A Clinical Observation of Endocrine Adrenal Tumors
- Author:
Hye Young PARK
;
Tae Suk KIM
;
Soo Jin LEE
;
Dong Gu CHOI
;
Moon Ho KANG
- Publication Type:Original Article
- Keywords:
Cushing's syndrome;
Aldosterone;
Pheochromocytoma;
Paraganglioma
- MeSH:
Adenoma;
Adrenal Glands;
Aldosterone;
Cause of Death;
Cushing Syndrome;
Diagnosis;
Diagnosis, Differential;
Early Diagnosis;
Ganglia;
Humans;
Hyperaldosteronism;
Hypotension;
Liver;
Mothers;
Paraganglioma;
Pheochromocytoma;
Pregnancy;
Pulmonary Edema;
Spironolactone
- From:Journal of Korean Society of Endocrinology
1994;9(3):228-238
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Endocrine adrenal tumors are uncommon but clinically significant because they can be managed successfully by surgical therapy. During pregnancy, adrenal tumors can be a cause of death for both mother and baby, unless they diagnoses antenatally and managed properly. To investigate clinical characteristics of endocrine adrenal tumors, we analyzed 26 cases of adrenal tumor diagnosed and managed in Chung Ang Gil Hospital including cases associated with pregnancy and also a rare case of paraganglioma in liver. 1) There were 7 cases of Cushing's syndrome among which two cases were due to Cushing's disease and five cases were due to adrenal adenoma. Six cases were managed successfully by appropriate surgery. Another one case was associated with pregnancy but the patient expired due to sudden development of pulmonary edema and hypotension during preoperative preparation.2) Among 9 cases of primary aldosteronism, 8 cases were aldosterone-producing adenoma(APA) and 1 case was idiopathic hyperaldosteronism(IHA). In differential diagnosis between APA and IHA, diagnostic accuracy of postural study and adrenal CT was 86%, 78% respectively. In each one case of APA and IHA, adrenal venous aldosterone sampling was used for the differential diagnosis. Six cases of APA were managed by appropriate surgery. One patient with APA who refuses surgery and one patient with IHA were placed on spironolactone with good response.3) Among 10 cases of pheochromocytoma, seven cases were from adrenal gland and three cases were paragangliomas including one case originating from liver and two cases from abdominal ganglia. One patient with pheochromocytoma was diagnosed in 1st trimester of pregnancy and she was successfully treated by surgery.We observed 26 cases of endocrine adrenal tumors which were successfully managed except one case. We think that it is important to pay attention to adrenal tumor for early diagnosis particulary when associated with pregnancy. Paraganglioma in liver, although very rare, should be included in the differential diagnosis of space occupying lesion in liver.
