Results 1 to 10 of about 27,401 (179)

Prenatal presentation of an adrenocortical tumor [PDF]

open access: yesCancer Reports, 2022
Background Prenatally identified suprarenal masses are most often found to be adrenal hemorrhage. The most common tumor in this situation is neuroblastoma. Case Presentation We report the case of a rare adrenocortical tumor found prenatally on ultrasound.
Jeffrey H. Schwartz, Erlyn Smith
doaj   +4 more sources

Biological Effects of EF24, a Curcumin Derivative, Alone or Combined with Mitotane in Adrenocortical Tumor Cell Lines [PDF]

open access: yesMolecules, 2019
Background: Curcumin has numerous properties and is used in many preclinical conditions, including cancer. It has low bioavailability, while its derivative EF24 shows enhanced solubility.
Loris Bertazza   +9 more
doaj   +2 more sources

Androgen producing oncocytic adrenocortical tumor in a 3.7-year-old female [PDF]

open access: yesEndocrinology, Diabetes & Metabolism Case Reports
We report a 3.7-year-old female who presented with clinical features of premature adrenarche. Workup revealed significantly elevated androgen levels and advanced bone maturation, prompting abdominal imaging that identified a 6.0 cm adrenal mass.
Kelli D Mans   +3 more
doaj   +2 more sources

Tumor adrenocortical:

open access: yesOncología, 2007
Hacemos breve revisión sobre Tumores de la Corteza Suprarrenal, sus aspectos macroscópico, microscópico, histopatológico e inmunohistoquímico, Se presenta un caso de Carcinoma de Corteza Suprarrenal, en una paciente de sexo femenino, de 57 años, con ...
Gabriela Picón C.   +2 more
doaj   +1 more source

Case Report: Surgery to remove adrenocortical oncocytic carcinoma from an Asian male

open access: yesFrontiers in Surgery, 2023
Adrenocortical oncocytic carcinoma is a rare type of adrenocortical tumor. Its clinical characteristics and biological behavior need to be further evaluated after the accumulation of cases.
Hongtao Liu   +3 more
doaj   +1 more source

A case of estrogen‐secreting adrenocortical carcinoma: Comprehensive immunohistochemical analysis of disorganized steroid genesis

open access: yesIJU Case Reports, 2021
Introduction Adrenocortical carcinoma rarely secretes estrogens, and little is known regarding the mechanism of intra‐tumor estrogen production. We report an estrogen‐secreting adrenocortical carcinoma in a postmenopausal woman, where comprehensive ...
Megumi Yokoyama   +8 more
doaj   +1 more source

Adrenocortical carcinoma with inferior vena cava tumor thrombus found during surgery

open access: yesIJU Case Reports, 2022
Introduction The safety and efficacy of minimally invasive approaches for adrenocortical carcinoma with inferior vena cava tumor thrombus have not yet been established.
Yuta Nabeshima   +9 more
doaj   +1 more source

Adrenocortical tumors in children [PDF]

open access: yesBrazilian Journal of Medical and Biological Research, 2000
Childhood adrenocortical tumors (ACT) are rare. In the USA, only about 25 new cases occur each year. In Southern Brazil, however, approximately 10 times that many cases are diagnosed each year. Most cases occur in the contiguous states of São Paulo and Paraná. The cause of this higher rate has not been identified.
Ribeiro, R.C.   +7 more
openaire   +5 more sources

DNA hypermethylation driven by DNMT1 and DNMT3A favors tumor immune escape contributing to the aggressiveness of adrenocortical carcinoma

open access: yesClinical Epigenetics, 2023
Background Adrenocortical carcinoma is rare and aggressive endocrine cancer of the adrenal gland. Within adrenocortical carcinoma, a recently described subtype characterized by a CpG island methylator phenotype (CIMP) has been associated with an ...
Gwenneg Kerdivel   +8 more
doaj   +1 more source

Ectopic adrenocortical adenoma in the renal hilum mimicking a renal cell carcinoma

open access: yesRadiology Case Reports, 2022
Ectopic adrenocortical tissue can arise along the path of embryonic migration, such as the celiac axis, broad ligament, adnexa of the testis, and spermatic cord.
Masashi Endo, MD   +7 more
doaj   +1 more source

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