Sarcoidosis
Sarcoidosis
Image 2
Image 2
Bilateral parotid gland enlargement.
Bilateral parotid gland enlargement.
Bilateral parotid involvement is the classic teaching pattern, but unilateral disease occurs in up to 86% of population-based cohorts and does not exclude sarcoidosis; painless enlargement is typical.
The diagnosis of parotid sarcoidosis cannot be made by granulomas on fine-needle aspiration alone—compatible clinical and imaging findings plus exclusion of other granulomatous causes (including sarcoid-like reactions from metastatic malignancy) are required.
The combined Ga-67 panda plus lambda signs or panda plus symmetric hilar adenopathy on chest imaging provide diagnostic specificity superior to panda sign alone, potentially avoiding diagnostic parotidectomy.
Heerfordt syndrome (parotid enlargement with anterior uveitis, facial palsy, and fever) is rare, occurring in only 0.3% of sarcoid cases in complete form and 1.3% in incomplete form.
Six of seven patients in a population-based cohort had intrathoracic sarcoidosis; therefore, chest imaging is essential to support the diagnosis and assess systemic disease burden.
Supportive imaging findings include lacrimal gland enlargement (present in ~10% of sarcoid patients) and posterior triangle cervical lymphadenopathy (palpable in ~one-third); labial gland biopsy shows 19% yield but effectively separates sarcoid from Sjögren syndrome.
Describe parotid sarcoidosis as "bilateral symmetric parotid enlargement with multiple hypoechoic nodules (or small hypodense foci on CT) representing granulomas and enlarged intraparotid nodes; no discrete dominant mass or periparotid inflammatory stranding is present," and note that supporting findings such as lacrimal gland enlargement and cervical lymphadenopathy strengthen the diagnosis; always recommend correlation with chest imaging for intrathoracic sarcoidosis.