Pili torti

Pili torti
  • 文章类型: Case Reports
    背景:要报告演示文稿,诊断过程,诊断为Bjornstad综合征伴深度感音神经性听力损失(SNHL)的患者人工耳蜗植入的治疗和结果。
    回顾性报道,两名患有Bjornstad综合征的兄弟姐妹患有严重的SNHL,对接受双侧同步人工耳蜗植入治疗的常规助听器无反应。
    方法:三级转诊中心。
    结果:对患有严重SNHL和双侧内耳异常(不完全分区类型1)的两个兄弟姐妹(四耳)进行人工耳蜗植入手术,无并发症。术后听力测量显示纯音阈值和单词识别得分显着提高。在文献综述中,以前没有报道过人工耳蜗植入治疗的Bjornstad综合征病例.
    结论:人工耳蜗植入是一种有效的,安全,和Bjornstad综合征的最终治疗选择,严重的SNHL对助听器无反应。
    BACKGROUND: To report the presentation, diagnostic process, management and results of cochlear implantation of patients diagnosed with Bjornstad syndrome with profound sensorineural hearing loss (SNHL).
    UNASSIGNED: A retrospective report of two siblings with Bjornstad syndrome suffering profound SNHL unresponsive to conventional hearing aids treated with bilateral simultaneous cochlear implantation.
    METHODS: Tertiary-referral center.
    RESULTS: Cochlear implant surgeries of two siblings (four ears) with profound SNHL and bilateral inner ear anomaly (incomplete partition type 1) were performed without complications. Postoperative audiometric measurements showed a significiant improvement in pure-tone threshold and a word recognition score. In the literature review, no previous case of Bjornstad syndrome treated with cochlear implantation has been reported.
    CONCLUSIONS: Cochlear implantation is an effective, safe, and ultimate treatment option for Bjornstad syndrome with profound SNHL not responding to hearing aids.
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  • 文章类型: Case Reports
    纤毛或“扭曲的头发”的特征是扁平的发干以不规则的间隔绕其长轴扭曲180度。它是遗传性或获得性毛干障碍,脆性增加。它可能与许多皮肤病和全身性疾病有关,也可能是药物诱导的。报道了一例孤立的菌毛torti病例,这是非常罕见的,并回顾了相关文献。
    Pili torti or \'twisted hair\' is characterized by flattened hair shaft twisted through 180 degree around their long axis at irregular intervals. It is inherited or acquired hair shaft disorder with increased fragility. It may be associated with numerous dermatological and systemic conditions or may be drug-induced. An isolated pili torti case is reported which is very rare and the related literature reviewed.
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  • 文章类型: Journal Article
    Although the clinical hair changes that occur under treatment with epidermal growth factor receptor inhibitors (EGFRIs) are documented, their trichoscopic features have not been reported.
    To evaluate the trichoscopic findings in scalp and facial hair, induced by EGFRI treatment.
    Patients treated with EGFRIs at a tertiary oncodermatology clinic in 2015 through 2017 were evaluated for macroscopic and trichoscopic changes.
    The cohort included 23 patients (13 women; median age, 68 years) treated with EGFRIs for an average of 13 months (range, 2-40 months). Macroscopically, 18 patients (78%) had dry, lusterless, coarse, kinky, brittle scalp hair, and 17 (74%) had trichomegaly of the eyebrows/eyelashes. Trichoscopic findings were of hair shaft anomalies including pili torti, affecting scalp hair in 20 patients (87%), eyebrows in 6 (26%), and eyelashes in 8 (50%), and asymmetric hyperpigmented fusiform widening of hair scalp in 3 (13%), eyebrows in 10 (43%), and eyelashes in 4 (25%). Dermoscopic findings of the peri- and interfollicular skin were scale, whitish erythematous structureless areas, and branching vessels.
    Lack of trichoscopic-histologic correlation, lack of baseline examination.
    The trichoscopic correlates of the macroscopic hair changes under EFGRI treatment include pili torti, and asymmetric hyperpigmented fusiform widening, with dermoscopic cutaneous manifestations of scale, whitish erythematous structureless areas, and branching vessels.
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