| Literature DB >> 29657688 |
Hui Yan Ong1, Liang Chye Goh1,2, Kalimuthu Santhi1, Mohamad Mokhtar Sha'ariyah1.
Abstract
Langerhans cell histiocytosis (LCH) is a rare proliferative disorder, which commonly arises in the bone and may involve other systems. To date, the diagnosis of temporal bone LCH remains a challenge as it may masquerade as a common ear infection. We report a case of a child who presented to us with persistent bilateral ear discharge for four months and was not responding to treatment. Her condition subsequently worsened, with clinical features and radiological findings suggestive of mastoid cellulitis. Nevertheless, further histopathology study revealed LCH.Entities:
Keywords: Cellulitis; Histiocytosis; Langerhans Cells; Temporal Bone
Year: 2018 PMID: 29657688 PMCID: PMC5889838 DOI: 10.5001/omj.2018.31
Source DB: PubMed Journal: Oman Med J ISSN: 1999-768X