Valenta L J, Sostrin R D, Eisenberg H, Tamkin J A, Elias A N
Am J Med. 1982 Jun;72(6):861-73. doi: 10.1016/0002-9343(82)90844-0.
One hundred and seventy patients with endocrine abnormalities, 29 males and 141 females, were studied by computerized tomography (CT) scanning of the pituitary and by pituitary hormone assays including basal and stimulated hormone concentrations in the blood. Pituitary macroadenoma was observed in 40 of the 170 patients, microadenoma in 49, primary empty sella in 46, secondary empty sella in 25, including 20 of the 40 patients with macroadenoma after surgical removal or radiation therapy of the tumor. Suprasellar tumor was present in four patients. In 23 women with menstrual abnormalities and 3 men with impotence and hyperprolactinemia, the results of CT scanning were normal. Of the 40 patients with macroadenoma, 24 presented with a hyperfunctioning syndrome (acromegaly or hyperprolactinemia). Among the 49 patients with microadenomas, 46 had the amenorrhea-galactorrhea syndrome, one male presented with acromegaly and one with Cushing's disease, and one female also had Cushing's disease. Primary empty sella was associated with the amenorrhea-galactorrhea syndrome in females and impotence in males. Only four female patients demonstrating an empty sella were asymptomatic. Distinctive biochemical findings were identified in certain groups of patients with different pituitary pathologic features. CT scanning was found very useful in the assessment of the size of the tumor, its suprasellar or parasellar extension and response to therapy, and in differential diagnosis of tumor and empty sella. Disappointing results were obtained in patients with endocrine abnormalities and normal results of CT scanning, and in patients following surgical treatment for a pituitary tumor, when the identification of recurrent tumor was impossible from a single examination. It is concluded that CT scanning is the most advanced technique in the diagnosis of anatomic pituitary abnormalities and it should replace the traditional invasive diagnostic procedures.
对170例内分泌异常患者(29例男性,141例女性)进行了垂体计算机断层扫描(CT)及垂体激素测定,包括血液中基础和刺激状态下的激素浓度。170例患者中,40例发现垂体大腺瘤,49例为微腺瘤,46例为原发性空蝶鞍,25例为继发性空蝶鞍,其中40例大腺瘤患者中有20例在肿瘤手术切除或放疗后出现继发性空蝶鞍。4例患者存在鞍上肿瘤。23例月经异常的女性和3例阳痿伴高催乳素血症的男性CT扫描结果正常。40例大腺瘤患者中,24例表现为功能亢进综合征(肢端肥大症或高催乳素血症)。49例微腺瘤患者中,46例有闭经 - 溢乳综合征,1例男性表现为肢端肥大症,1例患有库欣病,1例女性也患有库欣病。原发性空蝶鞍与女性闭经 - 溢乳综合征及男性阳痿相关。仅4例显示空蝶鞍的女性患者无症状。在具有不同垂体病理特征的特定患者组中发现了独特的生化表现。发现CT扫描在评估肿瘤大小、鞍上或鞍旁扩展情况及对治疗的反应以及肿瘤与空蝶鞍的鉴别诊断方面非常有用。对于内分泌异常但CT扫描结果正常的患者,以及垂体肿瘤手术后单次检查无法鉴别复发性肿瘤的患者,结果令人失望。结论是CT扫描是诊断垂体解剖异常的最先进技术,应取代传统的侵入性诊断程序。