Sialendoscopy
Few reports adequately estimate the effectiveness of sialendoscopy in halting recurrence of childhood Sjögren’s Disease (cSjD). Sialendoscopy is a safe, minimally invasive procedure which can be effective for addressing salivary issues in SjD. Benefits include direct visualization of ductal pathologies, including inflammation, stenosis, and stricture diagnosis. In addition to gathering images, the physician can also administer a treatment when indicated [
10]. The impact of sialendoscopy has been studied extensively in the adult population with SjD. However, to our knowledge, Iorio et al. are the only authors who have explored the impact of sialendoscopy and steroid irrigation on children [
11].
Currently, no guidelines establish sialendoscopy with irrigation as part of the standard of care for treatment, as both cSjD and SjD are often medically managed with anti-inflammatory treatments or immunomodulatory therapy. When reviewing outcomes in patients with recurrent juvenile parotitis, Schwarz et al. determined it is unclear whether steroid administration or sialendoscopy itself relieves severity of inflammatory symptoms [
10]. Du et al. performed a randomized controlled trial assessing the efficacy of sialendoscopy itself by comparing outcomes in adults with SjD between three treatments: those who did not undergo sialendoscopy, patients who received saline irrigation, and patients who received irrigation with triamcinolone acetate [
12]. Patients who underwent sialendoscopy, either with irrigation of saline or triamcinolone, showed significant improvement in salivary flow at one to eight weeks. However, the patients who received the triamcinolone treatment continued to experience consistent improvement in salivary flow at 16 to 24 weeks. Izumi et al. also noted that their patients who received corticosteroids showed greater efficacy in improving salivary flow rate in comparison to patients who started with saline irrigation [
13]. Thus, administration of triamcinolone appears to show clinically significant results in reducing inflammation.
The 2002 American-European Consensus Group (AECG) criteria [
14], 2012 American College of Rheumatology (ACR) classification criteria [
15], and the 2016 ACR/EULAR criteria [
6] do not incorporate sialendoscopy as a factor for the diagnosis or treatment of cSjD. With that said, many clinicians utilize sialendoscopy for the management of inflammatory parotitis. Faure et al. noted that sialendoscopy has a greater sensitivity than radiologic ultrasound or MRI, and Schiffer et al. have established that cSjD diagnoses can be based upon sialendoscopy when used in combination with histopathology from labial biopsy [
16‐
18]. While sialendoscopy offers an exceptional diagnostic and treatment modality, it is important to note that it is not sufficient for making a definitive diagnosis or providing a cure for all salivary gland disorders, particularly those resulting from autoimmune inflammatory processes. Therefore, clinical indicators of cSjD, as outlined by the ACR/EULAR criteria, should be included when determining a diagnosis. Patients with cSjD and autoimmune disorders are at a higher risk of symptom recurrence compared to those with obstructive salivary gland disorders, necessitating continued monitoring and follow-up examinations after treatment.
Patients diagnosed with cSjD present with a unique pathophysiology of the parotid glands in comparison to the adult population. Karagozoglu noted that the improvement of salivary flow is most likely dependent upon the presence of saliva-producing acinar cells, which may be lacking in patients with fibrotic tissue, secondary to long-standing disease [
19]. Therefore, pediatric patients with a recent onset of cSjD and increased salivary gland capacity would likely benefit from undergoing sialendoscopy, as their tissue would be less likely to exhibit fibrosis and resulting fatty infiltration.
Iorio et al. evaluated the long-term impacts of sialendoscopy with corticosteroid irrigation in children aged 6 to 13, and improvement in salivary flow was noticeable during an 18-month observation period [
11]. The biopsy report of our patient indicates normal glandular architecture throughout, without evidence of fibrotic change with normal-appearing acini, fulfilling the original guideline for SjD histological evaluations [
20]. Based on the results of our patient, along with the results of Iorio et al., further investigation comparing the effects of sialendoscopy between children and adults is warranted, considering the unique pathophysiology of cSjD and SjD, respectively.
Numerous studies have evaluated the efficacy of sialendoscopy over different timeframes. Karagozoglu et al. conducted follow-ups with patients for up to sixty weeks after undergoing sialendoscopy with triamcinolone acetate [
21]. Their results demonstrated a significant increase in salivary flow, indicating long-term efficacy considering the typical disease course. In a study by Du et al., saline provided immediate relief similar to triamcinolone at one to eight weeks, but patients who received triamcinolone irrigation showed continued improvement in salivary flow rate at sixteen and twenty-four weeks [
12].
Our patient experienced recurrence of right-sided parotitis at eleven months. However, overall improvement was noted over 48 weeks after her hydroxychloroquine dosage was increased to 300 mg. While cSjD is a rare condition, recurrence is not uncommon in other cases. Iorio reported recurrences of parotitis in two patients at five and three years. It is important to note that sialendoscopy is a treatment modality for managing salivary gland disorders and is focused on addressing specific concerns related to the salivary glands. Therefore, the optimal treatment plan for a patient with cSjD should remain multifactorial, encompassing both medical and procedural management, as each patient with an autoimmune condition presents uniquely with their own respective clinical presentation.
Salivary gland Ultrasonography
In 2005, Hocevar et al. set forth a novel scoring system through SGUS. Through SGUS, the inflammation of glandular tissue is quantified via observation of parenchymal echogenicity in comparison to the thyroid, homogeneity of tissue parenchyma, hypoechoic areas, hypoechoic foci, and delineation [
9]. According to Hocevar et al., a score of 17 or greater on a scale ranging from 0 to 48 indicates a diagnosis for Sjögren’s Disease (SjD), along with consideration of the broader clinical picture and plasma titers. Theander and Mandl note that SGUS is an effective method for diagnostic and prognostic purposes in diagnosing SjD, as it has a positive predictive value and specificity of 98% [
22].
In our patient, SGUS was utilized to offer not only a visual imaging but also provide a quantified score in assessing efficacy of treatment post-sialendoscopy. Our patient’s SGUS score decreased from 16 to 11, and she reported being asymptomatic without flares after one year. Her clinical improvement was reflected by subsequent SGUS results and a normal physical exam upon follow-up. We conclude SGUS is best utilized to monitor each patient’s individual progress via comparison of imaging and scoring with the first established baseline.
Notably, our patient presented with a baseline score of 16 in her SGUS, which is one point below the cutoff for Hocevar for SjD. With that said, half of the subjects with SjD in Hocevar et al’s study scored below 17 in their SGUS assessment. In addition, in Hocevar’s study all subjects were adults between the ages of 23–84 with a mean age of 51.5. As discussed, cSjD presents with unique pathophysiology. Therefore, further investigation is warranted on whether the cutoff or parameters for a diagnosis of cSjD via SGUS should be modified for the pediatric population. As seen in our patient, a reduction in five points suggested a curtailment of inflammatory processes within her parotid tissue. However, the degree of point reduction should be compared to more patients with cSjD who have undergone sialendoscopy. In addition, a modified SGUS for the pediatric population might reflect a greater difference in scoring.
It should be noted that SGUS does present with other limitations. Drawbacks can include missing early disease if disease severity is mild, and SGUS monitoring should be executed with the same technique, machine, technician, and standardized scoring system if long-term follow-up is planned. Since cSjD is a systematic inflammatory disease process, clinicians should also continue to monitor renal, neurologic, and musculoskeletal function in a thorough workup.