Purpose. To report favorable outcome of a case of acute posterior multifocal placoid pigment epitheliopathy (APMPPE) associated with cerebral vasculitis after treatment with immunosuppressive therapy by mitoxantrone. Design. Single case report. Method. A 22-year-old man presented with acute isolated bilateral loss of vision revealing APMPPE. Corticosteroid therapy was initiated and visual acuity gradually improved. Seventeen days later, visual function deteriorated again, associated with flu-like syndrome and severe headaches. A relapse of APMPPE was diagnosed, complicated with lymphocytic meningitis and cerebral ischemia. Intravenous therapy with mitoxantrone was performed in combination with methylprednisolone. Results. Headaches disappea...
Purpose To report a case with acute posterior multifocal placoid pigment epitheliopathy (APMPPE)-lik...
PURPOSE: Acute posterior multifocal placoid pigment epitheliopathy (APMPPE) is an acquired inflammat...
Acute multifocal placoid pigment epitheliopathy (AMPPE) is an autoimmune chorioretinal disease that ...
Purpose. To report favorable outcome of a case of acute posterior multifocal placoid pigment epithel...
APMPPE is a cause of rapid bilateral loss of vision in young adults found to have multifocal choroid...
A 21-year-old man experienced unilateral vision loss associated with multiple atrophic chorioretinal...
Artículo de publicación ISIAcute posterior multifocal placoid pigment epitheliopathy (APMPPE) is a c...
The purpose of this study was to report the rare presentation of bilateral acute posterior multifoca...
In this paper, we report a 43-year-old male patient presented with sudden decreased vision of both e...
Abstract Background Acute posterior multifocal placoid pigment epitheliopathy (APMPPE) is a rare inf...
WOS: 000305320400036In this paper, we report a 43-year-old male patient presented with sudden decrea...
Purpose: To report the functional and anatomic features of a case of acute posterior multifocal plac...
Purpose: To describe clinical characteristics and visual and anatomic outcomes of a syndrome clinica...
A 26-year-old man developed sequential left-sided numbness, left hand clumsiness, severe headache, a...
Abstract Background Acute Posterior Multifocal Placoid Pigment Epitheliopathy (APMPPE) is a rare inf...
Purpose To report a case with acute posterior multifocal placoid pigment epitheliopathy (APMPPE)-lik...
PURPOSE: Acute posterior multifocal placoid pigment epitheliopathy (APMPPE) is an acquired inflammat...
Acute multifocal placoid pigment epitheliopathy (AMPPE) is an autoimmune chorioretinal disease that ...
Purpose. To report favorable outcome of a case of acute posterior multifocal placoid pigment epithel...
APMPPE is a cause of rapid bilateral loss of vision in young adults found to have multifocal choroid...
A 21-year-old man experienced unilateral vision loss associated with multiple atrophic chorioretinal...
Artículo de publicación ISIAcute posterior multifocal placoid pigment epitheliopathy (APMPPE) is a c...
The purpose of this study was to report the rare presentation of bilateral acute posterior multifoca...
In this paper, we report a 43-year-old male patient presented with sudden decreased vision of both e...
Abstract Background Acute posterior multifocal placoid pigment epitheliopathy (APMPPE) is a rare inf...
WOS: 000305320400036In this paper, we report a 43-year-old male patient presented with sudden decrea...
Purpose: To report the functional and anatomic features of a case of acute posterior multifocal plac...
Purpose: To describe clinical characteristics and visual and anatomic outcomes of a syndrome clinica...
A 26-year-old man developed sequential left-sided numbness, left hand clumsiness, severe headache, a...
Abstract Background Acute Posterior Multifocal Placoid Pigment Epitheliopathy (APMPPE) is a rare inf...
Purpose To report a case with acute posterior multifocal placoid pigment epitheliopathy (APMPPE)-lik...
PURPOSE: Acute posterior multifocal placoid pigment epitheliopathy (APMPPE) is an acquired inflammat...
Acute multifocal placoid pigment epitheliopathy (AMPPE) is an autoimmune chorioretinal disease that ...