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Published in 2021 at "International Journal of Surgery Case Reports"
DOI: 10.1016/j.ijscr.2021.105763
Abstract: Highlights • Resection of large Pheochromocytoma with invasion or metastasis is now considered indicated.• Pheochromocytoma surgery combined organ resection is generally challenging for surgeons and anesthesiologists because the procedure is complex and life threatening cardiovascular… read more here.
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Published in 2022 at "Journal of palliative medicine"
DOI: 10.1089/jpm.2022.0402
Abstract: Background: Pheochromocytoma is a tumor arising from adrenomedullary chromaffin cells. Five-year survival with malignant pheochromocytoma is read more here.
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Published in 2017 at "Medicine"
DOI: 10.1097/md.0000000000008535
Abstract: Rationale: We present a rare case of malignant pheochromocytoma with thoracic metastases during pregnancy that presented with symptoms of myelopathy and was treated with circumferential decompression, stabilization, and radiation. The management of this unique case… read more here.
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Published in 2018 at "Medicine"
DOI: 10.1097/md.0000000000010614
Abstract: Rationale: Malignant pheochromocytoma is a rare disease and surgical resection is the only curative treatment. Patient concerns: An 81-year-old man of Chinese ethnicity was found to have a giant retroperitoneal tumor. Diagnoses: B-scan ultrasonography and… read more here.
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Published in 2018 at "Medicine"
DOI: 10.1097/md.0000000000012184
Abstract: Rationale: Malignant pheochromocytoma in the spine is a rare disease without standard curative managements so far. The objective of this article is to report a very rare case of malignant pheochromocytoma with sacrum metastases causing… read more here.
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Published in 2017 at "Journal of thoracic disease"
DOI: 10.21037/jtd.2017.02.71
Abstract: Pheochromocytomas are catecholamine-producing neuroendocrine tumors that usually occur in the adrenal medulla or sympathetic paraganglia. Anterior mediastinum involvement with pheochromocytoma is rare and may not present with typical symptoms. Its clinical manifestation may be unclear… read more here.
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Published in 2017 at "OncoTargets and therapy"
DOI: 10.2147/ott.s130236
Abstract: Purpose Malignant pheochromocytoma (PCC) is a rare tumor with a very poor prognosis and no effective treatments. The aim of this study was to assess the efficacy of a novel second-generation synthetic heat-shock protein 90… read more here.
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Published in 2021 at "Frontiers in Medicine"
DOI: 10.3389/fmed.2021.733553
Abstract: Introduction: Bone metastasis of malignant pheochromocytoma is a rare disease. We report a patient with a 10-year history who underwent 18F-FDG PET/CT to detect bone metastasis and receive radiotherapy and chemotherapy with complete response for… read more here.
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Published in 2017 at "Turkish journal of surgery"
DOI: 10.5152/ucd.2015.3011
Abstract: Pheochromocytoma is a rare tumor originating from the embryonic neural crest and secreting high levels of catecholamines. The average tumor size is approximately 7 cm, and the average weight is approximately 200 g in the… read more here.