Results 211 to 220 of about 117,431 (260)
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Adrenal Tumors in Adults

Surgical Pathology Clinics, 2015
Although most adrenal tumors are not diagnostic dilemmas, there are cases that are challenging. This may be due to the tissue provided, for example fragmented tissue received in the setting of morcellation, or it may be due to inherently challenging histology, such as in cases with equivocal features of malignancy.
Andre, Pinto, Justine A, Barletta
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Adrenal cortex tumors

The American Journal of Surgery, 1952
Abstract The aforementioned comments of the effects of adrenal cortical tumors have been necessarily limited by the extensiveness of the subject. However, we have mentioned briefly the relation of the adrenal cortex to electrolyte and carbohydrate metabolism and to the various changes in secondary sex characteristics which are seen in patients with ...
H, BERMAN, F S, MAINELLA
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Adrenal tumors in the elderly

Endocrine-Related Cancer
Graphical Abstract Abstract The incidence of adrenal tumors rises with age, but the link between adrenal aging and tumorigenesis is still not well defined. This mini-review summarizes age-related changes in both the adrenal cortex and
Abel Decmann   +3 more
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Malignant adrenal tumors

Seminars in Pediatric Surgery, 2006
Adrenal tumors, apart from neuroblastoma, are relatively rare in infancy and childhood. Most adrenal lesions are benign, and both benign and malignant tumors may be hormonally active thus, making accurate preoperative diagnosis difficult. The two main malignant tumors are adrenocortical carcinoma and pheochromocytoma.
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Tumors of the adrenal glands

The American Journal of Surgery, 1958
T HE pbeocbromocytoma is a tumor of the chromaffrn tissue of the body; and since chromaffrn tissue is rather widely distributed, it follows that the location of these tumors may also vary widely. Naturally, since most of the chromaffrn tissue is in the adrenal meduIla, this is by far the most common location for these tumors.
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Tumors of the Adrenals

Onkologie, 2009
Recent advances in imaging techniques (e.g. computed tomography, nuclear resonance imaging) have led to the discovery of unexpected adrenal tumors in about 2% of the patients. The incidental discovery of an adrenal tumor presents a complex diagnostic problem since the differentiation of the few endocrine active adrenal tumors (combined less than 6% of ...
F. Jockenhövel, R. Hoermann, K. Mann
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Tumors of the Adrenal Cortex

2009
Adrenal cortical tumors may present clinically with evidence of excess hormone secretion, local mass effects, or symptoms and signs associated with malignancy. They are now also identified incidentally when the abdomen is scanned in the investigation of other disease.
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Adrenal tumors.

Minerva endocrinologica, 2009
Adrenal tumors can be primary or secondary entities. Primary tumors are able to secrete hormones which may cause significant effects clinically. Typical tumor-related adrenal diseases are Conn's syndrome (hyperaldosteronism), Cushing's syndrome (hypercortisolism), and pheochromocytoma (catacholamine excess). Primary adrenal tumors are rarely malignant,
D, Rubello, M D, Gross
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Adrenal tumors

The American Journal of Surgery, 1958
P J, CONNOLLY   +2 more
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Brain and other central nervous system tumor statistics, 2021

Ca-A Cancer Journal for Clinicians, 2021
Rebecca L. Siegel   +2 more
exaly  

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