Ortner’s syndrome or cardiovocal hoarseness
Ortner’s syndrome or cardiovocal hoarseness
复制标题
奥特纳综合征或心声嘶哑
DOI:
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发表时间:
2007
期刊:
影响因子:
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通讯作者:
R. Strasser
中科院分区:
文献类型:
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作者:
C. Wunderlich;O. Wunderlich;A. Tausche;J. Fuhrmann;A. Boscheri;R. Strasser
A spontaneously occurring hoarseness prompted a 66-year-old Caucasian man to consult an outpatient ear, nose and throat specialist. As the result of a conspicuous paralysis of his left vocal cord the patient was hospitalized in a non-teaching hospital where the depicted chest radiograph was obtained (Fig. 1). Under suspicion of an aortic dissection the patient was referred to our intensive care unit. An immediate contrast-enhanced computed tomography (CT) scan indicated a false aneurysm of the aortic arch with the entry distal the left subclavian artery (Fig. 2A). Notably the patient did not remember a traumatic event. After having invasively ruled out a significant coronary artery disease the lesion wasuneventfully treatedwith anaorticwall stent covering the false aneurysm. A post-interventional CT image showed a complete thrombosis of the false lumen (Fig. 2 B). In the 6-month follow up his hoarseness also disappeared. To date only a few such cases have been described. As early as 1897 Ortner first described hoarseness in patients with left atrial enlargement due to mitral valve stenosis. Subsequently, this clinical entity was reported as a rare complication of various cardiovascular abnormalities, such as atrial septal defects, pulmonary hypertension and aortic aneurysms involving the aortic arch. In this syndrome the left recurrent laryngeal nerve is believed to be injured because of compression or traction caused by changes in the anatomy of the heart or great vessels. Although neoplasms and surgical interventions account for most of the recurrent laryngeal nerve palsies, cardiovascular pathologies can also Figure 1 Chest radiograph indicating a suspicious bulge of the aortic arch, which guided subsequent diagnostic steps.