Results 61 to 70 of about 38,208 (195)
Trapdoor Procedure for Benign Bone Lesions in the Femoral Head of Skeletally Immature Children
Orthopaedic Surgery, Volume 17, Issue 7, Page 2183-2192, July 2025.This finding of this study suggests that the trapdoor procedure for bone lesions of the femoral head is a safe and effective technique to completely remove the tumors. ABSTRACT Objective Benign bone lesions involving the femoral head are common in pediatric populations but pose significant challenges due to anatomical complexity and the need to ...
Qichao Ma +6 more
wiley +1 more source
High prevalence of myeloid neoplasms in adults with non-Langerhans cell histiocytosis.
Blood, 2017 Erdheim-Chester disease (ECD) is a rare non-Langerhans cell histiocytosis that most commonly affects adults and is driven by a high frequency of mutations in BRAF, MAP2K1, and kinases promoting MAPK signaling.
M. Papo +22 more
semanticscholar +1 more source
Histiocytoid Sweet Syndrome With Paradoxical Neutropenia in a Pediatric Patient
Pediatric Dermatology, EarlyView.ABSTRACT Histiocytoid Sweet syndrome (HSS) is a rare inflammatory skin condition characterized by the infiltration of mononuclear cells in the dermis and leukocytosis with neutrophilia. This uncommon variant of classic Sweet syndrome is rarely reported in the literature, especially in pediatric patients.
Shelby Boock +3 more
wiley +1 more source
Cancer Discovery, 2019 Langerhans cell histiocytosis (LCH) is a rare neoplasm predominantly affecting children. It occupies a hybrid position between cancers and inflammatory diseases, which makes it an attractive model for studying cancer development. To explore the molecular
F. Halbritter +16 more
semanticscholar +1 more source
Paediatric and Perinatal Epidemiology, EarlyView.Abstract Background Cancer is the leading cause of death in children aged 1–14 and the second in 15‐19‐year‐old adolescents in Spain. The Paediatric Population‐Based Cancer Registry of the Community of Madrid was created to monitor its incidence and survival.
Raquel López‐González +5 more
wiley +1 more source
Case Reports in Pathology, 2014 A 37-year-old male case was admitted with goiter. Ultrasonography of thyroid showed a 5 cm cystic nodule in the left lobe with a 1.5 cm solid component. Fine needle aspiration biopsy revealed atypia of undetermined significance or follicular lesion.
A. Bahar Ceyran +5 more
doaj +1 more source
مجله دانشکده پزشکی اصفهان, 2010 Background: Patients with Langerhans cell histiocytosis are at particularly high risk for central diabetes insipi-dus (CDI) due to hypothalamic-pituitary disease. Langerhans cell histiocytosis (LCH) is a group of idiopathic disorders characterized by the
Zahra Alian +2 more
doaj
A rare case of "switch on and off" multi-system Langerhans cell histiocytosis in an adult patient
Journal of Medical Case Reports, 2011 Introduction We report the case of a 24-year-old Greek woman with histologically proven osseous and pulmonary Langerhans cell histiocytosis whose lesions had progressively regressed with a "switch on and off" mode.
Froudarakis Marios E +2 more
doaj +1 more source
Hematopoietic origin of Langerhans cell histiocytosis and Erdheim-Chester disease in adults.
Blood, 2017 Langerhans cell histiocytosis (LCH) and Erdheim-Chester disease (ECD) are rare histiocytic disorders induced by somatic mutation of MAPK pathway genes. BRAFV600E mutation is the most common mutation in both conditions and also occurs in the hematopoietic
Paul Milne +16 more
semanticscholar +1 more source
A young man with multifocal brainstem leptomeningeal disease
Brain Pathology, EarlyView.
Burana Khiankaew +7 more
wiley +1 more source