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1.
Di Yi Jun Yi Da Xue Xue Bao ; 22(12): 1145-7, 2002 Dec.
Artigo em Chinês | MEDLINE | ID: mdl-12480602

RESUMO

Pathological changes usually occur independently in the adrenal cortex and medulla because of their distinct embryonic origins, and changes involving both the cortex and medulla are rare. We report 4 cases of corticomedullary mixed pathological changes adrenal glands. CT scanning of the adrenal glands showed unilateral abnormalities in all the 4 cases, 3 of which were diagnosed as aldosteronism and the other pheochromocytoma before surgery. Unilateral adrenalectomy was performed in the 4 patients 3 being cured and discharged. The other 1 had recurrence 18 months postoperatively with suspected pathological changes on the other side. Subsequent pathological examination confirmed the suspicion in both the cortex and medulla of the other adrenal gland. In cases with clinical presentations as simultaneous onset of aldosteronism and catecholamine responses, pathological changes in both the cortex and medulla of the adrenal glands should be considered. Perioperative management of such cases should be the same as that in cases of catecholamine responses, and the diagnosis relies on histopathological examination.


Assuntos
Córtex Suprarrenal/patologia , Neoplasias das Glândulas Suprarrenais/diagnóstico , Medula Suprarrenal/patologia , Erros de Diagnóstico , Feocromocitoma/diagnóstico , Doenças das Glândulas Suprarrenais/diagnóstico , Doenças das Glândulas Suprarrenais/patologia , Neoplasias das Glândulas Suprarrenais/patologia , Adulto , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Feocromocitoma/patologia
2.
Di Yi Jun Yi Da Xue Xue Bao ; 22(9): 849-50, 2002 Sep.
Artigo em Chinês | MEDLINE | ID: mdl-12297454

RESUMO

OBJECTIVE: To study the diagnosis and treatment of adrenal medullary hyperplasia (AMH). METHODS: An retrospective analysis of the clinical data of 8 patients with AMH admitted in our hospital from May 1998 to May 2002 were conducted with a review of the follow-up study. RESULTS: CT scanning of the adrenal gland showed unilateral abnormal appearance in all 8 cases. Diagnoses of AMH in 4 patients and pheochromocytoma in the other 4 patients were established before surgery. All the patients underwent unilateral adrenalectomy, among whom 7 were cured and 1 suffered recurrence 1 month after operation because of medullar hyperplasia in the contralateral adrenal gland. CONCLUSIONS: AMH should be differentiated from pheochromocytoma, especially from adrenal nodules shown by catecholamin assay. Definite diagnosis depends on pathological examination and surgical removal through abdominal approach is the best choice of treatment, in which both sides of the adrenal glands should be explored.


Assuntos
Neoplasias das Glândulas Suprarrenais/diagnóstico , Medula Suprarrenal/patologia , Feocromocitoma/diagnóstico , Neoplasias das Glândulas Suprarrenais/cirurgia , Medula Suprarrenal/cirurgia , Adrenalectomia , Adulto , Diagnóstico Diferencial , Feminino , Humanos , Hiperplasia/diagnóstico , Hiperplasia/cirurgia , Masculino , Pessoa de Meia-Idade , Feocromocitoma/cirurgia
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