Results 101 to 110 of about 22,024 (247)
11‐year‐old girl presenting with blurred vision and progressive right arm weakness
Brain Pathology, EarlyView.
Trung Toan Tran +6 more
wiley +1 more source
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
LCH-Histiocytosis from Langerhans Cells in Craniofacial Region
, 2005 The authors retrospectively analyze the occurrence of histiocytosis from Langerhans cells (LCH) in a group of patients from the Children Stomatological Clinic in Prague - Motol from the years 1998-2003.
J. Kozák, M. Hubáček
core
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 +1 more source
Clinical Case Reports, Volume 14, Issue 7, July 2026.ABSTRACT Pityriasis lichenoides (PL) is a benign, self‐limiting inflammatory condition, characterized by the appearance of papular, scaly, or necrotic lesions. Despite the rare incidence, clinicians should suspect its diagnosis in the presence of specific skin lesions and epidemiological contexts, as suggested by its association with infections and/or ...
Gregorio Serra +7 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
Acta Medica, 2018 Langerhans cell histiocytosis (LCH) is a very rare disease in adults and as well a very rare cause of sellar expansion. The clinical presentation can be heterogeneous, from a single bone lesion to potentially fatal, widespread disease.
Filip Gabalec +9 more
doaj +1 more source
, 2011 An elderly woman presented with anaemia, thrombocytopenia and multifocal lytic and sclerotic bone lesions. Trephine bone marrow biopsy demonstrated widespread involvement by systemic mastocytosis (SM).
Kudela, Andrzej +4 more
core
Journal of Cutaneous Pathology, Volume 53, Issue 7, Page 576-580, July 2026.ABSTRACT Cutaneous crystal‐storing histiocytosis (CSH) is an extremely rare histopathologic finding of histiocytes accumulating crystals of immunoglobulin or paraproteins, often associated with lymphoplasmacytic malignancies. It commonly presents in a wide age range of both female and male adults with a history of a lymphoproliferative disorder ...
Ashton Arlen +3 more
wiley +1 more source
Multifocal Langerhans Cell Histiocytosis in an Adult
, 2017 Eosinophilic granuloma (EG) is the most common and benign form of the spectrum of disorders referred to as Langerhans cell histiocytosis (LCH). Langerhans cell histiocytosis is primarily regarded as a pediatric disease, with few adult cases of multifocal
Nielsen, Natalie +3 more
core