Results 61 to 70 of about 24,931 (232)
CASES OF DISSEMINATED AND GIANT JUVENILE XANTHOGRANULOMA IN CHILDREN
Педиатрическая фармакология, 2014 Juvenile xanthogranuloma is the most common clinical variant of the class II histiocytosis. This article presents two clinical observationsof papulonodular juvenile xanthogranuloma, specification of epidemiological data, clinical and histological ...
E. I. Pil'gui +5 more
doaj +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
A Recurrent Indurated Plaque on the Thigh
JEADV Clinical Practice, EarlyView.
Tram T. Tran +3 more
wiley +1 more source
Tattoo Inflammation With Uveitis: From Recognition to Definition
Clinical &Experimental Ophthalmology, EarlyView.ABSTRACT Tattoo inflammation with uveitis (TIU) is increasingly recognised but growing case numbers have revealed substantial heterogeneity. Patients currently classified as TIU appear to include those with overt or evolving systemic sarcoidosis as well as those with isolated, pigment‐associated ocular inflammation.
Anthea Anantharajah +5 more
wiley +1 more source
Extraosseous langerhans cell histiocytosis in children
, 2008 Langerhans cell histiocytosis, a rare disease that occurs mainly in children, may produce a broad range of manifestations, from a single osseous lesion to multiple lesions involving more than one organ or system.
Letovanec, I. +36 more
core +1 more source
Langerhans cell histiocytosis: A rare cause of pathological rib fracture
, 2021 Langerhans cell histiocytosis, formerly known as histiocytosis X, represents clonal proliferations of the antigen-presenting dendritic cells, which are normally found in many organs. It is a rare disease which tends to affect children and adolescents. In
Yolcu A. +7 more
core +1 more source
Journal of Cutaneous Pathology, EarlyView.ABSTRACT Indeterminate cell histiocytosis (ICH) is a clonal proliferative disorder of mononuclear phagocyte cells that shows features of both dendritic and histiocytic cells. Only around 100 cases of ICH were reported, and among them, only 24% of reported cases involve pediatric patients, with a mean age at diagnosis of 50 years.
Seung‐Soo Lee +3 more
wiley +1 more source
Chronic Pruritic Papular Eruption in an Elderly Man
JEADV Clinical Practice, EarlyView.
Filipe Monteiro +6 more
wiley +1 more source
Journal of Cutaneous Pathology, EarlyView.ABSTRACT Several activating mutations and gene fusions involving the mitogen‐activated protein kinase (MAPK) pathway have appeared in the literature regarding histiocytic neoplasms. We identified a GAB2::BRAF fusion in a cutaneous lesion of a 36‐year‐old male who developed central diabetes insipidus and reddish‐pink grouped papules on the bilateral ...
Pauline C. Xu +3 more
wiley +1 more source
Case of Rosai — Dorfman Disease in a Child
Zdorovʹe Rebenka, 2014 Sinus histiocytosis with massive lymphadenopathy is rare in children. The article describes a case of Rosai — Dorfman disease in 3-year-old boy. The emergence of lymphadenopathy, mainly cervical one, with synchronous lesion of extranodal area — spleen ...
S.V. Vesyoly +6 more
doaj +1 more source