Hyperaldosteronism from adrenal carcinoma.
نویسندگان
چکیده
criteria for a diagnosis of infectious mononucleosis. In a more recent report of an outbreak of the disease Dunnet (1963) described 80 cases; the diagnostic criteria used were stringent. Though almost all of the 80 cases had evidence of hepatic involvement and 13 (16%) had electrocardiographic changes, only a few had the radiological appearances of enlarged hilar lymph nodes and none had pulmonary lesions. The present case satisfied the accepted diagnostic criteria for infectious mononucleosis. There was no direct evidence of infection other than of infectious mononucleosis, and the pulmonary changes coincided with the development and remission of the primary disease. It seems likely that the pulmonary opacities were due to foci of infiltration by mononuclear cells or atypical lymphocytes, as has been described in a minority of the few cases coming to necropsy (Ziegler, 1944; Allen and Kellner, 1947; Natvig, 1962). If these pulmonary opacities were indeed due to lymphocytic proliferation, we are reminded that the mechanism of proliferation and above all the limitation of lymphocytic proliferation in infectious mononucleosis is inadequately understood (Dameshek and Gunz, 1964).
منابع مشابه
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Primary hyperaldosteronism is one of the few causes of hypertension that can be cured by surgery. Primary hyperaldosteronism is caused by adrenocortical adenoma or hyperplasia. It is important to differentiate between adrenal adenoma and hyperplasia because the preferred treatments are different. In all patients with new-onest or worsening hypertension the primary hyperaldosteronism should be c...
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The conditions pathophysiology is to be traced in by far the largest share of cases (85%) to an aldosterone-producing adrenocortical adenoma, most often solitary and unilateral rather than multiple of bilateral. The syndrome may be accompanied also by cortical hyperplasia without nodules or at times with diffuse micronodules, or by carcinoma. Onset varies according to published series, ranging...
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BACKGROUND To determine differences in biological features among different adrenal tumors, we investigated the DNA ploidy, numerical chromosomal aberration and proliferative activity in human adrenal cortical neoplasms. METHODS Our study included six adrenal cortical adenomas with Cushing syndrome, 12 adenomas with hyperaldosteronism, three non-functioning adenomas and three adrenal cortical ...
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Aldosterone-producing adrenocortical carcinomas are an extremely rare cause of hyperaldosteronism (<1%). Coexistence of different endocrine tumors warrants additional screening for multiple endocrine neoplasia syndromes, especially in young patients with large or malignant masses. We present the case of a 40-year-old man with a history of hypertension that presented with an incidental left adre...
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عنوان ژورنال:
- British medical journal
دوره 1 5794 شماره
صفحات -
تاریخ انتشار 1972