaka 577-8502, Japan.

Minor acidic glycans, such as sulfated and phosphorylated glycans, constitute only a small fraction of biological glycome, making their analysis a considerable challenge. In this study, we developed a technique to analyze minor acidic -glycans in biological samples. First, efficient reaction conditions for the release of -glycans from the proteins were determined.

View Article and Find Full Text PDF

To investigate the clinical effect of retroauricular hairline approach in submandibular gland resection assisted by endoscope. A total of 18 patients with submandibular gland benign tumors treated in our hospital from September 2022 to September 2023 were selected. A 5 cm incision was designed in the retroauricular hairline, and the flap was turned over directly to the anterior edge of sternocleidomastoid muscle, then the flap was turned over to build the cavity through endoscopic surgery, and submandibular gland resection was completed with the assistance of endoscope.

View Article and Find Full Text PDF
Article Synopsis
  • Warthin tumor (WT) is a common non-cancerous tumor found in the salivary glands, especially near the ear, and usually doesn't cause pain.
  • A 70-year-old woman found a lump in her neck, which was confirmed to be WT along with a rare type of lymphoma called mantle cell lymphoma (MCL).
  • After surgery to remove the lump, the patient is stable and being watched closely to make sure her condition doesn’t get worse.
View Article and Find Full Text PDF

This case report delves into the intricate medical history of an 85-year-old male who experienced a myriad of health challenges throughout his years. With a medical history full of conditions, such as stroke, sinus bradycardia, chronic obstructive pulmonary disease, severe pulmonary hypertension, and chronic gastritis, the patient´s health profile is further complicated by prostatic hypertrophy, persistent dorsalgia and lumbalgia, the presence of a thyroid nodule, and a recent onset of hypothyroidism. Among the diverse medical conditions of this patient, our narrative is primarily centered on his latest diagnosis: non-Hodgkin´s lymphoma.

View Article and Find Full Text PDF

Synovial Sarcoma of the Submaxillary Salivary Gland: A Rare Location and Challenging Diagnosis.

Cureus

May 2024

Department of Pathology, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy of Oujda, Mohammed First University of Oujda, Oujda, MAR.

Synovial sarcoma is a high-grade sarcoma. The periarticular region, deep soft tissues, and the extremities are where it is most frequently found. The head and neck regions are rarely affected and salivary gland localization is rather rare, especially the submaxillary gland.

View Article and Find Full Text PDF

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!