Results 81 to 90 of about 14,204,460 (231)
Pediatric Blood &Cancer, Volume 73, Issue 10, October 2026.ABSTRACT Juvenile xanthogranuloma (JXG) of the central nervous system (CNS) is a rare non‐Langerhans cell histiocytosis. CSF1R mutations have been reported for peripheral JXG, but not in CNS JXG. A 3‐month‐old male presented with fever, lymphadenopathy, and macrocephaly with bulging fontanelles.
Sima Vazquez +8 more
wiley +1 more source
Uncommon preputial localization of Langerhans cell histiocytosis
, 2021 International audienceWe report a rare case of a 14-year-old boy with Langerhans cell histiocytosis localized to the prepuce. The patient was treated with a topical corticosteroid followed by imiquimod cream resulting in significant clinical improvement ...
Sebastien Barbarot +11 more
core +1 more source
Flat Topped Brown Papules on a Four-Year-Old Male
Revista da Sociedade Portuguesa de Dermatologia e Venereologia, 2020 .
Francisca Alves +3 more
doaj +1 more source
The Role of “Adult‐Onset” Cancer Predisposition Genes in Pediatric Cancer: A Comprehensive Review
Pediatric Blood &Cancer, Volume 73, Issue 9, September 2026.ABSTRACT Current literature estimates that 10% of pediatric cancers are caused by pathogenic or likely pathogenic (P/LP) germline variants in cancer predisposition genes (CPGs). Variants in CPGs thought to increase cancer risk exclusively during adulthood are referred to as “adult‐onset” CPGs (aoCPGs).
Maria Rozo +5 more
wiley +1 more source
Langerhans cell histiocytosis of the orbit
, 2013 Purpose: The management of Langerhans cell histiocytosis is controversial.
KIRATLI, HAYYAM +2 more
core +1 more source
Langerhans cell histiocytosis (histiocytosis X) [PDF]
, 1997 There has been a renewed interest in Langerhans cell histiocytosis in recent years due both to advances in basic research and to improvements in diagnostic and treatment approaches.
K Y Lam, Lam, KY
core +1 more source
Erdheim-Chester Disease Associated with Marginal Zone Lymphoma and Monoclonal Proteinemia
Case Reports in Hematology, 2011 Erdheim-Chester disease (ECD) is a rare non-Langerhans cell histiocytosis. We report a fatal case of ECD with extensive cardiac involvement associated with a marginal zone lymphoma and monoclonal proteinemia in a young man.
Peter G. Pavlidakey +3 more
doaj +1 more source
Cancer Medicine, Volume 15, Issue 9, September 2026.ABSTRACT Introduction Children treated with ifosfamide seem to have an increased risk for developing chronic kidney disease (CKD) already within the first years following chemotherapy. However, studies investigating CKD prevalence in this specific phase are scarce.
Lotte Pitlo +9 more
wiley +1 more source
Langerhans Cell Histiocytosis (LCH) and Diabetes Insipidus with Mandibular lesion
, 2012 Langerhans cell histicytosis (LCH) is a rare disorder that primarily affects children. Its occurrence in adult is very rare. We report a case of 42 year old female patient who presented polyuria and polydipsia, loosing teeth and diplopia added to symptom
Sayeh Alizad jahani +3 more
core
Craniofacial and intracranial Langerhans cell histiocytosis [PDF]
, 2020 Main Teaching Point: Multiple osteolytic calvarial lesions in a child raise suspicion of Langerhans cell ...
Lemmerling, Marc +2 more
core +1 more source