Recurring meningoencephalitis in sinusitis-associated acute posterior multifocal placoid pigment epitheliopathy under prednisone tapering.

نویسندگان

  • H Joswig
  • C Flueckiger
  • A Infanger
  • B Tettenborn
  • A Felbecker
چکیده

The authors describe a case of acute posterior multifocal placoid pigment epitheliopathy (APMPPE) with recurrent neurological complications. A 24-year-old man experienced subacute bilateral visual loss. Based on the characteristic findings in funduscopy and fluorescin angiography and after the exclusion of the differential diagnoses, APMPPE was diagnosed. During the course of the disease recurrent episodes of meningitis and encephalitis occurred when tapering of prednisone was attempted. Secondary to encephalitic lesions, the patient developed partial epileptic seizures, which made an anticonvulsive medication necessary. The authors considered a chronic sinusitis to be an aetiological factor of the underlying autoimmune process. Due to the complicated course of APMPPE, they decided to start long-term immunosuppressive therapy with azathioprine under which the patient remained stable and prednisone could be tapered successfully. Neurological complications of APMPPE are rare. Nevertheless, this case demonstrates that long-term immunosuppressive treatment might be necessary to prevent recurrent neurological complications in some cases.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Acute posterior multifocal placoid pigment epitheliopathy (APMPPE).

A 20-year-old female presented with distorted vision after a viral illness and was found to have acute posterior multifocal placoid pigment epitheliopathy (APMPPE). This case is described with presenting signs and symptoms and the final outcome. The general features and aetiology of APMPPE are discussed.

متن کامل

[Acute posterior multifocal placoid pigment epitheliopathy. Case report].

BACKGROUND Acute posterior multifocal placoid pigment epitheliopathy is an unusual, self-limited, inflammatory disease that affects the choriocapillaris, and external retinal layers. CLINICAL CASE A 26 year-old male patient complained of decreased visual acuity, as well as photopsia in both eyes for the past three days. Best corrected visual acuity was 20/200 in the right eye and 20/80 in the...

متن کامل

A syndrome resembling acute posterior multifocal placoid pigment epitheliopathy in older adults.

PURPOSE To describe clinical characteristics and visual and anatomic outcomes of a syndrome in older patients that is similar in its active stage to acute posterior multifocal placoid pigment epitheliopathy, but has a distinct clinical course. METHODS We retrospectively reviewed medical records and photographic studies of consecutive patients over the age of 50 who presented with acute-onset ...

متن کامل

Acute posterior multifocal placoid pigment epitheliopathy and sarcoidosis.

We report on a patient with acute posterior multifocal placoid pigment epitheliopathy and sarcoidosis. A review of the literature suggests that sarcoidosis may occur more commonly in this condition than previously suspected.

متن کامل

Acute posterior multifocal placoid pigment epitheliopathy complicated by central retinal vein occlusion.

A case of acute posterior multifocal placoid pigment epitheliopathy (APMPPE) complicated by a central retinal vein occlusion five weeks after presentation is described. After eight months' follow-up there was mild residual visual impairment, macular scarring, and angiographic changes. The association of these two conditions is discussed.

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:
  • BMJ case reports

دوره 2011  شماره 

صفحات  -

تاریخ انتشار 2011