The term “fibro-osseous lesions” is an umbrella term that is used to describe the
histopathological picture of certain lesions where normal bone is replaced by fibrous tissue …

Langerhans cell histiocytosis (LCH) is a rare inflammatory neoplasia in which somatic
mutations in components of the MAPK/ERK pathway have been identified. Osseous …

The aim of our paper is to present and discuss in detail the bony changes indicative of
tuberculosis (TB) that were identified in a skeleton (KB67), unearthed from grave 67 of the …

Background Langerhans cell histiocytosis (LCH) is an inflammatory myeloid neoplasm that
can involve multisystem organs. Positron emission tomography/computed tomography …

Background Xanthogranulomatous osteomyelitis (XO) is a rare disease characterized
radiologically by an osteolytic lesion with cortical expansion or disruption. Differentiating this …

Langerhans cell histiocytosis (LCH) is a rare disorder of clonal proliferation of dendritic cell
mostly seen in children. It consists in various clinical manifestations from a single lytic bone …

In adolescents periodontal destruction may be the primary manifestation of an as yet
unrecognized rare systemic disease, and it may be up to the periodontist to make the correct …

Objective To explore the clinical features, diagnosis, treatment and prognosis of Langerhans
cell histiocytosis (LCH) of the skull in children. Methods This study retrospectively …

Langerhans cell histiocytosis (LCH) is a rare neoplastic disorder marked by the uncontrolled
proliferation and accumulation of immature myeloid dendritic cells, which originate from the …

Langerhans cell histiocytosis is a rare disease with diverse clinical presentations. We report
a 4-year-old boy with progressive weakness in lower extremities, a large head lump, and …