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DOI: 10.1055/s-0040-1703620
AN UNUSUAL PRESENTATION OF LANGERHANS CELL HISTIOCYTOSIS
Authors

Abstract
Langerhans cell histiocytosis most commonly occurring in children, demonstrates a broad spectrum of clinical and radiologic features that may mimic those of infection as well as benign and malignant tumors. Osseous involvement is the most common manifestation. Recognition of the skeletal alterations is important so that the disease is considered as differential diagnosis. This disease is of unknown aetiology, non-specific clinical and imaging findings with diagnosis possible only on histopathological examination, will always pose a diagnostic challenge to the orthopaedic surgeon. Here by we are reporting two cases of eosinophilic granuloma that has presented with lytic lesion in the tibia and scapula. The clinico-radiological suspicion was either infection or tumour of the affected bones. Hence, core biopsy was done confirmed as eosinophilic granuloma on histopathology and immunohistochemistry.
Publikationsverlauf
Artikel online veröffentlicht:
29. April 2020
© .
Thieme Medical and Scientific Publishers Private Ltd.
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References
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