Results 141 to 150 of about 8,531 (170)

Cecal perforation and adrenocortical adenoma in a dog

Journal of the American Veterinary Medical Association, 1987
Cecal perforation was diagnosed in a dog with a history of acute vomiting. The dog also had an adrenocortical adenoma. Intestinal perforation can be a serious complication of cortico-steroid treatment in the dog, but has not been attributable to hyperadrenocorticism.
M P, Moore, J D, Robinette
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Myxoid adrenocortical adenoma with a pseudoglandular pattern

Virchows Archiv, 2004
Myxoid changes rarely occur in adrenocortical adenomas and carcinomas. Only eight benign tumours with such features have been described thus far, five of which also had a prominent pseudoglandular component. We report an additional pseudoglandular myxoid adenoma of the adrenal gland detected in a 58-year-old male patient who developed mild hypertension.
BOLLITO ER, PAPOTTI, Mauro Giulio, PORPIGLIA, Francesco, TERZOLO, Massimo, CRACCO, CECILIA MARIA, CAPPIA S, GUBETTA L, MIKUZ G.   +7 more
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Ultrastructural Features of an Aldosterone-Secreting Adrenocortical Adenoma

Hormone Research, 2008
An aldosterone-secreting adrenocortical adenoma was removed by surgery from a 15-year-old boy who exhibited signs characteristic of Conn’s syndrome including hypertension, potassium depletion and increased aldosterone production rate. The neoplasm was found to consist mainly of clear cells by light microscopy.
K, Kovacs, E, Horvath, N C, Delarue, J C, Laidlaw   +3 more
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Non‐functional adrenocortical adenoma with extensive degeneration

Pathology International, 2003
We report a case of non‐functional adrenocortical adenoma of 5.5 × 5.5 × 3.2 cm in size that had an unusual histopathological appearance in two respects. First, the tumor contained small adipose foci with osteogenesis and was suspected of being a myelolipoma based on its appearance on computerized tomography (CT) and magnetic resonance imaging. However,
Youhei, Masugi, Kaori, Kameyama, Motohiko, Aiba, Makio, Mukai, Satoshi, Hara, Takashi, Ohigashi, Masaru, Murai   +6 more
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MENARCHE AND PREGNANCY AFTER REMOVAL OF AN ADRENOCORTICAL ADENOMA*

The Journal of Clinical Endocrinology & Metabolism, 1951
THE clinical and laboratory manifestations of hyperfunctioning adrenocorticaltumors are variable, depending upon the character of the hormonal products of the neoplasm, the age and sex of the patient, and perhaps upon other factors (1, 2). Because of the relative rarity of such lesions and the diversity of their manifestations, the reporting of a case ...
L M, de PAIVA, J I, LOBO, A M, da SILVA
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STRUCTURAL CHANGE OF ADRENOCORTICAL ADENOMA IN CUSHING'S SYNDROME

Acta Pathologica Japonica, 1986
Eight adrenocortical adenomata from patients with Cushing's syndrome were examined by light and electron microscopy. Light microscopically, the reticulin fibers were markedly prominent in areas of the compact‐type cells and ran tangentially to the adenoma cells or parenchyma! cells.
K, Matsuo, H, Tsuchiyama
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Adrenal Pheochromocytoma With Contralateral Adrenocortical Adenoma in a Cat

Journal of the American Animal Hospital Association, 2010
A 7-year-old, neutered male cat was presented with a 6-month history of progressive polyuria, polydipsia, polyphagia, aggression, and weight gain. Previous blood work, urinalysis, and radiographs did not delineate a cause for the clinical signs. An ultrasound revealed bilateral adrenal gland enlargement.
Jon David R, Calsyn, Rebecca A, Green, Garrett J, Davis, Christopher M, Reilly   +3 more
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Plasma and tissue chromogranin in patients with adrenocortical adenomas

Journal of Endocrinological Investigation, 2004
Adrenal adenomas frequently arise from cortical islets in the medulla, and these islets seem to present a greater risk for pathological growth than cortical cells within the adrenal cortex. Chromogranin A (CgA), a glycoprotein co-stored in secreting granules and co-released with resident hormones of chromaffin cells, behaves as a prohormone, generating
BERNINI, GIAMPAOLO, MORETTI A, BORGIOLI M, BARDINI M, MICCOLI, PAOLO, BERTI, PIERO, BASOLO, FULVIO, FAVIANA, PINUCCIA, BIRINDELLI R, SALVETTI, ANTONIO   +9 more
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Congenital hemihypertrophy with adrenocortical adenoma.

Journal of the Medical Association of Thailand = Chotmaihet thangphaet, 1995
A rare case of adrenocortical adenoma in a 7-month-old female infant with congenital hemihypertrophy of left leg is described. Only 7 similar cases including the present one, are on record. The patients ranged in age from 7 weeks to 45 years. The male:female ratio was 3:4. The adrenal tumors were often detected after CH had become evident.
V, Kasantikul, S, Maneesri, S, Sriwatana, K, Vajarapongse   +3 more
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Characteristic Radiographic Shapes of Pheochromocytomas and Adrenocortical Adenomas

Radiology, 1966
In most organs of the body, the shape of a tumor radiologically demonstrated is not helpful in the preoperative histologic diagnosis. By virtue of its concentric growth, a noninfiltrative neoplasm tends to assume a spherical configuration. The parent organ usually offers no constant asymmetry contributing to a characteristic shape of a tumor developing
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