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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. ...The value of sustentacular cells and Ki67 labeling as prognost …
This review summarizes the classification of tumors of the adrenal medulla and extra-adrenal paraganglia as outlined in the 5t …
Adrenal pheochromocytoma: is it all or the tip of the iceberg?
Wang K, Tang G, Peng Y, Li C, Fu W, Li R, Guan J. Wang K, et al. Jpn J Radiol. 2022 Feb;40(2):120-134. doi: 10.1007/s11604-021-01199-1. Epub 2021 Sep 21. Jpn J Radiol. 2022. PMID: 34546504 Review.
Adrenal pheochromocytoma is not always a simple retroperitoneal tumor but may be part of a more complicated condition. ...A comprehensive understanding of the clinical, pathological, and variable imaging manifestations of pheochromocytoma can help radiologist …
Adrenal pheochromocytoma is not always a simple retroperitoneal tumor but may be part of a more complicated condition. ...A co …
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. ...Moreover, the novel 2022 WHO Classification of Endocrine and Neuroendocrine Tumor …
Adrenal paraganglioma (or "pheochromocytoma") and extra-adrenal paraganglioma, collectively abbreviated PPGL, are rare …
Presentation and outcomes of adrenal ganglioneuromas: A cohort study and a systematic review of literature.
Dages KN, Kohlenberg JD, Young WF Jr, Murad MH, Prokop L, Rivera M, Dy B, Foster T, Lyden M, McKenzie T, Thompson G, Bancos I. Dages KN, et al. Clin Endocrinol (Oxf). 2021 Jul;95(1):47-57. doi: 10.1111/cen.14460. Epub 2021 Mar 22. Clin Endocrinol (Oxf). 2021. PMID: 33721367 Free PMC article.
Subgroup analysis was performed on tumours with histologic elements of ganglioneuroma and pheochromocytoma (ie composite tumours). RESULTS: The cohort study included 45 patients with AGN, 20 (44%) of which had composite tumours. ...Imaging characteristics can …
Subgroup analysis was performed on tumours with histologic elements of ganglioneuroma and pheochromocytoma (ie composite tumou …
Differential diagnosis of pheochromocytomas and paragangliomas.
McNichol AM. McNichol AM. Endocr Pathol. 2001 Winter;12(4):407-15. doi: 10.1385/ep:12:4:407. Endocr Pathol. 2001. PMID: 11914474 Review.
Paragangliomas are of two types, sympathetic and parasympathetic, depending on the type of paraganglion in which they arise. The term pheochromocytoma is reserved for tumors arising in the adrenal medulla. ...Paragangliomas may have spindle cell morphology or contai …
Paragangliomas are of two types, sympathetic and parasympathetic, depending on the type of paraganglion in which they arise. The term phe …
Cardiovascular Complications in Pheochromocytoma and Paraganglioma: Does Phenotype Matter?
Petrák O, Krátká Z, Holaj R, Zítek M, Nguyen Nikrýnová T, Klímová J, Kološová B, Waldauf P, Michalský D, Novák K, Markvartová A, Zlatohlávek L, Grus T, Dušková J, Widimský J Jr, Zelinka T. Petrák O, et al. Hypertension. 2024 Mar;81(3):595-603. doi: 10.1161/HYPERTENSIONAHA.123.21902. Epub 2023 Dec 28. Hypertension. 2024. PMID: 38152977
METHODS: We retrospectively analyzed data on the prevalence of cardiovascular events in 341 consecutive patients with pheochromocytoma and paraganglioma treated from 1995 to 2023. Biochemical catecholamine phenotype was determined based on plasma or urinary catecholamines …
METHODS: We retrospectively analyzed data on the prevalence of cardiovascular events in 341 consecutive patients with pheochromocytoma …
Composite pheochromocytoma with spindle cell sarcoma - a rare tumor of the adrenal gland: case report.
Turk Y, Karimov Z, Ozdemir M, Ertan Y, Makay O. Turk Y, et al. Hormones (Athens). 2022 Sep;21(3):507-511. doi: 10.1007/s42000-022-00363-0. Epub 2022 Mar 18. Hormones (Athens). 2022. PMID: 35304732 Review.
Composite pheochromocytomas with a non-pheochromocytoma component stemming from an embryological origin other than the neural crest comprise a unique entity. We present a patient diagnosed with a composite pheochromocytoma with spindle cell sarc …
Composite pheochromocytomas with a non-pheochromocytoma component stemming from an embryological origin other than the …
Utility of GATA3 in the differential diagnosis of pheochromocytoma.
Perrino CM, Ho A, Dall CP, Zynger DL. Perrino CM, et al. Histopathology. 2017 Sep;71(3):475-479. doi: 10.1111/his.13229. Epub 2017 Jun 5. Histopathology. 2017. PMID: 28374498
GATA3 was negative in 90% of adrenal cortical carcinoma. In contrast, pheochromocytomas were frequently positive (71%), including benign pheochromocytoma, pheochromocytoma with features concerning for malignancy, malignant (metastatic) pheochromocyt …
GATA3 was negative in 90% of adrenal cortical carcinoma. In contrast, pheochromocytomas were frequently positive (71%), includ …
Case Report: Composite pheochromocytoma with ganglioneuroma component: A report of three cases.
Araujo PB, Carvallo MS, Vidal AP, Nascimento JB, Wo JM, Naliato EO, Cunha Neto SH, Conceição FL, Fontes R, de Lima VV, Carvalho DP, Soares P, Lima J, Lourenço DM Jr, Violante AHD. Araujo PB, et al. Front Endocrinol (Lausanne). 2022 Sep 14;13:903085. doi: 10.3389/fendo.2022.903085. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 36187102 Free PMC article.
Composite pheochromocytoma (CP) is a very rare tumor originating from neural crest cells, predominantly composed of pheochromocytoma (PCC), a chromaffin cell tumor arising in adrenal medulla, and ganglioneuroma, a tumor derived from autonomic ganglion …
Composite pheochromocytoma (CP) is a very rare tumor originating from neural crest cells, predominantly composed of pheochr …
Retroperitoneal composite pheochromocytoma-ganglioneuroma : a case report and review of literature.
Hu J, Wu J, Cai L, Jiang L, Lang Z, Qu G, Liu H, Yao W, Yu G. Hu J, et al. Diagn Pathol. 2013 Apr 15;8:63. doi: 10.1186/1746-1596-8-63. Diagn Pathol. 2013. PMID: 23587063 Free PMC article. Review.
Composite pheochromocytoma/paraganglioma is a rare tumor with elements of pheochromocytoma/paraganglioma and neurogenic tumor. Most were located in the adrenal glands, and extra-adrenal composite pheochromocytoma is extremel …
Composite pheochromocytoma/paraganglioma is a rare tumor with elements of pheochromocytoma/paraganglioma and neurogenic …
44 results