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SIMULTANEOUS BILATERAL ACUTE ANGLE-CLOSURE GLAUCOMA IN MILLER FISHER SYNDROME


Authors: J. Štěpánková 1;  L. Kinštová 2;  I. Gažová 2;  M. Kodetová 1;  J. Cendelín 1,3;  N. Ondrová 1;  D. Dotřelová 1
Authors‘ workplace: Oční klinika dětí a dospělých 2. LF UK a FN Motol, přednosta prof. MUDr. Dagmar Dotřelová, CSc., FEBO 1;  Neurologická klinika 2. LF UK a FN Motol, přednosta prof. MUDr. Petr Marusič, Ph. D. 2;  Oční centrum OFTA, Plzeň, primář MUDr. Jiří Cendelín, CSc. 3
Published in: Čes. a slov. Oftal., 75, 2019, No. 4, p. 210-218
Category: Case Report
doi: https://doi.org/10.31348/2019/4/5

Overview

Purpose: To report a case of patient with Miller Fisher syndrome, complicated by simultaneous bilateral acute angle-closure glaucoma in her slightly (+1.5) hyperopic eyes.

Methods: We present a case report of a 71-year-old female patient presenting with total ophthalmoplegia, areflexia, ataxia and bilateral acute angle-closure glaucoma.

Results: The initial ocular examination revealed hand motion in the both eyes and oedematic corneas. Initial intraocular pressure was immeasurable high (measurment by Tonopen Avia). Measurement was possible after intravenous Mannitol 20 % infusion on both eyes as 54 and 56 mm Hg, respectively. Local medical therapy of pilocarpine, timolol, dorsolamide and dexamethasone improve intraocular pressure into normal limits within several hours. Prophylactic peripheral Nd-YAG laser iridotomy was performed on a both eyes two days later. Systemic treatment involved plasma exchange and rehabilitation program. Subsequent cataract surgery on both eyes with posterior capsule lens implantation improve the best corrected visual acuity on right eye from 0.5 to 1.0 and the left eye from 0.5 to 0.8, respectively. Intraocular pressure is within normal limits without any glaucoma therapy. Follow up period is three years.

Conclusions: This is the second reported case of patient with Miller Fisher syndrome and simultaneous bilateral acute angle-closure glaucoma and the fifth reported case of Miller Fisher syndrome and acute angle-closure glaucoma. Treatment for both conditions made a very good recovery.

Keywords:

Miller Fisher syndrome – bilateral acute angle-closure glaucoma – acute angle-closure glaucoma

INTRODUCTION

Simultaneous bilateral acute angle-closure glaucoma ranks among rare findings. Miller Fisher syndrome (MFS) is described as a rare variant of Guillain-Barré syndrome (GBS). MFS is an acute post-infection immunity mediated polyradiculoneuropathy, characterised by ophthalmoplegia, ataxia and areflexia, which was first described by Fisher in 1956 (40). It is estimated that in Europe and the USA it represents 1-5% of cases of GBS, although in South-East Asia higher percentages have been published (2). MFS is different from other forms of GBS in its characteristic rapid onset of ophthalmoplegia, occurrence of anti-glycolipid antibodies (Anti-GQ1b antibodies) with an affinity for the oculomotor nerves and peripheral nervous system, and in its clinically good prognosis, with correction within a number of weeks to maximally months, regardless of the selected treatment. The described treatment may be symptomatic, intravenously administered immunoglobulins or plasmapheresis. If in rare cases MFS progresses to a mixed form with GBS, thus a form also with affliction of the respiratory muscles, it is designated as GBS with ophthalmoplegia (2). Ophthalmoplegia may be both total (extraocular muscles and simultaneously intraocular muscles), or extraocular muscles only. Ptosis is present in approximately only one third of cases. Similarly as in other forms of GBS, MFS is preceded by approximately two weeks mostly by respiratory or less commonly gastrointestinal infection, most often with serological occurrence of Campylobacter jejuni. Lesions also of other cranial nerves may be present, most commonly the facial nerve and the caudal bulbar nerves.

CASE REPORT

The described patient was a woman aged 71 years, being treated for hypertension (bisoprolol), hyperlipidemia (rosuvastatin) and gastroesophageal reflux (pantoprazol), under general anamnesis. Six years before this pathology she had suffered from herpes zoster in the neck and shoulder region.

Two weeks before the acute onset of the complaints in May 2015 she had suffered an illness accompanied by a cough, purulent inflammation of the conjunctivas and headache, which was considered to be sinusitis, but did not respond to the administered antibiotics (amoxicillin with conjugated linoleic acid). Headaches, strongest in the occipital lobe, did not subside, vertigo progressively appeared, with vomiting and blurred vision, and impaired ability of articulation. At an initial examination in June 2015, bilateral acute angle-closure glaucoma was diagnosed, together with total ophthalmoplegia, areflexia and ataxia. Also described in the neurological finding were bulbar syndrome, upper meningeal syndrome and neocerebellar and paleocerebellar syndrome. Predominant in the ocular finding was bilateral deterioration of vision to fingers in front of the eye, certa, with edema of both corneas and medium areactive mydriasis of both pupils. Initial intraocular pressure was immeasurably high (measurement by Tono-pen Avia). After intravenous one-off administration of 100 ml 20% Mannitol, intraocular pressure in the right eye was 54 mmHg and in the left eye 56 mmHg. Local treatment with pilocarpine, timolol, dorsolamide and dexamethasone improved intraocular pressure to the level of physiological values within the course of a few hours. Prophylactic peripheral Nd-YAG laser iridotomy (LI) was performed on both eyes two days later.

Systemic therapy covered 5 times performance of plasmapheresis, re-treatment with antibiotics, symptomatic treatment and a rehabilitation programme. Examination of spinal fluid demonstrated positivity of the antibodies GQ1b (Ig G) and GT 1a (IgG). CT angio, concordant with later performed MRI, demonstrated sinusitis on the right side, in addition MRI also showed multiple deposits of gliosis in supratentorial white matter bilaterally, attributed to vascular etiology.

Subsequent cataract surgery (in October 2015 in right eye and March 2016 in left eye, with implantation of a posterior chamber intraocular lens, improved best corrected visual acuity in the right eye from 0.5 to 1.0 and in the left eye from 0.5 to 0.8 (Fig. 1 – pseudophakia natively and in artificial mydriasis). Intraocular pressure is physiological without the need for treatment. General and local therapy led to normalisation of the neurological finding and adjustment of the ocular finding (Fig. 2 – physiological motility of eyes). The observation period is three years.

1. Pseudophakia – natively (A, B) and in artificial mydriasis (C, D)
Pseudophakia – natively (A, B) and in artificial
mydriasis (C, D)

2. Adjustment of ophthalmoplegia
Adjustment of ophthalmoplegia

METHOD

The finding on the patient was monitored continuously by means of a regular clinical examination making use of examination on a slit lamp (Nidek SL-250, Japan), biomicroscopic examination (non-contact VOLK Super Field NC lens, VOLK Optical, Ohio, USA), measurement of intraocular pressure by contact method (Tono-pen Avia), examination by indirect ophthalmoscopy (Sigma 150, Heine Optotechnik, Germany) with + 28 D lens (Ocular Instruments, Washington, USA) and photographically (retina camera Kowa VX-10α, Japan), biometric data Tomey (Tomey Corporation OA-2000 IOL cal. OPT).

In the PubMed database we used the key words Miller Fisher syndrome and glaucoma to search for references to studies on the issue in question published in journals indexed in MEDLINE.

Using the same method, in the PubMed database we used the key words acute angle-closure glaucoma and bilateral to search for references to studies describing simultaneous bilateral occurrence of acute angle-closure glaucoma.

DISCUSSION

The appearance of acute angle-closure glaucoma in MFS requires not only the occurrence of total ophthalmoplegia with bilateral mydriasis, but also predisposition of the patient in the form of age and hypermetropia. In the literature we found only four references describing acute angle-closure glaucoma in combination with MFS. Only Baxter et al. (11) in 2010 described acute angle-closure glaucoma as a bilateral ocular affliction in a 55-year-old man. Other authors described acute angle-closure glaucoma in MFS as unilateral – Brittain and Lake in 2005 in the left eye of a 64-year-old man, Ryu et al. in 2015 in the right eye of a 75-year-old man, and Han et al. in 2017 in the left eye of a 78-year-old woman (18, 120, 51). Our 71-year-old patient was also within the band of hypermetropia, axial length of the right eye was 22.38 mm, left eye 22.26 mm. According to our information, this case report is to date the second described case of a patient with simultaneous bilateral acute angle-closure glaucoma upon a background of MFS and to date the fifth described case with acute angle-closure glaucoma in this syndrome whatsoever.

Because ophthalmoplegia is an easily detected and determining symptom in MFS, from the perspective of MFS as such we could conclude the discussion here.

However, a surprisingly important factor is the issue of the very bilateral nature of acute angle-closure glaucoma, because this significantly influences both the diagnosis and the actual treatment.

If we encounter simultaneous bilateral acute angle-closure glaucoma, according to the published information there is a significant probability that this will not concern a case of primary acute angle-closure glaucoma, thus glaucoma incorporating pupillary block, as in the case in MFS, and therefore with a prompt response to the usual systemic and local anti-glaucomatous therapy covering intravenous mannitol (or peroral glycerol) and local pilocarpine, but secondary angle-closure glaucoma caused by a different mechanism, in which the usual treatment of primary angle-closure glaucoma is proving not only to be ineffective, but in many cases even worsens the condition.

In the case of this mechanism, it is possible to find swelling of the ciliary body, change of position of the lens-iris diaphragm, anterior rotation of the tips of the ciliary body, acute myopisation of the eyes, peripheral bulging of the iris and shallowing of the anterior chamber. Uveal effusion detectable by ultrasound biomicroscopy (UBM) has been described here, sometimes with signs of uveal irritation. Breach of the blood-brain barrier has also been described here (Viet Tran) (141). This finding may appear both in a systemically proceeding pathology, and also – far more frequently from the perspective of the literature – as pharmacologically iatrogenically induced. It is assumed that LI is not effective because pupillary block does not take place as such. Causal treatment is to influence the triggering causes, thus in the case of secondary effect of administered pharmaceutical its discontinuation, supporting therapy is to induce cycloplegia and local steroid treatment. With regard to the fact that pharmacologically induced bilateral acute angle-closure glaucoma has been described also in children in the case of topiramate (87, 24, 113), it is necessary to emphasise that in this mechanism, inducing cycloplegia does not directly influence myopisation (54). In terms of anterior rotation of the tips of the ciliary body and the effectiveness of local therapy with cycloplegic drugs and steroids, this mechanism is consistent with malignant glaucoma.

It is therefore necessary to divide pharmacological induction of bilateral acute angle-closure glaucoma into induction of primary acute angle-closure glaucoma (with pupillary block), thus after the administration of a pharmaceutical with a parasympatholytic or sympathomimetic effect and subsequent widening of the pupil in a predisposed individual (hypermetropia, age, prone head position), and induction of secondary acute angle-closure glaucoma following the administration of a pharmaceutical with an idiosyncratic effect, in which neither age nor original refraction of the eye play an important role.

Pharmacologically boosted or directly induced bilateral primary acute angle-closure glaucoma may occur in predisposed individuals (hypermetropia, age), most often in connection with general anaesthesia (e.g. Ates, Gayat) (7, 43), sometimes reinforced by the prone position of the head during spinal surgery (e.g. Singer) (125). It has also been described after blepharoplasty (e.g. Haverals) (53). It has further been described after local use of nasal drops (Fenox) containing phenylephrine and naphazoline (Khan) (68), or upon excessive use of cold remedies, the chief active substance of which was deadly nightshade (atropa belladonna) (Rudkin) (118), upon use of the anticholinergic drug oxybutynin (spasmolytic agent) in a predisposed individual (Haddad) (49), or ipratropium bromide either alone or in combination with salbutamol (Kola, Hall) (70, 50).

Simultaneous bilateral primary acute angle-closure glaucoma is not described often, furthermore the first authors to describe it are usually not ophthalmologists.

Pharmacologically induced secondary acute angle-closure glaucoma following the administration of a pharmaceutical and its idiosyncratic effect has been most widely described to date in the case of topiramate. This drug is used for the treatment of epilepsy (third generation anti-epileptic drug), migraine and off label as an anorectic drug. It is a sulfamate derivative of fructose, chemically classified as 2.3:4.5-bis-O-(1-methylethylidene)-ß-D-fructopyranose sulfamate. Bilateral acute angle-closure glaucoma in the case of topiramate was first described by Banta et al. in 2001 (10). We found more than forty studies (2001 – Banta, Rhee (10, 116), 2002 – Nemet (103), 2003 – Lin, Coats (87, 24), 2004 – Craig, Fraunfelder (26, 42), 2005 – Mansoor (92), 2006 – Viet Tran, Levy, Desai (141, 84, 34), 2007 – Stangler, Izambart, Guier, Parikh, Singh (131, 59, 48, 106, 126), 2008 – Aminlari, Chalam, Zalta, Boonyaleephan (5, 20, 150, 15), 2009 – Sbeity, Cruciani (121, 30), 2010 – Tahiri Joutei Hassani, Natesh, Acharya, Senthil (132, 102, 1, 122), 2011 – van Issum, Paciuc-Beja, Willet, Tanaka (139, 105, 145, 134), 2012 – Cole, Caglar, Muniesa Royo, Rodriguez-Blanco (25, 19, 100, 117), 2013 – Quagliato, Kulkarni (112, 74), 2014 – Czyz, Kamal, Reis, Rapoport, Pikkel, Katsimpris, Mitra (31, 63, 115, 113, 110, 64, 97), 2015 – Grewal, Dhar (45, 35), 2016 – Behl, Beaudry (14, 12), 2017 – Joshi, Lan, Meijer (61, 78, 95)), including cases of described incidence in children (Lin, Coats, Rapoport) (87, 24, 113).

Another large group of pharmaceuticals, also of compounds containing sulphur, in which an idiosyncratic effect of administration of the drug and induction of bilateral secondary acute angle-closure glaucoma by this mechanism has been described, is the group of sulphonamides.

Sulphonamides constitute a broad group of pharmaceuticals, including not only drugs with an antimicrobial effect, but also antidiabetic drugs on the basis of sulphonylurea, diuretics, anti-convulsive drugs, antiviral drugs and other substances, such as the anti-glaucomatous agents used in ophthalmology brinzolamide and dorsolamide. Tamsulosin, which increases the difficulty of cataract surgery by inducing a condition designated as IFIS (intraoperative floppy iris syndrome), is also a sulphonamide derivative.

Secondary acute angle-closure glaucoma has been most frequently described in the case of sulphonamides with a diuretic effect, in the case of acetazolamide (Grigera, Mancino, Malagola, Lee GC, Parthasarathi, Senthil) (46, 91, 90, 79, 107, 122), furosemide (Bondaoui) (15), hydrochlorothiazide (Chen, Geanon, Lee GC) (22, 44, 79), methazolamide (Aref, Kwon) (6, 77), indapamide (Senthil) (122) and chlorthalidone (Durai, Singer) (36, 124). In the case of sulphonamides with an anti-inflammatory effect, it has been described in connection with sulfasalazine in combination with trimethoprim (Lee GC) (79), in sulphonamides with an antimicrobial effect in the case of sulfamethoxazole (Spadoni, Waheeb) (128, 143), in sulphonamides with an anti-convulsive effect in the case of zonisamide (Weiler) (144), and also in the anti-migraine drug sumatriptan (Hsu) (55).

In the case of drugs used as antidepressants, secondary acute angle-closure glaucoma has been described in connection with venlafaxin (serotonin and norardrenaline reuptake inhibitor, SNRI) (de Guzman, Ezra, Ng) (32, 38, 104), duloxetine (SNRI) (Shifera, Mahmut) (123, 89), trazodone (serotonin reuptake inhibitor, SRI) (Hrčková) (54), citalopram and escitalopram (selective serotonin reuptake inhibitor, SSRI) (Croos, Massaoutis, Zelefsky (28, 93, 152), paroxetine (SRI) (Kirwan, Levy) (69, 85) and bupropion (aminoketone) (Takusagawa) (133). Acute angle-closure glaucoma has also been described in the case of tramadol (SNRI), which is used as a painkilling drug (Mahmoud) (88).

Secondary acute angle-closure glaucoma has been described in the case of two different serotonin agonists, namely the anti-migraine drug zolmitriptan (Lee JTL) (80) and the anorectic drug dexfenfluramine (Denis) (33).

We present other substances linked with secondary bilateral acute angle-closure glaucoma only in alphabetical order: cabergoline (lactation suppressor) (Razmjoo) (114), cyclosporine (Braun) (17), ecstasy (3.4-methylenedioxymethamphetamine (MDMA)) (Kumar, Trittibach) (76, 137), the plant ephedra (Ma-huang) (natural source of ephedrine) in a natural compound for slimming (Ryu) (119), ephedrine and phendimetrazine (anorectic drug) (Lee W) (82), flavoxate (spasmolytic agent for urinary tract) used on a patient already using indapamide (Mohammed) (98), flucloxacillin and carbamazepine (Chan) (21), isoretinoin (acne treatment) (Park) (108), mefenamic acid (Vishwakarma) (142), olsetamivir (Tamiflu), neuraminidase inhibitor (Lee JW, Yazdani) (81, 149), methylsulfonylmethane (MSM), used as a food supplement and source of biologically bound sulphur (Hwang) (57) and a poisonous bite from a further unspecified Indian snake (Srinivasan) (130).

Bilateral secondary angle-closure glaucoma in connection with change of position of the ciliary body due to its swelling has been described also in the case of systemic tumours, inflammatory and infectious diseases.

In the case of systemic tumorous pathologies, it has been described in connection with Hodgkin’s lymphoma (Belz, Baillif) (13, 9), lymphoma (Cristol) (27), myelofibrosis (Lin) (86) and myelodysplastic syndrome (Smith) (129).

In the case of systemic inflammatory pathologies it has been described in connection with leukocytoclastic vasculitis (Guerriero) (47), systemic lupus erythematodes (Han) (52), large cell arteritis (Hunter) (56), Wegener’s granulomatosis (Mete) (96) and several times in the case of Vogt-Koyanagi-Harada syndrome (Eibschitz-Tsimhoni, Forster, Yang, Yao) (37, 41, 147, 148).

In the case of systemic infectious pathologies it has been described in connection with acute retinal necrosis (Kaushik) (66), infection by Campylobacter iejuni (Mukherji) (99) herpes zoster (al Halel) (4), HIV infection and AIDS (Fineman, Joshi, Koster, Krzystolik, Meige, Nash, Ullman, Zambarakji) (39, 62, 71, 72, 94, 101, 138, 151), in haemorrhagic fevers – Dengue fever (Joob, Levaggi, Pierre Filho Pde) (60, 83, 109), Korean haemorrhagic fever and haemorrhagic fevers caused by hantavirus (Cho, Zimmermann) (23, 153). We do not have any explanation for the fact that in the case of HIV – AIDS infection all the studies came within a relatively short time interval, from 1986 (Ullman) (138) to 1997 (Fineman) (39).

To complete the list it is necessary to add that secondary bilateral angle-closure glaucoma has also been described in the case of congenital developmental defects, repeatedly in the case of bilateral and multiple occurrence of ciliary cysts (Azuara-Blanco, Tanihara, Kuchenbecker, Viestenz, Badlani, Crowston, Katsimpris) (3, 135, 73, 140, 8, 29, 65)) and sporadically in other congenital defects – Alagille syndrome (Potamitis) (111), spherophakia and Weill-Marchesani syndrome (Kaushik, Wright) (67, 146). It has also been described in iridoschisis (Iaccarino, Torricelli) (58, 136). It has also once been described in the case of phacomorphic glaucoma in the first identification of type 1 diabetes mellitus (Skrabic) (127) and as the first symptom of primary pulmonary hypertension (Kunjukunju) (75).

CONCLUSION

The Miller Fisher syndrome is a post-infection, self-limiting, immunity mediated pathology from the group of Guillain-Barré syndrome, which has a good prognosis. If total ophthalmoplegia in a patient of risk age with hypermetropia appears upon the background of Miller Fisher syndrome, this may lead to primary acute angle-closure glaucoma, either unilateral or bilateral. With regard to pupillary block, ocular treatment is standard.

If an ophthalmologist encounters simultaneous bilateral acute angle-closure glaucoma, it is necessary to evaluate the patient’s overall condition of health, the pharmaceuticals used, and in differential diagnostics not to overlook secondary acute angle-closure glaucoma.

Presented at the 26th annual congress of the Czech Ophthalmology Association, Czech Medical Association of J. E. Purkyně in Prague, 13-15 September 2018

The authors of the study declare that no conflict of interest exists in the compilation, theme and subsequent publication of this professional communication, and that it is not supported by any pharmaceuticals company.

Supported by a project (Ministry of Health) for conceptual development of research organisation 00064203 (Motol University Hospital) and CZ.2.16/3.1.00/24022

Received: 6. 5. 2019

Accepted: 26. 7. 2019

Available on-line: 6.1.2020

MUDr. Jana Štěpánková

Oční klinika dětí a dospělých FNM

V Úvalu 84,

150 08 Praha 5 - Motol

jana.stepankova@lfmotol.cuni.cz


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