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Arteritic Anterior Ischemic Optic Neuropathy Associated with Giant Cell Arteritis in an Elderly Korean Man

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239

Karen Kar-Wun Chan

Hospital Authority, Hong Kong

Jonathan Chun-Ho Ho, Irene Tak-Yee Yeung, Simon Tak-Chuen Ko

Department of Ophthalmology, Tung Wah Eastern Hospital, Hong Kong

E-mail (Jonathan Chun-Ho Ho): [email protected]

Conflict of Interest

No potential conflict of interest relevant to this article was reported.

References

1. Feldmann J, Prieur AM, Quartier P, et al. Chronic infantile neurological cutaneous and articular syndrome is caused

by mutations in CIAS1, a gene highly expressed in poly- morphonuclear cells and chondrocytes. Am J Hum Genet 2002;71:198-203.

2. Dollfus H, Hafner R, Hofmann HM, et al. Chronic infan- tile neurological cutaneous and articular/neonatal onset multisystem inflammatory disease syndrome: ocular mani- festations in a recently recognized chronic inflammatory disease of childhood. Arch Ophthalmol 2000;118:1386-92.

3. Terrada C, Neven B, Boddaert N, et al. Ocular modifica- tions in a young girl with cryopyrin-associated periodic syndromes responding to interleukin-1 receptor antagonist anakinra. J Ophthalmic Inflamm Infect 2011;1:133-6.

4. Espandar L, Boehlke CS, Kelly MP. First report of keratitis in familial cold autoinflammatory syndrome. Can J Oph- thalmol 2014;49:304-6.

Arteritic Anterior Ischemic Optic Neuropathy Associated with Giant Cell Arteritis in an Elderly Korean Man

Dear Editor,

Giant cell arteritis (GCA), also known as temporal arte- ritis, is a systemic autoimmune disease primarily affecting the elderly. It is characterized by granulomatous inflam- mation of large and medium-sized arteries [1]. Arteritic anterior ischemic optic neuropathy (AAION) is the most common type of ophthalmic complication of GCA, and can cause permanent visual loss [2]. Therefore, AAION represents a true ophthalmic emergency, because the pos- sibility of visual loss is very high if it is not recognized and treated promptly [3]. There have been few reports of GCA among Asians, and only one involving a patient with silent GCA-associated AAION in Korea [2]. Herein, we report a case of GCA-associated AAION with typical systemic

GCA symptoms in an elderly Korean man, as confirmed by temporal artery biopsy.

A 70-year-old man presented with sudden vision loss in his right eye (oculus dexter, OD), which had occurred the previous day. He had been suffering headaches for several months, and anorexia, general weakness and scalp tender- ness were also noted during this period. His best-corrected visual acuity (VA) was 10 / 20 in OD and 20 / 20 in the left eye (oculus sinister, OS). A relative afferent pupillary de- fect was also noted in OD and intraocular pressure was 14 mmHg in OD, 12 mmHg in OS. Both eyes were freely movable and non-tender upon eye movement. A chalky white swelling in OD was discovered upon fundus exam- ination (Fig. 1A), and visual field testing (Humphrey HFA II; Carl Zeiss Meditec, Jena, Germany) revealed a near to- tal field defect in the same eye. The Hardy-Rand-Rittler test showed total dyschromatopsia in OD and fluorescein angiography revealed delayed filling of the vertical water- shed zone at the adjacent nasal peripapillary choroid and optic disc leakage at late phase. The patient’s body tem- perature was 38.3°C and white blood cell count was 12,900/mm

3

. C-reactive protein levels, as well as the eryth- rocyte sedimentation rate, were also elevated to be 14.5

Korean J Ophthalmol 2016;30(3):239-241

http://dx.doi.org/10.3341/kjo.2016.30.3.239

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Korean J Ophthalmol Vol.30, No.3, 2016

mg/dL (upper normal limit, 0.5 mg/dL) and 108 mm/hr (upper normal limit, 20 mm/hr), respectively. The patient was admitted on the presumption of GCA with AAION, although we could not completely rule out systemic infec- tion, because AAION is very rare in Korea. For this rea- son, we systematically evaluated potential foci of infec- tion, and the patients was administered intravenous empirical antibiotics.

After 2 days, the patient’s VA in OD had decreased to finger-count. Disc swelling remained, and a disc hemor- rhage had newly developed. Computed tomography of the chest and abdomen revealed no definitive infection focus.

We planned temporal artery ultrasonography and bi- opsy, and the patient was referred to the Department of Rheumatology.

On hospital day 5, temporal artery ultrasonography re- vealed no evidence of temporal arteritis. The intravenous antibiotics were stopped, and a once-daily course of intra- venous methylprednisolone (62.5 mg) was started. A biop- sy was performed at the right temporal artery. It showed an intimal thickening and inflammatory cells within the media of arterial wall (Fig. 1B and 1C). GCA was thereby confirmed and intravenous steroid therapy was maintained.

The C-reactive protein and erythrocyte sedimentation rate

level had both decreased after 3 days of steroid treatment, to 2.86 mg/dL and 79 mm/hr, respectively.

On hospital day 13, the patient’s VA OD had improved to 6 / 20, and disc swelling had decreased. His general con- dition had also improved. Oral prednisolone therapy was slowly tapered from 60 mg per day to 15 mg per day. How- ever, after 1 month, the patient’s VA OD had decreased to 3 / 20, and visual field testing showed a progressed visual field defect. What is more, pale optic disc in OD was found upon fundus examination (Fig. 1D). Optical coherence to- mography revealed decreased macular ganglion cell layer thickness in OD. OS had not been affected.

In summary, we presents a case of AAION with typical systemic symptoms of GCA and pathological findings of diffuse inflammatory cell infiltration of the temporal ar- tery in an elderly Korean man. To our knowledge, there has only been one other report of a biopsy confirmed case of GCA-related AAION in Korea [2]. However, unlike our patient, the previous report involve silent GCA with no systemic symptoms. Therefore, this is the first biopsy con- firmed report of GCA-associated AAION with typical sys- temic symptoms of GCA in Korea.

In conclusion, although GCA-associated AAION is very rare in Koreans, it can indeed occur. A rapid diagnostic Fig. 1. (A) Fundus photograph taken at initial examination of the right eye shows a chalky, white disc swelling. (B,C) Histopathology presentations of a right temporal arterial biopsy. (B) Diffuse thickening of the intima and fragmentation of the internal elastic lamina of the arterial wall (elastin stain, ×40). (C) Inflammatory cells within the arterial wall, especially in the media (H&E, ×40). (D) After 1 month of treatment, a pale optic disc was found in the right eye.

A

C

B

D

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241 work-up involving erythrocyte sedimentation rate,

C-reactive protein and temporal artery biopsy, as well as prompt corticosteroid treatment, may be necessary to save the vision in the affected eye, and to prevent the involve- ment of the other eye.

Yeon-Soo Kang, Sang-Woo Park

Department of Ophthalmology, Chonnam National University Hospital, Chonnam National University Medical School, Gwangju, Korea

Ho-Kyun Lee

Department of Surgery, Chonnam National University Hospital, Chonnam National University Medical School, Gwangju, Korea

Yoo-Duk Choi

Department of Pathology, Chonnam National University Hospital, Chonnam National University Medical School, Gwangju, Korea

Hwan Heo

Department of Ophthalmology, Chonnam National University Hospital, Chonnam National University Medical School, Gwangju, Korea

E-mail: [email protected]

Conflict of Interest

No potential conflict of interest relevant to this article was reported.

References

1. Chacko JG, Chacko JA, Salter MW. Review of giant cell arteritis. Saudi J Ophthalmol 2015;29:48-52.

2. Cha DM, Lee T, Choe G, et al. Silent giant cell arteritis in an elderly Korean woman. Korean J Ophthalmol 2013;27:

224-7.

3. Rahman W, Rahman FZ. Giant cell (temporal) arteritis: an

overview and update. Surv Ophthalmol 2005;50:415-28.

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