Results 81 to 90 of about 15,155 (248)
Multiple Biliary Hamartomas: The ''Von Meyenburg Complexes''
, 2022 Multiple biliary hamartomas are rare benign malformations of the intrahepatic bile ducts first described by von Meyenburg in 1918. This due to the developmental malformation of the interlobular bile duct in the liver during the embryonic period, leading ...
Khadija Laasri*, Salma Marrakchi, Zakia El yousfi, Ittimade Nassar, Nabil Moatassim Billah
core +1 more source
Brunner’s gland hyperplasias and hamartomas in association with Helicobacter pylori
Background: The proliferative lesions of the Brunner’s glands (BGs) are hyperplasia and hamartomas, and they are usually asymptomatic and very rarely diagnosed. The aetiology of these lesions is not yet clear.
Destek, Sabahattin
core +2 more sources
Perspectives In Medical Research, 2018 Mammary gland hamartoma are uncommon benign tumour like lesions. The pathogenesis still poorly understood and because of its rarity, often under reported by clinicians and pathologist.
Surender Reddy T1 , Abhijeet I2 ; Majed B. Momin3 , Vijaya G4
doaj
A case report of non‐syndromic colonic ganglioneuroma in a patient with juvenile polyposis
JPGN Reports, EarlyView.Abstract Colonic ganglioneuromas in children are rare, particularly without associated hereditary syndromes like multiple endocrine neoplasia (MEN2B), neurofibromatosis type 1(NF1), or Phosphatase and tensin homolog hamartoma tumor syndrome (PHTS). We report a 12‐year‐old male with a history of juvenile polyposis syndrome (JPS) and segmental colonic ...
Holly Coffey +2 more
wiley +1 more source
Síndrome de Peutz-Jeghers, a propósito de un caso
Oncología, 2007 El síndrome de Peutz-Jeghers (SPJ) es una enfermedad hereditaria de etiología desconocida que se caracteriza por la presencia de pólipos hamartomatosos en el tracto gastrointestinal asociados a depósito mucocutáneo de melanina.
Edwin Guayasamín Ch. +2 more
doaj
Hamartomas and choristomas of the oral cavity soft tissues: case series and review of the literature
, 2022 Oral soft tissue-derived hamartomas and choristomas are relatively uncommon lesions, being more prevalent in childhood. They present themselves as self-limited growths that are proper and ectopic to the site of origin. OBJECTIVES: To investigate clinical
Jesus, Ianca Daniele Oliveira de
core +1 more source
Otolaryngology–Head and Neck Surgery, EarlyView.Abstract The American Thyroid Association (ATA) has published an update to the 2015 management guidelines for adult patients with thyroid nodules and differentiated thyroid cancer (DTC). This updated version focuses solely on the management of differentiated thyroid cancer, offering a comprehensive set of guidelines for all stakeholders in the care of ...
Chau Nguyen +2 more
wiley +1 more source
Monaldi Archives for Chest DiseaseBenign endobronchial tumors are rare clinical entities characterized by considerable variability in etiology and clinical presentation. The authors report four cases of endobronchial hamartomas treated and followed up from 2018 to 2023.
Cristiano Cesaro +9 more
doaj +1 more source
Pediatric Investigation, EarlyView.Pediatric nasal skull base tumors present diagnostic and therapeutic challenges due to their deep location, nonspecific symptoms, and the narrow nasal cavity in children. Although artificial intelligence (AI) and digital medicine have advanced early diagnosis, multidisciplinary treatment, and prognosis, their application in these rare tumors remains ...
Xiuping Wu +5 more
wiley +1 more source
, 2013 Tuberous sclerosis is an hereditary disease characterized by disseminated hamartomas involving the central nervous system, skin, kidney and eye. Astrocytic hamartomas are typical retinal lesions.We report a case of a child affected by tuberous ...
SPINUCCI, GIOVANNI +3 more
core +1 more source