The impact of mitotane therapy on serum-free proteins in patients with adrenocortical carcinoma [PDF]
Introduction: Adrenocortical carcinoma (ACC) is a rare malignancy of the adrenal cortex. Whilst surgery is the preferred treatment, adjunctive therapy with mitotane may be offered post-surgically to minimise the risk of recurrence or, in the absence of ...
Magdalena Lech +12 more
doaj +2 more sources
Recent Updates on the Management of Adrenal Incidentalomas [PDF]
Adrenal incidentalomas represent an increasingly common clinical conundrum with significant implications for patients. The revised 2023 European Society of Endocrinology (ESE) guideline incorporates cutting-edge evidence for managing adrenal ...
Seung Shin Park, Jung Hee Kim
doaj +1 more source
A Histopathological Study on Adrenal Tumours in a Tertiary Care Centre in Chenna [PDF]
Introduction: The lesions of the adrenal gland are quite rarely encountered in surgical pathology. Primary adrenal neoplasms have a varied clinical presentation, being functional or nonfunctional, symptomatic or asymptomatic, or detected as ...
Deepa Krishnan, Sudha Venkatesh
doaj +1 more source
[Adrenal cortex neoplasms in children: diagnostic and therapeutic difficulties].
Two cases of adrenal cortical carcinoma in the pediatric age group are reported: the first case regards a fourteen month old female patient which presented with virilization and Cushing's syndrome: the second case regards a twelve year old boy with severe hypertension.
Caldarella A +4 more
openaire +3 more sources
Androgen deficiency in women with adrenal insufficiency. Dehydroepiandrosterone. Review [PDF]
It is known that adrenal insufficiency (AI) is a severe life-threatening disease due to the exceptional role of glucocorticoids and mineralocorticoids in the human body. At the same time, according to some reports, the deficit of androgens synthesized by
N F Nuralieva +3 more
doaj +1 more source
Hypersecretor oncocytic tumor of adrenal cortex
Introducción: El carcinoma adrenocortical es una entidad rara con una incidencia anual de 1- 2 casos por millón de personas. Las neoplasias oncocíticas que surgen en las glándulas suprarrenales son extremadamente raras, y por lo general se descubren como
García Hernández, Mildrey +2 more
core +1 more source
The new histological system for the diagnosis of adrenocortical cancer
IntroductionAdrenocortical cancer (ACC) is a rare malignant tumor that originates in the adrenal cortex. Despite extensive molecular-genetic, pathomorphological, and clinical research, assessing the malignant potential of adrenal neoplasms in clinical ...
Liliya Urusova +5 more
doaj +1 more source
Background: Prolonged episodes of uncontrolled congenital adrenal hyperplasia (CAH) have been shown to result in the occurrence of secondary adrenal neoplasms.
Zulfiya R. Shafigullina +7 more
doaj +1 more source
Robot‐Assisted Laparoscopic Partial Adrenalectomy Utilizing Intraoperative Indocyanine Green Near‐Infrared Fluorescence Imaging for Pheochromocytoma: A Case Report [PDF]
ABSTRACT Introduction Indocyanine green (ICG) near‐infrared fluorescence (NIRF) imaging facilitates pheochromocytoma identification during adrenal surgery. Case Presentation We report a 21‐year‐old woman with multiple endocrine neoplasia type 2A and bilateral adrenal tumors who underwent ICG‐NIRF–guided, robot‐assisted partial adrenalectomy for ...
Takizawa N +5 more
europepmc +2 more sources
Embolization in an adrenocortical carcinoma as palliative therapy [PDF]
Background: With an annual incidence of 0.2% of new cases per 100,000 inhabitants, adrenocortical carcinoma is rare. In advanced tumor only palliative treatment modalities are practicable. Because of scarcity of the tumor, standard treatment has not been
Kühl, M. +5 more
core +1 more source

