Danovitch G M, Le Roith D, Sikuler S E, Straus R
Clin Endocrinol (Oxf). 1979 Dec;11(6):595-601. doi: 10.1111/j.1365-2265.1979.tb03113.x.
Three patients known to suffer from familial Mediterranean fever (FMF), systemic amyloidosis and chronic renal failure developed large amyloid goitres. Amyloid goitre is an extremely rare complication of systemic amyloidosis not previously described in FMF. The clinical and pathological features of these three cases were similar to those previously described in amyloid goitre. In two of the patients abnormalities in thyroid function were consistent with those documented in chronic renal failure. There was evidence of hypothyroidism in a third patient. There was no evidence of amyloid induced dysfunction of other endocrine organs.
三名已知患有家族性地中海热(FMF)、系统性淀粉样变性和慢性肾衰竭的患者出现了巨大的淀粉样甲状腺肿。淀粉样甲状腺肿是系统性淀粉样变性极为罕见的并发症,此前在FMF中未曾有过描述。这三例病例的临床和病理特征与先前报道的淀粉样甲状腺肿相似。其中两名患者的甲状腺功能异常与慢性肾衰竭中记录的情况一致。第三名患者有甲状腺功能减退的证据。没有证据表明淀粉样物质会导致其他内分泌器官功能障碍。