INTRODUCTION We report the case of a 24-year-old Greek woman with histologically proven osseous and pulmonary Langerhans cell histiocytosis whose lesions had progressively regressed with a "switch on and off" mode. This is the first report in the literature of this mode of presentation of Langerhans cell histiocytosis. CASE PRESENTATION The patient had first presented at the age of 20 years w...

Solitary pulmonary Langerhans cell histiocytosis occurs predominantly in young adults, who are frequently heavy smokers. Besides the strong association to smoking, it differs from childhood Langerhans cell histiocytosis as well in that it is a polyclonal disorder, and the lesional Langerhans cells in this form of disease are reported to display mature markers. Thus, in this study we set out to ...

vertebra plana is a radiological diagnosis that indicates complete compression of the vertebral body.(1,2) this condition was reported in langerhans cell histiocytosis including eosino-philic granuloma,(3, 12) ewing's sarcoma,(2,13,14) tuberculosis,(15,16) vertebral osteomyelitis,(17) aseptic necrosis,(18) aneurysmal bone cyst,(19) osteosarcoma,(20) neuroblastoma,(21) acute leu-kemia,(22) rhabd...

BACKGROUND Langerhans cell histiocytosis (LCH) is a rare histiocytic disorder of unknown etiopathogenesis. Its clinical presentation is variable and ranges from isolated skin or bone disease to a life-threatening multisystem condition. LCH can occur at any age but is more frequent in the pediatric population. A neoplastic origin of this disease has been suggested due to the discovery of the mut...

Langerhans cell histiocytosis (LCH) combines in one nosological category a group of diseases that have widely disparate clinical manifestations but are all characterized by accumulation of proliferating cells with surface markers and ultrastructural features similar to cutaneous Langerhans cells (LCs). In particular, careful molecular analyses of mouse models and human LCH samples suggest that ...

Langerhans cell histiocytosis (LCH) is a rare disease of unknown cause, characterized by the proliferation of pathogenic Langerhans cells and cytokine overproduction causing inflammation, infiltration and destruction of many tissues of the body. LCH is a heterogeneous condition and may present with simple painful bony lesions, often affecting the skull or long bones, chronic otitis, proptosis o...

Langerhans' cell histiocytosis (LCH) is one of the 'histiocytosis disorders', as defined by the Histiocyte Society. LCH is an abnormal proliferation and dissemination of clonal Langerhans' cells in which they accumulate, along with other inflammatory cells, and form tissue granulomas in different organs. It is named after the appearance of the cells, which resemble the normal dendritic cells fo...

Histiocytosis X, or Langerhans cell histiocytosis (LCH), is a rare disease, with an estimated incidence of 1/200,000 per year in children under 15 years of age. It has a wide clinical spectrum, from single bone involvement (eosinophilic granuloma) to multisystemic disease with organ failure. The treatment of LCH is still controversial. While single system disease may spontaneously recover or re...