Results 61 to 70 of about 14,672 (261)

Kimura Disease With Eosinophilic Granulomatosis With Polyangiitis Successfully Treated by Mepolizumab

Clinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT Diagnosis of Kimura's disease should be considered if a middle‐aged Asian male patient presents with painless enlargement of cervical lymph nodes, eosinophilia, and elevated serum total IgE level. Patients with Kimura's disease can have concurrent EGPA or presentations consistent with EGPA.
Wei Du, Ranran Dai, Xiaoyan Chen, Wei Tang   +3 more
wiley   +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

Thoracotomies in Children in Low to Middle Income Countries: The Indications for Surgery

Pediatric Pulmonology, Volume 60, Issue 10, October 2025.
ABSTRACT Introduction There is a scarcity of data on the utilization of thoracotomy for lung pathology in children in low‐ and middle‐income countries (LMICs). These countries have high burdens of infectious diseases, especially tuberculosis, hydatic disease and Human immunodeficiency virus (HIV).
Jacobus Botha, Pierre Goussard, Jacques Janson, Zane Ismail, Jin Kim, Francois Retief, Jonathan Burke, André Gie, Delano Rhode, Pawel Schubert, Savvas Andronikou   +10 more
wiley   +1 more source

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  

Physical fitness and clinically assessed disease burden in long‐term childhood cancer survivors—The SURfit study

Cancer, Volume 131, Issue 17, 1 September 2025.
Abstract Background Identifying disease burden among childhood cancer survivors (CCS) can guide tailored care. Physical fitness predicts health and mortality and may help reduce disease burden in CCS. This study aimed to 1) describe the burden of clinically ascertained adverse health outcomes in long‐term CCS, and 2) investigate the association between
Anna K. Mayr, Simeon Zürcher, Iris Bänteli, Helge Hebestreit, Rahel Kasteler, Nicolas X. von der Weid, Susi Kriemler, Christina Schindera, Corina S. Rueegg   +8 more
wiley   +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

Histiocytosis X: Langerhans’ Cell Histiocytosis

Hematology/Oncology Clinics of North America, 1987
Histiocytosis X is a complex and poorly understood entity. Nevertheless, it would appear as if certain themes are found recurrently throughout the literature dealing with this disease and a review of them serves as a useful summary. 1. Problems with Nomenclature.
openaire   +2 more sources

Results in pediatric T‐ALL patients treated in trial AIEOP‐BFM ALL 2009: Prognostic factors in the context of modern risk‐adapted therapy

HemaSphere, Volume 9, Issue 9, September 2025.
Abstract To improve the outcome of pediatric T‐cell acute lymphoblastic leukemia (T‐ALL) patients, the AIEOP‐BFM ALL 2009 trial modified T‐ALL stratification and treatment based on AIEOP‐BFM ALL 2000 and other pediatric ALL groups' results. This report aims to describe the outcome of T‐ALL patients in trial AIEOP‐BFM ALL 2009 and evaluate prognostic ...
Gunnar Cario, Maria Grazia Valsecchi, Valentino Conter, Giacomo Gotti, Anja Möricke, Martin Stanulla, Michaela Vossen‐Gajcy, Lennart Lenk, Jan Stary, Ondrej Hrusak, Michael Dworzak, Andishe Attarbaschi, Draga Barbaric, Franco Locatelli, Nicole Bodmer, Sarah Elitzur, Daniela Silvestri, Luciano Dalla‐Pozza, Franca Fagioli, Andreas E. Kulozik, Shai Izraeli, Carmelo Rizzari, Annika Rademacher, Barbara Buldini, Jean‐Pierre Bourquin, Martin Zimmermann, Martin Schrappe, Andrea Biondi   +27 more
wiley   +1 more source

Diagnostic problems and surgical treatment of histiocytosis X [PDF]

Medicinski Glasnik, 2007
A 16-year-old boy, with swelling and pain in the left submandibular region was treated at the Clinic for Maxillofacial Surgery. The x-ray examination showed destructive bone lesion of the mandibulae left side and oval lesions on the left hand bone and ...
Alkhalil M, A. Redžić, A. Smajilagić
doaj  

Secondary aneurysmal bone cyst in Langerhans cell histiocytosis: Case report, literature review

European Journal of Radiology Open, 2019
Langerhans cell histiocytosis (LCH) is a rare disease of the myeloid precursor cells, it predominantly occurs in the skull and long bones as unifocal bone lesions. Aneurysmal bone cysts (ABC) are benign, expansive and lytic bone. Reports of secondary ABC
P. Lomoro, I. Simonetti, G. Vinci, V. Fichera, L. Tarotto, P. Trovato, M.S. Prevedoni Gorone   +6 more
doaj   +1 more source