Intraparotid plexiform neurofibroma: A rare diagnostic challenge.
Diagn Cytopathol
; 52(7): E164-E167, 2024 Jul.
Article
de En
| MEDLINE
| ID: mdl-38595111
ABSTRACT
Isolated intraparotid neurofibromas are exceptionally rare and often associated with neurofibromatosis type 1 (NF1). Diagnosing these tumors proves challenging because of the clinical resemblance to primary salivary gland masses. This case report details an 18-year-old with a painful, enlarging parotid mass, diagnosed through fine needle aspiration biopsy (FNAB) revealing myxoid stroma and spindle cells. Magnetic resonance imaging confirmed a plexiform neurofibroma involving the parotid gland and facial nerve. Histopathology validated the diagnosis, emphasizing the importance of cytological and radiological correlation. Notably, the absent NF1 association makes this case unique. Surgical excision with facial nerve reconstruction was performed, highlighting the complexity of managing such rare intraparotid neurofibromas. Awareness of this entity is crucial for accurate diagnosis and appropriate management.
Mots clés
Texte intégral:
1
Collection:
01-internacional
Base de données:
MEDLINE
Sujet principal:
Tumeurs de la parotide
/
Neurofibrome plexiforme
Limites:
Adolescent
/
Female
/
Humans
/
Male
Langue:
En
Journal:
Diagn Cytopathol
Sujet du journal:
PATOLOGIA
Année:
2024
Type de document:
Article
Pays d'affiliation:
Inde