Results 31 to 40 of about 9,012 (189)
Unusual facial lesions in H syndrome
Clinical Case Reports, 2022 H Syndrome is a rare genodermatosis. It may include facial involvement such as: facial telangiectasia, both hypo‐ and hyperpigmented lesions, hirsutism, swollen cheeks due to subcutaneous infiltration and eczematous lesions.
Mariem Rekik +7 more
doaj +1 more source
A rare cutaneous lesion in the neonatal period: The non-Langerhans cell histiocytosis
Marmara Medical Journal, 2020 The non-Langerhans cell histiocytosis (non-LCH) is a group of diseases characterized by cutaneous involvement in the neonatal period. The non-LCH affects less than 1 in 200,000 children born each year. A definitive diagnosis is important for the treatment of the disease.
Adnan BARUTCU +3 more
openaire +4 more sources
Clinical experience in an infant with Langerhans cell histiocytosis
Universidad Médica Pinareña, 2021 Introduction: Langerhans cell histiocytosis (LCH) or Histiocytosis X is a benign proliferative disease affecting dendritic cells. It presents a wide clinical spectrum, from isolated eosinophilic bone granuloma to multisystem involvement with multiple ...
Yamilka Pita Barrios +2 more
doaj
Indeterminate cell histocytosis with naïve cells
Rare Tumors, 2013 Histiocytoses are a heterogeneous group of disorders characterized by proliferation and accumulation of cells of mononuclearmacrophage system and dendritic cells.
Sheren F Younes +3 more
doaj +1 more source
Erdheim-Chester disease detected with 99MTC MDP bone SPECT/CT
Journal of the Belgian Society of Radiology, 2012 Erdheim-Chester disease (ECD) is a rare non-Langerhans’ cell histiocytosis. Mild but permanent juxta-articular bone pain in mainly knees and ankles is the most frequent associated symptom.
G Ceulemans +8 more
doaj +1 more source
Blood Advances, 2023 Abstract Erdheim-Chester disease (ECD) and Rosai-Dorfman disease (RDD) are rare non-Langerhans cell histiocytoses (non-LCHs), for which therapeutic options are limited. MAPK pathway activation through BRAFV600E mutation or other genomic alterations is a histiocytosis hallmark and correlates with a favorable response to BRAF inhibitors ...
Ashley Aaroe +12 more
openaire +2 more sources
Advances in Oral and Maxillofacial Surgery, 2022 Langerhans cell histiocytosis, is a rare disorder characterized by an aberrant proliferation of Langerhans-type cells that infiltrates and replaces the involved tissues.
Soukaïna Oujdad +3 more
doaj
Multiple adult xanthogranuloma: case report of successful treatment with CO2 Laser [PDF]
Surgical & Cosmetic Dermatology, 2020 Multiple adult xanthogranuloma is a rare and late variant of Juvenile xanthogranuloma, a non-Langerhans cell histiocytosis. It usually corresponds to a single lesion in adults, and the manifestation of multiples lesions is uncommon.
Alessandra Jaccottet Piriz +2 more
doaj +1 more source
Choroidal Neovascular Membrane Formation and Retinochoroidopathy in a Patient with Systemic Langerhans Cell Histiocytosis: A Case Report and Review of the Literature [PDF]
, 2012 We report a case of bilateral atrophic retinochoroidopathy with choroidal neovascular membrane (CNVM) formation in a patient with systemic Langerhans cell histiocytosis (LCH).
Foster, Charles Stephen +3 more
core +2 more sources
Journal of orthopaedic case reports, 2020 Histiocytoses are rare disorders and most orthopedic surgeons are unfamiliar with this diagnosis. We report a case of synovial non-Langerhans cell histiocytosis (LCH) located in the shoulder, which has not been reported in the literature previously.A 24-year-old female patient presented to our clinic with shoulder pain and decreased range of motion ...
Gokhan Gedikoglu +3 more
openaire +3 more sources