Results 11 to 20 of about 117,113 (304)

Adrenal oncocytoma

open access: yesRevista Cubana de Medicina Militar, 2021
Introduction: Adrenal oncocytoma is a rare and incidental tumor without its own clinical manifestations. Objective: To present a case of adrenal oncocytoma and its diagnostic and therapeutic characteristics. Clinical case: 34-year-old male patient with a
Roxana Soranyer Horroutinel Scull   +3 more
doaj   +2 more sources

Case of extragonadal germ cell tumor mimicking left adrenal tumor. [PDF]

open access: yesUrol Case Rep, 2023
A 30-year-old man presented to his previous physician with left abdominal pain. Computed tomography revealed a left retroperitoneal mass with calcification, measuring 15 × 9 × 6 cm, and the patient was referred to our hospital for further examination ...
Ito H   +5 more
europepmc   +2 more sources

The ADRENAL score: A comprehensive scoring system for standardized evaluation of adrenal tumor. [PDF]

open access: yesFront Endocrinol (Lausanne), 2022
OBJECTIVES: To propose an original and standardized scoring system to quantify the functional and anatomical characteristics of adrenal tumor. MATERIALS AND METHODS: Four groups of consecutive adrenalectomies (n = 458) with heterogeneity in tumor ...
Zhou X   +12 more
europepmc   +2 more sources

Differentiation of adrenal adenomas from adrenal metastases in single-phased staging dual-energy CT and radiomics [PDF]

open access: yes, 2022
PURPOSE Differentiation of incidental adrenal lesions remains a challenge in diagnostic imaging, especially on single-phase portal venous computed tomography (CT) in the oncological setting.
Malte N. Bongers   +15 more
core   +1 more source

Impairment of adrenocortical function associated with increased plasma tumor necrosis factor-alpha and interleukin 6 concentrations in African trypanosomiasis [PDF]

open access: yes, 1994
African sleeping sickness (SS) is a severe, potentially lethal parasitic disease. The treatments of choice are the antiparasitic agents suramin, which is adrenotoxic, and/or melarsoprol. We evaluated the functional integrity of the hypothalamic-pituitary-
Winkelmann, W.   +19 more
core   +1 more source

Tumors OF THE Adrenals [PDF]

open access: yesThe Journal of Nervous and Mental Disease, 1934
A review of 371 cases of malignant tumors coming to autopsy at the State Institute for the Study of Malignant Disease revealed 49 cases in which the adrenal gland showed metastatic involvement. Two cases of primary adrenal tumors, one a medullary type tumor in a three-year-old boy, the other arising in the cortex of the right adrenal of a female of ...
openaire   +1 more source

Adrenal Tumor Mimicking Non-Classic Congenital Adrenal Hyperplasia

open access: yesFrontiers in Endocrinology, 2020
Elevated 17-hydroxyprogesterone may be caused by congenital adrenal hyperplasia, ovarian or adrenal tumors. A positive cosyntropin stimulation test result for 17-hydroxyprogesterone may be found in functional or non-functional tumors and be related to ...
Wen-Hsuan Tsai   +5 more
doaj   +1 more source

European multicentre study on outcome of surgery for sporadic primary hyperparathyroidism

open access: yesBJS (British Journal of Surgery), EarlyView., 2020
Some 5861 patients undergoing first‐time surgery for sporadic primary hyperparathyroidism were registered in the Eurocrine® database between 2015 and 2018. The use of intraoperative parathyroid hormone measurement decreased the risk of conversion and persistent hypercalcaemia.
A. Bergenfelz   +3 more
wiley   +1 more source

Complications after medullary thyroid carcinoma surgery: multicentre study of the SQRTPA and EUROCRINE® databases

open access: yesBJS (British Journal of Surgery), EarlyView., 2020
This study investigated postoperative complications after surgery for medullary thyroid carcinoma (MTC) in Europe. Hypoparathyroidism, recurrent laryngeal nerve palsy and bleeding requiring reoperation occurred in 170 (26·2 per cent), 62 (13·7 per cent) and 17 (2·6 per cent) patients respectively.
D.‐J. van Beek   +18 more
wiley   +1 more source

Laparoscopic excision of a large Adrenal Ganglioneuroma masquerading as Pheochromocytoma- A case report & review of literature

open access: yesUrology Case Reports, 2020
Adrenal Ganglioneuromas are rare. Evaluation for hormone secretion followed by complete excision is the treatment of choice for such masses. We present our experience of a symptomatic large Adrenal Ganglioneuroma, which was removed with laparoscopic ...
K. Santosh   +5 more
doaj   +1 more source

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