腎上腺皮質(zhì)腺瘤合并髓脂肪瘤的臨床病理分析
[Abstract]:Objective there are few reports of adrenal cortical adenoma complicated with myelolipoma at home and abroad. The clinicopathological features of the tumor are discussed in order to provide more evidences for correct diagnosis and treatment. Methods the histological and clinical data of 11 cases of adrenocortical adenoma with myelolipoma diagnosed in Nanjing General Hospital and Jiangning Hospital from June 1, 2005 to June 30, 2016 were retrospectively analyzed. The results were compared with the related literature. Results among 11 patients with adrenal cortical adenoma and myelolipoma, there were 4 males and 7 females with an average age of (49.0 鹵9.5) years. Cushing's syndrome was found in 3 cases, dizziness in 1 case with hypertension for more than 10 years, and physical examination in 7 cases. Imaging findings revealed adrenal mass. Under light microscope, myelolipoma appeared as solitary nodular distribution and / or mixed distribution in cortical adenoma. Myelolipoma was composed of mature adipose tissue and different proportion of hematopoietic cells. There was no recurrence of tumor after 2 months to 11 years follow-up. Conclusion adrenal cortical adenoma complicated with myelolipoma is rare in clinic, and is more common in women. Cushing's syndrome may occur in the patients with hypertension or no obvious clinical symptoms, and the prognosis of surgical resection is good.
【作者單位】: 南京軍區(qū)南京總醫(yī)院病理科;南京市江寧醫(yī)院;南京醫(yī)科大學(xué)病理學(xué)系;
【分類號(hào)】:R736.6
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