激光治疗早产儿视网膜病变后迟发继发性闭角型青光眼引起的伴有偏头痛特征的头痛

Christina J. Su, Carley Gilman, Andrew R. Lee, Shannon C. Agner
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He denied vision changes, waking up from sleep due to headaches, numbness, tingling, or weakness. He had no prior headache history or family history of chronic headaches. His exam was notable for the oblong appearance of the left pupil, but his neurological exam was otherwise nonfocal. His symptoms and exam were thought to be most consistent with migraine headaches.</p><p>Due to the positional component of his headaches, further evaluation was pursued, including imaging and consultation with ophthalmology. Brain magnetic resonance imaging revealed no structural explanation for his headaches. Eye exams during this period revealed normal intraocular pressure (IOP) bilaterally and no optic disc edema. There were notable iris abnormalities and iridocorneal adhesions in his left eye consistent with prior history of retinal laser treatment. 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引用次数: 0

摘要

随着早产儿存活率的不断提高,面临早产儿并发症风险的儿童人数也在增加。早产儿视网膜病变(ROP)是一种视网膜血管发育异常的疾病,是早产儿可预防性失明的主要原因之一。9 岁时,他的左眼后部开始出现新的间歇性头痛,描述为疼痛和钝痛。头痛伴有光敏感、恶心和呕吐,头向前移动时头痛加剧。他否认视力有变化,否认因头痛、麻木、刺痛或虚弱而从睡梦中惊醒。他以前没有头痛病史,也没有慢性头痛家族史。他的检查结果是左眼瞳孔呈长圆形,但其他神经系统检查均无异常。他的症状和检查结果被认为与偏头痛最为吻合。由于他的头痛具有位置性,医生对他进行了进一步评估,包括影像学检查和眼科会诊。脑磁共振成像显示,他的头痛在结构上无法解释。在此期间进行的眼科检查显示双侧眼压(IOP)正常,无视盘水肿。左眼有明显的虹膜异常和虹膜角膜粘连,与之前的视网膜激光治疗史一致。在接下来的一个月里,患者尝试了多种偏头痛治疗方法,但症状缓解不明显,包括对乙酰氨基酚联合丙氯丙嗪、苯海拉明、丙戊酸钠和普萘洛尔。由于他有慢性肾病史,因此避免使用非甾体抗炎药。大约一个月后,他的头痛迅速加重,左侧额部和颞部出现搏动性疼痛。他的神经系统检查保持稳定。然而,在眼科检查中,他的左眼眼压升高至 34 mmHg(正常值≤ 21 mmHg)。一周后,他的头痛、视力模糊、恶心和呕吐症状进一步加重。他左眼的眼压升至 46 mmHg,对药物降眼压疗法没有反应。患者入院后紧急在左眼植入艾哈迈德青光眼引流装置(New World Medical),术后头痛症状立即缓解。闭角型青光眼的症状首先表现为间歇性头痛,原因是眼压周期性升高,随后自发恢复正常。这些头痛经常发生在额部和颞部,并可能伴有恶心和呕吐。6 手术后一年多,患者的眼压测量值一直保持稳定。术后一年多,患者的眼压测量值一直保持稳定。他偶尔会感到头痛,但术后头痛的频率和严重程度都有所减轻。他的头痛恶化与测量到的眼压升高之间的时间关系,以及术后头痛的改善,证明闭角型青光眼是他头痛的主要病因,可能是直接原因,也可能是偏头痛的诱因。总之,这名患者的情况突出说明了偏头痛和闭角型青光眼症状的重叠,而偏头痛和闭角型青光眼可能是激光视网膜光凝治疗 ROP 的结果。对于新发头痛并有 ROP 病史的患者,应考虑眼部病因,眼科团队的早期参与可能有助于确诊:视觉化;写作(原稿);写作(审阅和编辑)。Carley Gilman:写作(审阅和编辑)。Andrew R. Lee:构思;写作(审阅和编辑);获取资金。香农-C-艾格纳作者声明无利益冲突。
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Headache with migrainous features caused by delayed onset secondary angle closure glaucoma following laser treatment for retinopathy of prematurity

As survival among preterm infants has increased over time, the number of children at risk of complications of prematurity has increased as well. Retinopathy of prematurity (ROP) is a disease of abnormal retinal blood vessel development and is one of the leading causes of preventable blindness in preterm babies.1, 2

We present a former 24-week premature infant who received left laser retinal photocoagulation at 2 months of age for ROP. At 9 years of age, he began experiencing new intermittent headaches behind the left eye that were described as achy and dull. The headaches were associated with light sensitivity, nausea, and vomiting, and they worsened when he moved his head forward. He denied vision changes, waking up from sleep due to headaches, numbness, tingling, or weakness. He had no prior headache history or family history of chronic headaches. His exam was notable for the oblong appearance of the left pupil, but his neurological exam was otherwise nonfocal. His symptoms and exam were thought to be most consistent with migraine headaches.

Due to the positional component of his headaches, further evaluation was pursued, including imaging and consultation with ophthalmology. Brain magnetic resonance imaging revealed no structural explanation for his headaches. Eye exams during this period revealed normal intraocular pressure (IOP) bilaterally and no optic disc edema. There were notable iris abnormalities and iridocorneal adhesions in his left eye consistent with prior history of retinal laser treatment. A lumbar puncture was not pursued due to no other signs or symptoms of increased intracranial pressure aside from the positional features.

Over the next month, several migraine treatments were trialed with inconsistent symptom relief, including acetaminophen in combination with prochlorperazine, diphenhydramine, valproate, and propranolol. Nonsteroidal anti-inflammatory drugs were avoided due to his history of chronic kidney disease. Approximately one month later, his headaches rapidly worsened to throbbing in the left frontal and temporal region. His neurological examination remained stable. However, his left eye pressure was elevated at 34 mmHg (normal ≤ 21 mmHg) during ophthalmologic evaluation. He developed further worsening headaches, blurred vision, nausea, and vomiting one week later. IOP of his left eye had increased to 46 mmHg and did not respond to pharmacologic IOP-lowering therapies. The patient was admitted for urgent Ahmed glaucoma drainage device implantation (New World Medical) in the left eye and experienced immediate headache relief after surgery.

Angle-closure glaucoma can present as early as two weeks after treatment of ROP. However, presentations have been reported anywhere from 12 to 45 years of age.3, 4 Angle-closure glaucoma symptoms can first present with intermittent headaches due to periodic elevation of IOP followed by spontaneous normalization.5, 6 This likely explains the normal IOP measurements during our patient's initial exams. These headaches are frequently localized to the frontal and temporal regions and can be associated with nausea and vomiting.6

More than a year after surgery, the patient's IOP measurements have remained stable. He has experienced occasional headaches, but these have decreased in both frequency and severity postsurgically. The temporal relationship between his worsening headaches and measured increase in IOP with the subsequent improvement of his headaches postsurgically supports angle-closure glaucoma as the primary etiology of his headaches, either as a direct cause or as a trigger for migraine headaches. It is alternatively possible that the patient had concurrent presence of both angle-closure glaucoma and migraine headaches.

Overall, this patient highlights the overlapping symptomatology of migraine headaches and angle-closure glaucoma that may result from laser retinal photocoagulation for ROP. For patients with new headaches and a history of ROP, ocular etiologies should be considered, and early involvement of ophthalmology teams may help establish a diagnosis.

Christina J. Su: Visualization; writing (original draft); writing (review and editing). Carley Gilman: Writing (review and editing). Andrew R. Lee: Conceptualization; writing (review and editing); funding acquisition. Shannon C. Agner: Conceptualization; project administration; supervision; writing (review and editing).

The authors declare no conflicts of interest.

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