Results 61 to 70 of about 9,723 (177)
An unusual Erdheim-Chester disease with orbital involvement: A case report [PDF]
, 2016 Erdheim-Chester disease is a rare non-Langerhans cell histiocytosis with multiorgan involvement and a specific tropism for perivascular and fatty connective tissue, of unclear origin, with poor response to therapy. Its identification is difficult because
Bencivinni, F. +5 more
core +2 more sources
Histiocytes: Multifaceted Regulators of Health and Disease
Veterinary Clinical Pathology, EarlyView.ABSTRACT The mononuclear phagocyte system encompasses macrophages, dendritic cells (DCs), and monocytes. Tissue‐resident macrophages and dendritic cells arise during embryogenesis and are replenished either through self‐renewal or by monocytes during inflammation.
Erika J. Gruber
wiley +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
International Journal of Cancer, Volume 158, Issue 6, Page 1541-1554, 15 March 2026.What's new? Childhood cancer ranks among the leading causes of disease‐related deaths in children in high‐income countries. Established risk factors, however, account for only a small proportion of incident childhood cancers. In this report, the authors present the first long‐term assessment of temporal trends in childhood cancer incidence rates in ...
Friederike Erdmann +8 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
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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
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
Langerhans cell histiocytosis with oral manifestations: a rare and unusual case report [PDF]
, 2012 Langerhans cell histiocytosis (LCH), is a rare, proliferative disorder in which the accumulation of pathologic Langerhans cells leads to local tissue infiltration and destruction.
Agarwal, Manjushree +2 more
core +1 more source
Pediatric Blood &Cancer, Volume 73, Issue 2, February 2026.ABSTRACT Purpose Infants with cancer are rare and face unique challenges. Our study aims to describe the incidence of infantile cancers in Canada and to compare treatment‐related mortality (TRM) and their outcomes with those of older children. Methods We conducted a retrospective cohort study using the Cancer in Young People in Canada database ...
Samuel Sassine +22 more
wiley +1 more source
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
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