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PubmedHPO

Id Subject Object Predicate Lexical cue
T1 323-332 HP_0003470 denotes paralysis

PubMed_Structured_Abstracts

Id Subject Object Predicate Lexical cue
T1 123-573 OBJECTIVE denotes The posterior cricoarytenoid (PCA) muscle is one of the intrinsic muscles of the larynx innervated by the recurrent laryngeal nerve. As such, recurrent laryngeal nerve palsy should not only result in paralysis of the true vocal cord or thyroarytenoid muscle but also in a similar change in the PCA muscle. The ability of CT and MR imaging to depict denervation atrophy in the PCA muscle in patients with recurrent laryngeal nerve palsy was evaluated.
T2 583-1104 METHODS denotes Two investigators reviewed the CT and/or MR studies of 20 patients with a clinical history of vocal cord paralysis. The appearance of the PCA muscle was given a rating of 0, 1, 2, 3, or 4, with 0 being definitely normal and 4 being definitely abnormal or atrophic. Each study was also reviewed for the presence or absence of other features of vocal cord paralysis: thyroarytenoid muscle atrophy, anteromedial deviation of the arytenoid cartilage, an enlarged piriform sinus and laryngeal ventricle, and a paramedian cord.
T3 1114-1503 RESULTS denotes Atrophy of the PCA muscle was shown unequivocally in 65% of the cases and was most likely present in an additional 20%. The frequency with which other features of vocal cord paralysis were seen was as follows: thyroarytenoid atrophy, 95%; anteromedial deviation of the arytenoid cartilage, 70%; enlarged piriform sinus, 100%; enlarged laryngeal ventricle, 90%; and a paramedian cord, 100%.
T4 1516-1872 CONCLUSIONS denotes Atrophy of the PCA muscle may be commonly documented on CT and MR studies in patients with recurrent laryngeal nerve palsy and vocal cord paralysis, and therefore should be part of the constellation of imaging features of vocal cord paralysis. This finding is particularly useful when other imaging findings of vocal cord paralysis are absent or equivocal.

PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T1 92-97 DiseaseOrPhenotypicFeature denotes palsy 0006496
T2 153-156 DiseaseOrPhenotypicFeature denotes PCA 0012155|0018899|0024522
T5 291-296 DiseaseOrPhenotypicFeature denotes palsy 0006496
T6 417-420 DiseaseOrPhenotypicFeature denotes PCA 0012155|0018899|0024522
T9 499-502 DiseaseOrPhenotypicFeature denotes PCA 0012155|0018899|0024522
T12 553-558 DiseaseOrPhenotypicFeature denotes palsy 0006496
T13 721-724 DiseaseOrPhenotypicFeature denotes PCA 0012155|0018899|0024522
T16 1129-1132 DiseaseOrPhenotypicFeature denotes PCA 0012155|0018899|0024522
T19 1531-1534 DiseaseOrPhenotypicFeature denotes PCA 0012155|0018899|0024522
T22 1633-1638 DiseaseOrPhenotypicFeature denotes palsy 0006496