Your browser doesn't support javascript.
loading
Presumed atypical peripapillary Vogt-Koyanagi-Harada disease.
Abucham-Neto, Julio Zaki; Masson, Andressa Passos; Nascimento, Priscila Alves; Barbosa Ferraz, Aline Alves; Cunha de Souza, Eduardo.
Afiliação
  • Abucham-Neto JZ; Medical Faculty of the ABC - Faculdade de Medicina do ABC, Av. Príncipe de Gales, 821, Santo André, SP, Brazil.
  • Masson AP; Medical Faculty of the ABC - Faculdade de Medicina do ABC, Av. Príncipe de Gales, 821, Santo André, SP, Brazil.
  • Nascimento PA; Medical Faculty of the ABC - Faculdade de Medicina do ABC, Av. Príncipe de Gales, 821, Santo André, SP, Brazil.
  • Barbosa Ferraz AA; Medical Faculty of the ABC - Faculdade de Medicina do ABC, Av. Príncipe de Gales, 821, Santo André, SP, Brazil.
  • Cunha de Souza E; University of Sao Paulo Hospital of Clinics - Universidade de São Paulo, Av. Dr. Enéas Carvalho de Aguiar, 255, São Paulo, SP, Brazil.
Am J Ophthalmol Case Rep ; 16: 100548, 2019 Dec.
Article em En | MEDLINE | ID: mdl-31517139
ABSTRACT

PURPOSE:

To describe a case of bilateral presumed atypical Harada disease with sequential, not simultaneous, involvement of the peripapillary retina (subretinal fluid) in a healthy patient with no systemic complaints. OBSERVATION A 35-year-old healthy white man presented with sudden paracentral visual loss in the left eye. His medical history was unremarkable. However, he reported a similar episode 20 months earlier in the right eye that was associated with macular serous retinal detachment. The right eye showed evidence of reactive peripapillary atrophy and pigmentary alteration in the macula. Optical coherence tomography scans of the posterior left eye segment revealed a diffuse thickened choroid, papillomacular subretinal exudate and discontinuity of the ellipsoid layer with suggestion of vitreous cellularity. Autofluorescence imaging of the left eye showed peripapillary hyperautofluorescence. A fluorescein angiogram revealed progressive staining and pooling of the peripapillary retina with corresponding retinal vasculitis. Indocyanine green angiography revealed multiple hypocyanescent lesions with an area of hypercyanescence temporal to the disc. Rheumatologic evaluation and laboratory tests were all negative. Chest tomography was normal. Considering the apparent absence of infectious diseases, the patient was started on 60 mg/day prednisone. After 8 days, visual acuity improved to 20/250, improving to 20/20 vision six months after a slow steroid wean.

CONCLUSION:

We believe our case represented a variant of the Vogt-Koyanagi-Harada syndrome in an atypical situation, because the patient fulfilled the presumed criteria. Furthermore, the findings of clinical and complementary examinations led to this nosological entity to the exclusion of others. IMPORTANCE The point of this case is to alert ophthalmologists to the existence of this atypical presentation of the disease so that it should be included among the differential diagnoses of pathologies that present with these findings.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article