A Reza Gohari, Sara P Modjtahedi, Caleb R Telander, Max X Kong
{"title":"ADRENAL CORTICAL CARCINOMA PRESENTING AS CENTRAL SEROUS CHORIORETINOPATHY.","authors":"A Reza Gohari, Sara P Modjtahedi, Caleb R Telander, Max X Kong","doi":"10.1097/ICB.0000000000001668","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>The authors describe a case of bilateral chronic central serous chorioretinopathy secondary to adrenal cortical carcinoma.</p><p><strong>Methods: </strong>A case report of a 70-year-old Hispanic man presenting with bilateral multifocal central serous chorioretinopathy.</p><p><strong>Results: </strong>Clinical findings of bilateral chronic central serous chorioretinopathy along with 160 µ m of subretinal fluid and choroidal thickness greater than 400 µ m without enhanced depth optical coherence tomography were noted in a patient presenting with distortion in vision in both eyes and a weight gain of 15 pounds, weakness, and fatigue starting 8 months before. Further endocrine testing showed an elevated 24-hour urinary free cortisol level of 137 µ g with no change in serum cortisol levels following the low-dose dexamethasone suppression test and undetectable serum adrenocorticotropic hormone levels consistent with adrenocorticotropic hormone-independent Cushing syndrome. Imaging of the abdomen revealed heterogeneously enhancing masses, and the biopsy of the adrenal tumor led to the diagnosis of adrenal cortical carcinoma. He died 3 weeks after starting hospice care and only completed one round of chemotherapy.</p><p><strong>Conclusion: </strong>Adrenal tumors, including adrenal cortical carcinoma, may present as bilateral chronic central serous chorioretinopathy.</p>","PeriodicalId":53580,"journal":{"name":"Retinal Cases and Brief Reports","volume":" ","pages":"761-765"},"PeriodicalIF":0.0000,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Retinal Cases and Brief Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1097/ICB.0000000000001668","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
Abstract
Purpose: The authors describe a case of bilateral chronic central serous chorioretinopathy secondary to adrenal cortical carcinoma.
Methods: A case report of a 70-year-old Hispanic man presenting with bilateral multifocal central serous chorioretinopathy.
Results: Clinical findings of bilateral chronic central serous chorioretinopathy along with 160 µ m of subretinal fluid and choroidal thickness greater than 400 µ m without enhanced depth optical coherence tomography were noted in a patient presenting with distortion in vision in both eyes and a weight gain of 15 pounds, weakness, and fatigue starting 8 months before. Further endocrine testing showed an elevated 24-hour urinary free cortisol level of 137 µ g with no change in serum cortisol levels following the low-dose dexamethasone suppression test and undetectable serum adrenocorticotropic hormone levels consistent with adrenocorticotropic hormone-independent Cushing syndrome. Imaging of the abdomen revealed heterogeneously enhancing masses, and the biopsy of the adrenal tumor led to the diagnosis of adrenal cortical carcinoma. He died 3 weeks after starting hospice care and only completed one round of chemotherapy.
Conclusion: Adrenal tumors, including adrenal cortical carcinoma, may present as bilateral chronic central serous chorioretinopathy.