Results 101 to 110 of about 56,324 (305)
Acute leukemia in association with Langerhans cell histiocytosis [PDF]
, 1994 Langerhans cell histiocytosis (LCH) and malignancy occurring in the same individual is unusual and has generally been the subject of isolated case reports.
Aricò, M. (Maurizio) +5 more
core +1 more source
How I treat Langerhans cell histiocytosis.
Blood, 2015 "Langerhans cell histiocytosis" (LCH) describes a spectrum of clinical presentations ranging from a single bone lesion or trivial skin rash to an explosive disseminated disease.
C. Allen, S. Ladisch, K. McClain
semanticscholar +1 more source
A young man with multifocal brainstem leptomeningeal disease
Brain Pathology, EarlyView.
Burana Khiankaew +7 more
wiley +1 more source
Changes in multi‐gene cancer panels for children: A 4‐year retrospective review
Journal of Genetic Counseling, Volume 34, Issue 4, August 2025.Abstract The multi‐gene panel is the most utilized genetic test to evaluate for germline cancer predisposition syndromes. However, the rate of change of commercial multigene panels is not well understood, and its value as a standalone test has also not been investigated.
Elise G. Williams +4 more
wiley +1 more source
Emergence of solitary juvenile xanthogranuloma on the corneoscleral limbus
Journal of Clinical Ophthalmology and Research, 2018 Juvenile xanthogranuloma (JXG) is the most frequent form of non-Langerhans histiocytosis, a rare benign inflammatory skin disorder. Eye involvement is the most frequent extracutaneous manifestation of the disease.
Raul Alfaro-Rangel +2 more
doaj +1 more source
Dendritic Cells Cause Bone Lesions in a New Mouse Model of Histiocytosis. [PDF]
, 2015 Langerhans cell histiocytosis (LCH) is a rare disease caused by the clonal accumulation of dendritic Langerhans cells, which is often accompanied by osteolytic lesions.
Acha-Orbea, H. +11 more
core +3 more sources
Oral manifestation of Langerhans cell histiocytosis: a case report
BMC Oral Health, 2018 Bone necrosis of the jaw is a serious condition with a broad differential diagnosis of pathologies such as cutaneous histiocytosis, bone metastases or malignant tumours.
J. Luz +5 more
semanticscholar +1 more source
Histopathology, Volume 87, Issue 2, Page 258-269, August 2025.Pathohistological analysis of FDCS revealed a morphological spectrum and led to the identification of the adhesion molecule L1CAM as a novel diagnostic immunomarker for FDCS. Sequencing identified NFKBIA as the most frequently altered gene, of note, exclusively in cases with a predominant epithelioid cytomorphology.
Selina Schelbert +12 more
wiley +1 more source
A case of Erdheim Chester disease with central nervous system involvement
Annals of Indian Academy of Neurology, 2015 Erdheim Chester disease (ECD) is a rare non-Langerhans cell histiocytosis, commonly involving the musculoskeletal system. Other tissue can also be involved, including the central nervous system with wide spectrum of clinical features, at times being ...
Anil Kumar Patil +6 more
doaj +1 more source
Isolated Langerhans cell histiocytosis of the vulva: a case report and review of the literature [PDF]
, 2018 Isolated Langerhans cell histiocytosis (LCH) of the female genital tract is very rare. A review of the literature revealed that only 15 cases of primary vulvar LCH have previously been published in the English literature.
Beer, Karl +5 more
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