Search results for "Scleroderma"
showing 10 items of 70 documents
Parry Romberg Syndrome with localized scleroderma: a case report
2014
Parry Romberg syndrome(PRS) is a rare acquired poorly understood neurocutaneous syndrome of unknown etiology characterized by slow progressive atrophic changes commonly affecting one half of the face. The exact incidence and etiology towards the syndrome remains unclear. Apart from the multifactorial etiology proposed, the possible primary cause is mainly attributed to the cerebral disturbance of the fat metabolism. The syndrome overlaps with “en coup de sabre” morphea, with an ill defined relationship existing between the two. Parry Romberg Syndrome is an invalidating lesion that may be associated with different neurological, cutaneous, ocular, dental and autoimmune abnormalities. This rep…
The "Renocentric Theory" of Renal Resistive Index: Is It Time for a Copernican Revolution?
2020
Ultrasound (US) with duplex Doppler scanning has spread to the capillary level, becoming an irreplaceable tool in daily clinical practice thanks to its characteristics: low cost, repeatability, and noninvasiveness. Moreover, US has become over time more sensitive and accurate; it can be considered an extension of the clinician’s hand. For this reason, it currently represents the ideal tool for first-level diagnostic use in several fields, and is the simplest and most flexible instrument for obtaining morphological and functional information on different organs, including the kidneys. In this issue of The Journal , Gigante, et al 1 propose to assess renal involvement in patients with systemi…
Bestimmung der Myokinase und der Kreatin-Phosphokinase im Serum bei experimentellem Lathyrismus, bei Dermatomyositis und bei progressiver Sklerodermie
1965
Mittels einer Bestimmung der muskelspezifischen Fermente Kreatin-Phosphokinase (CPK) und Myokinase (MK) im Serum lathyritischer Ratten wird bei dieser experimentellen akuten Mesenchymschadigung die erhebliche stoffwechselmasige Beteiligung der Muskulatur enzymologisch erfast und dem histomorphologischen Befund in der Skelet-Muskulatur gegenubergestellt.
Platelet-rich gel for the adjuvant treatment of wound healing of transposed flap for arteriovenous fistula in systemic scleroderma
2017
LETTER TO EDITOR
Enzymatic Determination in Serum of Lathyritic and Prednisone-treated Lathyritic Rats
1966
WHILE a remarkably raised serum-level of transaminases and aldolase is found in dermatomyositis, such augmentation, as a rule, is not found in cases of severe muscular involvement of scleroderma and disseminated lupus erythematosus (acutus)1–3.
Interleukin-32 in systemic sclerosis, a potential new biomarker for pulmonary arterial hypertension
2020
Abstract Background Pulmonary arterial hypertension (PAH) is a severe complication of systemic sclerosis (SSc), associated with a progressive elevation in pulmonary vascular resistance and subsequent right heart failure and death. Due to unspecific symptoms, the diagnosis of PAH is often delayed. On this basis, it is of great value to improve current diagnostic methods and develop new strategies for evaluating patients with suspected PAH. Interleukin-32 (IL-32) is a proinflammatory cytokine expressed in damaged vascular cells, and the present study aimed to assess if this cytokine could be a new biomarker of PAH during SSc. Methods The IL-32 expression was evaluated in the sera and skin sam…
Manometric assessment of oesophageal involvement in progressive systemic sclerosis, morphoea and Raynaud's disease.
1982
SUMMARY Oesophageal function was studied by radiography and manometry in fifty-one patients with progressive systemic sclerosis (PSS), fourteen patients with morphoea, twelve patients with Raynaud's disease and twenty-one normal subjects. Upper oesophageal sphincter pressure was not affected. Peristaltic contractions of the upper third of the oesophagus were significantly decreased in PSS and morphoea, but the lower two-thirds were affected only in PSS. Lower oesophageal sphincter pressure was significantly decreased in PSS but was normal in morphoea and Raynaud's disease. There was a significant correlation between oesophageal dysfunction and the duration of PSS. Manometry was better than …
Nutritional evaluation and physical activity in scleroderma patients
2010
SCLERODERMA-ASSOCIATED SYNDROME: ORAL MANIFESTATIONS
2021
Introduction: The authors propose to evaluate the existence of a correlation between Sjogren’s syndrome and progressive systemic sclerosis, and to describe oral manifest- ations of scleroderma- associated syndrome. Material and methods: 24 patients with progressive systemic sclerosis were examined: 22 women and 2 men. All the patients examined met the diagnostic criteria for progressive systemic sclerosis. A diagnosis of Sjogren’s syndrome was made based on a positive histological examination of biopsy specimens of the accessory salivary glands of the lower lip, associated with dry keratoconjunctivitis and/or xerostomia, and the detection of serum autoantibody. Each patient underwent a care…