Results 41 to 50 of about 4,903,700 (215)

Spontaneous pneumothorax with isolated pulmonary Langerhans cell histiocytosis in an adult case: A common manifestation of rare disease

Clinical Case Reports, 2023
Key Clinical Message Pulmonary Langerhans cell histiocytosis should be evaluated even in adults with no previous medical history and no history of cigarette smoking who have spontaneous pneumothorax and evidence of multiple lung cystic lesions, and other
Mitra Samareh Fekri, Faranak Salajegheh, Mohsen Nakhaie, Mohammad Rezaei Zadeh Rukerd   +3 more
doaj   +1 more source

Nail Toxicities Associated With Anticancer Therapies in Children

JEADV Clinical Practice, EarlyView.
ABSTRACT Nail toxicities are a frequent yet often underrecognized component of dermatologic adverse events in children receiving anticancer therapies. Both conventional cytotoxic chemotherapy and newer targeted agents can affect the nail matrix, nail bed and periungual tissues, producing a broad spectrum of clinical manifestations that range from ...
Luca Rapparini, Michela Starace
wiley   +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

Gastrointestinal Tract Involvement of Langerhans Cell Histiocytosis: Concerning Point of Diagnosis

Journal of Health Science and Medical Research (JHSMR), 2020
An 8-month-old girl presented with chronic mucous bloody diarrhea for 3 months. She was diagnosed as infective gastroenteritis and did not improve after antibiotic treatment.
Shevachut Chavananon, Pornpun Sripornsawan, Thirachit Chotsampancharoen   +2 more
doaj   +1 more source

Cutaneous Rosai‐Dorfman Disease With MAP2K1 Mutation Treated With Encorafenib and Binimetinib

JEADV Clinical Practice, EarlyView.
ABSTRACT Rosai‐Dorfman disease (RDD) is a rare histiocytic disorder with unifocal to multisystemic involvement. Activating mutations in the MAPK/ERK pathway can occur in up to 50% of RDD cases. We report a case of cutaneous RDD (C‐RDD) with facial and truncal lesions harboring an activating MAP2K1 (MEK1) mutation that showed a complete response to a ...
Melike Ak, Reinhard Dummer, Egle Ramelyte   +2 more
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

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

Extraosseous langerhans cell histiocytosis in children

, 2008
Langerhans cell histiocytosis, a rare disease that occurs mainly in children, may produce a broad range of manifestations, from a single osseous lesion to multiple lesions involving more than one organ or system.
Letovanec, I., Geoffray, A., Letovanec, Igor, Waibel, Peter, Georg Eich, Peter Waibel, Schmidt, S., Gudinchet, Francois, Hanquinet, Sylviane, Eich, Georg, Anne Geoffray, Wolf, R., Rainer Wolf, Sabine Schmidt, Geoffray, Anne, Hanquinet, S., Schmidt, Sabine, Alamo-Maestre, L., Francois Gudinchet, Alamo-Maestre, Leonore, Eich, G., Gudinchet, F., Igor Letovanec, Leonore Alamo-Maestre, Waibel, P., Wolf, Rainer, Sylviane Hanquinet   +26 more
core   +1 more source

Pregnancy in CTD‐interstitial lung disease: Current evidence, clinical challenges, and a proposed management algorithm

Rheumatology &Autoimmunity, EarlyView.
Summary of pregnancy management in CTD‐ILD across preconception, antenatal, and postpartum phases, emphasizing risk stratification and multidisciplinary care. 6MWT, 6‐min walk test; CTD‐ILD: connective tissue disease‐interstitial lung disease; DLCO, diffusion capacity of the lung for carbon monoxide; FVC, forced vital capacity; MDT, multidisciplinary ...
Khaled Aldhuaina, Ghaydaa Aldabie, Mohammad Abdulsalam, Ali Jawad   +3 more
wiley   +1 more source

Langerhans Cell Histiocytosis of the Mandible

Cureus, 2022
The unusual disorder known as Langerhans cell histiocytosis, which is most frequently seen in children and young adults, is caused by the clonal proliferation of Langerhans cells. Even if clinical signs and radiographic evidence of destructive bone lesions may raise suspicion of the disease, a reliable diagnosis without a thorough pathological ...
Padmanaban, Kamalakannan, Kamalakaran, Arunkumar, Raghavan, Priyadharshini, Palani, Triveni, Rajiah, Davidson   +4 more
openaire   +2 more sources