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2942 search results for:

Adrenocortical Carcinoma 

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  1. 23-04-2024 | Adrenocortical Carcinoma | Online First

    Prognostic factors of adrenocortical carcinoma in children and adolescents: a population-based study

    Adrenocortical carcinoma (ACC) is a rare and aggressive form of cancer that develops in the adrenal cortex, which is the outer layer of the adrenal glands [ 1 ]. It is rare in the pediatric population, with an incidence of 0.2–0.3 patients per …

  2. 21-02-2024 | Adrenocortical Carcinoma | ReviewPaper

    Current Status and Future Direction in the Treatment of Advanced Adrenocortical Carcinoma

    Adrenocortical carcinoma (ACC) is an extremely rare tumor originating in the cortex of adrenal glands and has a very poor prognosis. The annual incidence of ACC is reported to be approximately 1 to 2 cases per million people [ 1 ]. Although …

  3. Open Access 21-02-2024 | Adrenocortical Carcinoma | Online First

    Prognostic role of quantitative [18F]FDG PET/CT parameters in adrenocortical carcinoma

    Adrenocortical carcinoma (ACC) is a rare endocrine malignancy (incidence of 0.7–2 cases per million population/year) [ 1 , 2 ]. Five-year survival rates are heterogeneous, ranging from 0% to 80%, and depend mainly on tumor stage, resection status …

  4. 05-11-2023 | Adrenocortical Carcinoma | OriginalPaper

    Defining Optimal Management of Non-metastatic Adrenocortical Carcinoma

  5. 17-11-2023 | Abstract

    ASO Visual Abstract: Defining Optimal Management of Nonmetastatic Adrenocortical Carcinoma

  6. 22-11-2023 | Adrenocortical Carcinoma | BriefCommunication

    ASO Author Reflections: Surgical Decision-Making in Adrenocortical Carcinoma: When Less is More

    Adrenocortical carcinoma (ACC) is an aggressive cancer with poor outcomes. 1 ACC is also rare, limiting the feasibility of randomized prospective trials. In non-metastatic ACC, complete surgical resection is the only potentially curative therapy; …

  7. Open Access 01-12-2023 | Metastasis | OriginalPaper

    Coincidence of primary adrenocortical carcinoma and melanoma: three CASE reports

    Adrenocortical carcinoma (ACC) is a rare and aggressive endocrine malignancy with an incidence of 0.7–2.0 cases/million/year. It commonly arises sporadically, but in rare cases, may also be a part of familial syndromes [ 1 , 2 ]. ACC has been …

  8. Open Access 24-06-2023 | Adrenocortical Carcinoma | OriginalPaper

    Outcome of brain metastases from adrenocortical carcinoma: a pooled analysis

    Adrenocortical carcinoma (ACC) is a rare malignancy affecting around 0.7–2 persons per one million population per year. [ 1 , 2 ] The incidence shows a bimodal distribution with the first peak in childhood (1–6 years old) and the second peak in …

  9. Open Access 01-12-2023 | Adrenocortical Carcinoma | OriginalPaper

    Pediatric adrenocortical carcinoma: clinical features and application of neoadjuvant chemotherapy

    Adrenal cortical carcinoma (ACC) is an aggressive malignant tumor with one of the incidence peaks in children and adolescents, with 0.5–2.0 new cases per 1 million children per year, accounting for 0.2% of childhood malignant tumors [ 1 , 2 ]. Due …

  10. 20-10-2023 | Adrenocortical Carcinoma | Online First

    Surgery for Adrenocortical Carcinoma: Do We Have Enough Evidence to Perform Robotic Approach? A Systematic Review

    Surgery is the treatment of choice for adrenocortical carcinoma (stage I–III). In recent years, many authors demonstrated the safety and feasibility of minimally invasive approaches when applied to highly selected cases. The aim of the present …

  11. Open Access 01-12-2023 | Adrenocortical Carcinoma | OriginalPaper

    Exploring the role of the disulfidptosis-related gene SLC7A11 in adrenocortical carcinoma: implications for prognosis, immune infiltration, and therapeutic strategies

    Adrenocortical carcinoma (ACC) is a malignant endocrine tumour that occurs in the adrenal cortex and accounts for approximately 14% of primary adrenal tumours [ 1 ]. It generally has specific biological characteristics, such as hormone activity and …

  12. Open Access 01-07-2023 | Adrenocortical Carcinoma | OriginalPaper

    Carbonic anhydrases III and IX are new players in the crosstalk between adrenocortical carcinoma and its altered adipose microenvironment

    The adipose tissue (AT) is a pivotal endocrine organ for the regulation not only of energetic and metabolic equilibrium, but it is also involved in solid tumor development and progression. A different sensitivity to metabolic dysregulation …

  13. Open Access 01-12-2022 | Adrenocortical Carcinoma | OriginalPaper

    Massive adrenocortical carcinoma presenting as peripheral edema: a case report

    Peripheral edema is often caused by diminished cardiac output, sodium and water retention due to kidney or liver failure, decreased serum albumin concentration (for example, due to nephrotic syndrome), or medications such as vasodilators …

  14. Open Access 01-12-2022 | Adrenocortical Carcinoma | OriginalPaper

    Tumor mutational burden presents limiting effects on predicting the efficacy of immune checkpoint inhibitors and prognostic assessment in adrenocortical carcinoma

    Adrenocortical carcinoma (ACC) is a highly malignant urologic cancer and tends to metastasize. The overall survival (OS) time of ACC patients is commonly less than 30 months, while the 5-year overall survival rate (OSR) of patients with clinical …

  15. 01-12-2023 | Adrenocortical Carcinoma | ReviewPaper

    Minimally invasive versus open adrenalectomy for adrenocortical carcinoma: the keys surgical factors influencing the outcomes—a collective overview

    Adrenocortical carcinoma (A.C.C.) is a rare and aggressive endocrine malignancy, with an annual incidence of approximately 1–2/1,000,000 people worldwide, accounting for 0.05–0.2% of all malignancies. In a recent Japanese nationwide survey …

  16. 12-09-2022 | Metastasis | OriginalPaper

    Metastatic adrenocortical carcinoma of the interventricular septum

  17. Open Access 14-05-2022 | Nausea | ReviewPaper

    Supportive therapies in patients with advanced adrenocortical carcinoma submitted to standard EDP-M regimen

    EDP-M (etoposide, doxorubicin, cisplatin combined with mitotane) is the standard first-line regimen in the management of patients with advanced adrenocortical carcinoma (ACC), an extremely rare disease [ 1 , 2 ]. The efficacy of this regimen is …

  18. 01-01-2022 | Adrenocortical Carcinoma | OriginalPaper

    Revisiting the AJCC staging system of adrenocortical carcinoma

    Adrenocortical carcinoma is a rare disease entity with limited information about prognostic variables and treatment strategies [ 1 , 2 ]. Factors shown to play a prognostic role among those patients include anatomic stage, grade (through Weiss …

  19. Open Access 01-12-2021 | Adrenocortical Carcinoma | OriginalPaper

    Upregulation of TCF21 inhibits migration of adrenocortical carcinoma cells

    Adrenocortical tumors are usually incidentally diagnosed in 6–7% of the population [ 1 ]. Most of them are benign and non-functioning classified as adenomas (ACA), requiring only clinical monitoring [ 2 ]. In contrast, adrenocortical carcinomas …

  20. 01-02-2024 | Adrenal Cancer | OriginalPaper

    Adrenocortical carcinoma with venous tumor invasion: is there a role for mini-invasive surgery?

    Adrenocortical carcinoma (ACC) is a rare disease combined with a poor prognosis [ 1 ]. The increasing use of abdominal imaging decreases the percentage of metastatic tumors at the diagnosis to 25% [ 2 ]; the lesions are often extensive with …

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