Erdheim-Chester disease with multisystem involvement in a 4-year-old

Erdheim-Chester disease is a rare form of non-Langerhans histiocytosis of unknown origin occurring mainly in adults. It is extremely rare in children. We report a case of a 4-year-old boy with Erdheim-Chester disease that initially presented as hemifacial palsy and bone pain with multisystem involve...

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Veröffentlicht in:Pediatric radiology 2012-05, Vol.42 (5), p.632-635
Hauptverfasser: Song, Sook Yun, Lee, Sun Wha, Ryu, Kyung-ha, Sung, Sun Hee
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creator Song, Sook Yun
Lee, Sun Wha
Ryu, Kyung-ha
Sung, Sun Hee
description Erdheim-Chester disease is a rare form of non-Langerhans histiocytosis of unknown origin occurring mainly in adults. It is extremely rare in children. We report a case of a 4-year-old boy with Erdheim-Chester disease that initially presented as hemifacial palsy and bone pain with multisystem involvement. We describe radiographic findings of bones that show characteristic bilateral symmetrical osteosclerosis with atypical osteolytic lesions in addition to CT findings for pulmonary involvement and MR findings for intracranial lesions.
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source MEDLINE; Springer Nature - Complete Springer Journals
subjects Case Report
Child, Preschool
Diagnosis, Differential
Erdheim-Chester Disease - diagnosis
Erdheim-Chester Disease - drug therapy
Humans
Imaging
Magnetic Resonance Imaging
Male
Medicine
Medicine & Public Health
Neuroradiology
Nuclear Medicine
Oncology
Pediatrics
Radiology
Tomography, X-Ray Computed
Ultrasound
title Erdheim-Chester disease with multisystem involvement in a 4-year-old
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