angiogenesis inhibitors

血管生成抑制剂
  • 文章类型: Case Reports
    背景:玻璃体腔注射抗血管内皮生长因子被认为是息肉状脉络膜血管病变的一线治疗方法。它对循环系统有潜在的风险,这应该特别仔细评估老年患者。在这个案例研究中,我们旨在讨论该治疗方案对心脏健康的潜在影响.
    方法:本病例报告描述了一位没有心脏病史的老年患者,他表现出意外的心脏扩大和功能障碍。在病人住院期间,调查了各种潜在的原因,产生了这样的假设,即玻璃体内注射抗血管内皮生长因子的10年历史可能与观察到的临床表现有关。病人被建议停止这种治疗,经过2个月的随访,患者的心脏结构和功能逐渐改善。
    结论:这篇手稿强调了在抗血管内皮生长因子治疗前后进行心脏检查的重要性,特别是对于像老年人这样有心脏病风险的人。它强调需要仔细权衡治疗方案的益处和风险,以确保最佳治疗结果。
    BACKGROUND: Intravitreal injection of anti-vascular endothelial growth factor is considered the first-line treatment for polypoidal choroidal vasculopathy. It has potential risks for circulatory system, which should be particularly carefully evaluated in older patients. In this case study, we aim to discuss the potential impact of this treatment regimen on cardiac health.
    METHODS: This case report describes an elderly patient with no prior history of heart disease who exhibited unexpected heart enlargement and dysfunction. Throughout the patient\'s hospital stay, various potential causes were investigated, leading to the hypothesis that a 10-year history of intravitreal injections of anti-vascular endothelial growth factor could be related to the observed clinical manifestations. The patient was advised to discontinue this treatment, and after a 2-month follow-up period, there was a gradual improvement in the patient\'s cardiac structure and function.
    CONCLUSIONS: This manuscript highlights the importance of conducting cardiac examinations before and after anti-vascular endothelial growth factor treatment, especially for individuals at risk of heart diseases like the elderly. It emphasizes the need to carefully weigh the benefits and risks of treatment regimens to ensure optimal therapeutic outcomes.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Case Reports
    目的:本病例报告旨在描述注射后眼内炎的异常临床表现和组织病理学特征。方法:一名56岁的男性糖尿病性视网膜病变患者接受了玻璃体内注射(根据患者的贝伐单抗),用于其他地方的新生血管性青光眼,并在给药hypopyon后一天被送往我们的中心。眼睛相对较白,没有疼痛或眼睑水肿。患者被治疗为注射后眼内炎的病例,间隔48小时服用两剂玻璃体内抗生素。在后续行动中,他患上了Covid感染.一周后,当媒体清除时,在视网膜相对健康的玻璃体腔中观察到白色渗出物。他接受了平坦部玻璃体切除术和玻璃体活检以进行组织病理学研究。结果:玻璃体抽吸物的显微镜检查显示结晶沉积物,没有任何微生物。两张控制幻灯片,一种是玻璃体内抗生素的混合物,以前注射过,另一个用新鲜的曲安奈德也进行了检查。尽管药物混合物的发现与玻璃体抽吸物不匹配,他们配用曲安奈德,将其确定为由于在其他地方注射曲安奈德而引起的假性眼内炎。讨论:最初,这似乎是一个简单的注射后眼内炎病例,但对玻璃体抽吸物的进一步检查显示,这是玻璃体内注射曲安奈德所致的假性眼内炎。尽管病人是有病的,新生血管形成或眼内压升高可能导致血眼屏障的破坏和曲安奈德向前房的迁移。结论:该病例的独特性在于是第一例有晶状体虹膜隔膜完整的有晶状体患者的假性眼内炎病例。此案还强调了对可用资源的明智利用和开箱即用的想法,以得出可能并不总是显而易见的诊断。缩写:TA=曲安奈德,AC=前房,IVB=玻璃体内注射贝伐单抗,PL=光的感知。
    Objective: This case report aimed to describe the unusual clinical presentation and histopathological features of post-injection endophthalmitis. Methods: A 56-year-old male phakic patient with diabetic retinopathy received an intravitreal injection (Bevacizumab as per the patient) for neovascular glaucoma elsewhere and presented to our center one day after the dose with hypopyon. The eye was relatively white without pain or lid oedema. The patient was treated as a case of post-injection endophthalmitis with two doses of intravitreal antibiotics 48 hours apart. During the follow-up, he developed a Covid infection. After one week, when the media cleared, white exudates were seen in the vitreous cavity with a relatively healthy retina. He was taken up for pars plana vitrectomy and vitreous biopsy for histopathological study. Results: The microscopic examination of vitreous aspirate revealed crystalline deposits without any microorganisms. Two control slides, one with a mixture of intravitreal antibiotics, which were previously injected, and the other with fresh Triamcinolone were also examined. Although the findings of the drug mixture did not match the vitreous aspirate, they matched with triamcinolone, which established it as a case of pseudo endophthalmitis due to triamcinolone injected elsewhere. Discussion: Initially, it seemed like a straightforward case of post-injection endophthalmitis, but a further examination of the vitreous aspirate showed that it was pseudoendophthalmitis due to an intravitreal triamcinolone injection. Despite the patient being phakic, neovascularization or elevated intraocular pressure may have led to the disruption of the blood-ocular barrier and the migration of Triamcinolone into the anterior chamber. Conclusion: The case\'s uniqueness lies in being the first reported case of pseudo endophthalmitis in a phakic patient with an intact lens iris diaphragm. The case also highlighted the judicious use of available resources and out-of-the-box thinking to reach a diagnosis that may not always be obvious. Abbreviations: TA = Triamcinolone acetonide, AC = Anterior chamber, IVB = Intravitreal Bevacizumab, PL = Perception of light.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Journal Article
    成人发作的中央眼窝卵黄样营养不良(AOFVD)是一种罕见的疾病,其特征是黄斑中淡黄色沉积物的积累。很少,它可能是复杂的脉络膜新生血管(CNV)。CNV病例可能与年龄相关性黄斑变性的隐匿性CNV混淆。在我们的案例中,我们将介绍AOVF相关CNV患者的视觉和解剖学结果,其中我们给予3剂玻璃体内雷珠单抗(IVR)。一名59岁的女性患者,他因双眼视力下降而去了我们的诊所,双眼均诊断为AOVF相关CNV,并接受3剂IVR治疗3个月。尽管第一次给药后1个月视觉和解剖功能有所改善,视力下降,和解剖功能在连续注射中回归到注射前状态。IVR疗法不是治疗AOVF相关CNV的适当治疗选择。
    Adult-onset foveomacular vitelliform dystrophy (AOFVD) is a rare disease characterized by accumulation of yellowish deposits in the macula. Rarely, it may be complicated by choroidal neovascularization (CNV). Cases with CNV may be confused with occult CNV in age-related macular degeneration. In our case, we will present the visual and anatomical results of a patient with AOVF-related CNV, in which we administered 3 doses of intravitreal ranibizumab (IVR). A 59-year-old female patient, who attended our clinic with the complaint of decreased vision in both eyes, was diagnosed with AOVF-related CNV in both eyes and was treated with 3 doses of IVR for 3 months. Despite the improvement in visual and anatomical functions 1 month after the first dose, vision decreased, and anatomical functions regressed to the pre-injection state in continued injections. IVR therapy is not an appropriate treatment option in the treatment of AOVF-associated CNV.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Journal Article
    背景:眼皮肤白化病(OCA)是一组影响黑色素生物合成的常染色体隐性遗传性疾病,导致头发异常,皮肤,和眼睛。早产儿视网膜病变(ROP)是一种增殖性视网膜病变,主要见于低出生体重和胎龄较早的早产儿。但它也会影响足月婴儿或体重正常的儿童,特别是在发展中国家。ROP和OCA的共存是罕见的。关于治疗方法的文件有限,由于缺乏黑色素,很少有研究报告激光治疗的积极结果。这项研究讨论了诊断为ROP和OCA的女婴的治疗挑战,并强调了遗传分析在指导这种罕见的合并症的治疗决策中的重要性。
    方法:本研究报告1例ROP与OCA同时发生。基因检测显示两种变异,c.727C>T(p。R243C)和c.1832T>C(p。L611P),在OCA2基因中,从病人的母亲和父亲那里继承下来,分别。鉴定的突变与OCA2的诊断一致,被分类为OCA的亚型。患者最初接受玻璃体内注射抗血管内皮生长因子(抗VEGF),然后是激光光凝治疗复发事件.在2个月的随访期间观察到良好的结果。
    结论:ROP和OCA的同时出现是一种罕见的现象,这是中国人口中记录的第一例。当前病例支持使用激光作为部分色素沉着受损的OCA2患者ROP的主要治疗方式。此外,遗传分析可以帮助预测该患者人群中激光光凝的有效性.
    BACKGROUND: Oculocutaneous albinism (OCA) is a group of autosomal recessive hereditary disorders that affect melanin biosynthesis, resulting in abnormalities in hair, skin, and eyes. Retinopathy of prematurity (ROP) is a proliferative retinopathy mainly observed in premature infants with low birth weight and early gestational age, but it can also affect full-term infants or children with normal weight, particularly in developing countries. The coexistence of ROP and OCA is rare. There is limited documentation regarding treatment approaches, with few studies reporting positive outcomes with laser treatment due to the absence of melanin pigment. This study discusses the treatment challenges in a female infant diagnosed with ROP and OCA, and underscores the importance of genetic analysis in guiding therapeutic decisions for this rare comorbid condition.
    METHODS: The study presents a case of ROP occurring concurrently with OCA. Genetic testing revealed two variants, c.727C > T (p.R243C) and c.1832 T > C (p.L611P), in the OCA2 gene, inherited from the patient\'s mother and father, respectively. The identified mutations were consistent with a diagnosis of OCA2, classified as a subtype of OCA. The patient initially received intravitreal anti-vascular endothelial growth factor (anti-VEGF) injection, followed by laser photocoagulation therapy for a recurrent event. A favorable outcome was observed during the 2-month follow-up period.
    CONCLUSIONS: The co-occurrence of ROP and OCA is a rare phenomenon, and this is the first recorded case in the Chinese population. The current case supports the use of laser as the primary treatment modality for ROP in OCA2 patients with partial pigmentation impairment. Furthermore, genetic analysis can aid in predicting the effectiveness of laser photocoagulation in this patient population.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Journal Article
    背景:黄斑视网膜裂孔(MRS)和近视黄斑新生血管(mMNV)都是高度近视的潜在致盲并发症。在这个案例报告中,我们强调了玻璃体内抗血管内皮生长因子(抗VEGF)治疗mMNV后MRS的进展,以及对有关该主题的文献的广泛评论。
    方法:一名49岁的女性近期出现了两周的右眼模糊和变形。她双眼高度近视(右眼-20/60与-16D,左眼-20/20与-13D)。裂隙灯检眼镜在双眼中发现正常的眼前段。眼底检查,双眼均观察到病理性近视伴后葡萄肿和乳头周围萎缩的特征。活跃的mMNV,以及视网膜内液体,最小中央凹内部和外部MRS,和沿着下颞区视网膜拱廊的局灶性玻璃体后部牵引,在右眼的光学相干断层扫描(OCT)上检测到。患者接受玻璃体内注射阿柏西普(2mg/0.05ml)。
    结果:两个月和四个月随访时的OCT扫描显示mMNV消退,视网膜前膜拉紧,外MRS逐渐恶化,以及位于中央凹下方的多个中央凹视网膜脱离的发展。在手术后的最后一个月就诊时,对进行性MRS进行了平坦部玻璃体切除术,具有良好的解剖学(已解决的MRS)和功能结果(维持视力为20/60)。
    结论:玻璃体内注射抗VEGF治疗mMNV可引起玻璃体视网膜界面改变,加剧MRS并导致视力下降。MRS的玻璃体切除术可能是几种治疗选择之一。
    BACKGROUND: Macular retinoschisis (MRS) and myopic macular neovascularization (mMNV) are both potentially blinding complications of high myopia. In this case report, we highlight the progression of MRS after intravitreal anti-vascular endothelial growth factor (anti-VEGF) treatment for mMNV, as well as an extensive review of the literature on this topic.
    METHODS: A 49-year-old woman presented with two weeks of recent onset blurring and metamorphopsia in her right eye. She had high myopia in both eyes (right eye - 20/60 with - 16D, left eye - 20/20 with - 13D). Slit-lamp ophthalmoscopy found a normal anterior segment in both eyes. On fundus examination, features of pathological myopia with posterior staphyloma and peripapillary atrophy were observed in both eyes. An active mMNV, as well as intraretinal fluid, minimal perifoveal inner and outer MRS, and focal posterior vitreous traction along the inferotemporal retinal arcade, were detected on optical coherence tomography (OCT) of the right eye. The patient received an intravitreal injection of Aflibercept (2 mg/0.05 ml).
    RESULTS: OCT scans at two- and four-month follow-up visits revealed regressed mMNV with a taut epiretinal membrane, progressive worsening of outer MRS, and the development of multiple perifoveal retinal detachment inferior to the fovea. Pars plana vitrectomy surgery was performed for the progressive MRS with good anatomical (resolved MRS) and functional outcome (maintained visual acuity at 20/60) at the last one-month post-surgery visit.
    CONCLUSIONS: Intravitreal anti-VEGF injections for mMNV can cause vitreoretinal interface changes, exacerbating MRS and causing visual deterioration. Vitrectomy for MRS could be one of several treatment options.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Journal Article
    背景:确定与新生血管性年龄相关性黄斑变性(nAMD)相关的基因型,并研究基因型变异与抗血管内皮生长因子(VEGF)治疗反应之间的关系。
    方法:这种观察,回顾性,病例系列研究纳入了在国立台湾大学医院接受抗VEGF治疗的诊断为nAMD的患者,并在2012年至2020年间进行了至少1年的随访.对入组患者和对照组进行全基因组关联研究(GWAS)。从GWAS鉴定的基因型与功能/解剖生物标志物的治疗反应之间的相关性,包括视敏度(VA),存在视网膜内或视网膜下液(SRF),浆液性或纤维血管色素上皮脱离(PED),和椭球区(EZ)的破坏,进行了分析。
    结果:总计,纳入182例nAMD患者和1748例对照。GWAS显示16个单核苷酸多态性(SNPs)为nAMD的风险位点,包括CFH和ARMS2/HTRA1中的七个基因座和九个新基因座,包括rs117517872和rs79835234(COPB2-DT),rs7525578(RAP1A),rs2123738(LOC105376755),rs1374879(CNTN3),rs3812692(SAR1A),rs117501587(PRKCA),rs9965945(CNDP1),和RS189769231(MATK)。我们的研究显示rs800292(CFH),rs11200638(HTRA1),rs2123738(LOC105376755)与VA的不良治疗反应相关(P=0.005),SRF(P=0.044),和纤维血管PED(P=0.007),分别。Rs9965945(CNDP1)与EZ(P=0.046)和浆液性PED(P=0.049)破坏反应不良相关。
    结论:在GWAS中发现的16个SNP中,四个基因座-CFH,ARMS2/HTRA1和两个新基因座与抗VEGF治疗后nAMD的易感性和解剖/功能反应相关。
    BACKGROUND: To identify genotypes associated with neovascular age-related macular degeneration (nAMD) and investigate the associations between genotype variations and anti-vascular endothelial growth factor (VEGF) treatment response.
    METHODS: This observational, retrospective, case series study enrolled patients diagnosed with nAMD who received anti-VEGF treatment in National Taiwan University Hospital with at least one-year follow-up between 2012 and 2020. A genome-wide association study (GWAS) was conducted on enrolled patients and controls. Correlations between the genotypes identified from GWAS and the treatment response of functional/anatomical biomarkers, including visual acuity (VA), presence of intraretinal or subretinal fluid (SRF), serous or fibrovascular pigmented epithelium detachment (PED), and disruption of the ellipsoid zone (EZ), were analysed.
    RESULTS: In total, 182 patients with nAMD and 1748 controls were enrolled. GWAS revealed 16 single nucleotide polymorphisms (SNPs) as risk loci for nAMD, including seven loci in CFH and ARMS2/HTRA1 and nine novel loci, including rs117517872 and rs79835234(COPB2-DT), rs7525578(RAP1A), rs2123738(LOC105376755), rs1374879(CNTN3), rs3812692(SAR1A), rs117501587(PRKCA), rs9965945(CNDP1), and rs189769231(MATK). Our study revealed rs800292(CFH), rs11200638(HTRA1), and rs2123738(LOC105376755) correlated with poor treatment response in VA (P = 0.005), SRF (P = 0.044), and fibrovascular PED (P = 0.007), respectively. Rs9965945(CNDP1) was correlated with poor response in disruption of EZ (P = 0.046) and serous PED (P = 0.049).
    CONCLUSIONS: Among the 16 SNPs found in the GWAS, four loci-CFH, ARMS2/HTRA1, and two novel loci-were correlated with the susceptibility of nAMD and anatomical/functional responses after anti-VEGF treatment.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Case Reports
    目前的研究表明,三阴性乳腺癌的发病率占乳腺浸润性导管癌的10-17%。没有具体的治疗目标,发病年龄相对较小,复发率相对较快。不同亚型乳腺癌的预后最不理想,5年生存率低于15%。我们报告了一个典型的转移性晚期三阴性乳腺癌病例,化疗失败后对甲磺酸阿帕替尼反应良好,并实现了显著的无进展生存期。这在治疗手段有限的三阴性乳腺癌中相对罕见。
    2015年4月17日,一名55岁女性被手术诊断为三阴性乳腺癌。手术后,标准辅助化疗和放疗后出现肺转移.在接受NX方案(长春瑞滨,卡培他滨)8个周期,她进步了。因为病人后来拒绝了,她调整了甲磺酸阿帕替尼,治疗过程中出现严重不良反应。通过调整药物剂量,和低剂量阿帕替尼治疗,肺部病变接近完全缓解(CR),达到45个月的无进展生存期。
    低剂量阿帕替尼对于三阴性乳腺癌患者可能是一种有前途的抗肿瘤药物,这需要更多的样本来验证。该病例可为今后三阴性转移性乳腺癌的治疗选择提供参考。
    UNASSIGNED: The current study shows that the incidence rate of triple-negative breast cancer accounts for 10-17% of invasive ductal carcinoma of the breast. There is no specific treatment target, the age of onset is relatively small, and the recurrence rate is relatively fast. The prognosis of breast cancer in different subtypes is the most unsatisfactory, with a 5-year survival rate of less than 15%. We report a typical case of metastatic advanced triple-negative breast cancer who responded well to apatinib mesylate after chemotherapy failure and achieved significant progression-free survival, which is relatively rare in triple-negative breast cancer with limited treatment means.
    UNASSIGNED: A 55-year-old female was surgically diagnosed as triple-negative breast cancer on April 17, 2015. After surgery, she had lung metastasis after standard adjuvant chemotherapy and radiotherapy. After receiving the NX regimen (vinorelbine, capecitabine) for 8 cycles, she progressed. Because the patient refused later, she was adjusted to apatinib mesylate, and serious adverse reactions occurred during the treatment process. By adjusting the drug dose, and low-dose apatinib treatment, the lung lesions were close to complete response (CR), reaching a progression-free survival period of 45 months.
    UNASSIGNED: Low-dose apatinib may be a promising anti-tumor drug for triple-negative breast cancer patients, which needs more samples to verify. This case may provide a reference for the treatment selection of triple-negative metastatic breast cancer in the future.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Journal Article
    目的:评估临床特征,治疗方案,结果,以及在该病例系列中出现的并发症,这些患者包括玻璃体内注射贝伐单抗(IVB)后连续出现无菌性眼内炎的24例患者。
    方法:在本回顾性病例系列中,IVB以来自同一天使用的三个批次的单独等分试样重新包装。由于糖尿病性黄斑水肿,对26例患者的26只眼注射IVB,年龄相关性黄斑变性,和视网膜分支静脉阻塞.所有患者均有眼内炎症。根据眼内炎症将患者分为重度和中度炎症两组。对所有患者的医疗记录进行审查。在每次后续访问中,进行了完整的眼科检查,包括最佳矫正视力(BCVA),眼内压,生物显微镜,和后眼底检查。
    结果:26例患者中有24例纳入研究。两名患者被排除在本研究之外,因为他们没有来随访。IVB前平均BCVA为1.00±0.52LogMAR单位。在最后一次访问中,BCVA为1.04±0.47LogMAR单位。这些差异不显著(p=0.58)。在24只眼睛中,16眼严重,8只眼有中度眼内炎症。严重炎症组中的11只眼由于强烈的玻璃体混浊而接受了平坦部玻璃体切除术。涂片,文化结果,聚合酶链反应结果为阴性。
    结论:IVB注射后可能发生无菌眼内炎。无菌性眼内炎与感染性眼内炎的鉴别诊断对于调整适当的治疗方法和防止因不必要的治疗而导致的长期并发症至关重要。
    OBJECTIVE: To evaluate clinical features, treatment protocol, outcomes, and complications that developed in this case series of 24 patients who had consecutive sterile endophthalmitis after intravitreal bevacizumab (IVB) injection.
    METHODS: In this retrospective case series, IVB was repackaged in individual aliquots from the three batches that were used on the same day. IVB was injected into 26 eyes of 26 patients due to diabetic macular edema, age-related macular degeneration, and branch retinal vein occlusion. All patients had intraocular inflammation. Patients were divided into two groups severe and moderate inflammation according to the intraocular inflammation. The medical records of all patients were reviewed. At each follow-up visit, the complete ophthalmologic examination was performed, including best corrected visual acuity (BCVA), intraocular pressure, biomicroscopy, and posterior fundus examination.
    RESULTS: Twenty-four of 26 patients were included in the study. Two patients were excluded from this study since they didn\'t come to follow-up visits. The mean BCVA was 1.00 ± 0.52 Log MAR units before IVB. At the final visit, the BCVA was 1.04 ± 0.47 Log MAR units. These differences were not significant (p = 0.58). Of the 24 eyes, 16 eyes had severe, and 8 eyes had moderate intraocular inflammation. Eleven eyes in the severe inflammation group underwent pars plana vitrectomy due to intense vitreous opacity. Smear, culture results, and polymerase chain reaction results were negative.
    CONCLUSIONS: Sterile endophthalmitis may occur after IVB injection. Differential diagnosis of sterile endophthalmitis from infective endophthalmitis is crucial to adjust the appropriate treatment and prevent long-term complications due to unnecessary treatment.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Case Reports
    背景:报告1例视网膜中央动脉阻塞(CRAO),在玻璃体内注射布罗珠单抗治疗初治新生血管性年龄相关性黄斑变性(nAMD)患者后,无共同心血管疾病史。
    方法:一名79岁的亚洲男性,没有心血管疾病史,如糖尿病或高血压,每月连续3次玻璃体内注射布卢珠单抗,用于治疗左眼进展性nAMD。第三次注射两天后,患者出现急性无痛性视力丧失。在眼底照片上观察到典型的具有樱桃红色斑点的视网膜白化,在光学相干断层扫描(OCT)扫描中也发现了具有高反射率的视网膜肿胀.在荧光素眼底血管造影术上,臂至视网膜时间和动静脉通过时间明显延迟,但未观察到提示眼内炎症(IOI)的临床发现。因此,CRAO被诊断出来,并立即进行前房穿刺。然而,在三个月的随访期间,视力没有改善,尽管长期口服类固醇和抗血小板药物。
    结论:在极少数情况下,没有心血管合并症的患者在玻璃体内注射布卢珠单抗后可发生CRAO,而没有IOI的确证.因此,对于老年nAMD患者,玻璃体内注射布卢珠单抗后,应始终考虑CRAO,需要仔细观察。即使患者没有任何其他心血管疾病史。
    BACKGROUND: To report a case of central retinal artery occlusion (CRAO) after intravitreal injection of brolucizumab for a treatment-naïve neovascular age-related macular degeneration (nAMD) patient without comorbid cardiovascular disease history.
    METHODS: A 79-year-old Asian male without a cardiovascular disease history such as diabetes or hypertension underwent three times of monthly consecutive intravitreal brolucizumab injections for treatment of progressed nAMD in his left eye. Two days after the third injection, the patient presented with acute painless visual loss. Typical retinal whitening with a cherry red spot was observed on the fundus photograph, and retinal swelling with hyper-reflectivity was also identified on the optical coherence tomography (OCT) scan. On the fundus fluorescein angiography, arm-to-retina time and arteriovenous transit time were remarkedly delayed, but clinical findings suggesting an intraocular inflammation (IOI) were not observed. Therefore, CRAO was diagnosed, and anterior chamber paracentesis was administrated immediately. However, there had been no improvement in visual acuity during the follow-up period of three months, despite prolonged oral steroid and anti-platelet agent medication.
    CONCLUSIONS: In rare cases, patients without cardiovascular comorbidities can develop CRAO after intravitreal brolucizumab injection without gross evidence of IOI. Therefore, CRAO should always be in consideration and careful observation is required after intravitreal brolucizumab injection for nAMD patients with old age, even if the patient does not have any other cardiovascular disease history.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Case Reports
    卵巢小细胞癌,高血钙型(SCCOHT)是一种罕见但高度侵袭性的卵巢恶性肿瘤,缺乏统一的临床治疗流程。大多数患者被诊断为晚期,预后极差,总生存率低于10%。这里,我们描述了1例晚期SCCOHT患者在接受多周期免疫治疗联合抗血管生成治疗或CDK4/6抑制剂治疗后生存超过5年.同时,我们还总结了SCCOHT免疫治疗的病例报告和临床试验.
    Small cell carcinoma of the ovary, hypercalcemic type (SCCOHT) is a rare but highly aggressive ovarian malignant neoplasm lacking a unified clinical management process. Most patients are diagnosed at an advanced stage and have an extremely poor prognosis with an overall probability of survival less than 10 %. Here, we describe the case of a patient with advanced SCCOHT achieved a survival of over 5 years after receiving multiple cycles of immunotherapy combined with anti-angiogenic therapy or CDK4/6 inhibitors. At the same time, we also summarized the case reports and clinical trials of immunotherapy in SCCOHT.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

公众号