Langerhans cell histiocytosis in childhood - Review, symptoms in the oral cavity, differential diagnosis and report of two cases

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11140%2F14%3A10145569" target="_blank" >RIV/00216208:11140/14:10145569 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/00669806:_____/14:10145569

Výsledek na webu

<a href="http://www.sciencedirect.com/science/article/pii/S1010518213000917#" target="_blank" >http://www.sciencedirect.com/science/article/pii/S1010518213000917#</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1016/j.jcms.2013.03.005" target="_blank" >10.1016/j.jcms.2013.03.005</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Langerhans cell histiocytosis in childhood - Review, symptoms in the oral cavity, differential diagnosis and report of two cases

Popis výsledku v původním jazyce

Langerhans cell histiocytosis is a rare disease characterized by monoclonal proliferation and migration of special dendritic cells. This disease primarily affects bones, but occurs less frequently in other organ systems or may manifest as a multisystem disease. Extraoral and intraoral symptoms of Langerhans cell histiocytosis are described in a 13-month-old female and a 5-month-old male infant. Dermatitis was found on the scalp, abdomen, flexures and in intertrigineous areas in both patients. The intraoral examination of the 13-month-old infant showed premature eruption of all maxillary deciduous molars, loosening and significant damage of periodontal tissues (gingivitis with bleeding, swelling of palatal mucosa, periodontal pockets) resembling severeperiodontitis. In the oral cavity of the 5-month-old predentate infant bilateral swellings of maxillary alveolar mucosa with deep ulcerations were seen. The oral and skin symptoms in both infants were indications for biopsy. Langerhans ce

Název v anglickém jazyce

Langerhans cell histiocytosis in childhood - Review, symptoms in the oral cavity, differential diagnosis and report of two cases

Popis výsledku anglicky

Langerhans cell histiocytosis is a rare disease characterized by monoclonal proliferation and migration of special dendritic cells. This disease primarily affects bones, but occurs less frequently in other organ systems or may manifest as a multisystem disease. Extraoral and intraoral symptoms of Langerhans cell histiocytosis are described in a 13-month-old female and a 5-month-old male infant. Dermatitis was found on the scalp, abdomen, flexures and in intertrigineous areas in both patients. The intraoral examination of the 13-month-old infant showed premature eruption of all maxillary deciduous molars, loosening and significant damage of periodontal tissues (gingivitis with bleeding, swelling of palatal mucosa, periodontal pockets) resembling severeperiodontitis. In the oral cavity of the 5-month-old predentate infant bilateral swellings of maxillary alveolar mucosa with deep ulcerations were seen. The oral and skin symptoms in both infants were indications for biopsy. Langerhans ce

Druh

J_x - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

CEP obor

FF - ORL, oftalmologie, stomatologie

OECD FORD obor

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Projekt

—

Návaznosti

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2014

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Journal of Cranio-Maxillofacial Surgery

ISSN

1010-5182

e-ISSN

—

Svazek periodika

42

Číslo periodika v rámci svazku

2

Stát vydavatele periodika

GB - Spojené království Velké Británie a Severního Irska

Počet stran výsledku

8

Strana od-do

93-100

Kód UT WoS článku

000331683200001

EID výsledku v databázi Scopus

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