Junejo Shoaib, Ali Yasir, Abrudescu Adriana
, Icahn School of Medicine at Mount Sinai-Queens Hospital Center, Jamaica, NY, USA.
Department of Endocrinology, NYC Health and Queens Hospital Center, Jamaica, NY, USA.
Am J Case Rep. 2017 Nov 22;18:1233-1237. doi: 10.12659/AJCR.907174.
['Patient: Male, 66', 'Final Diagnosis: Giant cell arteritis', 'Symptoms: Hearing loss', 'Medication: —', 'Clinical Procedure: —', 'Specialty: Rheumatology']
: Unusual clinical course
: The classical picture of giant cell (temporal) arteritis (GCA) is not always evident. A wide variety of unusual presentations have been increasingly reported. Sensorineural hearing loss (SNHL) as an initial manifestation of GCA is a rare, yet important entity. Similar to blindness, SNHL also deserves serious attention as timely intervention may play a key role in overall prognosis. Only a few cases of SNHL associated with GCA have been reported in the literature, the majority of them were diagnosed early and responded well to glucocorticoid therapy. Our report focuses on a case of persistent audiometry-proven SNHL despite optimal doses and duration of glucocorticoids required in GCA patients with ischemic complications.
: We present the case of a 66-year-old male with severe bi-temporal headache, left jaw claudication, and progressively worsening hearing loss, the latter symptom reported over the preceding year. Examination of his temporal artery remained insignificant, but the laboratory data showed raised erythrocyte sedimentation rate (ESR) of 52 mm/hour. Audiometry performed and the interpretations were coincided with the bilateral high frequency mild to moderately-severe SNHL. Prompt administration of IV methylprednisolone started at high-optimum doses that were gradually tapered over the subsequent six months. On biopsy of the left temporal artery, the findings were consistent with the GCA. The patient responded well in terms of headache and general condition improvement, but results of repeat audiometry at follow-up visits proved disappointing and the interpretations were that there was no change in the audiometry results based on first presentation.
: This case is purposefully reported to draw the attention of practicing physicians, and encourage them not only to better understand atypical presentations of GCA but also to intervene in a timely fashion. This case should encourage literature to reset recommendations and encourage have high-indexed suspicion when elderly patients present with deafness since early diagnosis and treatment may have profound effects on overall long-term prognosis of other cranial ischemic complications as well.
['患者:男性,66岁', '最终诊断:巨细胞动脉炎', '症状:听力丧失', '用药:—', '临床操作:—', '专科:风湿病学']
不寻常的临床病程
巨细胞(颞)动脉炎(GCA)的典型表现并不总是很明显。越来越多的各种不寻常表现被报道。感音神经性听力丧失(SNHL)作为GCA的初始表现是一种罕见但重要的情况。与失明类似,SNHL也值得认真关注,因为及时干预可能在总体预后中起关键作用。文献中仅报道了少数几例与GCA相关的SNHL病例,其中大多数早期被诊断并对糖皮质激素治疗反应良好。我们的报告重点关注一例尽管给予GCA缺血性并发症患者最佳剂量和疗程的糖皮质激素,但听力测定证实SNHL仍持续存在的病例。
我们报告一例66岁男性,有严重双侧颞部头痛、左侧颌部跛行以及听力丧失逐渐加重,后者症状在前一年就已出现。对其颞动脉检查无异常,但实验室数据显示红细胞沉降率(ESR)升高至52毫米/小时。进行了听力测定,结果显示双侧高频轻度至中度重度SNHL。立即给予静脉注射甲泼尼龙,起始剂量为高最佳剂量,随后六个月逐渐减量。对左侧颞动脉进行活检,结果符合GCA。患者在头痛和一般状况改善方面反应良好,但随访时重复听力测定结果令人失望,结果显示与首次检查时的听力测定结果无变化。
特意报告此病例以引起执业医师的注意,并鼓励他们不仅要更好地了解GCA的非典型表现,还要及时进行干预。该病例应促使文献重新设定建议,并鼓励在老年患者出现耳聋时高度怀疑,因为早期诊断和治疗可能对其他颅脑缺血性并发症的总体长期预后也有深远影响。