Results 111 to 120 of about 56,324 (305)
Unusual presentation of Rosai-Dorfman disease in a 14-month-old Italian child: a case report and review of the literature [PDF]
, 2016 Background: Rosai-Dorfman disease (RDD) is a rare form of histiocytosis characterized by histiocyte proliferation within lymph nodes and extranodal tissue. Here we report an unusual presentation of RDD in an Italian toddler.
Bruzzi, Patrizia +5 more
core +2 more sources
Trapdoor Procedure for Benign Bone Lesions in the Femoral Head of Skeletally Immature Children
Orthopaedic Surgery, Volume 17, Issue 7, Page 2183-2192, July 2025.This finding of this study suggests that the trapdoor procedure for bone lesions of the femoral head is a safe and effective technique to completely remove the tumors. ABSTRACT Objective Benign bone lesions involving the femoral head are common in pediatric populations but pose significant challenges due to anatomical complexity and the need to ...
Qichao Ma +6 more
wiley +1 more source
Soft Tissue Rosai-Dorfman Disease: Case report
Sultan Qaboos University Medical Journal, 2018 Rosai-Dorfman disease (RDD) is a rare benign proliferative histiocytic disorder characterised by massive lymphadenopathy. While extranodal involvement can occur in generalised RDD, isolated soft tissue RDD (STRDD) is extremely rare.
Rubyath C. Rajib +3 more
doaj +1 more source
Diffuse plane xanthomas as the first manifestation of multiple myeloma
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Eleni Koutra +5 more
wiley +1 more source
مجله دانشکده پزشکی اصفهان, 2010 Background: Patients with Langerhans cell histiocytosis are at particularly high risk for central diabetes insipi-dus (CDI) due to hypothalamic-pituitary disease. Langerhans cell histiocytosis (LCH) is a group of idiopathic disorders characterized by the
Zahra Alian +2 more
doaj
Histiocytosis of Langerhans Cells in Children
Zdorovʹe Rebenka, 2016 The article presents the modern concepts of the etiology, pathogenesis and clinical manifestations of histiocytosis in children. There is provided a description of ten children, who were under supervision for 10 years.
Yu.V. Odynets +2 more
doaj +1 more source
How I manage pulmonary Langerhans cell histiocytosis
European Respiratory Review, 2017 Pulmonary Langerhans cell histiocytosis (PLCH) is a rare sporadic cystic lung disease of unknown aetiology that is characterised by the infiltration and destruction of the wall of distal bronchioles by CD1a+ Langerhans-like cells.
G. Lorillon, A. Tazi
semanticscholar +1 more source
Langerhans cell histiocytosis: current concepts in dentistry and case report [PDF]
, 2016 Langerhans cell histiocytosis (LCH), which is a rare granulomatous pediatric disease of unknown etiology, is characterized by the idiopathic proliferation and accumulation of abnormal and clonal Langerhans cells or their ...
Alejo-Gonzalez, Francisco +4 more
core
Indian Dermatology Online Journal, 2013 A one and a half year old girl born of a non-consanguineous marriage presented with multiple asymptomatic erythematous to hyperpigmented and skin colored papules on both cheeks slowly increasing in number of 1 year duration. On the basis of clinical, histopathological, and immunohistochemistry findings, a diagnosis of benign cephalic histiocytosis was ...
Puthenveedu Salahudeen Simi +3 more
openaire +4 more sources