Background: Nowadays luetic infections are rarely seen by ophthalmologists. We report on an immunocompetent ophthalmologically asymptomatic patient with bilateral papilledema due to perineuritis optici in lues cerebrospinalis.
Patient: A 47-year old female patient presented with presbyopic complaints. Additionally she reported occasional dizziness with nausea and hearing loss with tinnitus. Visual acuity measured 16/20. There was a bilateral prominent optic disc with indistinct margins and papillary hemorrhagies on the right side and corresponding enlargement of the blind spot in the visual field. Echography revealed bilateral optic drusen. Serological examination suggested lues (TPHA 1:5120, IgM-FTA-Abs-Test 1:320, Cardiolipin 1:640). Cerebrospinal fluid examination indicated an inflammatory process in the CNS without proof of an autochthonous antibody production.
Conclusion: Even nowadays lues cerebrospinalis must be suspected in patients with bilateral papilledema without visual loss. The ophthalmologist holds an important diagnostic position, because adequate treatment is able to prevent disease progression.
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http://dx.doi.org/10.1055/s-2000-10517 | DOI Listing |
Am J Ophthalmol Case Rep
December 2024
California Pacific Medical Center Department of Ophthalmology, 711 Van Ness, Suite 250, San Francisco, CA, 94102, USA.
Purpose: To report the case of a woman in her fifties whose presenting symptom of idiopathic intracranial hypertension was engorgement of the eyelid veins.
Observations: Bilateral engorged palpebral veins were visible through the skin. Dilated fundus examination revealed bilateral optic disc edema.
J Med Case Rep
January 2025
Headache Department, Iranian Center of Neurological Research, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran.
Background: Idiopathic intracranial hypertension (IIH) is a condition where the pressure of the cerebrospinal fluid in the brain increases without a known cause. It typically affects adults but can also occur in adolescents and children, although it is less common. Numerous elements, including coagulopathy, have been documented in previous cases as potential etiological factors of IIH.
View Article and Find Full Text PDFMedicine (Baltimore)
November 2024
Department of Ophthalmology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Front Pediatr
November 2024
Department of Pediatrics, Golisano Children's Hospital, University of Rochester, Rochester, NY, United States.
Juvenile dermatomyositis is a systemic autoimmune disease characterized by progressive proximal muscle weakness, pathognomonic rashes, and often the presence of myositis-specific antibodies. Consensus treatment plans for pediatric patients with juvenile dermatomyositis recommend steroids and methotrexate as initial therapy. Patients with anti-transcription intermediary factor 1 gamma (anti-TIF-1γ) antibodies tend to have more refractory disease requiring more aggressive treatment with intravenous immunoglobulin, which is typically well tolerated.
View Article and Find Full Text PDFJ Neuroophthalmol
November 2024
Ruiz Department of Ophthalmology and Visual Science (ALC, AZC, O-oA), McGovern Medical School at UTHealth Houston, Houston, Texas; Robert Cizik Eye Clinic (ALC, AZC, O-oA), Houston, Texas; and Texas Children's Hospital (JLM, RPP), Baylor College of Medicine, Houston, Texas.
Background: Pseudotumor cerebri (PTC) syndrome is a disorder of increased intracranial pressure, most commonly affecting overweight women of childbearing age. Malignant PTC (MPTC) is a rare presentation that involves rapidly worsening vision, often necessitating surgical intervention to prevent permanent vision loss. The goal of this study was to determine whether radiographic findings of PTC are predictive of MPTC and the final visual outcome.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!