Klin Monbl Augenheilkd 2020; 237(04): 431-440
DOI: 10.1055/a-1081-1683
Kasuistik
Georg Thieme Verlag KG Stuttgart · New York

Advanced Cases of Birdshot HLA-A29 Retinochoroiditis: Prevalence and Characteristics

Fortgeschrittene Fälle von Birdshot-HLA-A29-Retinochoroiditis: Prävalenz und Eigenschaften
Sina Elahi
1   Ophthalmology, Centre dʼOphtalmologie Spécialisée, Lausanne, Switzerland
,
Vania Lages
2   Ophthalmology, Centro Hospitalar do Porto, Porto, Portugal
,
Bruno Jeannin
3   Retinal and Inflammatory Eye Diseases, Centre for Ophthalmic Specialized Care (COS), Clinic Montchoisi Teaching Centre, Lausanne, Switzerland
,
Carl Peter Herbort
1   Ophthalmology, Centre dʼOphtalmologie Spécialisée, Lausanne, Switzerland
3   Retinal and Inflammatory Eye Diseases, Centre for Ophthalmic Specialized Care (COS), Clinic Montchoisi Teaching Centre, Lausanne, Switzerland
› Author Affiliations
Further Information

Publication History

received 25 September 2019

accepted 07 December 2019

Publication Date:
24 April 2020 (online)

Abstract

Purpose To establish the prevalence, morphological, and functional characteristics and evolution of advanced cases of birdshot retinochoroiditis (BRC).

Methods A retrospective review of all BRC cases seen at the Centre for Ophthalmic Specialized Care, Lausanne, Switzerland, with at least 3 years of follow-up since the onset of symptoms. The following parameters were evaluated: demographic characteristics, best-corrected visual acuity (BCVA), fundus photographs, fluorescein (FA) and indocyanine green (ICGA) angiography frames, and visual field evaluation from initial visit to last follow-up.

Results Out of the 1920 patients with uveitis who were followed from 1995 until 2018, 32 (1.67%) were diagnosed with BRC; 20 of these 32 patients had sufficient data to be included. Three of these twenty patients (15.0%) had severe forms of the disease. Two patients had received insufficient treatment and one progressed despite attempted maximal therapy. The mean BCVA was 0.62 (± 0.42) at presentation, which was already at an advanced stage of the disease, and 0.51 (± 0.37) at last follow-up. The average visual field mean defect (VFMD) was 19.65 (± 4.71 dB) at presentation and 21.40 (± 2.45 dB) at last follow-up. Choroidal inflammatory activity monitored by ICGA decreased from 10.67 (± 9.18) at presentation to 6.67 (± 5.61) at last follow-up. FA revealed mild retinal vasculitis at 6.50 (± 4.76), which remained stable to 4.67 (± 3.20). EDI-OCT estimated choroidal thickness (EDI-OCT-CT) measurements were 246.36 (± 116.93 µm) at presentation and 231.30 (± 120.70 µm) at the last follow-up.

Conclusions In our setting, 15% of BRC cases had a severe course and suffered extensive irreversible chorioretinal damage, obviously due to insufficient treatment in two cases. This underlines the importance of correctly diagnosing BRC and initiating therapy as promptly as possible to avoid such outcomes in an otherwise possibly controllable disease.

Zusammenfassung

Ziel Das Ziel war es, die Prävalenz, morphologische und funktionelle Eigenschaften und die Entwicklung fortgeschrittener Fälle von Birdshot-Retinochoroiditis (BRC) zu bestimmen.

Methode Eine retrospektive Überprüfung aller BRC-Fälle eines Zentrums für Augenheilkunde, Lausanne, Schweiz, mit mindestens 3 Jahren Follow-up seit dem Beginn von Symptomen. Die folgenden Parameter wurden bewertet: demografische Eigenschaften, bestkorrigierte Sehschärfe, Fundusbilder, Fluorescein- und Indocyaningrün-Angiografie sowie Gesichtsfeldauswertung vom 1. Besuch bis zum letzten Follow-up.

Ergebnisse Von den 1920 Patienten mit Uveitis, die von 1995 bis 2018 beobachtet wurden, wurde bei 32 (1,67%) Patienten eine Birdshot-Diagnose gestellt; 20 dieser 32 Patienten hatten ausreichende Daten, um eingeschlossen werden zu können. Drei dieser 20 Patienten (15,0%) hatten schwere Formen der Krankheit. Zwei Patienten hatten eine unzureichende Behandlung erhalten und bei 1 Patienten schritt die Entzündung trotz des Versuchs der maximalen Therapie fort. Der mittlere Visus betrug bei Präsentation 0,62 (± 0,42) bei Patienten, die bereits in einem fortgeschrittenen Stadium der Krankheit waren, und 0,51 (± 0,37) bei der letzten Nachuntersuchung. Der durchschnittliche Gesichtsfeldmittelwertdefekt (VFMD) betrug bei Präsentation 19,65 (± 4,71 dB) und 21,40 (± 2,45 dB) bei der letzten Nachuntersuchung. Der Aderhautentzündungsscore, durch ICGA monitoriert, nahm von 10,67 (± 9,18) bei Präsentation auf 6,67 (± 5,61) ab bei der letzten Nachuntersuchung. Die FA zeigte eine leichte Netzhautvaskulitis, deren Score leicht abnahm unter Therapie: 6,50 (± 4,76) vs. 4,67 (± 3,20). Die mit EDI-OCT gemessenen Dicken der Aderhaut (EDI-OCT-CT) betrugen 246,36 (± 116,93 µm) bei Präsentation und 231,30 (± 120,70 µm) bei der letzten Nachuntersuchung.

Schlussfolgerungen In unserem Krankengut erlitten 15% der BRC-Fälle schwere, umfangreiche, irreversible, chorioretinale Schäden, offensichtlich aufgrund unzureichender Behandlung in 2 Fällen und schlechter Compliance in 1 Fall. Dies unterstreicht, wie wichtig es ist, bei  BRC eine schnelle Diagnose zu stellen und eine prompte Therapie zu starten, um eine solche schädliche Entwicklung zu vermeiden bei einer ansonsten möglicherweise kontrollierbaren Krankheit.

 
  • References

  • 1 Franceschetti A, Babel J. [Chorioretinitis with “candle spots,” a manifestation of Besnier-Boeck disease]. Ophthalmologica 1949; 118: 701-710
  • 2 Ryan SJ, Maumenee AE. Birdshot retinochoroidopathy. Am J Ophthalmol 1980; 89: 31-45
  • 3 Gass JD. Vitiliginous chorioretinitis. 1981. Retina 2003; 23 (6 Suppl): 1778-1787
  • 4 Papadia M, Herbort CP. Reappraisal of birdshot retinochoroiditis (BRC): a global approach. Graefes Arch Clin Exp Ophthalmol 2013; 251: 861-869
  • 5 Guex-Crosier Y, Herbort CP. Prolonged retinal arterio-venous circulation time by fluorescein but not by indocyanine green angiography in birdshot chorioretinopathy. Ocul Immunol Inflamm 1997; 5: 203-206
  • 6 Gasch AT, Smith JA, Whitcup SM. Birdshot retinochoroidopathy. Br J Ophthalmol 1999; 83: 241-249
  • 7 Baarsma GS, Priem HA, Kijlstra A. Association of birdshot retinochoroidopathy and HLA-A29 antigen. Curr Eye Res 1990; 9 (Suppl) 63-68
  • 8 Brezin AP, Monnet D, Cohen JH. et al. HLA-A29 and birdshot chorioretinopathy. Ocul Immunol Inflamm 2011; 19: 397-400
  • 9 LeHoang P, Ozdemir N, Benhamou A. et al. HLA-A29.2 subtype associated with birdshot retinochoroidopathy. Am J Ophthalmol 1992; 113: 33-35
  • 10 Nussenblatt RB, Mittal KK, Ryan S. et al. Birdshot retinochoroidopathy associated with HLA-A29 antigen and immune responsiveness to retinal S-antigen. Am J Ophthalmol 1982; 94: 147-158
  • 11 Wender JD, Fu AD, Jumper JM. et al. False negative antibody-based HLA-A29 typing in two patients with birdshot chorioretinopathy. Br J Ophthalmol 2008; 92: 1153-1154
  • 12 Herbort CP, Mantovani A, Papadia M. Use of indocyanine green angiography in uveitis. Int Ophthalmol Clin 2012; 52: 13-31
  • 13 Papadia M, Herbort CP. New concepts in the appraisal and management of birdshot retinochoroiditis, a global perspective. Int Ophthalmol 2015; 35: 287-301
  • 14 Herbort CP, Pavesio C, LeHoang P. et al. Why birdshot retinochoroiditis should rather be called ʼHLA-A29 uveitisʼ?. Br J Ophthalmol 2017; 101: 851-855
  • 15 Herbort CP, Probst K, Cimino L. et al. Differential inflammatory involvement in retina and choroid in birdshot chorioretinopathy. Klin Monatsbl Augenheilkd 2004; 221: 351-356
  • 16 Herbort CP, Papadia M, Mantovani A. Classification of choroiditis based on inflammatory lesion process rather than fundus appearance: enhanced comprehension through the ICGA concepts of the iceberg and jellyfish effects. Klin Monatsbl Augenheilkd 2012; 229: 306-313
  • 17 Skvortsova N, Gasc A, Jeannin B. et al. Evolution of choroidal thickness over time and effect of early and sustained therapy in birdshot retinochoroiditis. Eye (Lond) 2017; 31: 1205-1211
  • 18 Nussenblatt RB, Whitcup SM, Palestine AG. Birdshot retinochoroidopathy. In: Nussenblatt RB, Whitcup SM, Palestine AG. eds. Uveitis, Fundamentals and Clinical Practice. Second ed. St. Louis: Mosby; 1996: 325-333
  • 19 Priem HA, Oosterhuis JA. Birdshot chorioretinopathy: clinical characteristics and evolution. Br J Ophthalmol 1988; 72: 646-659
  • 20 Rothova A, Berendschot TT, Probst K. et al. Birdshot chorioretinopathy: long-term manifestations and visual prognosis. Ophthalmology 2004; 111: 954-959
  • 21 Cervantes-Castaneda RA, Gonzalez-Gonzalez LA, Cordero-Coma M. et al. Combined therapy of cyclosporine A and mycophenolate mofetil for the treatment of birdshot retinochoroidopathy: a 12-month follow-up. Br J Ophthalmol 2013; 97: 637-643
  • 22 Kiss S, Ahmed M, Letko E. et al. Long-term follow-up of patients with birdshot retinochoroidopathy treated with corticosteroid-sparing systemic immunomodulatory therapy. Ophthalmology 2005; 112: 1066-1071
  • 23 Knecht PB, Papadia M, Herbort CP. Early and sustained treatment modifies the phenotype of birdshot retinochoroiditis. Int Ophthalmol 2014; 34: 563-574
  • 24 de Courten C, Herbort CP. Potential role of computerized visual field testing for the appraisal and follow-up of birdshot chorioretinopathy. Arch Ophthalmol 1998; 116: 1389-1391
  • 25 Thorne JE, Jabs DA, Kedhar SR. et al. Loss of visual field among patients with birdshot chorioretinopathy. Am J Ophthalmol 2008; 145: 23-28
  • 26 Lages V, Skvortsova N, Jeannin B. et al. Low-grade “benign” birdshot retinochoroiditis: prevalence and characteristics. Int Ophthalmol 2019; 39: 2111-2120
  • 27 Fabro F, Herbort CP. Need for Quantitative Measurement Methods for Posterior Uveitis: Comparison of Dual FA/ICGA Angiography, EDI-OCT Choroidal Thickness and SUN Vitreous Haze Evaluation in Stromal Choroiditis. Klin Monatsbl Augenheilkd 2018; 235: 424-435
  • 28 Tugal-Tutkun I, Herbort CP, Khairallah M. et al. Interobserver agreement in scoring of dual fluorescein and ICG inflammatory angiographic signs for the grading of posterior segment inflammation. Ocul Immunol Inflamm 2010; 18: 385-389
  • 29 Trusko B, Thorne J, Jabs D. et al. The Standardization of Uveitis Nomenclature (SUN) Project. Development of a clinical evidence base utilizing informatics tools and techniques. Methods Inf Med 2013; 52: 259-265 S1–S6
  • 30 Fuerst DJ, Tessler HH, Fishman GA. et al. Birdshot retinochoroidopathy. Arch Ophthalmol 1984; 102: 214-219
  • 31 Oh KT, Christmas NJ, Folk JC. Birdshot retinochoroiditis: long term follow-up of a chronically progressive disease. Am J Ophthalmol 2002; 133: 622-629
  • 32 Leder HA, Galor A, Thorne JE. et al. Disappearance of classic birdshot spots after immunosuppression with tacrolimus and mycophenolate mofetil. Br J Ophthalmol 2008; 92: 291
  • 33 Artornsombudh P, Gevorgyan O, Payal A. et al. Infliximab treatment of patients with birdshot retinochoroidopathy. Ophthalmology 2013; 120: 588-592
  • 34 Balci O, Gasc A, Jeannin B. et al. Enhanced depth imaging is less suited than indocyanine green angiography for close monitoring of primary stromal choroiditis: a pilot report. Int Ophthalmol 2017; 37: 737-748
  • 35 Balci O, Jeannin B, Herbort CP. Contribution of dual fluorescein and indocyanine green angiography to the appraisal of posterior involvement in birdshot retinochoroiditis and Vogt-Koyanagi-Harada disease. Int Ophthalmol 2018; 38: 527-539
  • 36 Cao JH, Silpa-Archa S, Freitas-Neto CA. et al. Birdshot chorioretinitis lesions on indocyanine green angiography as an indicator of disease activity. Retina 2016; 36: 1751-1757
  • 37 Fardeau C, Herbort CP, Kullmann N. et al. Indocyanine green angiography in birdshot chorioretinopathy. Ophthalmology 1999; 106: 1928-1934
  • 38 Papadia M, Herbort CP. Indocyanine green angiography (ICGA) is essential for the early diagnosis of birdshot chorioretinopathy. Klin Monatsbl Augenheilkd 2012; 229: 348-352
  • 39 Elahi S, Gillmann K, Gasc A. et al. Sensitivity of indocyanine green angiography compared to fluorescein angiography and enhanced depth imaging optical coherence tomography during tapering and fine-tuning of therapy in primary stromal choroiditis: A case series. J Curr Ophthalmol 2019; 31: 180-187 doi:10.1016/j.joco.2018.12.006
  • 40 Willermain F, Greiner K, Forrester JV. Atypical end-stage birdshot retinochoroidopathy. Ocul Immunol Inflamm 2003; 11: 305-307