Kurihara K, Mizuseki K, Kondo T, Ohoka H, Mannami M, Kawai K
Department of Pathology, Uwajima City Hospital, Japan.
Acta Pathol Jpn. 1990 Sep;40(9):683-6. doi: 10.1111/j.1440-1827.1990.tb01616.x.
We present a case of unilateral adrenal medullary hyperplasia in a 63-year-old woman with clinical signs and symptoms of pheochromocytoma unassociated with multiple endocrine neoplasia. The surgically removed adrenal gland revealed diffuse medullary hyperplasia with multiple micronodules measuring up to 2 mm. The micronodules were composed of enlarged chromaffin cells with atypia, histologically similar to those of pheochromocytoma, forming small solid alveolar patterns separated by a fibrovascular stroma. Removal of the hyperplastic adrenal gland resulted in disappearance of paroxysmal nocturnal hypertension and palpitation. These results suggest that diffuse and nodular medullary hyperplasia is the precursor of pheochromocytoma.
我们报告一例63岁女性的单侧肾上腺髓质增生病例,该患者有嗜铬细胞瘤的临床症状和体征,与多发性内分泌肿瘤无关。手术切除的肾上腺显示弥漫性髓质增生,伴有多个直径达2毫米的微结节。微结节由增大的嗜铬细胞组成,具有异型性,组织学上与嗜铬细胞瘤相似,形成由纤维血管间质分隔的小实性肺泡样结构。切除增生的肾上腺后,阵发性夜间高血压和心悸消失。这些结果表明弥漫性和结节性髓质增生是嗜铬细胞瘤的前驱病变。