scholarly journals Chinese medicine, Gui Lu Er Xian Jiao – related serous retinal detachment 2nd to circumscribed choroidal hemangioma a case report

2021 ◽  
pp. 101135
Author(s):  
Hsin Hui Huang ◽  
Shiuh-Liang Hsu ◽  
Shwu-Jiuan Sheu
Keyword(s):  
Case Report ◽  
Chinese Medicine ◽  
Retinal Detachment ◽  
Serous Retinal Detachment ◽  
Choroidal Hemangioma

scholarly journals Choroidal Hemangioma Associated with Hepatic Hemangioma: A Case Report and Literature Review

2021 ◽  
pp. 425-432
Author(s):  
Ana Boned-Murillo ◽  
Maria Dolores Diaz-Barreda ◽  
Ana Honrubia-Grijalbo ◽  
Olivia Esteban-Floria ◽  
Francisco Javier Ascaso Puyuelo
Keyword(s):  
Case Report ◽  
Retinal Detachment ◽  
Serous Retinal Detachment ◽  
Hepatic Hemangioma ◽  
Tumor Type ◽  
Central Scotoma ◽  
Blurred Vision ◽  
Choroidal Hemangioma ◽  
Elevated Lesion ◽  
History Of

Circumscribed choroidal hemangioma (CCH) is a rare congenital ocular tumor type that is usually benign and asymptomatic. CCH has only been reported once previously in the literature in association with a visceral neoplasm. Here, we present a newly described association between CCH and hepatic hemangioma (HH). We report the case of a 57-year-old woman diagnosed with asymptomatic HHs who presented with a 2- to 3-month history of central scotoma and blurred vision in her left eye. Assessment identified an orange-red elevated lesion with a central serous retinal detachment and subretinal edema. Complementary tests suggested a CCH. To our knowledge, CCH has only been reported once previously in association with a visceral neoplasm, making this newly described association between CCH and HH of clinical relevance. Ophthalmologists should be aware of the possible association between CCH and other visceral tumors as this association offers an opportunity for the early detection of this pathology.

scholarly journals Preeclamptic serous retinal detachment without hypertension: A case report

2019 ◽  
Vol 21 ◽  
pp. e00098
Author(s):  
S. Ahmed Hussain ◽  
Brendan J. O'Shea ◽  
Andrew S. Thagard
Keyword(s):  
Case Report ◽  
Retinal Detachment ◽  
Serous Retinal Detachment

Bilateral Serous Retinal Detachment in Preeclampsia: Case Report

2017 ◽  
Vol 71 (2) ◽  
pp. 143-145
Author(s):  
Ivo Kjaev ◽  
Jana Kjaeva Nivicka ◽  
Sasha Kjaeva ◽  
Dafina Karadjova ◽  
Irena Aleksioska ◽  
...  
Keyword(s):  
Blood Pressure ◽  
Case Report ◽  
Retinal Detachment ◽  
Medical Condition ◽  
Post Partum ◽  
Rare Complication ◽  
Serous Retinal Detachment ◽  
Initial Assessment ◽  
Ocular Involvement ◽  
Ocular Ultrasound

Abstract Introduction. Preeclampsia presents a medical condition in pregnancy that is manifested with increased blood pressure and protein urine. Ocular involvement is rare. Retinal detachment in preeclampsia is a rare complication; it only occurs in 1-2% of severe preeclampsia but in 10% of those with eclamptic seizures. Case report. A pregnant patient G1P0 visited the outpatient clinic of the University Clinic for Ophthalmology complaining on visual disturbances. The chief complaint was blurred vision and headaches. She was in 31 week of gestation and complained that she had increased blood pressure over the last month. After initial assessment she was suspected of central serous retinal ablation (CSCR). Ocular ultrasound and posterior segment OCT (optical coherence tomography) confirmed the diagnosis. Treatment and outcome. Obstetric examination confirmed high blood (TA180/130) pressure with dipstick urine showing(+++). Unfortunately, the ultrasound showed an eutrophic pregnancy in 31 g.w. with fetus mortus inutero. The patient was administered to the intensive care unit. She had an ophthalmologic check-upat 2 weeks and one month post-partum that showed regression and visual acuity was getting better. The final check-up after 6 months revealed that retina was in place with no subretinal substantial fluid and no macular edema. Conclusion. Serous retinal detachment is a rare complication of preeclampsia. In most case it resolves spontaneously few weeks post delivery.

SPONTANEOUS REGRESSION OF SEROUS RETINAL DETACHMENT ASSOCIATED WITH CIRCUMSCRIBED CHOROIDAL HEMANGIOMA AFTER CHILDBIRTH

2017 ◽  
Vol 11 (1) ◽  
pp. 7-11 ◽  
Author(s):  
Isil Sayman Muslubas ◽  
Serra Arf ◽  
Mumin Hocaoglu ◽  
Hakan Ozdemir ◽  
Murat Karacorlu
Keyword(s):  
Retinal Detachment ◽  
Spontaneous Regression ◽  
Serous Retinal Detachment ◽  
Choroidal Hemangioma

scholarly journals Unilateral Vogt-Koyanagi-Harada Disease: A Clinical Case Report

2015 ◽  
Vol 6 (3) ◽  
pp. 361-365 ◽  
Author(s):  
Arminda Neves ◽  
Ana Cardoso ◽  
Mariana Almeida ◽  
Joana Campos ◽  
António Campos ◽  
...  
Keyword(s):  
Visual Acuity ◽  
Case Report ◽  
Retinal Detachment ◽  
Serous Retinal Detachment ◽  
Subretinal Fluid ◽  
Posterior Pole ◽  
Exudative Retinal Detachment ◽  
The Right ◽  
Clinical Records ◽  
Vkh Disease

Purpose: To report a case of a 20-year-old female with decreased visual acuity (VA) in the left eye (LE). Methods: This is a retrospective and descriptive case report based on data from clinical records, patient observation and analysis of diagnostic tests. Results: A 20-year-old female presented with decreased VA in the LE for 3 days. Best-corrected visual acuity (BCVA) was 20/20 in the right eye (RE) and 20/40 in the LE. Pupillary function, intraocular pressure, results of external segment examinations and slit-lamp biomicroscopy were normal, bilaterally. RE fundoscopy was normal, and in the LE it revealed papillitis and posterior pole exudative retinal detachment. Optical coherence tomography (OCT) confirmed the macular serous retinal detachment and showed thickening of the posterior choroid also revealed by orbital ultrasound and magnetic resonance imaging (MRI). Fluorescein angiography showed angiographic features typical of Vogt-Koyanagi-Harada (VKH) disease: disseminated spotted choroidal hyperfluorescence and choroidal multifocal hypofluorescence, multifocal profuse leakage in the retina with pooling, serous retinal detachment and optic disc hyperfluorescence. Serological testing for the diagnosis of infectious pathologies was negative, and the review of systems was normal. The patient received systemic steroids and cyclosporine. LE BCVA improved up to 20/20 at 18 months after the diagnosis, with complete reabsorption of subretinal fluid and normal retinal and choroidal thickness by OCT. Conclusion: Despite the unilateral involvement, the clinical and angiographic features were typical of VKH disease, and ophthalmologists should be aware to recognize this rare clinical variant of the disease.

scholarly journals Post typhoid fever neuroretinitis with serous retinal detachment and choroidal involvement-A case report

2021 ◽  
Vol 21 ◽  
pp. 101025
Author(s):  
Anadi Khatri ◽  
Bivek Wagle ◽  
K.C. Hony ◽  
Babu Dhanendra Chaurasiya ◽  
Satish Timalsena ◽  
...  
Keyword(s):  
Case Report ◽  
Retinal Detachment ◽  
Typhoid Fever ◽  
Serous Retinal Detachment

scholarly journals Recurrence of Pancreatic Cancer Presenting as Choroidal Metastasis: A Case Report

2021 ◽  
pp. 854-858
Author(s):  
Ebony Smith ◽  
Tuan Tran
Keyword(s):  
Pancreatic Cancer ◽  
Case Report ◽  
Retinal Detachment ◽  
Clinical Assessment ◽  
Central Serous Chorioretinopathy ◽  
Early Recognition ◽  
Locally Advanced ◽  
Serous Retinal Detachment ◽  
Advanced Pancreatic Cancer ◽  
Choroidal Metastasis

A patient initially diagnosed as having central serous chorioretinopathy (CSC) presented to a clinic with recurrence of pancreatic cancer manifesting as choroidal metastasis. He was initially diagnosed with CSC by a local ophthalmologist 8 weeks earlier and subsequently presented to our clinic for second opinion after further loss of vision. His medical history was significant for locally advanced pancreatic cancer that was resected by pancreaticoduodenectomy and was treated with adjuvant Folfirinox chemotherapy that was completed 12 months earlier. On examination, there was a large serous retinal detachment overlying a large pale ill-defined elevated choroidal lesion. A diagnosis of choroidal metastasis from recurrence of his pancreatic cancer was made. The diagnosis of choroidal metastasis of his pancreatic cancer represented recurrence of his pancreatic cancer that is associated with high mortality. Early recognition by clinical assessment may allow timely management with chemotherapy and radiation, and potentially prolong survival.

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