Intraparotid plexiform neurofibroma: A rare diagnostic challenge.
Diagn Cytopathol
; 52(7): E164-E167, 2024 Jul.
Article
em 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.
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Base de dados:
MEDLINE
Assunto principal:
Neoplasias Parotídeas
/
Neurofibroma Plexiforme
Idioma:
En
Ano de publicação:
2024
Tipo de documento:
Article