Rosai-Dorfman disease mimicking molluscum contagiosum in a patient with prior kappa light chain multiple myeloma. [PDF]
Rivas S +6 more
europepmc +1 more source
Prognostic factor analysis of oral and maxillofacial Langerhans cell histiocytosis based on clinical findings and tumour microenvironment. [PDF]
Ogawa M +7 more
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Pediatric hemophagocytic lymphohistiocytosis with predominant CNS involvement: MRI features and differential diagnosis. [PDF]
Bulut OS +3 more
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Multisystem Langerhans cell Histiocytosis presenting with spontaneous pneumothorax in a toddler: case report and literature review. [PDF]
Tard SC +3 more
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Expanding the Toolbox: Utility of HistioTrak for Minimal Residual Monitoring in Pediatric Patients with Langerhans Cell Histiocytosis Treated with Targeted Therapy. [PDF]
Nevers R +5 more
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Spinal relapse of Erdheim-Chester disease detected on <sup>18</sup>F-FDG PET/CT. [PDF]
Benameur Y +6 more
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Spontaneous regression of a presumed orbitocranial eosinophilic granuloma in an adult patient: illustrative case. [PDF]
Lin LY +5 more
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Biology of Langerhans Cells and Langerhans Cell Histiocytosis
International Review of Cytology, 2006Langerhans cells (LC) are epidermal dendritic cells (DC). They play an important role in the initiation of immune responses through antigen uptake, processing, and presentation to T cells. Langerhans cell histiocytosis (LCH) is a rare disease in which accumulation of cells with LC characteristics (LCH cells) occur. LCH lesions are further characterized
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