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Publikováno v:
Rare ILD / DPLD.
Publikováno v:
Rare ILD/DPLD.
Pulmonary Langerhans cell histiocytosis (PLCH) is a disease of the reticulohistiocytic system of unknown etiology, characterized by primary proliferation of atypical histiocytes and the formation of histiocytic granulomas in the lungs, also in other