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Quoted phrase not found in phrase index: "Recurrent Adrenal Cortical Carcinoma"
Page 1
European Society of Endocrinology Clinical Practice Guidelines on the management of adrenocortical carcinoma in adults, in collaboration with the European Network for the Study of Adrenal Tumors.
Fassnacht M, Dekkers OM, Else T, Baudin E, Berruti A, de Krijger R, Haak HR, Mihai R, Assie G, Terzolo M. Fassnacht M, et al. Eur J Endocrinol. 2018 Oct 1;179(4):G1-G46. doi: 10.1530/EJE-18-0608. Eur J Endocrinol. 2018. PMID: 30299884 Free article.
Adrenocortical carcinoma (ACC) is a rare and in most cases steroid hormone-producing tumor with variable prognosis. ...(iv) We suggest that all suspected ACC should be reviewed by an expert adrenal pathologist using the Weiss score and providing Ki67 i …
Adrenocortical carcinoma (ACC) is a rare and in most cases steroid hormone-producing tumor with variable prognosis. ...(iv) We …
Pembrolizumab in paediatric patients with advanced melanoma or a PD-L1-positive, advanced, relapsed, or refractory solid tumour or lymphoma (KEYNOTE-051): interim analysis of an open-label, single-arm, phase 1-2 trial.
Geoerger B, Kang HJ, Yalon-Oren M, Marshall LV, Vezina C, Pappo A, Laetsch TW, Petrilli AS, Ebinger M, Toporski J, Glade-Bender J, Nicholls W, Fox E, DuBois SG, Macy ME, Cohn SL, Pathiraja K, Diede SJ, Ebbinghaus S, Pinto N. Geoerger B, et al. Lancet Oncol. 2020 Jan;21(1):121-133. doi: 10.1016/S1470-2045(19)30671-0. Epub 2019 Dec 4. Lancet Oncol. 2020. PMID: 31812554 Clinical Trial.
Patients with melanoma or a centrally confirmed, PD-L1-positive, relapsed or refractory solid tumour or lymphoma, and a Lansky Play/Karnofsky Performance status score of 50 or higher, received intravenous pembrolizumab at an initial dose of 2 mg/kg every 3 weeks. ...Of 136 …
Patients with melanoma or a centrally confirmed, PD-L1-positive, relapsed or refractory solid tumour or lymphoma, and a Lansky Play/Karnofsk …
Adrenocortical Carcinoma: A Clinician's Perspective.
Elfiky A. Elfiky A. Surg Pathol Clin. 2015 Dec;8(4):751-4. doi: 10.1016/j.path.2015.07.002. Surg Pathol Clin. 2015. PMID: 26612225 Review.
Within the category of orphan diseases and rare malignancies, adrenocortical carcinoma (ACC) represents an aggressive entity with high mortality and morbidity. While localized tumors which are diagnosed early can be cured with surgical intervention, there are progno …
Within the category of orphan diseases and rare malignancies, adrenocortical carcinoma (ACC) represents an aggressive entity w …
Multimodality Imaging of Abdominopelvic Tumors with Venous Invasion.
LeGout JD, Bailey RE, Bolan CW, Bowman AW, Chen F, Cernigliaro JG, Alexander LF. LeGout JD, et al. Radiographics. 2020 Nov-Dec;40(7):2098-2116. doi: 10.1148/rg.2020200047. Epub 2020 Oct 16. Radiographics. 2020. PMID: 33064623 Review.
Venous invasion is a distinctive feature of hepatocellular carcinoma and renal cell carcinoma with known prognostic and treatment implications; however, this finding remains an underrecognized characteristic of multiple other malignancies-including cholangiocarcinom …
Venous invasion is a distinctive feature of hepatocellular carcinoma and renal cell carcinoma with known prognostic and treatm …
Management of functioning pediatric adrenal tumors.
Lopes RI, Suartz CV, Neto RP, Berjeaut RH, Mendonca B, Almeida MQ, Fragoso MCV, Dénes FT. Lopes RI, et al. J Pediatr Surg. 2021 Apr;56(4):768-771. doi: 10.1016/j.jpedsurg.2020.08.020. Epub 2020 Sep 1. J Pediatr Surg. 2021. PMID: 32972741
Tumor recurrence occurred in 6 patients (10.3%), and there were three disease-related deaths (5%). ...During a median follow-up of 180 (range: 127-300) months, recurrence was observed in 6 cases (35.3%) and disease-related death in 1 case (5.9%). ...
Tumor recurrence occurred in 6 patients (10.3%), and there were three disease-related deaths (5%). ...During a median follow-up of 18 …
Functioning metastasis from adrenocortical carcinoma.
Cunha C, Donato S, Silva T, Leite V. Cunha C, et al. BMJ Case Rep. 2022 Jan 25;15(1):e246742. doi: 10.1136/bcr-2021-246742. BMJ Case Rep. 2022. PMID: 35078872 Free PMC article.
Recurrence of Cushing's syndrome due to functional metastasis from adrenocortical carcinoma (ACC) after adrenalectomy is extremely rare. ...Patient underwent bilateral adrenalectomy with R0 resection. Pathological examination revealed a left ACC with a Weiss' …
Recurrence of Cushing's syndrome due to functional metastasis from adrenocortical carcinoma (ACC) after adrenalectomy i …
Prognostic Value of Microscopic Tumor Necrosis in Adrenal Cortical Carcinoma.
Luconi M, Cantini G, van Leeuwaarde RS, Roebaar R, Fei L, Propato AP, Santi R, Ercolino T, Mannelli M, Canu L, de Krijger RR, Nesi G. Luconi M, et al. Endocr Pathol. 2023 Jun;34(2):224-233. doi: 10.1007/s12022-023-09760-6. Epub 2023 Mar 23. Endocr Pathol. 2023. PMID: 36952130 Free PMC article.
Adrenal cortical carcinoma (ACC) is an uncommon neoplasm with variable prognosis. Several histologic criteria have been identified as predictors of malignancy in adrenal cortical tumors. The Weiss score is the system most widely em …
Adrenal cortical carcinoma (ACC) is an uncommon neoplasm with variable prognosis. Several histologic criteria have been …
Radiotherapy in adrenocortical carcinoma.
Polat B, Fassnacht M, Pfreundner L, Guckenberger M, Bratengeier K, Johanssen S, Kenn W, Hahner S, Allolio B, Flentje M. Polat B, et al. Cancer. 2009 Jul 1;115(13):2816-23. doi: 10.1002/cncr.24331. Cancer. 2009. PMID: 19402169 Free article. Review.
Adrenocortical carcinoma (ACC) is a rare malignancy, and patients with ACC have a poor prognosis. ...In an adjuvant setting, postoperative radiotherapy was able to prevent local recurrence in the majority of patients. In those with advanced disease, a respons …
Adrenocortical carcinoma (ACC) is a rare malignancy, and patients with ACC have a poor prognosis. ...In an adjuvant setting, p …
Adrenocortical carcinoma: a clinician's update.
Fassnacht M, Libé R, Kroiss M, Allolio B. Fassnacht M, et al. Nat Rev Endocrinol. 2011 Jun;7(6):323-35. doi: 10.1038/nrendo.2010.235. Epub 2011 Mar 8. Nat Rev Endocrinol. 2011. PMID: 21386792 Review.
Adrenocortical carcinoma is a rare heterogeneous neoplasm with an incompletely understood pathogenesis and a poor prognosis. ...No general consensus on the diagnostic and therapeutic measures for adrenocortical carcinoma exists, but collaborative effor …
Adrenocortical carcinoma is a rare heterogeneous neoplasm with an incompletely understood pathogenesis and a poor prognosis. . …
Molecular Imaging in the Management of Adrenocortical Cancer: A Systematic Review.
Wong KK, Miller BS, Viglianti BL, Dwamena BA, Gauger PG, Cook GJ, Colletti PM, Rubello D, Gross MD. Wong KK, et al. Clin Nucl Med. 2016 Aug;41(8):e368-82. doi: 10.1097/RLU.0000000000001112. Clin Nucl Med. 2016. PMID: 26825212 Review.
Adrenocortical cancer (ACC) is an uncommon primary neoplasm of the adrenal cortex with dismal prognosis. It often presents with symptoms and signs of adrenal cortical hormone hypersecretion and abdominal mass effect or is incidentally detected as an …
Adrenocortical cancer (ACC) is an uncommon primary neoplasm of the adrenal cortex with dismal prognosis. It often presents wit …
164 results