Primary Bilateral Macronodular Adrenal Hyperplasia Associated With <i>ARMC5</i> Variant and Pituitary Microadenoma. [PDF]
O'Connor-Ramiro L +5 more
europepmc +1 more source
Autoimmune Polyglandular Syndrome Type 2 With Hurthle Cell Adenoma: A Rare Association. [PDF]
Pandya SS, Shah K, Chavda H, Shah K.
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Secondary bilateral adrenal Burkitt lymphoma with hepatic and renal involvement in a 17-year-old patient: A rare case report and literature review. [PDF]
Elmassoudi N +9 more
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Ganglioneuroma has a potential for lymph node metastasis, not impacting recurrence. [PDF]
Ozcelik EE +7 more
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Computed Tomography Accuracy for Prediction of Adrenal Tumor Adhesion With Organs and Vessels in Dogs and Cats. [PDF]
Baldinetti M +10 more
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Primary Angiosarcoma of the Adrenal Gland: Report of 2 Cases and Review of the Literature
International Journal of Surgical Pathology, 2021Primary adrenal angiosarcoma is a rare, malignant, vascular neoplasm. These neoplasms typically arise in middle age (median age of 60 years) and are more common in males (65%) than in females.
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Adrenal gland haemangioma, a rare entity difficult to differentiate from malignancy
BJR|case reportsAdrenal haemangioma is a rare benign vascular lesion, which is usually asymptomatic and it is typically discovered incidentally on radiographic imaging.
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Background: Oncocytic lesions of the adrenal gland pose several diagnostic challenges as they can be associated with both functional and non-functional adrenal disorders and may be either benign or malignant. Summary: Oncocytic tumors are predominantly (>
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