Results 51 to 60 of about 14,204,415 (185)
Respirology, EarlyView.This study demonstrates that the Single Time Point Prediction score, a novel machine learning–based imaging biomarker, along with established quantitative CT measures, is significantly associated with disease progression in non‐IPF ILD. This imaging metric may enable earlier identification of high‐risk patients and support personalised treatment ...
Ju Hyun Oh +11 more
wiley +1 more source
The clinicopathological characteristics and differential diagnosis of histiocytosis
Chinese Journal of Contemporary Neurology and Neurosurgery, 2015 The histiocytosis is divided into Langerhans' cell histiocytosis (histiocytosis X) and non-Langerhans' cell histiocytosis (NLCH). The former mainly occurs in lymphatic hematopoietic tissue and often involves central nervous system (CNS).
Shi-zhu YU
doaj
Journal of Cutaneous Pathology, EarlyView.ABSTRACT Indeterminate cell histiocytosis (ICH) is a clonal proliferative disorder of mononuclear phagocyte cells that shows features of both dendritic and histiocytic cells. Only around 100 cases of ICH were reported, and among them, only 24% of reported cases involve pediatric patients, with a mean age at diagnosis of 50 years.
Seung‐Soo Lee +3 more
wiley +1 more source
[Unusual pulmonary presentation of systemic Langerhans cell histiocytosis]
, 2008 An 80-year-old nonsmoking man was referred to our hospital with bilateral perihilar pulmonary opacities. He had a history of epilepsy, sclerosing cholangitis, cutaneous lesions previously diagnosed as localised Langerhans cell histiocytosis.
Schuller, A +11 more
core +1 more source
Pulmonary Langerhans Cell Histiocytosis
, 2010 Pulmonary Langerhans cell histiocytosis is an uncommon interstitial lung disease that results from the accumulation of cells known as Langerhans cells in the lung. It primarily affects young smokers. High resolution chest computed tomography findings are
Furtun K. +5 more
core +2 more sources
Scabies mimicking mastocytosis in two infants
The Turkish Journal of Pediatrics, 2013 Scabies is a common parasitic human infection in infants and children. However, diagnostic pitfalls are frequent in infants, in whom the clinical presentation is usually atypical and different from that in adults.
Emine Cölgeçen-Özel +3 more
doaj
Pericardial Effusion and Tamponade as the Manifestation of Erdheim–Chester Disease
Annals of Internal Medicine: Clinical CasesWe hereby report the case of a 77-year-old man hospitalized due to pericardial effusion and tamponade. Upon investigating potential etiologies of the pericardial effusion, we diagnosed him with non-Langerhans cell histiocytosis, also known as Erdheim ...
María Andreo Galera +6 more
doaj +1 more source
Indeterminate Cell Histiocytosis in Association with Acute Myeloid Leukemia
Dermatology Research and Practice, 2010 Indeterminate cell histiocytosis (ICH) is a rare proliferative disorder, in which the predominant cells share morphologic and immunophenotypic features from both Langerhans and non-Langerhans cell histiocytosis. We describe a 62-year-old man presenting a
Filipa Ventura +5 more
doaj +1 more source
Histiocitosis de células de Langerhans del adulto [PDF]
, 2019 Langerhans cell histiocytosis, previously called histiocytosis X, is a disease characterized by the proliferation of CD1a dendritic cells. Its nature, reactive or neoplastic, is still discussed. Its onset in adulthood is uncommon.
Donatti, Lucila +5 more
core
Erdheim-Chester Disease: Utility of 18F-FDG Positron Emission Tomography [PDF]
Journal of Clinical and Diagnostic Research, 2018 Erdheim-Chester Disease (ECD) is a rare non Langerhans cell histiocytosis of unknown origin with multiorgan involvement. We report a case of a man who presented to us with haematuria, asthenia, fever, nausea and malleolar oedema.
Angelina Cistaro +4 more
doaj +1 more source