Parosmia como debut de una displasia fibrosa

Introduction: Fibrous Dysplasia is a rare benign bone disorder with unknown aetiology; consists in replacement of normal medullary bone by fibroosseous tissue, causing distortion and overgrowth of the bones involved. Entity with nonspecific clinical presentation (whose symptoms may include olfactory...

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Autores: Samarà Piñol, Laura, Galindo Ortego, Xavier, Bellera Vilar, Patricia
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2015
País:España
Institución:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:10459.1/58397
Acceso en línea:http://hdl.handle.net/10459.1/58397
Access Level:acceso abierto
Palabra clave:Fibrous Dysplasia
Olfaction disorders
Paraosmia
Displàsia fibrosa òssia
Olfacte
Fibrous dysplasia of bone
Smell
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spelling Parosmia como debut de una displasia fibrosa Paraosmia as a fibrous dysplasia debut Samarà Piñol, Laura Galindo Ortego, Xavier Bellera Vilar, Patricia Fibrous Dysplasia Olfaction disorders Paraosmia Displàsia fibrosa òssia Olfacte Fibrous dysplasia of bone Smell Introduction: Fibrous Dysplasia is a rare benign bone disorder with unknown aetiology; consists in replacement of normal medullary bone by fibroosseous tissue, causing distortion and overgrowth of the bones involved. Entity with nonspecific clinical presentation (whose symptoms may include olfactory disorders - due to involvement of the cribriform plate or surrounding areas); whose suspected diagnosis is established by test-imaging and definitive diagnosis requires histological confirmation. Treatment depends on symptoms' severity, location and impact on patient quality of life and it goes from conservative treatment (in asymptomatic or mild cases) till surgical excision (in severe ones). It has a 0.4% malignancy incidence rate and a capacity for local recurrence of up to 25%. Therefore, requires a long-term follow-up. Case Report: A 78-year-old woman was referred for evaluation of an olfaction disorder that began six months earlier, with no other neurological or ENT associated symptoms. After a detailed anamnesis and a complete physical examination, which turned out to be normal, test-imaging was requested reporting an altered signal in the right sphenoethmoidal junction, with no apparent intracranial extension, associated with a pattern consistent with Fibrous Dysplasia. Due to mild patient symptomatology's (only parosmias), medical treatment (oxcarbazepine) was proposed -with improvement thereof-, and later controls. Keywords: Fibrous Dysplasia, Olfaction Disorders, Paraosmia. 2 Sociedad Gallega de Otorrinolaringología http://hdl.handle.net/10459.1/58397
title Parosmia como debut de una displasia fibrosa
spellingShingle Parosmia como debut de una displasia fibrosa
Samarà Piñol, Laura
Fibrous Dysplasia
Olfaction disorders
Paraosmia
Displàsia fibrosa òssia
Olfacte
Fibrous dysplasia of bone
Smell
title_short Parosmia como debut de una displasia fibrosa
title_full Parosmia como debut de una displasia fibrosa
title_fullStr Parosmia como debut de una displasia fibrosa
title_full_unstemmed Parosmia como debut de una displasia fibrosa
title_sort Parosmia como debut de una displasia fibrosa
author Samarà Piñol, Laura
author_facet Samarà Piñol, Laura
Galindo Ortego, Xavier
Bellera Vilar, Patricia
author_role author
author2 Galindo Ortego, Xavier
Bellera Vilar, Patricia
author2_role author
author
topic Fibrous Dysplasia
Olfaction disorders
Paraosmia
Displàsia fibrosa òssia
Olfacte
Fibrous dysplasia of bone
Smell
topic_facet Fibrous Dysplasia
Olfaction disorders
Paraosmia
Displàsia fibrosa òssia
Olfacte
Fibrous dysplasia of bone
Smell
description Introduction: Fibrous Dysplasia is a rare benign bone disorder with unknown aetiology; consists in replacement of normal medullary bone by fibroosseous tissue, causing distortion and overgrowth of the bones involved. Entity with nonspecific clinical presentation (whose symptoms may include olfactory disorders - due to involvement of the cribriform plate or surrounding areas); whose suspected diagnosis is established by test-imaging and definitive diagnosis requires histological confirmation. Treatment depends on symptoms' severity, location and impact on patient quality of life and it goes from conservative treatment (in asymptomatic or mild cases) till surgical excision (in severe ones). It has a 0.4% malignancy incidence rate and a capacity for local recurrence of up to 25%. Therefore, requires a long-term follow-up. Case Report: A 78-year-old woman was referred for evaluation of an olfaction disorder that began six months earlier, with no other neurological or ENT associated symptoms. After a detailed anamnesis and a complete physical examination, which turned out to be normal, test-imaging was requested reporting an altered signal in the right sphenoethmoidal junction, with no apparent intracranial extension, associated with a pattern consistent with Fibrous Dysplasia. Due to mild patient symptomatology's (only parosmias), medical treatment (oxcarbazepine) was proposed -with improvement thereof-, and later controls. Keywords: Fibrous Dysplasia, Olfaction Disorders, Paraosmia. 2
publishDate 2015
format article
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url http://hdl.handle.net/10459.1/58397
eu_rights_str_mv openAccess
publisher Sociedad Gallega de Otorrinolaringología
institution Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
collection Recercat. Dipósit de la Recerca de Catalunya
reponame_str Recercat. Dipósit de la Recerca de Catalunya
instname_str Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
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publishDateSort 2015
author_browse Bellera Vilar, Patricia
Galindo Ortego, Xavier
Samarà Piñol, Laura
publisherStr Sociedad Gallega de Otorrinolaringología
score 6,924472