Publications by authors named "Cedric Landron"

Article Synopsis
  • Giant cell arteritis (GCA) is a common condition in individuals over 50 that can lead to serious issues like vision loss if not diagnosed quickly.
  • This study assesses the effectiveness of using color Doppler ultrasound as the first step for diagnosing GCA, followed by temporal artery biopsy for those who test negative on the ultrasound.
  • The findings showed that ultrasound confirmed GCA in 44% of cases, compared to 17% for biopsy and 21% for other methods, but the study had limitations like a small sample size and no objective gold-standard for comparison.
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Background: IgG4-related kidney disease is a major manifestation of IgG4-related disease, a systemic fibroinflammatory disorder. However, the clinical and prognostic kidney-related factors in patients with IgG4-related kidney disease are insufficiently defined.

Methods: We conducted an observational cohort study using data from 35 sites in two European countries.

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Background: Giant cell arteritis (GCA) is frequently associated with aortic involvement that is likely to cause life-threatening structural complications (aneurysm, dissection). Few studies have investigated the occurrence of these complications, and no predictive factor has been identified so far. The aim of this study was to investigate factors associated with the risk of aortic complications in a cohort of GCA aortitis.

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Background: Trephine bone marrow biopsy (BMB) in internal medicine has only been studied in fever of unknown origin and inflammation of unknown origin. The aim was to assess BMB diagnostic yield according to main indications and patient characteristics in internal medicine. Quality of BMB and contribution of bone marrow aspiration (BMA) to BMB were also analyzed.

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Objective: Temporal arteritis (TA) is a typical manifestation of giant cell arteritis (GCA). Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAVs) are rarely revealed by TA manifestations, leading to a risk of misdiagnosis of GCA and inappropriate treatments. This study was undertaken to describe the clinical, biologic, and histologic presentations and outcomes in cases of TA revealing AAV (TA-AAV) compared to controls with classic GCA.

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Calcinosis is a complication of systemic sclerosis, most often occurring more than several years after diagnosis. We report the case of a man who developed severe calcinosis in shoulders and hips occurring before other systemic sclerosis' symptoms.

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Article Synopsis
  • - The relapse rates for antiphospholipid syndrome (APS) are significant, with 20%-21% for thrombotic APS and 20-28% for obstetrical APS over five years.
  • - Hydroxychloroquine (HCQ) is being explored as a potential treatment due to its immunomodulatory and anti-thrombotic properties, and it has received orphan designation from the European Medicines Agency for APS.
  • - An international study called HIBISCUS is underway, involving 53 centers in 16 countries, to investigate the use of HCQ in preventing obstetrical and thrombotic events in primary APS, consisting of both retrospective and prospective components.
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Objectives: To assess the efficacy of tocilizumab in patients with Takayasu arteritis (TA).

Methods: We conducted a retrospective multicenter study in 46 TA patients treated with tocilizumab. We analyzed factors associated with response to tocilizumab (assessed using NIH score).

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Background: Cogan syndrome is mainly treated with steroids. We aimed to determine the place of DMARDs and biologic-targeted treatments.

Patients And Methods: We conducted a French nationwide retrospective study of patients with Cogan syndrome (n=40) and a literature review of cases (n=22) and analyzed the efficacy of disease-modifying anti-rheumatic drugs (DMARDs) and tumor necrosis factor α (TNF-α) antagonists.

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Article Synopsis
  • The study compared clinical and imaging outcomes in patients with idiopathic aortitis (IA) and giant cell arteritis (GCA)-related aortitis, focusing on findings from 191 patients treated in 11 French departments.
  • Results showed that IA patients were generally younger, had higher rates of aortic aneurysms at diagnosis, and experienced worse long-term outcomes compared to GCA patients.
  • Despite differences in younger patients, those aged 60 and older with IA shared similar characteristics and outcomes with GCA patients, indicating some overlap in the progression of the diseases.
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Objective: Kawasaki disease (KD) is a vasculitis that mostly occurs in young children and rarely in adults. We analyzed the characteristics of adult-onset KD (AKD) in France.

Methods: We collected retrospective and prospective data for patients with a diagnosis of KD occurring after the age of 18 years.

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Unlabelled: Revascularization aims at improving walking ability in patients with arterial claudication. The highest measured distance between 2 stops (highest-MDCW), the average walking speed (average-WSCW), and the average stop duration (average-DSCW) can be measured by global positioning system, but their evolution after revascularization is unknown.We included 251 peripheral artery diseased patients with self-reported limiting claudication.

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Objectives: The aim of the present study was to assess the outcome in anti-PL12 patients with antisynthetase syndrome (ASS).

Methods: The medical records of anti-PL12 (n=5) patients with ASS were retrospectively analyzed without prior selection. To exclude false-positive patients, we included patients who were successively tested positive for anti-PL12 antibody at least twice by immunodot and/or Western blot.

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IgG4-related systemic disease is now recognized as a systemic disease that may affect various organs. The diagnosis is usually made in patients who present with elevated IgG4 in serum and tissue infiltration of diseased organs by numerous IgG4+ plasma cells, in the absence of validated diagnosis criteria. We report the clinical, laboratory, and histologic characteristics of 25 patients from a French nationwide cohort.

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Kawasaki disease (KD) is an acute multisystemic vasculitis occurring predominantly in children and rarely in adults. Diagnosis is made clinically using diagnostic guidelines; no specific test is available. "Incomplete" KD is a more recent concept, which refers to patients with fever lasting > or =5 days and 2 or 3 clinical criteria (rash, conjunctivitis, oral mucosal changes, changes of extremities, adenopathy), without reasonable explanation for the illness.

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A 28-year-old Zairian woman was presented with a diurnal somnolence, cervical polyadenopathy, splenomegaly, eosinophilia, and elevated IgM. A diagnosis of West African trypanosomiasis was confirmed and the patient improved after treatment with eflornithine.

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In view of its localization, brain abscess (BA) usually requires medical and surgical care. A broad spectrum of bacteria is involved. Recent reports stress the increasing frequency of anaerobes, but their impact has not been well evaluated.

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Introduction: Infections due to subspecies arizonae Salmonella enterica are rare. These infections are transmitted by reptiles. We report the case of S.

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We describe a case of meningitis due to Capnocytophaga canimorsus and review 18 cases with attention to risk factors, clinical features, diagnosis, treatment, and outcome. In most of the reported cases, contact with dogs and predisposing factors were found. Clinical manifestations and the findings of examinations of cerebrospinal fluid specimens were similar to those of classic bacterial meningitis; however, the mortality rate for C.

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We report 2 cases of Agrobacterium radiobacter bacteremia in immunocompromised patients. Removal of the central venous catheter and administration of antimicrobial therapy led to favorable outcomes in both patients. Infections due to A.

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