2012
DOI: 10.1016/j.otoeng.2012.07.012
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Otolaryngologic Manifestations of Systemic Vasculitis

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Cited by 9 publications
(14 citation statements)
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“…Although otolaryngologic manifestations of various rheumatic diseases have been well described, awareness among otolaryngologists regarding these manifestations is negligible. [2][3][4][5][6][7][8][9] Early and accurate diagnosis with prompt treatment or referral to specialists may prevent morbidity and mortality related to these diseases. The present study was designed to assess the understanding and practice about various ENT problems of rheumatic diseases amongst otolaryngologists.…”
Section: Introductionmentioning
confidence: 99%
“…Although otolaryngologic manifestations of various rheumatic diseases have been well described, awareness among otolaryngologists regarding these manifestations is negligible. [2][3][4][5][6][7][8][9] Early and accurate diagnosis with prompt treatment or referral to specialists may prevent morbidity and mortality related to these diseases. The present study was designed to assess the understanding and practice about various ENT problems of rheumatic diseases amongst otolaryngologists.…”
Section: Introductionmentioning
confidence: 99%
“…KD is a type of systemic vasculitis, although here we focused on cervical symptoms. Most (65%) patients showing otolaryngologic manifestations of KD present with cervical lymphadenopathy [4]. Three previous reports describe parotitis associated with KD [57].…”
Section: Discussionmentioning
confidence: 99%
“…37 CREST syndrome is a variant of systemic sclerosis with its own acronym defined as calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly and telangiectasia. [1][2][3][4][5] The association of this disease with malignancyis well established. [2][3][4][5] There is smooth muscle atrophy and fibrosis of the esophagus with reduced or absent peristaltic contractions.…”
Section: Systemic Sclerosis (Scleroderma)mentioning
confidence: 99%
“…Reactive hemophagocytic syndrome is a hematological disorder characterized by the activation of differentiated macrophages to be involved in the phagocytosis of hematopoietic cells. [3][4][5][6] In the head and neck, this disorder shows enlarged cervical lymphadenopathy. Nodes have an oblong appearance with a central hyperechogenic hilum that is associated with a central flow pattern, seen via color duplex examination (Figure 11).…”
Section: Antiphospholipid Antibody Syndromementioning
confidence: 99%
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