Histopathologic clues to the etiopathogenesis of orbital inflammatory disease: Idiopathic, IgG4-related, neoplastic, autoimmune and beyond.
Semin Diagn Pathol
; 41(2): 66-71, 2024 Mar.
Article
en En
| MEDLINE
| ID: mdl-38341348
ABSTRACT
Orbital inflammatory diseases represent a heterogenous group of idiopathic, autoimmune-related, and sometimes neoplastic conditions with overlapping clinical and histopathologic features, as well as variable levels of IgG4-positive plasma cells detected within tissue biopsies. Some histopathologic features, especially in an appropriate clinical context, may point to a specific diagnosis in a given patient. Diagnoses of non-specific orbital inflammation, orbital inflammation related to autoimmune diseases such as granulomatosis with polyangiitis and IgG4-related disease, lymphoma, and xanthogranulomatous diseases are discussed, contrasted and illustrated.
Palabras clave
Texto completo:
1
Colección:
01-internacional
Banco de datos:
MEDLINE
Asunto principal:
Enfermedades Autoinmunes
/
Enfermedad Relacionada con Inmunoglobulina G4
/
Linfoma
Límite:
Humans
Idioma:
En
Revista:
Semin Diagn Pathol
/
Semin. diagn. pathol
/
Seminars in diagnostic pathology
Asunto de la revista:
PATOLOGIA
Año:
2024
Tipo del documento:
Article