Abstract
A 64-year-old hypertensive woman presented with complaints of a painless, progressive decrease in vision, headache, dizziness for the last month. She was a known case of diabetes mellitus on insulin therapy. On examination, best-corrected visual acuity was 6/12 in the right eye and 6/18 in the left eye. The fundus examination in both eyes revealed features of grade IV hypertensive retinopathy. Systemic examination revealed the raised blood pressure of 200/110 mm Hg. Diagnosis of pheochromocytoma was made on the basis of increased urinary norepinephrine (892.8 mg/dL) and mass in the left adrenal gland (measuring 31×28 mm) at contrast-enhanced CT. Medical management to control hypertension was done and ultimately, she underwent left laparoscopic adrenalectomy. After 10 months of surgery, the patient was asymptomatic, blood pressure was within normal limit and her vision improved to 6/6 in both the eyes. The retinal features of hypertensive retinopathy had completely disappeared.
Reference10 articles.
1. Pheochromocytoma: clinical review based on a rare case in adolescence;Alface;BMJ Case Rep,2015
2. [Pheochromocytoma];Pereira;Arq Bras Endocrinol Metabol,2004
3. Pheochromocytoma: presentation, diagnosis and treatment;Reisch;J Hypertens,2006
4. Hypertensive retinopathy. description, classification, and prognosis;Walsh;Ophthalmology,1982
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