OBJECTIVE: Solid organ transplant (SOT) and hematopoietic stem cell transplant (HSCT) recipients are at risk of several diseases, principally attributable to immunosuppression. This global overview of SOT/HSCT-associated orofacial diseases is aimed at providing a practical instrument for the oral healthcare management of SOT/HSCT recipients. Methods: Literature search was made through MEDLINE. The associations between orofacial diseases and SOT/HSCT were assessed using observational studies and case series and were classified into association, no association, and unclear association. Results: Lip/oral cancers, drug-induced gingival overgrowth (DIGO), infections, including hairy leukoplakia and, less frequently, post-transplantation lymphoproliferative disorders (PTLDs) and oral lichenoid lesions of graft-versus-host disease (GVHD), were associated with SOT. Lip/oral cancers, GVHD, mucositis, DIGO, infections and, less frequently, PTLDs were associated with HSCT. Associations of orofacial granulomatosis-like lesions and oral mucosa-associated lymphoid tissue-type lymphoma with SOT, and of pyogenic granuloma and hairy leukoplakia with HSCT were unclear. Periodontal disease and dental caries were not associated with SOT/HSCT. For none of the local treatments was there a strong evidence of effectiveness. Conclusions: Solid organ transplant/HSCT recipients are at risk of orofacial diseases. Adequate management of these patients alleviates local symptoms responsible for impaired eating, helps prevent systemic and lethal complications, and helps where dental healthcare has been neglected. Oral Diseases (2012) 19, 1836

Orofacial diseases in solid organ and hematopoietic stem cell transplant recipients / Petti, Stefano; Polimeni, Antonella; Berloco, Pasquale Bartolomeo; C., Scully. - In: ORAL DISEASES. - ISSN 1354-523X. - STAMPA. - 19:1(2013), pp. 18-36. [10.1111/j.1601-0825.2012.01925.x]

Orofacial diseases in solid organ and hematopoietic stem cell transplant recipients

PETTI, Stefano;POLIMENI, Antonella;BERLOCO, Pasquale Bartolomeo;
2013

Abstract

OBJECTIVE: Solid organ transplant (SOT) and hematopoietic stem cell transplant (HSCT) recipients are at risk of several diseases, principally attributable to immunosuppression. This global overview of SOT/HSCT-associated orofacial diseases is aimed at providing a practical instrument for the oral healthcare management of SOT/HSCT recipients. Methods: Literature search was made through MEDLINE. The associations between orofacial diseases and SOT/HSCT were assessed using observational studies and case series and were classified into association, no association, and unclear association. Results: Lip/oral cancers, drug-induced gingival overgrowth (DIGO), infections, including hairy leukoplakia and, less frequently, post-transplantation lymphoproliferative disorders (PTLDs) and oral lichenoid lesions of graft-versus-host disease (GVHD), were associated with SOT. Lip/oral cancers, GVHD, mucositis, DIGO, infections and, less frequently, PTLDs were associated with HSCT. Associations of orofacial granulomatosis-like lesions and oral mucosa-associated lymphoid tissue-type lymphoma with SOT, and of pyogenic granuloma and hairy leukoplakia with HSCT were unclear. Periodontal disease and dental caries were not associated with SOT/HSCT. For none of the local treatments was there a strong evidence of effectiveness. Conclusions: Solid organ transplant/HSCT recipients are at risk of orofacial diseases. Adequate management of these patients alleviates local symptoms responsible for impaired eating, helps prevent systemic and lethal complications, and helps where dental healthcare has been neglected. Oral Diseases (2012) 19, 1836
2013
solid organ transplant; oral health; haematopoietic stem cell transplant; oral disease
01 Pubblicazione su rivista::01a Articolo in rivista
Orofacial diseases in solid organ and hematopoietic stem cell transplant recipients / Petti, Stefano; Polimeni, Antonella; Berloco, Pasquale Bartolomeo; C., Scully. - In: ORAL DISEASES. - ISSN 1354-523X. - STAMPA. - 19:1(2013), pp. 18-36. [10.1111/j.1601-0825.2012.01925.x]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/446781
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