25 results match your criteria: "Santa Maria Nuova Hospital IRCCS[Affiliation]"

Article Synopsis
  • Necrobiosis Lipoidica (NL) is a rare skin condition that causes yellowish-brown plaques, mostly affecting middle-aged women on their shins, and is marked by inflammation and collagen degeneration.
  • A study conducted on 17 NL patients treated with photodynamic therapy (PDT) from 2013 to 2023 showed varied treatment outcomes, with 29% achieving complete lesion clearance and 59% experiencing partial clearance.
  • The findings highlight the need for personalized treatment approaches and standardized protocols to improve the effectiveness of PDT for NL, as current evidence in literature is limited.
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Article Synopsis
  • Tolosa-Hunt syndrome (THS) and recurrent painful ophthalmoplegic neuropathy (RPON) are rare conditions that can make diagnosing and managing initial painful attacks challenging, especially in young patients.
  • A new case study reported a 13-year-old with THS and a 14-year-old with RPON, both presenting with unilateral periorbital headache and third cranial nerve issues that did not respond well to NSAIDs, leading to the utilization of brain MRI and steroids for effective treatment.
  • The study suggests that a thorough investigation including brain MRI with TOF angiography should be conducted for patients with unilateral headaches and cranial nerve paresis from the first episode, while also considering watchful waiting in negative MRI cases before initiating
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Pterostilbene Promotes Mean Lifespan in Both Male and Female Modulating Different Proteins in the Two Sexes.

Oxid Med Cell Longev

March 2022

Department for Life Quality Studies, Alma Mater Studiorum, University of Bologna, Corso d'Augusto 237, 47921 Rimini (RN), Italy.

Aging is a multifactorial phenomenon characterized by degenerative processes closely connected to oxidative damage and chronic inflammation. Recently, many studies have shown that natural bioactive compounds are useful in delaying the aging process. In this work, we studied the effects of an supplementation of the stilbenoid pterostilbene on lifespan extension in .

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Background: Molecular technologies are expanding our knowledge about genetic variability underlying early-onset non-progressive choreic syndromes. Focusing on NKX2-1-related chorea, the clinical phenotype and sleep related disorders have been only partially characterized.

Methods: We propose a retrospective and longitudinal observational study in 7 patients with non-progressive chorea due to NKX2-1 mutations.

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Purpose: To determine long-term results of vitrectomy for lamellar macular holes (LMH). To evaluate how the type of lamellar macular hole (tractional vs. degenerative) and the crystalline lens status might influence visual outcomes.

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: To assess the efficacy and tolerability of interferon (IFN) alpha-2a in post-infectious uveitis secondary to presumed intraocular tuberculosis (IOTB). : Patients with chronic uveitis secondary to presumed IOTB who, after completing an antitubercular treatment, showed poor response to treatments or recurred after tapering oral corticosteroids to ≤7.5 mg/day were enrolled.

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We tested baseline positron emission tomography (PET)/computed tomography (CT) as a measure of total tumor burden to better identify high-risk patients with early-stage Hodgkin lymphoma (HL). Patients with stage I-II HL enrolled in the standard arm (combined modality treatment) of the H10 trial (NCT00433433) with available baseline PET and interim PET (iPET2) after 2 cycles of doxorubicin, bleomycin, vinblastine, and dacarbazine were included. Total metabolic tumor volume (TMTV) was measured on baseline PET.

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Article Synopsis
  • Clinical factors like MGMT methylation status, age, KPS, and surgical resection are key in predicting glioblastoma (GBM) prognosis, with a noted advantage for female patients in survival rates.
  • In a study of 169 GBM patients, those with MGMT methylation showed longer survival, especially females compared to males; survival differences were not significant among unmethylated individuals.
  • Multivariate analysis confirmed that both gender and MGMT status, along with age and KPS, are important predictive factors for patient survival in GBM cases.
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Purpose: The aim of the present study was to evaluate the added diagnostic value of respiratory-gated 4D18F-FDG PET/CT in liver lesion detection and characterization in a European multicenter retrospective study.

Methods: Fifty-six oncological patients (29 males and 27 females, mean age, 61.2 ± 11.

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Purpose: To describe vitreal, retinal, and choroidal features of eyes affected by Endogenous candida endophthalmitis (ECE) analyzed by spectral domain optical coherence tomography (SD-OCT) and to evaluate their clinical impact.

Methods: Medical records and SD-OCT images from eyes diagnosed with ECE at four retina and uveitis tertiary referral centers were retrospectively evaluated. Spectral domain optical coherence tomography images were analyzed to evaluate the structural changes occurring in the vitreous, the retina, and the choroid in areas involved by ECE.

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Unlabelled: Background Systemic lupus erythematosus (SLE) and antiphospholipid antibody syndrome (APS) are autoimmune diseases that affect women of childbearing age. Maternal IgG antiphospholipid antibodies (aPL) can cross the placenta during pregnancy and theoretically reach the fetal brain. Some studies showed an increased number of learning disabilities in these children.

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Glycaemic index, glycaemic load and risk of cutaneous melanoma in a population-based, case-control study.

Br J Nutr

February 2017

1Department of Biomedical, Metabolic and Neural Sciences,Research Center for Environmental, Genetic, and Nutritional Epidemiology (CREAGEN), University of Modena and Reggio Emilia,41125 Modena,Italy.

Glycaemic index (GI) and glycaemic load (GL) are indicators of dietary carbohydrate quantity and quality and have been associated with increased risk of certain cancers and type 2 diabetes. Insulin resistance has been associated with increased melanoma risk. However, GI and GL have not been investigated for melanoma.

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Infantile neuroaxonal dystrophy is a rare neurodegenerative disorder characterized by infantile onset of rapid motor and cognitive regression and hypotonia evolving into spasticity. Recessively inherited mutations of the PLA2G6 gene are causative of infantile neuroaxonal dystrophy and other PLA2G6-associated neurodegeneration, which includes conditions known as atypical neuroaxonal dystrophy, Karak syndrome and early-onset dystonia-parkinsonism with cognitive impairment. Phenotypic spectrum continues to evolve and genotype-phenotype correlations are currently limited.

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Purpose: To present challenging cases of vitreoretinal lymphoma (VRL) that was misdiagnosed as uveitis because of the apparent intraocular inflammation. At the light of the new classification of intraocular lymphomas, we detail the characteristics that masqueraded the tumors and the clinical aspects that guided us to the correct diagnosis.

Materials And Methods: We retrospectively reviewed the patients referred to our uveitis service between January 2006 and December 2014.

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Purpose: Clinical risk management is the basis of safety procedures also in radiological workflows. In the literature, it has been documented that the incidence of reconciled radiological studies ranges between 0.2 and 0.

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Curcuminoids represent new perspectives for the development of novel therapeutics for Alzheimer's disease (AD), one probable mechanism of action is related to their metal complexing ability. In this work we examined the metal complexing ability of substituted curcuminoids to propose new chelating molecules with biological properties comparable with curcumin but with improved stability as new potential AD therapeutic agents. The K2T derivatives originate from the insertion of a -CH2COOC(CH3)3 group on the central atom of the diketonic moiety of curcumin.

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On X-ray modalities, the information concerning the dose delivered to the patient is usually available in image headers or in structured reports stored in the picture archiving and communication system (PACS). Sometimes this information is sent in the Modality Performed Procedure Step message. By saving the information inside the Radiological Information System, it can be linked to the patient and to his/her episode/request.

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Clinical and biochemical features guiding the diagnostics in neurometabolic cutis laxa.

Eur J Hum Genet

July 2014

1] Department of Pediatrics, Institute for Metabolic and Genetic Disease, Radboud University Medical Centre, Nijmegen, The Netherlands [2] Hayward Genetics Center, Tulane University Medical Center, New Orleans, LA, USA.

Patients with cutis laxa (CL) have wrinkled, sagging skin with decreased elasticity. Skin symptoms are associated with variable systemic involvement. The most common, genetically highly heterogeneous form of autosomal recessive CL, ARCL2, is frequently associated with variable metabolic and neurological symptoms.

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Objectives: The treatment of tumours expressing somatostatin receptors with yttrium-90 (90Y)-labelled and lutetium-177 (177Lu)-labelled somatostatin analogues is one of the most interesting therapeutic approaches adopted in nuclear medicine in recent years. However, the process of synthesis and fractionation of these radiopharmaceuticals is still mainly carried out manually despite the high radiation exposure to the operators and the need to comply with good manufacturing practices. In this study a semiautomatic synthesizer [automatic dose dispenser (ADD-2)] using only disposable syringes and vials has been presented.

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Objectives: Biocytin analogues labelled with indium-111, yttrium-90 and lutetium-177 have shown their effectiveness in the imaging of infections/inflammation in patients with osteomyelitis and function as efficient tools in pretargeted antibody-guided radioimmunotherapy. In this study, the labelling of a biocytin analogue coupled with DOTA (1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid), namely, r-BHD, with gallium-68 (68Ga) was optimized, and the quality and stability of the preparations were assessed for clinical use.

Materials And Methods: Synthesis of 68Ga-r-BHD was carried out by heating a fraction of the 68Ge/68Ga eluate in a reactor containing the biocytin analogue with the appropriate buffer.

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Using pathology-specific laboratory profiles in clinical pathology to reduce inappropriate test requesting: two completed audit cycles.

BMC Health Serv Res

July 2012

Education and Clinical Innovation Department, Healthcare Library - Clinical Governance Documentation Centre of the Healthcare Trusts of the Province of Reggio Emilia, Arcispedale Santa Maria Nuova Hospital (IRCCS), Reggio Emilia, Italy.

Background: Systematic reviews have shown that, although well prepared, the Consensus Guidelines have failed to change clinical practice. In the healthcare district of Castelnovo né Monti (Reggio Emilia, Italy), it became necessary for the GPs and Clinical Pathologists to work together to jointly define laboratory profiles.

Methods: Observational study with two cycles of retrospective audit on test request forms, in a primary care setting.

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Clinical and pharmacoeconomic aspects of omalizumab: a 4-year follow-up.

Ther Adv Respir Dis

April 2012

Department of Cardiac-Thoracic-Vascular and Intensive Care Medicine, Pneumology Unit, Santa Maria Nuova Hospital-IRCCS, Viale Risorgimento 80, 42123, Reggio Emilia, Italy. menzella.francesco@ asmn.re.it

Objectives: The aim of this study was to assess the stability of the effectiveness of omalizumab as add-on treatment in 11 patients with severe persistent allergic asthma followed for 4 years. Secondary outcomes were safety and economic impact, in terms of use of healthcare resources.

Methods: This retrospective study was designed to analyse a series of patients with severe allergic asthma treated with omalizumab.

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