Results 31 to 40 of about 9,723 (177)

Clinical experience in an infant with Langerhans cell histiocytosis

Universidad Médica Pinareña, 2021
Introduction: Langerhans cell histiocytosis (LCH) or Histiocytosis X is a benign proliferative disease affecting dendritic cells. It presents a wide clinical spectrum, from isolated eosinophilic bone granuloma to multisystem involvement with multiple ...
Yamilka Pita Barrios, Surelys Peralta Santiesteban, César Adrián Blanco-Gómez   +2 more
doaj  

Common Acute Lymphoblastic Leukemia Ph＋ Following Langerhans Cell Histiocytosis in a Multi-Malformed Child with INV (9) (p12;q13) (mat):Case Report [PDF]

, 2010
The occurrence of Langerhans cell histiocytosis (LCH) and another malignancy in the same patient is infrequent but has been recognized. The genetic changes that could be responsible for LCH and/or concomitant leukemia development are obscure. To the best
Pavelić, Jasminka, Čulić, Srdjana, Čulić, Vida   +2 more
core   +1 more source

Indeterminate cell histocytosis with naïve cells

Rare Tumors, 2013
Histiocytoses are a heterogeneous group of disorders characterized by proliferation and accumulation of cells of mononuclearmacrophage system and dendritic cells.
Sheren F Younes, Mona A Kandil, Rehab M Samaka, Ola A Bakry   +3 more
doaj   +1 more source

Localized Langerhans cell histiocytosis masquerading as Brodie s abscess in a 2-year-old child: a case report [PDF]

, 2016
Langerhans cell histiocytosis (LCH), formerly known as histiocytosis X, refers to a spectrum of diseases characterized by idiopathic proliferation of histiocytes that produce either focal (localized LCH) or systemic manifestations (Hand–Schüller ...
Chang, Wei-Fang, Hsu, Yi-Chih, Huang, Guo-Shu, Kuo, Chun-Lang, Wu, Yi-Der   +4 more
core   +1 more source

Erdheim-Chester disease detected with 99MTC MDP bone SPECT/CT

Journal of the Belgian Society of Radiology, 2012
Erdheim-Chester disease (ECD) is a rare non-Langerhans’ cell histiocytosis. Mild but permanent juxta-articular bone pain in mainly knees and ankles is the most frequent associated symptom.
G Ceulemans, M Keyaerts, L Verbruggen, A Hoorens, C Boulet, D Verdries, M De Maeseneer, B Ilsen, H Everaert   +8 more
doaj   +1 more source

Growth of children with Langerhans cell histiocytosis [PDF]

, 1995
Conclusion: GH deficiency is not a common manifestation of LCH in childhood and GH provocation tests are only indicated when there is a poor or decelerating growth rate.
Egeler, R.M. (Maarten), Hoek, A.C.J. (A. C J) van den, Hählen, K. (Karel), Karstens, A. (A.)   +3 more
core   +1 more source

Somatic mutations in solid tumors: a spectrum at the service of diagnostic armamentarium or an indecipherable puzzle? The morphological eyes looking for BRAF and somatic molecular detections on cyto-histological samples [PDF]

, 2016
This review article deals with the analysis and the detection of the morphological features associated with somatic mutations, mostly BRAF(V600E) mutation, on both cytological and histological samples of carcinomas.
Abildgaard, Al-Maghrabi, Amoura, Auclair, Baker, Baltazar, Baltazar, Baltazar, Baltazar, Baltazar, Baltazar, Basolo, Basolo, Bedossa, Biegel, Birner, Birner, Catovsky, Cerutti, Chen, Chiarle, Cho, Choi, Christensen, Ciarrocchi, Clegg, Cornillon, Cox, Cramer, Czyz, Dexter, Diebold, Draetta, Fadda, Fadda, Falini, Fend, Fisher, Flaherty, Frankel, Ghossein, Gilliland, Godeau, Hahn, Hoffmann, Hwang, Iseki, James, Jo, Johnston, Kebebew, Kitamura, Kumar, Kurman, Kurman, Lam, Lee, Leite, Marais, Marais, Marais, Maruyama, McCarthy, Mechtersheimer, Miccoli, Mino-Kenudson, Miziorko, Naidu, Nikiforov, Nikiforov, Nikiforov, Nikiforov, Nikiforova, Odze, Pai, Park do, Pelizzo, Picarsic, Pignata, Prasad, Pujade-Lauraine, Raab, Rollins, Rossi, Saki, Santagata, Santoro, Schmitt, Schmitt, Schmitt, Sciot, Sepulveda, Sharrock, Shih, Shoenfeld, Shong, Sobrinho-Simões, Stokloza, Suh, Tagawa, Tóth, Vandenberghe, Vandenberghe, Vitale, Ward, Waxman, Weitzman, Westerman, White, White, Widlund, Xing, Zenz   +112 more
core   +1 more source

An unusual case of intertrigo in an adult caused by purely cutaneous Langerhans cell histiocytosis [PDF]

, 2016
We report a case of persistent intertrigo in an adult, eventually diagnosed as cutaneous Langerhans cell histiocytosis (LCH). It is known that LCH has a predilection for intertriginous areas, however purely cutaneous disease as in our case, is uncommon ...
Baldacchino, Godfrey, Betts, Alexandra, Boffa, Michael J., Gatt, Alex   +3 more
core  

CD207‐Positive Dendritic Cells Promote Emphysema Through CD8+ T Cell Pathway in Chronic Obstructive Pulmonary Disease

Advanced Science, EarlyView.
CD207+ dendritic cells (DCs) drive emphysema by promoting CD8⁺ T cell cytotoxicity via Birbeck granule‐dependent MHC‐I antigen presentation. This DC subset is expanded by cigarette smoke‐induced oxidative stress, which triggers granulocyte‐macrophage colony‐stimulating factor (GM‐CSF) release from airway epithelium.
Shurui Xuan, Yunhui Wu, Feng Liu, Heng Fu, Yaqi Meng, Yingwei Ou, Xijing Yuan, Ian M. Adcock, Man Jia, Xiaoning Zeng, Xin Yao   +10 more
wiley   +1 more source

Laryngeal involvement with fatal outcome in progressive nodular histiocytosis: A rare case report

Indian Dermatology Online Journal, 2016
Progressive nodular histiocytosis (PNH) represents a very rare type of non-Langerhans cell histiocytosis. It is characterized by progressive appearance of papules and nodules without spontaneous resolution.
Aarti Salunke, Vasudha Belgaumkar, Ravindranath Chavan, Rinkesh Dobariya   +3 more
doaj   +1 more source