Results 41 to 50 of about 18,178 (224)

Multisystem Langerhans cell histiocytosis coexisting with metastasizing adenocarcinoma of the lung: A case report [PDF]

, 2013
Introduction. Langerhans cell histiocytosis (LCH) is an uncommon disease of unknown etiology characterized by uncontrolled proliferation and infiltration of various organs by Langerhans cells. Case report. We presented a 54-year-old man, heavy smoker,
Eri Živka, Klem Ištvan, Lovrenski Aleksandra, Panjković Milana, Považan Đorđe, Tegeltija Dragana, Đurić Mirna   +6 more
core   +1 more source

Paediatric development of radiopharmaceutical imaging agents and radioligand therapeutics

British Journal of Clinical Pharmacology, EarlyView.
Abstract This review focuses on the development of radiopharmaceutical imaging agents and radioligand therapeutics for paediatric use. Nuclear medicine plays an important role in the diagnosis and treatment of various childhood conditions, including cancers, infections and brain disorders.
Justin L. Hay, Amandine Manon, Hunter Stephens, S. Y. Amy Cheung, Bart de Keizer, Erik T. te Beek   +5 more
wiley   +1 more source

Langerhans cell histiocytosis (histiocytosis x) – in the mandible

Brazilian Dental Science, 2013
This article reports a case of 65 year-old man consultedin a private radiology dental clinic for a panoramicradiography, where was indicated a radiolucent area,extending into the periapical region of the teeth 35 to 43 to the base of the mandible ...
Angela Jordão Camargo, Mayara Cheade, Celso Martinelli, Solange Aparecida Caldeira Monteiro, Christiano de Oliveira Santos, Plauto Christopher Aranha Watanabe   +5 more
doaj   +1 more source

BRAF V600E mutations in urine and plasma cell-free DNA from patients with Erdheim-Chester disease. [PDF]

, 2014
Erdheim-Chester disease (ECD) is a rare histiocytosis with a high prevalence of BRAF V600E mutation (>50% of patients). Patients with BRAF-mutant ECD can respond to BRAF inhibitors.
Cabrilo, Goran, Erlander, Mark G, Hassaine, Latifa, Holley, Veronica R, Janku, Filip, Kosco, Karena, Kurzrock, Razelle, Leppin, Lorieta, Lin, Patrick P, Meric-Bernstam, Funda, Poole, Jason C, Stepanek, Vanda M, Vibat, Cecile Rose T   +12 more
core   +6 more sources

Surveillance of Isolated Colonic Langerhans Cell Histiocytosis in an Adult: A Case Report

Journal of Investigative Medicine High Impact Case Reports, 2022
Langerhans cell histiocytosis (LCH) is a rare disorder involving the proliferation of myeloid-derived dendritic cells. It most commonly affects children aged less than 1 to 2 years old.
Sandhya Kolagatla MD, Joshua K. Jenkins MS, Joseph Elsoueidi MD, Nagabhishek Moka MD   +3 more
doaj   +1 more source

Clinical quiz. [PDF]

, 2005
J Pediatr Gastroenterol Nutr. 2005 Oct;41(4):483-4, 484. Clinical quiz. Prior AC, Selores M, Pina R, Dias JA, Costa FM, Vale L, Gomes L. Department of Pediatrics, Hospital Geral de Santo António, Portugal.
COSTA, F.M., DIAS, J.A., GOMES, L., PINA, R., PRIOR, A.C., SELORES, M., VALE, L.   +6 more
core   +1 more source

A Review of Bioarcheological Investigations in Iron Age Cambodia

International Journal of Osteoarchaeology, EarlyView.
ABSTRACT Archeological research within Cambodia is quite extensive, with significant projects led by both Cambodian archeologists and international researchers alike. Many of these projects have uncovered human skeletal remains. This article reviews archeological human skeletal studies in Cambodia, synthesizing published and unpublished data, primarily
Sophorn Nhoem, Kate Domett, Nigel Chang
wiley   +1 more source

Langerhans cell histiocytosis present in a 1-day-old girl: a case report

Journal of Medical Case Reports
Background Langerhans cell histiocytosis is a rare condition characterized by diverse clinical manifestations, ranging from cutaneous lesions to systemic involvement.
Yang Meng
doaj   +1 more source

Otic Langerhans' Cell Histiocytosis in an Adult: A Case Report and Review of the Literature

Case Reports in Otolaryngology, 2013
Objective. To present a case of otic Langerhans' cell histiocytosis in an adult. Also included the diagnosis and management of the condition and a review of the relevant literature. Case Report.
Anil Gungadeen, Peter Kullar, Philip Yates   +2 more
doaj   +1 more source

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