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1.
Acta Ophthalmol ; 95(5): e366-e372, 2017 Aug.
Article in English | MEDLINE | ID: mdl-27775242

ABSTRACT

PURPOSE: To evaluate light backscattering (LB) in corneal layers in patients with primary Sjögren's syndrome dry eye (SSDE) utilizing in vivo corneal confocal microscopy (IVCM) and to determine the eventual association with the lacrimal functional test values. METHODS: A complete ophthalmic evaluation, Schirmer test with and without stimulation, break-up time (BUT) and IVCM were performed on 55 patients affected by SSDE and in an age- and sex-matched cohort of healthy participants (HP). Light backscattering, measures as light reflectivity unit (LRU), detected by IVCM at Bowman's membrane (BM) at 50 µm, at 100 µm and at 200 µm deeper than BM was compared in the two groups. The correlations between LB values and lacrimal function results were evaluated. RESULTS: In patients affected by SSDE, LB was significantly higher (p < 0.001) in each corneal layer examined (+14 ± 6.33 LRU at BM), compared with HP. A good reverse correlation between the light reflectivity measures at BM with Schirmer test with (r = -0.91) and without (r = -0.90) stimulation and BUT (r = -0.88) was found. Correlations were lower in the deeper corneal layers. CONCLUSION: Even if our results should be confirmed in further studies with a larger population, these findings show that IVCM is a device able to detect alterations in corneal layers in SSDE patients related to the lacrimal function. Light backscattering (LB) could be very useful for clinical diagnosis and management of SSDE.


Subject(s)
Cornea/pathology , Dry Eye Syndromes/diagnosis , Microscopy, Confocal/methods , Sjogren's Syndrome/complications , Adult , Aged , Cornea/metabolism , Dry Eye Syndromes/etiology , Female , Follow-Up Studies , Humans , Male , Middle Aged , Reproducibility of Results , Retrospective Studies , Sjogren's Syndrome/diagnosis , Sjogren's Syndrome/metabolism , Tears/metabolism , Young Adult
2.
Eur J Intern Med ; 25(2): 103-11, 2014 Feb.
Article in English | MEDLINE | ID: mdl-24041708

ABSTRACT

In primary care and internal medicine settings clinicians are often reluctant to take advantage of the resources that ultrasonography (US) offers as a diagnostic tool in the initial management of patients with inflammatory arthritis, despite the recognised importance of an accurate and timely diagnosis of rheumatoid arthritis (RA) and of early referral to ensure optimal patient management. Both grey-scale (GS) and power Doppler (PD) imaging have been extensively used in early detection of synovitis and bone erosions in patients with inflammatory arthritides. We reviewed the main data on the clinical use of US in the initial management of patients with inflammatory arthritis, focusing on RA diagnosis in patients with undifferentiated arthritis, prediction of disease severity, differential diagnoses and assessment of synovitis in children with juvenile idiopathic arthritis (JIA). The role of US in assessing treatment response and monitoring disease activity in clinical remission was also briefly evaluated. The reliability of US as a diagnostic tool in rheumatological diseases has greatly advanced in the last years and the use of this imaging technique, in association with conventional assessments such as physical examination and serological tests, should be considered more often also in primary care settings.


Subject(s)
Arthritis, Juvenile/diagnostic imaging , Arthritis, Rheumatoid/diagnostic imaging , Synovitis/diagnostic imaging , Antirheumatic Agents/therapeutic use , Arthritis/diagnostic imaging , Arthritis/drug therapy , Arthritis, Juvenile/complications , Arthritis, Juvenile/drug therapy , Arthritis, Rheumatoid/complications , Arthritis, Rheumatoid/drug therapy , Disease Management , Humans , Severity of Illness Index , Synovitis/drug therapy , Synovitis/etiology , Ultrasonography, Doppler , Ultrasonography, Doppler, Color
3.
Ann Ital Med Int ; 19(1): 58-62, 2004.
Article in English | MEDLINE | ID: mdl-15176710

ABSTRACT

Interferon (IFN)-alpha with or without ribavirin is the treatment of choice for patients with chronic HCV-related hepatitis. Cough and dyspnea during IFN therapy are often regarded as a side effect and not as a possible sign of the onset of a pulmonary interstitial disease. It may therefore be claimed that the likelihood that patients treated with IFN develop sarcoidosis is being underestimated. Although they are not conventionally classified as etiopathologic agents of sarcoidosis, the IFNs have been proven to be capable of triggering macrophages and of promoting the expression of class II HLA antigens. It is therefore possible that IFN-alpha treatment could trigger macrophages and promote the polarization of the immune response towards Th1 in the presence of particular susceptibility conditions, thus starting the series of events that lead to the onset of sarcoidosis. We describe a case of pulmonary sarcoidosis in a 33-year-old patient treated with IFN-alpha2b and ribavirin for chronic HCV-related hepatitis after 6 months of therapy. The case we report here brings forth the issue of a possible underestimation of the real incidence of sarcoidosis during IFN therapy and highlights the need for more attention to and a more careful evaluation of respiratory symptoms manifesting in treated patients.


Subject(s)
Hepatitis C, Chronic/drug therapy , Interferon-alpha/adverse effects , Sarcoidosis, Pulmonary/chemically induced , Adult , Cough/etiology , Drug Therapy, Combination , Dyspnea/etiology , Gallium Radioisotopes , Hepatitis C, Chronic/complications , Humans , Immunosuppressive Agents/therapeutic use , Interferon alpha-2 , Interferon-alpha/administration & dosage , Interferon-alpha/therapeutic use , Macrophage Activation , Male , Prednisone/therapeutic use , RNA, Viral/blood , Radiopharmaceuticals , Recombinant Proteins , Ribavirin/administration & dosage , Ribavirin/adverse effects , Ribavirin/therapeutic use , Sarcoidosis, Pulmonary/complications , Sarcoidosis, Pulmonary/diagnosis , Sarcoidosis, Pulmonary/drug therapy , Sarcoidosis, Pulmonary/epidemiology , Viremia/complications , Viremia/drug therapy
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