Literature DB >> 26222111

Idiopathic polypoidal choroidal vasculopathy masquerading as choroidal tumors: one year follow-up of a peripheral lesion.

Rony Carlos Preti1, Mario Luiz Ribeiro Monteiro1, Celso Morita1, John Helal Junior1, Leandro Cabral Zacharias1, Daniel Araújo Ferraz1, David E Pelayes2, Walter Yukihiko Takahashi1.   

Abstract

This case report describes peripheral idiopathic polypoidal choroidal vasculopathy (IPCV) with a collection of small aneurysmal dilations that masqueraded as choroidal tumors in an elderly patient. A 68-year-old African American woman was referred to us with a suspected diagnosis of asymptomatic vascular choroidal tumor and choroidal capillary hemangioma, affecting the temporal peripheral fundus. Upon examination, optical coherence tomography (OCT) revealed two large hemorrhagic pigment epithelium detachments (PED), and indocyanine green angiography (ICG) confirmed the diagnosis of IPCV. One year later, there was reduction in the hemorrhagic pigment epithelium detachments and the lesion took on a different appearance, resembling a choroidal osteoma. No treatment was necessary despite the presence of multiple polyps. IPCV is a rare condition that can resemble other choroidal diseases depending on the stage of presentation. OCT is the best tool to determine the characteristics of the lesions, and indocyanine green angiography should be used to confirm the diagnosis. Not all cases require treatment.

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Year:  2015        PMID: 26222111     DOI: 10.5935/0004-2749.20150048

Source DB:  PubMed          Journal:  Arq Bras Oftalmol        ISSN: 0004-2749            Impact factor:   0.872


  1 in total

1.  [Unclear serous retinal detachment].

Authors:  M Alnawaiseh; G Wirths; L Lahme; P Nelis; N Eter
Journal:  Ophthalmologe       Date:  2017-10       Impact factor: 1.059

  1 in total

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