Results 121 to 130 of about 6,950 (277)
Imaging characterization of non-hypersecreting adrenal masses. Comparison between MR and radionuclide techniques. [PDF]
AIM: In patients with non-hypersecreting adrenal masses, tumor characterization is clinically relevant to establish the appropriate treatment planning. The aim of this study was to comparatively characterize such adrenal lesions using MR and radionuclide
Caracò C +5 more
core
Continua com: Baròmetre semestral de ...
Direcció de Serveis d'Estudis i Avaluació
core +3 more sources
Bilateral giant adrenal myelolipoma associated with congenital adrenal hyperplasia
Isabela Milagres Guimarães +4 more
openalex +1 more source
Giant adrenal myelolipomas: a literature review
Myelolipomas are described as small tumors, with some authors referring to sizes less than 4 cm in diameter. However, when greater than 10 cm, myelolipomas are labeled as giant tumors and thus, have a definite indication for surgical resection ...
Mircea Hogea +5 more
doaj +1 more source
Laparoscopic management of adrenal tumors: a four-year experience in a single center [PDF]
AIM: Today laparoscopy is considered the first choice treatment of many adrenal tumors, although its use is still controversial for large adrenal masses and incidentally found adrenal cortical carcinoma.
AGRUSA, Antonino +6 more
core
Transradial Embolization of Hemorrhagic Adrenal Myelolipoma [PDF]
Griffin Mcnamara +6 more
openalex +1 more source
Evaluation of adrenal tumors by magnetic resonance imaging with histological correlation [PDF]
A ressonância magnética é ferramenta importante para a detecção e caracterização dos tumores adrenais. O conhecimento das diferentes apresentações dos tumores primários e secundários à ressonância magnética e sua correlação com dados da histologia são ...
BARONI, Ronaldo Hueb +9 more
core +2 more sources
Robotic treatment of giant adrenal myelolipoma: A case report and review of the literature
Adrenal myelolipoma is a rare mesenchymal tumour with benign biological behaviour that is mainly composed of mature adipose and myeloid tissue. Both sexes are equally affected, most commonly between the fifth and seventh decades of life. The diagnosis of
G. Cochetti +6 more
semanticscholar +1 more source
Adrenocortical neoplasia: evolving concepts in tumorigenesis with an emphasis on adrenal cortical carcinoma variants [PDF]
Adrenocortical carcinoma (ACC) is a rare, heterogeneous malignancy with a poor prognosis. According to WHO classification 2004, ACC variants include oncocytic ACCs, myxoid ACCs and ACCs with sarcomatous areas. Herein, we provide a comprehensive review of
Ronald R. de Krijger +1 more
core +1 more source

