Results 61 to 70 of about 14,204,460 (231)

[Unusual pulmonary presentation of systemic Langerhans cell histiocytosis]

, 2008
An 80-year-old nonsmoking man was referred to our hospital with bilateral perihilar pulmonary opacities. He had a history of epilepsy, sclerosing cholangitis, cutaneous lesions previously diagnosed as localised Langerhans cell histiocytosis.
Schuller, A, Lega, J-C, Schuller, Aurélien, Lazor, R, Lega, Jean-Christophe, Cottin, Vincent, Cordier, J F, Cordier, Jean-François, Jullien, D, Lazor, Romain, Jullien, Denis, Cottin, V   +11 more
core   +1 more source

Pulmonary Langerhans Cell Histiocytosis

, 2010
Pulmonary Langerhans cell histiocytosis is an uncommon interstitial lung disease that results from the accumulation of cells known as Langerhans cells in the lung. It primarily affects young smokers. High resolution chest computed tomography findings are
Furtun K., Salih Bilgin, Burcin Celik, Kamil Furtun, Bilgin S., Çelik B.   +5 more
core   +2 more sources

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  

Pericardial Effusion and Tamponade as the Manifestation of Erdheim–Chester Disease

Annals of Internal Medicine: Clinical Cases
We 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, Daniela D'Urso Soriano, Selene Falcón-Vega, Ana Quiles-Recuenco, Fernando Lidón Pérez, Francisco López García, Félix Gutiérrez Rodero   +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, Teresa Pereira, Maria da Luz Duarte, Herlander Marques, Fernando Pardal, Celeste Brito   +5 more
doaj   +1 more source

Management of Non‐Plaque‐Induced Gingival Conditions: A Systematic Review—Part 2: Inflammatory and Immune Conditions; Neoplasms; and Gingival Pigmentation

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, Cecile Wasielewski, Bruno Špiljak, Maja Sabalić‐Schoener, Sebastien Jungo, Ivan Alajbeg   +5 more
wiley   +1 more source

Histiocitosis de células de Langerhans del adulto [PDF]

, 2019
Langerhans cell histiocytosis, previously called histiocytosis X, is a disease characterized by the proliferation of CD1a dendritic cells. Its nature, reactive or neoplastic, is still discussed. Its onset in adulthood is uncommon.
Donatti, Lucila, Marini, Mario, Cesaroni, Estefanía, Allevato, Miguel, Infante, Lucrecia, Martínez del Sel, Juliana   +5 more
core  

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

Hypermanganesemia in Children With Liver and Portosystemic Circulation Disorders: A Systematic Review

Journal of Paediatrics and Child Health, EarlyView.
ABSTRACT Aim Children with chronic liver disease and portosystemic circulation disorders may have long‐term neurocognitive problems. Hypermanganesemia, reported in this group, could be a contributor. This systematic review aimed to characterise liver and portosystemic circulation disorders associated with hypermanganesemia and reported neurocognitive ...
Helena J. Kim, Susan M. Siew, Ji Hyun Moon, Tracey A. Williams, S. Murthy Chennapragada, Gordon Thomas, Shekeeb S. Mohammad   +6 more
wiley   +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