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THE SALIVARY GLANDS AND SARCOIDOSIS
Sarcoidosis is a chronic systemic granulomatous disease of unknown
origin with a special predilection for the lungs and hilar lymph
nodes. The varied clinical symptomatology results from infiltration
of specific organs. Because the initial manifestation is usually
respiratory, an exogenous airborne agent is the suspected culprit.
Diagnosis is based upon radiologic identifications of both the
distinctive lung infiltrates and hilar lymphadenopathy and biochemical
changes. Final diagnosis awaits the histologic demonstration of
the granulomas in other organ structures. Non caseating granulomas
with a core of epithelioid and giant cells and a periphery of lymphocytes
and fibroblasts are characteristic.
The Salivary Gland Center (SGC) has seen a varied clinical picture
of salivary gland involvement in sarcoidosis. The spectrum can be
classified into 4 symptom complexes. First, patients already diagnosed
with sarcoidosis often develop salivary gland swelling. Usually,
bilateral parotid gland swelling is seen. The glands tend to be
firm, only slightly tender, and do not fluctuate in size when eating.
Spontaneous resolution can be expected but steroids may be prescribed.
Second, although most cases of sarcoidosis do not have clinical
sialadenopathy, biopsy of a labial salivary gland reveals granulomas
in 58% of the specimens. The third pattern observed in known cases
of sarcoidosis, uveoparotid fever (HeerfordtÌs Syndrome),
is characterized by the triad of uveitis, parotid swelling and cranial
nerve involvement.
Recently, the SGC has become aware of a fourth pattern of salivary
gland involvement in sarcoidosis. Patients have been referred with
bilateral salivary gland swellings (parotid or submandibular) who
were unaware of their sarcoid disease. No subjective respiratory
or other systemic complaints were present. Sarcoidosis was diagnosed
when the patient was referred for chest films and was confirmed
by histologic examination of salivary gland tissue. In these cases,
sialadenopathy serves as a clinical herald of a clinically occult
sarcoidosis.
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The SGC was developed because a void existed in the diagnosis and
comprehensive care of patients with salivary gland problems and/or
secretory dysfunction. Since the diversity of salivary gland problems
presents challenges to the clinician, the SGC is available for referrals
at Columbia Presbyterian Medical Center, 630 West 168th Street,
New York City 10032, N.Y. Phone (212) 305-9982.
Louis Mandel DDS
Director, Salivary Gland Center
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