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Case report: Langerhans cell histiocytosis of the temporal bone in children: Challenging diagnosis of a rare disease with some pitfalls

A 4‐year‐old girl was admitted to hospital with disturbance of balance. After being questioned, parents remembered an otitis with effusion 3 months earlier. CT‐scans revealed destruction of both temporal bones. Initial biopsy showed granulomatous, necrotic inflammation, which led to comprehensive di...

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Detalles Bibliográficos
Autores principales: Pähler vor der Holte, Anja, Welkoborsky´, Hans‐Jürgen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9556999/
https://www.ncbi.nlm.nih.gov/pubmed/36254150
http://dx.doi.org/10.1002/ccr3.6057
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author Pähler vor der Holte, Anja
Welkoborsky´, Hans‐Jürgen
author_facet Pähler vor der Holte, Anja
Welkoborsky´, Hans‐Jürgen
author_sort Pähler vor der Holte, Anja
collection PubMed
description A 4‐year‐old girl was admitted to hospital with disturbance of balance. After being questioned, parents remembered an otitis with effusion 3 months earlier. CT‐scans revealed destruction of both temporal bones. Initial biopsy showed granulomatous, necrotic inflammation, which led to comprehensive differential diagnoses. A second tissue sample confirmed Langerhans cell histiocytosis.
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spelling pubmed-95569992022-10-16 Case report: Langerhans cell histiocytosis of the temporal bone in children: Challenging diagnosis of a rare disease with some pitfalls Pähler vor der Holte, Anja Welkoborsky´, Hans‐Jürgen Clin Case Rep Case Report A 4‐year‐old girl was admitted to hospital with disturbance of balance. After being questioned, parents remembered an otitis with effusion 3 months earlier. CT‐scans revealed destruction of both temporal bones. Initial biopsy showed granulomatous, necrotic inflammation, which led to comprehensive differential diagnoses. A second tissue sample confirmed Langerhans cell histiocytosis. John Wiley and Sons Inc. 2022-10-12 /pmc/articles/PMC9556999/ /pubmed/36254150 http://dx.doi.org/10.1002/ccr3.6057 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Case Report
Pähler vor der Holte, Anja
Welkoborsky´, Hans‐Jürgen
Case report: Langerhans cell histiocytosis of the temporal bone in children: Challenging diagnosis of a rare disease with some pitfalls
title Case report: Langerhans cell histiocytosis of the temporal bone in children: Challenging diagnosis of a rare disease with some pitfalls
title_full Case report: Langerhans cell histiocytosis of the temporal bone in children: Challenging diagnosis of a rare disease with some pitfalls
title_fullStr Case report: Langerhans cell histiocytosis of the temporal bone in children: Challenging diagnosis of a rare disease with some pitfalls
title_full_unstemmed Case report: Langerhans cell histiocytosis of the temporal bone in children: Challenging diagnosis of a rare disease with some pitfalls
title_short Case report: Langerhans cell histiocytosis of the temporal bone in children: Challenging diagnosis of a rare disease with some pitfalls
title_sort case report: langerhans cell histiocytosis of the temporal bone in children: challenging diagnosis of a rare disease with some pitfalls
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9556999/
https://www.ncbi.nlm.nih.gov/pubmed/36254150
http://dx.doi.org/10.1002/ccr3.6057
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