A patient with a large recurrent pheochromocytoma demonstrating the pitfalls of diagnosis
暂无分享,去创建一个
R. Paschke | T. Lincke | R. Kluge | G. Eisenhofer | K. Schierle | M. Seiwerts | P. Lamesch | G. Borte | W. Kassahun | J. Singer | C. Koch
[1] R. Lloyd. Adrenal cortical tumors, pheochromocytomas and paragangliomas , 2011, Modern Pathology.
[2] J. Lombard,et al. 123I-meta-iodobenzylguanidine scintigraphy for the detection of neuroblastoma and pheochromocytoma: results of a meta-analysis. , 2010, The Journal of clinical endocrinology and metabolism.
[3] Erin E. Chambers,et al. Performance of plasma free metanephrines measured by liquid chromatography-tandem mass spectrometry in the diagnosis of pheochromocytoma. , 2010, Clinica chimica acta; international journal of clinical chemistry.
[4] R. Dullaart,et al. New imaging approaches to phaeochromocytomas and paragangliomas , 2010, Clinical endocrinology.
[5] S. Callen,et al. Pilot quality assurance programme for plasma metanephrines , 2010, Annals of clinical biochemistry.
[6] S. Majumdar,et al. Compound heterozygous mutation with a novel splice donor region DNA sequence variant in the succinate dehydrogenase subunit B gene in malignant paraganglioma , 2010, Pediatric blood & cancer.
[7] Fiona Douglas,et al. Tumor risks and genotype–phenotype–proteotype analysis in 358 patients with germline mutations in SDHB and SDHD , 2010, Human mutation.
[8] D. Schteingart. 6-[F-18]Fluoro-l-Dihydroxyphenylalanine Positron Emission Tomography Is Superior to Conventional Imaging with 123I-Metaiodobenzylguanidine Scintigraphy, Computer Tomography, and Magnetic Resonance Imaging in Localizing Tumors Causing Catecholamine Excess , 2010 .
[9] E. D. de Vries,et al. 6-[F-18]Fluoro-L-dihydroxyphenylalanine positron emission tomography is superior to conventional imaging with (123)I-metaiodobenzylguanidine scintigraphy, computer tomography, and magnetic resonance imaging in localizing tumors causing catecholamine excess. , 2009, The Journal of clinical endocrinology and metabolism.
[10] K. Buddavarapu,et al. Pheochromocytomas: From Genetic Diversity to New Paradigms , 2009, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.
[11] J. Carrasquillo,et al. Comparison of 18F-fluoro-L-DOPA, 18F-fluoro-deoxyglucose, and 18F-fluorodopamine PET and 123I-MIBG scintigraphy in the localization of pheochromocytoma and paraganglioma. , 2009, The Journal of clinical endocrinology and metabolism.
[12] S. Steinberg,et al. Treatment of malignant pheochromocytoma/paraganglioma with cyclophosphamide, vincristine, and dacarbazine , 2008, Cancer.
[13] R. Reznek,et al. 123I‐metaiodobenzylguanidine (MIBG) scintigraphy for the detection of adrenal and extra‐adrenal phaeochromocytomas: CT and MRI correlation , 2008, Clinical endocrinology.
[14] Laura H. Tang,et al. Prognostic indicators of malignancy in adrenal pheochromocytomas: clinical, histopathologic, and cell cycle/apoptosis gene expression analysis. , 2008, Surgery.
[15] T. Abe,et al. Immunohistochemistry of a proliferation marker Ki67/MIB1 in adrenocortical carcinomas: Ki67/MIB1 labeling index is a predictor for recurrence of adrenocortical carcinomas. , 2008, Endocrine journal.
[16] W. Young,et al. Plasma chromogranin A or urine fractionated metanephrines follow-up testing improves the diagnostic accuracy of plasma fractionated metanephrines for pheochromocytoma. , 2008, The Journal of clinical endocrinology and metabolism.
[17] Yanxia Sun,et al. A logistic regression model for predicting malignant pheochromocytomas , 2008, Journal of Cancer Research and Clinical Oncology.
[18] A. Elkahloun,et al. Identification of potential gene markers and insights into the pathophysiology of pheochromocytoma malignancy. , 2007, The Journal of clinical endocrinology and metabolism.
[19] E. Baudin,et al. Succinate dehydrogenase B gene mutations predict survival in patients with malignant pheochromocytomas or paragangliomas. , 2007, The Journal of clinical endocrinology and metabolism.
[20] R. Onders,et al. Analysis of large versus small pheochromocytomas: operative approaches and patient outcomes. , 2006, Surgery.
[21] Haifeng Zhao,et al. Development and validation of pheochromocytoma of the adrenal gland scaled score for predicting malignant pheochromocytomas. , 2006, Urology.
[22] H. Neumann,et al. Clinical and genetic characteristics of patients with neurofibromatosis type 1 and pheochromocytoma. , 2006, The New England journal of medicine.
[23] K. Schmid,et al. Diagnostic value of various biochemical parameters for the diagnosis of pheochromocytoma in patients with adrenal mass. , 2004, European journal of endocrinology.
[24] M. Walther,et al. Pheochromocytoma catecholamine phenotypes and prediction of tumor size and location by use of plasma free metanephrines. , 2005, Clinical chemistry.
[25] Q. Duh,et al. Should pheochromocytoma size influence surgical approach? A comparison of 90 malignant and 60 benign pheochromocytomas. , 2004, Surgery.
[26] A. Gafni,et al. A systematic review of the literature examining the diagnostic efficacy of measurement of fractionated plasma free metanephrines in the biochemical diagnosis of pheochromocytoma , 2004, BMC endocrine disorders.
[27] R. Paschke,et al. Does tumor heterogeneity limit the use of the Weiss criteria in the evaluation of adrenocortical tumors? , 2004, Journal of endocrinological investigation.
[28] M. Walther,et al. Biochemical diagnosis of pheochromocytoma: how to distinguish true- from false-positive test results. , 2003, The Journal of clinical endocrinology and metabolism.
[29] 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.
[30] J. Doppman,et al. A "pheo" lurks: novel approaches for locating occult pheochromocytoma. , 2001, The Journal of clinical endocrinology and metabolism.