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本文报告我院1957～1979年收治的肢端肥大症35例,男22例,女13例。年龄大多在20～29岁之间。本病发病缓慢,大多在出现肢端肥大症状3～5年后才来就诊,临床表现以肢端指、趾增粗,增大为本病最早而具有特征性的变化,见于全部病人,至疾病形成后则呈典型面貌:眶上嵴、颧骨增大突出,下颌突出在上颌之前,牙齿稀疏。头痛(54％)及视力减退(40％)也较多见,视野缩小者60％,蝶鞍扩大及床突吸收者82％,本组合并高血压者5
This article reports 35 cases of acromegaly in our hospital from 1957 to 1979, including 22 males and 13 females. Most of them are between 20 and 29 years old. The onset of this disease is slow. Most of them come to the clinic 3 to 5 years after the symptoms of acromegaly appear. The clinical manifestations are the earliest and characteristic changes in the acromegaly and toes, which are seen in all patients. After the formation of the disease, the typical appearance is: the supraorbital palate and the cheekbones enlarge and protrude, and the jaws are sparse before the jaws protrude from the maxilla. Headache (54%) and vision loss (40%) are also more common, 60% of the visual field is reduced, and the sella enlargement and bed socket absorption are 82%.