1995
DOI: 10.5980/jpnjurol1989.86.1064
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A Case of Adrenal Angiosarcoma

Abstract: A 62-year-old male with slight fever, anorexia and easy fatigability was found to have a tumor in the left adrenal gland by computed tomogram of abdomen. Further study of angiogram suggesting neoplasm of the left adrenal gland, eventually he was underwent surgical extirpation. Histological study, combined with immunohistochemical staining, revealed that the tumor measuring 8 x 4 x 6 cm was an angiosarcoma. The patient died of pulmonary dysfunction 42 days after the operation. Autopsy was not done. In the liter… Show more

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Cited by 7 publications
(3 citation statements)
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“…1 b, PCH-3: De 21.1) cannot be used for active matrix diplays. The cyano group tends to solvate ubiquituous ionic impurities [4] resulting in a low voltage holding ratio [5] and observable flicker and contrast loss in the display panel.…”
mentioning
confidence: 99%
“…1 b, PCH-3: De 21.1) cannot be used for active matrix diplays. The cyano group tends to solvate ubiquituous ionic impurities [4] resulting in a low voltage holding ratio [5] and observable flicker and contrast loss in the display panel.…”
mentioning
confidence: 99%
“…Their irregular histological and immunological attributes as well as their relatively low incidence can cause pathologists to mistake them for adrenal epithelial neoplasms. In clinical practice these neoplasms should always be differentiated from other vascular neoplasms, pheochromocytoma, adrenal cortical carcinoma, metastatic adenocarcinoma, metastatic malignant melanoma and other metastatic tumors as well as from benign neoplasms such as adrenal adenomas with hemorrhage and epithelioidhemangioendothelioma 36 , 38 , 40 , 50 , 51 , 52 ) . The safest and easiest way to confirm or rule out this malignancy is by using immunohistochemistry.…”
Section: Discussionmentioning
confidence: 99%
“…Recurrences and metastases frequently evolve within 2 years of diagnosis and death occurs either by local tumor extension or by development of lymph node, lung, liver or spleen metastases. The first report of an adrenal angiosarcoma was published in 1967 [16], and clinical and pathological characteristics of the 21 patients who have been reported so far are shown in table 1 [16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29]. Of interest, adrenal function was normal in all patients in whom it was evaluated (patients 4, 7, 12–21).…”
Section: Discussionmentioning
confidence: 99%