Results 61 to 70 of about 5,875,026 (205)
Secondary aneurysmal bone cyst in Langerhans cell histiocytosis: Case report, literature review
European Journal of Radiology Open, 2019 Langerhans cell histiocytosis (LCH) is a rare disease of the myeloid precursor cells, it predominantly occurs in the skull and long bones as unifocal bone lesions. Aneurysmal bone cysts (ABC) are benign, expansive and lytic bone. Reports of secondary ABC
P. Lomoro +6 more
doaj +1 more source
Показатели иммунореактивности у больных гистиоцитозом X [PDF]
, 2022 Developed blood immunodeficiencies and activation of immunological processes in BAL-fluid were revaled in 28 patients with Histiocytosis-X during immunological examination.
А. А. Бажанов +11 more
core
Synthetic Ligands of Myeloid C‐Type Lectin Receptors
ChemBioChem, Volume 27, Issue 13, 14 July 2026.Binding of ligands to C‐type lectin receptors (CLRs) on myeloid cells can lead to an array of cellular responses. Exploitation of these receptors for therapeutic purposes requires high‐affinity ligands. This review surveys the diversity of synthetic ligands of myeloid CLRs in the context of binding, signaling, and downstream effects, as well as ...
James Suri, Bernd Lepenies
wiley +1 more source
Bone marrow transplantation for refractory Langerhans' cell histiocytosis
Haematologica, 1996 Langerhans' cell histiocytosis (LCH) is an uncommon disorder of childhood, formerly referred to histiocytosis X. A significant proportion of children with disseminated disease may undergo progression to a fatal outcome despite chemotherapy with single or
V Conter +5 more
doaj
Pulmonary Langerhans Cell Hysiocytosis: A Rare Pathology in The Practice of a Pulmonologist
Архивъ внутренней медициныPulmonary Langerhans cell histiocytosis is a rare disease with insidious onset and nonspecific manifestations. The article discusses two clinical cases of patients with a rare pathology — pulmonary histiocytosis from Langerhans cells.
E. S. Rvanina, N. A. Karoli
doaj +1 more source
A CASE OF HISTIOCYTOSIS IN THE PATIENT SUSPECTED TO HAVE PULMONARY TUBERCULOSIS
Туберкулез и болезни лёгких, 2019 The article describes the clinical case of Langerhans cell histiocytosis with lesions in lungs and flat bones in a 40-year-old smoker. During 4 years, all stages of the disease were followed.
M. A. Karnaushkina +2 more
doaj +1 more source
Commentary: "Histiocytosis X" [PDF]
Thorax, 1998 Pulmonary Langerhans’ cell granulomatosis (LCG) is a diffuse, smoking-related lung disease characterised pathologically by bronchiolocentric inflammation, cyst formation, and widespread vascular abnormalities, and physiologically by exercise limitation. Pulmonary fibrosis is a long term sequel.
openaire +2 more sources
, 2005 Ulcerated nodules are often seen in the flexural areas of patients with Langerhans cell histiocytosis, or histiocytosis X (2,5-7). Infants with this condition have widespread cutaneous disease with a seborrheic rash involving the scalp and flexural ...
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Late-Onset Langerhans Cell Histiocytosis Presenting with Seizures and Bilateral Temporal Involvement
, 2022 Langerhans cell histiocytosis is known as a rare childhood disease. In this case, we wanted to share our patient’s experience whose first symptom was an epileptic seizure, which attracted attention at an advanced age and revealed bilateral temporal lobe ...
Özge Öcek, Hasan Kuş, Pınar Ortan
core +1 more source