Results 41 to 50 of about 6,770 (190)
Cutaneous Rosai‐Dorfman Disease With MAP2K1 Mutation Treated With Encorafenib and Binimetinib
JEADV Clinical Practice, EarlyView.ABSTRACT Rosai‐Dorfman disease (RDD) is a rare histiocytic disorder with unifocal to multisystemic involvement. Activating mutations in the MAPK/ERK pathway can occur in up to 50% of RDD cases. We report a case of cutaneous RDD (C‐RDD) with facial and truncal lesions harboring an activating MAP2K1 (MEK1) mutation that showed a complete response to a ...
Melike Ak +2 more
wiley +1 more source
Indeterminate Cell Histiocytosis: Report of a Case
Acta Medica Iranica, 2014 Indeterminate cell histiocytosis is a very rare disorder of histiocytes proliferation. It has both Langerhans and non-Langerhans cell histiocytosis immunophenotypic features.
Alireza Ghanadan +8 more
doaj
Rheumatology &Autoimmunity, EarlyView.Summary of pregnancy management in CTD‐ILD across preconception, antenatal, and postpartum phases, emphasizing risk stratification and multidisciplinary care. 6MWT, 6‐min walk test; CTD‐ILD: connective tissue disease‐interstitial lung disease; DLCO, diffusion capacity of the lung for carbon monoxide; FVC, forced vital capacity; MDT, multidisciplinary ...
Khaled Aldhuaina +3 more
wiley +1 more source
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 Clinical Periodontology, EarlyView.ABSTRACT Aims This systematic review assesses current evidence on the management of non‐plaque (dental biofilm)‐induced gingival diseases and conditions (NPIGDs), including (i) inflammatory and immune conditions, (ii) neoplasms and (iii) gingival pigmentations.
Maria Clotilde Carra +5 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
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
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