Renal dynamic scintigraphy is a crucial diagnostic tool for assessing renal function, yet unexpected findings can provide additional insights into extrarenal conditions. We report 2 rare cases of extrarenal 99mTc-DTPA uptake associated with adrenal tumors: one adrenal cortical carcinoma and one pheochromocytoma. In both cases, significant tracer accumulation in the adrenal region was observed, highlighting an uncommon but noteworthy diagnostic consideration. These cases emphasize the importance of including adrenal tumors in the differential diagnosis when encountering abnormal 99mTc-DTPA uptake patterns, offering valuable clinical insights for interpreting atypical imaging findings and broadening diagnostic perspectives.
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http://dx.doi.org/10.1097/RLU.0000000000005811 | DOI Listing |
J Endocr Soc
March 2025
Division of Endocrinology and Metabolism, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Context: Cells derived from neural crest populate several organs. A particular precursor cell, sympathogonia, gives rise to pheochromoblasts and neuroblasts. Due to common origin, tumors originating from pheochromoblasts, such as pheochromocytoma (PHEO) and paraganglioma (PGL), may rarely coexist with ganglioneuroma (GN).
View Article and Find Full Text PDFInt J Endocrinol Metab
October 2024
Clinic for Endocrine Surgery, University Clinical Centre of Serbia, Belgrade, Serbia.
Introduction: Sertoli cell tumors are rare sex cord-stromal tumors, accounting for less than 1% of primary testicular tumors. They typically arise in the testes and ovaries, with other localizations being uncommon. We present the case of a Sertoli cell tumor in the adrenal gland, which, to our knowledge, is the first reported in the literature.
View Article and Find Full Text PDFAnn Noninvasive Electrocardiol
March 2025
Xiamen Cardiovascular Hospital, Division of Cardiology, Xiamen University, Xiamen, Fujian, China.
Pheochromocytoma, a type of neuroendocrine tumor, can cause numerous symptoms and signs similar to those of other clinical conditions, with the classic triad being palpitations, headache, and diaphoresis. Patients with pheochromocytoma can present with various cardiac complications, including myocarditis, acute coronary syndromes, cardiomyopathy, heart failure, and arrhythmias. Here we report a case of pheochromocytoma that first presented with bidirectional ventricular tachycardia.
View Article and Find Full Text PDFInt Urol Nephrol
March 2025
Department of Urology, Gansu Province Clinical Research Center for Urinary System Disease, Lanzhou University Second Hospital, Cuiying Men 80, Chengguan District, Lanzhou, 730030, Gansu, China.
Background: The application of robotic adrenalectomy (RA) is increasing. However, there is still controversy over whether RA is more feasible than laparoscopic adrenalectomy (LA) for large adrenal tumors (LATs).
Methods: This meta-analysis compares the efficacy and safety of RA versus LA for LATs.
Hypertens Res
March 2025
Renal Division, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Emerging evidence has suggested a significant prevalence of mild autonomous cortisol secretion (MACS) among patients diagnosed with primary aldosteronism (PA). However, MACS's clinical characteristics and implications in PA patients remain largely unexplored. To investigate the prevalence, comorbidities, and indicators of MACS in PA patients, we conducted a retrospective cohort study including 874 PA patients with dexamethasone suppression test results in the Taiwan Primary Aldosteronism Investigators (TAIPAI) cohort between February 2011 and February 2024.
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