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1.
J Autoimmun ; 146: 103242, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38761452

ABSTRACT

OBJECTIVE: To assess the prognosis and outcome of patients with isolated carotid vasculitis. METHODS: We performed a retrospective multicenter study of 36 patients (median age at diagnosis was 37 [IQR 27-45] years and 11 [31 %] patients were men) with initial presentation as isolated carotid vasculitis. Study endpoints included vascular complications, relapses, and progression to large vessel vasculitis (i.e. Giant cell arteritis or Takayasu). RESULTS: The most frequent involvement was the left internal carotid artery (39 %), and 81 % had stenosis. After a median follow-up of 32 months [IQR 12-96], 21 (58 %) patients had a vascular event, including 31 % of new onset vascular lesions and 25 % of stroke/transient ischemic attack. Patients with stroke had less carotidynia at diagnosis (33 % vs 74 %, p = 0.046), higher significant carotid stenosis (i.e. > 50 %) (89 % vs. 30 %, p = 0.026) and higher severe carotid stenosis (i.e. >70 %) (67 % vs 19 %, p = 0.012), compared to those without stroke. Twenty (52 %) patients experienced relapses. High CRP at diagnosis was associated with relapses (p = 0.022). At the end of follow-up, 21 (58 %) patients were classified as having Takayasu arteritis, 13 (36 %) as isolated carotid vasculitis, and two (6 %) as giant cell arteritis. CONCLUSION: Carotid vasculitis may occur as a topographically limited lesion and is associated with significant rate of vascular complications.


Subject(s)
Giant Cell Arteritis , Humans , Male , Female , Prognosis , Middle Aged , Retrospective Studies , Adult , Giant Cell Arteritis/diagnosis , Takayasu Arteritis/diagnosis , Recurrence , Vasculitis/diagnosis , Follow-Up Studies , Stroke/etiology , Stroke/diagnosis , Carotid Stenosis/diagnosis , Disease Progression
3.
Rev Med Interne ; 41(2): 130-133, 2020 Feb.
Article in French | MEDLINE | ID: mdl-31635978

ABSTRACT

INTRODUCTION: Encapsulating peritonitis is a rare but severe chronic fibrotic condition related to the development of a white fibrous membrane surrounding the digestive tract. Idiopathic forms have been described, however the disease is most often secondary to peritoneal dialysis or more rarely to surgery. Treatment is difficult and not codified. CASE REPORT: We report here the observation of a 36-year-old patient whose diagnosis of encapsulating peritonitis was made after a long sub-occlusive history, eight years after a gastric ulcer perforation. DISCUSSION: We discuss the possible etiologies and we present a focus on this rare and little-known entity.


Subject(s)
Intestinal Obstruction/diagnosis , Peritoneal Fibrosis/diagnosis , Peritonitis/diagnosis , Adult , Delayed Diagnosis , Diagnosis, Differential , Humans , Intestinal Obstruction/complications , Intestinal Obstruction/drug therapy , Intestinal Obstruction/surgery , Laparotomy , Male , Peptic Ulcer/complications , Peptic Ulcer/diagnosis , Peptic Ulcer/drug therapy , Peptic Ulcer/surgery , Peptic Ulcer Perforation/complications , Peptic Ulcer Perforation/diagnosis , Peptic Ulcer Perforation/drug therapy , Peptic Ulcer Perforation/surgery , Peritoneal Fibrosis/drug therapy , Peritoneal Fibrosis/surgery , Peritonitis/complications , Peritonitis/drug therapy , Peritonitis/surgery , Tamoxifen/therapeutic use
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