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R.I. Fox et al.

 

 

ANCA always represent overlap syndromes with other conditions such as progressive systemic sclerosis (PSS) or Wegener’s granulomatosis [8].

Comments: Although patients may develop an overlap syndrome with other autoimmune disorders such as PSS, the pattern of autoantibodies in patients with SS correlates more closely with their HLA-DR than with their clinical presentation [9, 10].

 

Ramos-Casals et al. [5, 6] studied 402 patients

diagnosed with primary SS.

¥

Eighty-two (20%) patients showed atypi-

 

cal autoantibodies (36 had antiphospholipid

 

(aPL), 21 anti-DNA, 13 ANCA, 10 anti-RNP,

 

8 ACA, 6 anti-Sm, 2 anti-Scl70, and 1 anti-Jo-

 

1 antibodies).

 

¥

Patients with

atypical autoantibodies had

 

no statistical

differences in extraglandular

manifestations (except for a higher prevalence of RaynaudÕs phenomenon, 28% vs 7%).

3.2.5 Pearl

3.2.6 Pearl

Salivary flow rates can be evaluated by nonor minimally invasive methods.

Comments: This is important to correlate measurements of patientÕs symptoms with objective signs of dryness. Technetium scans of salivary function are performed after coating the tongue with a lemon concentrate [13Ð15]. The uptake of contrast material and its rate of secretion into the gland can be quantitated.

Although the decreased ßow rate is not speciÞc to SS (i.e., many processes can contribute to decreased uptake or secretion), the method is useful in the evaluation of the patient who complains that ÒI donÕt feel any saliva in my mouth,Ó but the oral mucosal tissues appear to be relatively intact. The Þnding of a normal technetium scan should point the rheumatologist toward other causes of the patientÕs severe mouth complaints.

3.2.7 Pearl

MRI sialography can be used to visualize the ductal structure of the major salivary glands. Comments: It is not necessary to perform a sialogram to assess the salivary status of SS patients or to visualize the ductal structures for punctual sialadenitis. This is important since most US academic centers do not have experience in retrograde sialography that is mentioned in consensus diagnostic criteria and this invasive method may have morbidity if done by inexperienced radiologists or ENT.

MRI of the parotid and submandibular glands has vastly improved. If an MRI of the soft tissues of the neck is required (for example, in a case of parotid gland swelling), then we ask for a gadolinium contrast study with Òfat suppressionÓ views that provides a nice evaluation of the glandular tissues [11, 12]. Although ultrasound of the glands has proven useful at certain research centers (particularly in Europe), a great deal of experience is required to obtain reproducible results. As a result of readily available MRI at most academic medical centers in the United States, experience with ultrasound imaging of the glands has not been fully developed.

There is significant variation when collecting saliva by oral expectoration or “sponge” methods [16, 17].

Comments: Simple expectorated saliva can be collected on a preweighed sponge placed under the tongue (called the Saxon test) [18]. However, there is signiÞcant variability in these measurements in the same patient over the course of the day or when measurements are repeated [16]. The reasons for the variability include

¥time since last meal

¥last oral stimulation (including tooth brushing)

¥history of smoking as well as

¥medications taken for other medical problems [5, 6, 19]

Although the variability in ßow rates in both normal and SS is noted above, it is worth pointing out that the Ònormal salivary ßow rateÓ for unstipulated saliva from the parotid gland is 0.4Ð0.5 mL/min/gland. The normal ßow rate for unstipulated, Òresting,Ó or ÒwholeÓ saliva is 0.3Ð 0.5 mol/min; for stimulated saliva, 1Ð2 mol/min. Values less than 0.1 mol/min are typically considered xerostomia, although reduced ßow may not always be associated with complaints of dryness.

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