Complete surgical removal of multiple tumor lesions in malignant pheochromocytomas produces a good prognosis
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T. Naiki | S. Nozaki | T. Etani | N. Kawai | T. Yasui | Y. Moritoki | S. Hamamoto | A. Okada | R. Unno | K. Iida
[1] W. Young,et al. Malignant Pheochromocytoma and Paraganglioma: 272 Patients Over 55 Years , 2017, The Journal of clinical endocrinology and metabolism.
[2] Tae Yong Kim,et al. Clinical course and prognostic factors in patients with malignant pheochromocytoma and paraganglioma: A single institution experience , 2015, Journal of surgical oncology.
[3] A. Hernigou,et al. Peritoneal implantation of pheochromocytoma following tumor capsule rupture during surgery. , 2014, The Journal of clinical endocrinology and metabolism.
[4] S. Steinberg,et al. Response after surgical resection of metastatic pheochromocytoma and paraganglioma: can postoperative biochemical remission be predicted? , 2013, Journal of the American College of Surgeons.
[5] P. Levillain,et al. Malignant pheochromocytoma: new malignancy criteria , 2012, Langenbeck's Archives of Surgery.
[6] A. Harari,et al. Malignant pheochromocytoma: a review. , 2011, American journal of surgery.
[7] Herb Chen,et al. Pheochromocytoma: current approaches and future directions. , 2008, The oncologist.
[8] L. Thompson. Pheochromocytoma of the Adrenal Gland Scaled Score (PASS) to Separate Benign From Malignant Neoplasms: A Clinicopathologic and Immunophenotypic Study of 100 Cases , 2002, The American journal of surgical pathology.
[9] P. Dicpinigaitis,et al. Hypertensive crises induced by treatment of malignant pheochromocytoma with a combination of cyclophosphamide, vincristine, and dacarbazine. , 1994, Medical and pediatric oncology.