Results 71 to 80 of about 4,912 (206)
Angiofibroma nasofaríngeo juvenil : perspetiva atual
Trabalho Final do Curso de Mestrado Integrado em Medicina, Faculdade de Medicina, Universidade de Lisboa, 2019O angiofibroma nasofaríngeo juvenil é um tumor benigno que apresenta como principal abordagem terapêutica com intuito curativo a intervenção ...
Peixe, Carolina Ribeiro
core +2 more sources
We found key differences between tuberous sclerosis patients with TSC1 and TSC2 variants. Patients carrying TSC2 variants had more severe and earlier‐onset symptoms. We also identified two distinct clinical subgroups which follow different disease courses: one characterized by predominant renal involvement and the other by more pronounced neurological ...
Hila Weisblum Neuman +6 more
wiley +1 more source
Summary Background and Objectives Deep learning‐convolutional neural networks (DL‐CNNs) have demonstrated high diagnostic accuracy within the domain of dermoscopy. However, many clinical settings lack dermoscopic devices, requiring reliance on close‐up images. This study evaluates the robustness of a DL‐CNN trained on dermoscopic images when challenged
Anastasia Sophie Vollmer +6 more
wiley +1 more source
European Society of Neuroendocrine Tumors (ENETS) 2025 guidance paper for lung and thymic carcinoids
Abstract This ENETS guidance paper, developed by a multidisciplinary working group, provides up‐to‐date and practical advice on the diagnosis and management of lung and thymic carcinoids, based on recent developments and study results. These recommendations aim to provide practical recommendations for the diagnosis, treatment and follow‐up of these ...
Eric Baudin +12 more
wiley +1 more source
Cellular Angiofibroma of the Prostate: A Rare Tumor in an Unusual Location
We report the unusual occurrence of a cellular angiofibroma in prostatic tissue. In this case, a 84-year-old man presented in the emergency room with urinary retention.
Inez Wyn +3 more
doaj +1 more source
Severe Renal Phenotype Across A Multigenerational Tuberous Sclerosis Complex (TSC) Family
A five generation family with a known pathogenic variant (c.1372C>T; p.Arg458*) in TSC2 displaying a severe renal phenotype characterized by large angiomyolipomas, renal cystic disease, and chronic kidney disease leading to renal failure. Our report illustrates a possible genotype–phenotype and highlights the importance of establishing genotype ...
Elena Tuller +3 more
wiley +1 more source
Anesthesia in juvenile angiofibroma: an challenge for the anesthesiologist
Introduction:Anesthesia for juvenile angiofibroma is one of the most complex interventions within otolaryngology, since incoercible bleeding causes acute hypovolemia, which occurs in a short period and leads to hypovolemic shock and death if not treated ...
Idoris Cordero Escobar, Areli Pérez Cue
doaj +2 more sources
Impact of prenatal sirolimus on cardiac rhabdomyomas and brain tubers
ABSTRACT Objective To document the natural progression of fetal cardiac rhabdomyomas and evaluate the impact of prenatal sirolimus (PNS) on tumor size, cardiac complications and brain‐tuber size. Methods This was a single‐center retrospective cohort study of pregnancies with suspected fetal cardiac rhabdomyoma referred to our center from April 2013 to ...
S. Vergote +6 more
wiley +1 more source
Reflectance confocal microscopy features of facial angiofibromas
Facial angiofibromas are benign tumors presenting as firm, dome-shaped flesh-colored to pink papules, typically on the nose and adjoining central face.
José-Francisco Millán-Cayetano +4 more
doaj +1 more source
Dermatologic Features of Endocrine Tumor Syndromes—Systematic Review and Meta‐Analysis
ABSTRACT Endocrine tumor syndromes, including multiple endocrine neoplasia types 1, 2A, and 2B (MEN1, MEN2A, MEN2B), Carney complex (CNC), and PTEN hamartoma tumor syndrome (PHTS), are hereditary conditions characterized by multisystem tumor development.
Sára Pálla +8 more
wiley +1 more source

