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Quoted phrase not found in phrase index: "Adrenal Gland Composite Pheochromocytoma"
Page 1
Overview of the 2022 WHO Classification of Paragangliomas and Pheochromocytomas.
Mete O, Asa SL, Gill AJ, Kimura N, de Krijger RR, Tischler A. Mete O, et al. Endocr Pathol. 2022 Mar;33(1):90-114. doi: 10.1007/s12022-022-09704-6. Epub 2022 Mar 13. Endocr Pathol. 2022. PMID: 35285002 Review.
This review summarizes the classification of tumors of the adrenal medulla and extra-adrenal paraganglia as outlined in the 5th series of the WHO Classification of Endocrine and Neuroendocrine Tumors. ...This review adopts a practical question-answer framework to pr …
This review summarizes the classification of tumors of the adrenal medulla and extra-adrenal paraganglia as outlined in the 5t …
Advances in Adrenal and Extra-adrenal Paraganglioma: Practical Synopsis for Pathologists.
Juhlin CC, Mete O. Juhlin CC, et al. Adv Anat Pathol. 2023 Jan 1;30(1):47-57. doi: 10.1097/PAP.0000000000000365. Epub 2022 Sep 23. Adv Anat Pathol. 2023. PMID: 36136370 Review.
Adrenal paraganglioma (or "pheochromocytoma") and extra-adrenal paraganglioma, collectively abbreviated PPGL, are rare but spectacular nonepithelial neuroendocrine neoplasms. ...This review focuses on updated key diagnostic and prognostic concepts that …
Adrenal paraganglioma (or "pheochromocytoma") and extra-adrenal paraganglioma, collectively abbreviated PPGL, are rare …
Composite pheochromocytoma of the adrenal gland-a review of published cases.
Costa J, Jácome M, Souteiro P, Santos C, Cunha AL. Costa J, et al. Virchows Arch. 2023 Aug;483(2):267-275. doi: 10.1007/s00428-023-03492-y. Epub 2023 Jan 16. Virchows Arch. 2023. PMID: 36645463 Review.
Composite pheochromocytoma (CP) is a rare adrenal tumor, composed of ordinary pheochromocytoma and neuroblastic components. ...We report the case of a 56-year-old woman with a CP of the left adrenal gland with a ganglioneuroma component. …
Composite pheochromocytoma (CP) is a rare adrenal tumor, composed of ordinary pheochromocytoma and neuroblastic …
Update on Adrenal Tumours in 2017 World Health Organization (WHO) of Endocrine Tumours.
Lam AK. Lam AK. Endocr Pathol. 2017 Sep;28(3):213-227. doi: 10.1007/s12022-017-9484-5. Endocr Pathol. 2017. PMID: 28477311 Review.
Also, a system for differentiation of oncocytoma from oncocytic cortical carcinoma is adopted. Tumours of the adrenal medulla and extra-adrenal paraganglia comprise pheochromocytoma, paraganglioma (head and neck paraganglioma and sympathetic paraganglioma), n …
Also, a system for differentiation of oncocytoma from oncocytic cortical carcinoma is adopted. Tumours of the adrenal medulla and ext …
Impact of body composition and genotype on haemodynamics during surgery for pheochromocytoma and paraganglioma.
Pang Y, Li M, Jiang J, Chen X, Fu Y, Wang C, He Y, Zhao Y, Wang Y, Guan X, Zhang L, Xu X, Gan Y, Liu Y, Xie Y, Tang T, Wang J, Xie B, Liang Z, Chen D, Liu H, Chen C, Eisenhofer G, Liu L, Yi X, Chen BT. Pang Y, et al. J Cachexia Sarcopenia Muscle. 2022 Dec;13(6):2843-2853. doi: 10.1002/jcsm.13071. Epub 2022 Sep 6. J Cachexia Sarcopenia Muscle. 2022. PMID: 36068986 Free PMC article.
BACKGROUND: Maintaining intraoperative haemodynamic stability can reduce cardiovascular complications during surgery for pheochromocytoma and paraganglioma (PPGL). Risk factors such as tumour size and catecholamine levels are reported to predict haemodynamic respons …
BACKGROUND: Maintaining intraoperative haemodynamic stability can reduce cardiovascular complications during surgery for pheochromocytoma …
Composite pheochromocytoma with a malignant peripheral nerve sheath tumor: Case report and review of the literature.
Namekawa T, Utsumi T, Imamoto T, Kawamura K, Oide T, Tanaka T, Nihei N, Suzuki H, Nakatani Y, Ichikawa T. Namekawa T, et al. Asian J Surg. 2016 Jul;39(3):187-90. doi: 10.1016/j.asjsur.2012.11.003. Epub 2013 Feb 20. Asian J Surg. 2016. PMID: 27338175 Free article. Review.
Furthermore, an adrenal tumor composed of a pheochromocytoma and a malignant peripheral nerve sheath tumor is extremely rare. A composite pheochromocytoma with malignant peripheral nerve sheath tumor in a 42-year-old man is reported here. ...
Furthermore, an adrenal tumor composed of a pheochromocytoma and a malignant peripheral nerve sheath tumor is extremely rare. …
Changes in energy metabolism in pheochromocytoma.
Petrák O, Haluzíková D, Kaválková P, Štrauch B, Rosa J, Holaj R, Brabcová Vránková A, Michalsky D, Haluzík M, Zelinka T, Widimsky J Jr. Petrák O, et al. J Clin Endocrinol Metab. 2013 Apr;98(4):1651-8. doi: 10.1210/jc.2012-3625. Epub 2013 Feb 22. J Clin Endocrinol Metab. 2013. PMID: 23436923 Clinical Trial.
CONTEXT: Catecholamine overproduction in pheochromocytoma affects basal metabolism, resulting in weight loss despite normal food intake. ...Inflammatory markers (leukocytes count and C-reactive protein) and cytokines (TNF-alpha, IL-6, and IL-8) were analyzed with a Luminex …
CONTEXT: Catecholamine overproduction in pheochromocytoma affects basal metabolism, resulting in weight loss despite normal food inta …
Composite pheochromocytoma: a clinicopathologic and molecular comparison with ordinary pheochromocytoma and neuroblastoma.
Comstock JM, Willmore-Payne C, Holden JA, Coffin CM. Comstock JM, et al. Am J Clin Pathol. 2009 Jul;132(1):69-73. doi: 10.1309/AJCPN76VTIGWPOAG. Am J Clin Pathol. 2009. PMID: 19864235
Composite pheochromocytoma is a rare adrenal tumor composed of ordinary pheochromocytoma and other components, most frequently neuroblastic elements. ...This study investigates the clinical characteristics and N-myc amplification status of 4 cases of …
Composite pheochromocytoma is a rare adrenal tumor composed of ordinary pheochromocytoma and other components, m …
The utility of (68)Ga-DOTATATE PET/CT in localizing primary/metastatic pheochromocytoma and paraganglioma in children and adolescents - a single-center experience.
Jaiswal SK, Sarathi V, Malhotra G, Hira P, Shah R, Patil VA, Dalvi A, Prakash G, Lila AR, Shah NS, Bandgar T. Jaiswal SK, et al. J Pediatr Endocrinol Metab. 2020 Nov 12;34(1):109-119. doi: 10.1515/jpem-2020-0354. Print 2021 Jan 27. J Pediatr Endocrinol Metab. 2020. PMID: 33180042 Clinical Trial.
OBJECTIVES: Pediatric pheochromocytoma and paraganglioma (PPGL) are rare tumors with limited data on the diagnostic performance of (68)Ga-DOTA(0)-Tyr(3)-octreotate positron emission tomography-computed tomography ((68)Ga-DOTATATE PET/CT). ...METHODS: Retrospective evaluati …
OBJECTIVES: Pediatric pheochromocytoma and paraganglioma (PPGL) are rare tumors with limited data on the diagnostic performance of (6 …
COPPS, a composite score integrating pathological features, PS100 and SDHB losses, predicts the risk of metastasis and progression-free survival in pheochromocytomas/paragangliomas.
Pierre C, Agopiantz M, Brunaud L, Battaglia-Hsu SF, Max A, Pouget C, Nomine C, Lomazzi S, Vignaud JM, Weryha G, Oussalah A, Gauchotte G, Busby-Venner H. Pierre C, et al. Virchows Arch. 2019 Jun;474(6):721-734. doi: 10.1007/s00428-019-02553-5. Epub 2019 Mar 13. Virchows Arch. 2019. PMID: 30868297
Here, using a series of 147 cases of paraganglioma and pheochromocytoma, we designed and evaluated the potential of a new score, the COPPS (COmposite Pheochromocytoma/paraganglioma Prognostic Score), by taking into consideration three clinico-pathologi …
Here, using a series of 147 cases of paraganglioma and pheochromocytoma, we designed and evaluated the potential of a new score, the …
27 results