Background And Study Aims: Endoscopic mucosal resection (EMR) has been applied to the treatment of superficial esophageal squamous cell carcinoma (SCC). The incidence and characteristics of metachronous multiple esophageal SCCs and Lugol-voiding lesions (LVLs) were investigated in a retrospective study in patients who had undergone EMR for superficial esophageal SCC.

Patients And Methods: 96 patients with esophageal SCC who had been treated by EMR were followed up by endoscopy for 12 months or longer. Clinicopathologic parameters such as tumor size and location and presence of LVLs were examined.

Results: 10 patients (10 %) had synchronous multiple SCCs, and 12 (13 %) developed metachronous multiple SCCs. The mean annual incidence of newly diagnosed tumor was 4.4 %. The incidence of a speckled pattern of LVLs was 20/74 (27 %) in patients with solitary SCC, 5/10 (50 %) in synchronous multiple SCC, and 10/12 (83 %) in metachronous multiple SCC. The incidence of the presence of speckled pattern of LVLs was significantly higher in patients with multiple SCCs than in those with solitary SCC (68 % vs. 27 %, P = 0.0004).

Conclusions: Patients who have undergone EMR for esophageal SCC, especially those with metachronous multiple LVLs in the background mucosa, should undergo follow-up with close endoscopic observation using Lugol staining.

Download full-text PDF

Source
http://dx.doi.org/10.1055/s-0029-1214477DOI Listing

Publication Analysis

Top Keywords

metachronous multiple
20
multiple sccs
12
multiple esophageal
8
esophageal squamous
8
squamous cell
8
lugol-voiding lesions
8
endoscopic mucosal
8
mucosal resection
8
superficial esophageal
8
scc incidence
8

Similar Publications

Chapter 6: SYNDROMIC PRIMARY HYPERPARATHYROIDISM.

Ann Endocrinol (Paris)

January 2025

Endocrinology Department, Huriez Hospital, Lille University Hospital, France. Electronic address:

Syndromic primary hyperparathyroidism has several features in common: younger age at diagnosis when compared with sporadic primary hyperparathyroidism, often synchronous or metachronous multi-glandular involvement, higher possibility of recurrence, association with other endocrine or extra-endocrine disorders, and suggestive family background with autosomal dominant inheritance. Hyperparathyroidism in multiple endocrine neoplasia type 1 is the most common syndromic hyperparathyroidism. It is often asymptomatic in adolescents and young adults, but may be responsible for recurrent lithiasis and/or bone loss.

View Article and Find Full Text PDF

Triple spinal dural arteriovenous fistula.

BMJ Case Rep

January 2025

Neurosurgery, ASST Grande Ospedale Metropolitano Niguarda, Milano, Italy.

Spinal dural arteriovenous fistulas (SDAVFs) are the most common type of spinal vascular malformations. Multiple SDAVFs are unusual and can occur either synchronously or metachronously, as reported in the literature. We report on the unusual case of a woman with three separate SDAVFs, which were surgically treated within the same setting; the postoperative course was characterised by unexplained repeated haematoma formation within the surgical sites.

View Article and Find Full Text PDF

Precision Treatment of Metachronous Multiple Primary Malignancies Based on Constructing Patient Tumor-Derived Organoids.

Biomedicines

November 2024

Department of Urology, Shanghai Tenth People's Hospital, School of Medicine, Tongji University, Shanghai 200072, China.

Article Synopsis
  • Patients with multiple primary malignant neoplasms (MPMNs) have two or more distinct primary tumors, and this report highlights a rare case of a patient with four primary tumors—three in the urinary tract (renal, prostate, bladder) and one in the lung.
  • The tumors developed over 13 years, and surgeries confirmed the tumors as primary rather than metastatic.
  • Patient-derived organoids (PDOs) were created from tumor samples, showing consistency with the original tumors and potential for personalizing treatment strategies based on their characteristics.
View Article and Find Full Text PDF

Clinicopathological features of Lynch syndrome pedigrees with MSH2 c.351G>A gene variant.

Mol Genet Genomic Med

January 2025

Department of General Surgery, The Fourth Affiliated Hospital, China Medical University, Shenyang, Liaoning, China.

Background: Lynch syndrome (LS) is an autosomal-dominant disorder that increases the risk of many cancers. To identify novel or rare pathogenic variants of MMR genes associated with LS, especially in Chinese pedigrees.

Methods: One four-generation Chinese Han family from northeast China with 29 members was enrolled.

View Article and Find Full Text PDF
Article Synopsis
  • The SEER registry uses criteria like laterality and histology to distinguish between second primary breast cancers, affecting how accurately tumors are classified.
  • Analysis of receptor status in a large sample of contralateral and ipsilateral tumors indicated that ipsilateral tumors may actually be recurrences due to their higher receptor dependence and younger patient demographics.
  • While SEER's criteria enhance specificity, they may also lead to inaccuracies in classifying tumors, highlighting the need for better datasets to compare classification methods.
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!