Your browser doesn't support javascript.
loading
Etiological diagnosis of macroglossia: Systematic review and diagnostic algorithm.
Dietrich, E; Grimaux, X; Martin, L; Samimi, M.
Afiliación
  • Dietrich E; Dermatology Department, Centre Hospitalier Universitaire d'Angers, 4 rue Larrey, 49000 Angers, France. Electronic address: elisemdietrich@gmail.com.
  • Grimaux X; Dermatology Department, Centre Hospitalier Universitaire d'Angers, 4 rue Larrey, 49000 Angers, France.
  • Martin L; Dermatology Department, Centre Hospitalier Universitaire d'Angers, 4 rue Larrey, 49000 Angers, France.
  • Samimi M; Dermatology Department, Centre Hospitalier Universitaire de Tours, 2 boulevard Tonnellé, 37000 Tours, France.
Ann Dermatol Venereol ; 149(4): 228-237, 2022 Dec.
Article en En | MEDLINE | ID: mdl-36229262
ABSTRACT

BACKGROUND:

The objective of this literature review was to list the different etiologies of macroglossia reported in the literature, to identify characteristics that might guide diagnosis, and to create a diagnostic algorithm.

METHODS:

The bibliographic search was carried out between October 2019 and July 2020 in the PubMed research base using the keywords "macroglossia" (MESH) and/or "tongue enlargement".

RESULTS:

Of the 1711 references identified, 615 articles were excluded, and 1096 abstracts were reviewed. We classified the different etiologies identified according to their mechanism and whether they were congenital or acquired. The etiologies are divided into the following categories genetic malformation syndromes, non-syndromic congenital malformations, endocrinopathies, neuromuscular diseases, storage disorders, infectious, inflammatory, traumatic, and iatrogenic diseases.

CONCLUSION:

Based on this review, we propose a diagnostic algorithm for macroglossia according to the characteristics described. The most common diagnoses among acquired causes were amyloidosis (13.7%), endocrinopathies (8.8%), myopathies (4%) and tongue tumors (6.7%). The most common congenital causes were aneuploidy, lymphatic malformations, and Beckwith-Wiedemann syndrome, which is the main cause of congenital macroglossia, even if it appears isolated.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Macroglosia Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Ann Dermatol Venereol Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Macroglosia Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Ann Dermatol Venereol Año: 2022 Tipo del documento: Article
...