Retinal Disease with Massive Exudation
نویسندگان
چکیده
منابع مشابه
Massive lipid exudation and retinal detachment after combined brachytherapy and transpupillary thermotherapy in choroidal melanoma.
CASE REPORT A 59 year-old male with choroidal melanoma in the left eye who underwent plaque brachytherapy (iodine 125). One week after surgery, massive exudation with retinal detachment and lipid exudation was observed. Evolution was assessed with funduscopy and ultrasound every month. Nine months after surgery transpupillary thermotherapy (TTT) was performed over the fluid-free irradiated resi...
متن کاملMassive osteolysis ( Gorham,s disease) and report a case
Gotham's disease or vanishing bone is a rare disease with unknown etiology. Frequently, children and young adults are affected. It is characterized by proliferation of vascular or lymphatic tissue which results in destruction and resorption of bone. In this disease, the destructed bone is replaced either by hemangiomatous or lymphangiomatous tissue ( s) and in a later stage, fibrosis occurs. It...
متن کاملSinus Histiocytosis with Massive Lymphadenpathy
In this paper the authors reported 2 cases of Sinus Histiocy-tosis . The first , an 11 year s o1d gir1 with massive 1ymphadnopathy of 10 CM diameter and 3 months duration otherwise normal. Paraclinic exams wer normal including BM. Diagnosis was confirmed by cervical node biopsy. She was followed clinically and was cured in 8 months. The second case, a 6 years old boy with massive cervical lymph...
متن کاملHypertensive crisis with massive retinal and choroidal infarction
A 30-year-old female with no prior ophthalmic complaints presented with a 1-week history of bilateral gradual painless vision loss. Her blood pressure was 225/115 mmHg (Hypertensive crisis is defined as a systolic reading of 180 mm Hg or higher or a diastolic reading of 110 mm Hg or higher). Past medical history included chronic renal failure from IgA nephropathy requiring hemodialysis for the ...
متن کاملMassive retinal gliosis in neurofibromatosis type 1.
Massive Retinal Gliosis in Neurofibromatosis Type 1 Neurofibromatosis type 1 (NF1), an autosomal dominant syndrome, has major extraocular expressions of bilateral ptosis, diffuse and plexiform neurofibromas, optic nerve gliomas, and dysplasia of the sphenoid bone. With respect to the eyeball, the spectrum of involvement includes enlarged corneal nerves, Lisch iris nodules, dysplasia of the ante...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Proceedings of the Royal Society of Medicine
سال: 1928
ISSN: 0035-9157
DOI: 10.1177/003591572802100742