Results 31 to 40 of about 34,931 (220)

Case Report: Adrenocortical carcinoma in children—symptoms, diagnosis, and treatment

open access: yesFrontiers in Endocrinology, 2023
Adrenocortical carcinomas are extremely rare in the paediatric population. Most of them are hormone-secretive lesions; therefore, they should be taken into consideration in a child with signs of precocious puberty and/or Cushing’s syndrome symptoms ...
Estera Zagojska   +3 more
doaj   +1 more source

New directions for the treatment of adrenal insufficiency [PDF]

open access: yes, 2015
The following funding bodies supported this work: Biotechnology and Biological Sciences Research Council (BBSRC BB/L00267/1, to LG), Rosetrees Trust (to LG), Barts and The London Charity (417/2235, to LG), EU COFUND (PCOFUND-GA-2013-608765, to LG and GRB)
Allen   +69 more
core   +2 more sources

18F-FDG PET/CT image findings of a dog with adrenocortical carcinoma

open access: yesBMC Veterinary Research, 2022
Background In human medicine, 18F-fluorodeoxyglucose (FDG) positron emission tomography (PET) has been used to differentiate between benign and malignant adrenal tumors and to identify metastases.
Dohee Lee   +7 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

Physiopathological Implications of 7TM Receptors [PDF]

open access: yes, 2010
Seven-transmembrane (7TM) receptors are one of the most important proteins involved in perception of extracellular stimuli and regulation of variety of intracellular signaling pathways.
Cygankiewicz, Adam
core   +2 more sources

Radiotherapy in adrenocortical carcinoma [PDF]

open access: yesCancer, 2009
AbstractAdrenocortical carcinoma (ACC) is a rare malignancy, and patients with ACC have a poor prognosis. Even after radical surgery, up to 85% of patients develop recurrent disease. Systemic treatment options still have limited efficacy. Because the role of radiotherapy is not defined well and because ACC often is considered radioresistant, the ...
Buelent, Polat   +9 more
openaire   +2 more sources

Virilizing adrenocortical carcinoma in a child: A rare enigma

open access: yesIndian Journal of Endocrinology and Metabolism, 2012
Adrenocortical carcinomas are rare tumors with an incidence of one to two cases per million population and are still more rarer in the pediatric age group.
Varuna Sipayya   +4 more
doaj   +1 more source

Surgical approach to an adrenocortical carcinoma with right atrial extension in a nine-year old male: Our experience

open access: yesJournal of Pediatric Surgery Case Reports, 2020
Adrenocortical carcinoma with intracaval and intra atrial extension is an extremely rare occurrence in the pediatric population. We report the case of a nine‐year‐old male who presented to our outpatient department with facial swelling, weight gain, and ...
Ayesha Saleem   +3 more
doaj   +1 more source

Durable response to pembrolizumab in microsatellite instability‐high advanced adrenocortical carcinoma

open access: yesIJU Case Reports, 2023
Introduction Advanced adrenocortical carcinoma has a poor prognosis and is treated with chemotherapy that includes mitotane with etoposide, doxorubicin, and cisplatin as first‐line therapy.
Masaya Senda   +5 more
doaj   +1 more source

Robot-Assisted Laparoscopic Adrenalectomy for Rare Myxoid Adrenocortical Carcinoma

open access: yesCase Reports in Urology, 2019
Background. Surgical resection remains the standard treatment for adrenocortical carcinoma. Higher rates of local and peritoneal recurrence have been reported with the laparoscopic approach compared to open resection, although the evidence is limited.
Grant Johnson   +3 more
doaj   +1 more source

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