Results 81 to 90 of about 22,368 (237)

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, Maria Licari, Simone Margotti, Daniele Penna, Vincenzo Arena   +4 more
doaj   +1 more source

An unusual Erdheim-Chester disease with orbital involvement: A case report [PDF]

, 2016
Erdheim-Chester disease is a rare non-Langerhans cell histiocytosis with multiorgan involvement and a specific tropism for perivascular and fatty connective tissue, of unclear origin, with poor response to therapy. Its identification is difficult because
Bencivinni, F., Brunori, G., Giannitrapani, L., Seidita, A., Serruto, A., Soresi, M.   +5 more
core   +2 more sources

A multidisciplinary non-invasive approach to monitor response to intravenous immunoglobulin treatment in neurodegenerative Langerhans cell histiocytosis: a real-world study

Frontiers in Immunology
Aims Early detection and treatment of neurodegenerative Langerhans cell histiocytosis (ND-LCH) have been suggested to prevent neurodegenerative progression.
Irene Trambusti, Carmen Barba, Marzia Mortilla, Susanna Rizzi, Katiuscia Romano, M. L. Coniglio, E. Lucenteforte, A. Tondo, R. Guerrini, E. Sieni   +9 more
semanticscholar   +1 more source

Incidence and Outcome of Infants With Cancer in Canada: A Report From Cancer in Young People in Canada Database

Pediatric Blood &Cancer, Volume 73, Issue 2, February 2026.
ABSTRACT Purpose Infants with cancer are rare and face unique challenges. Our study aims to describe the incidence of infantile cancers in Canada and to compare treatment‐related mortality (TRM) and their outcomes with those of older children. Methods We conducted a retrospective cohort study using the Cancer in Young People in Canada database ...
Samuel Sassine, Hallie Coltin, Maria Kondyli, Monia Marzouki, Nicolas Prud'homme, Nida Usmani, Sylvia Cheng, Lesleigh Abbott, Tony Truong, Sapna Oberoi, Ketan Kulkarni, Josée Brossard, Lynette Bowes, Paul Gibson, Donna L. Johnston, Sarah McKillop, Roona Sinha, Lillian Sung, Catherine Vezina, Laura Wheaton, Alexandra P. Zorzi, Marie‐Claude Pelland‐Marcotte, Thai Hoa Tran   +22 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, Ragıp Ertaş, Serap Utaş, Olgun Kontaş   +3 more
doaj  

Multisystem Langerhans cell histiocytosis in an adult non‐smoker treated with steroid therapy

Respirology Case Reports, 2020
We describe the case of a 29‐year‐old female non‐smoker who was treated with steroid therapy for a subacute exacerbation of multisystem Langerhans cell histiocytosis (MS‐LCH) with worsening lung, skin, and oral mucosal lesions.
Haruka Ito, Masaru Ito, Y. Kakuta, T. Kaneko, K. Okudera, T. Ogura   +5 more
semanticscholar   +1 more source

Langerhans cell histiocytosis in children: a case report and brief review of the literature

PAMJ Clinical Medicine, 2019
Langerhans cell histiocytosis (LCH), formerly known as histiocytosis X, is a non-malignant disease involving clonal proliferation of Langerhans cells. It is an orphan disease affecting mainly the child and the young adult.
Zakaria El Ouali, Nisrine Khoubila, Siham Cherkaoui, Mohamed Rachid, Mouna Lamchahab, Meryem Qachouh, Abdellah Madani, Asmaa Quessar   +7 more
doaj   +1 more source

Dermoscopy in the diagnosis of juvenile xanthogranuloma [PDF]

Anais Brasileiros de Dermatologia, 2018
: Juvenile xanthogranuloma is the most common form of non-Langerhans cell histiocytosis. It manifests clinically as a red-yellow papule, usually showing spontaneous remission. The diagnosis is based on clinical and histological findings.
Thaís Erance de Oliveira, Roberto Gomes Tarlé, Lismary Aparecida de Forville Mesquita   +2 more
doaj   +1 more source

Gastrointestinal Langerhans cell histiocytosis responding to cladribine and imatinib mesylate [PDF]

, 2010
Gastrointestinal involvement in Langerhans cells histiocytosis (LCH) is extremely rare. An optimal treatment regimen is not defined yet and its prognosis is relatively poor.
Agreda Vásquez, Gladys Patricia, Lome Maldonado, Carmen, Oviedo, Edgar, Popoca Barriga, Ulises, Sánchez Guerrero, Sergio Arturo   +4 more
core  

Erdheim-Chester Disease: a comprehensive review of the literature [PDF]

, 2013
Erdheim-Chester Disease (ECD) is a rare form of non Langerhans' cell histiocytosis. Individuals affected by this disease are typically adults between their 5th and 7th decades of life. Males and females are almost equally affected.
Mirra Manevich-Mazor, Roei D Mazor, Yehuda Shoenfeld   +2 more
core   +1 more source