Samaan N A, Hickey R C, Sethi M R, Yang K P, Wallace S
Surgery. 1976 Sep;80(3):382-9.
In 82 patients, a preoperative diagnosis of primary hyperparathyroidism has been established by means of transfemoral neck vein catheterization and measurement of serum immunoreactive parathyroid hormone (iPTH). Twenty-five of these patients have had cancer in other parts of the body but with no evidence of recurrence or metastasis. One patient had carcinoma of the colon with metastases, and four were members of families with multiple endocrine adenomatosis (MEA, Types I and II). In six other hypercalcemic patients, high levels of iPTH were found also in the effluent blood from cancer sites other than the parathyroid gland, secondary to ectopic hormone production or pseudohyperparathyroidism. In addition, a high serum level of iPTH was found in the superior vena cava of a seventh patient who had carcinoma of the breast but no clinical or radiological signs of recurrence or metastasis with the exception of an enlarged liver. This iPTH finding was interpreted as being, probably, the result of parathyroid adenoma in either the neck or the mediastinum. At the time of operation, a transcervical mediastinal search was made. Four normal cervical parathyroid glands were found; three were removed. Hypercalcemia persisted after operation, and the patient died. At postmortem examination, microscopic study revealed that the disease had metastasized to lungs and hilar lymph nodes. There was massive metastasis in the liver; the liver contained a large amount of iPTH. The results of these investigations suggest that (1) venous catheterization of the neck veins and the effluent blood from extraparathyroid tumors aid in identifying and localizing iPTH production; (2) primary benign hyperparathyroidism is not uncommon in patients with cancer, and its co-existence must be recognized; (3) high serum iPTH level in the superior vena cava may be found in patients with metastatic or primary cancer of the thoracic cavity; and (4) hyperparathyroidism may be the first hint of a familial multiple endocrine syndrome.
在82例患者中,通过经股颈静脉插管及测定血清免疫反应性甲状旁腺激素(iPTH),术前确诊为原发性甲状旁腺功能亢进。其中25例患者身体其他部位曾患癌症,但无复发或转移迹象。1例患者患有结肠癌伴转移,4例为多发性内分泌腺瘤病(MEA,Ⅰ型和Ⅱ型)家族成员。另外6例高钙血症患者,除甲状旁腺外,其他癌症部位的流出血液中也发现iPTH水平升高,继发于异位激素分泌或假性甲状旁腺功能亢进。此外,第7例乳腺癌患者上腔静脉中发现血清iPTH水平升高,除肝脏肿大外无临床或影像学复发或转移迹象。该iPTH结果可能被解释为颈部或纵隔甲状旁腺腺瘤的结果。手术时,进行了经颈纵隔探查。发现4枚正常的颈部甲状旁腺;切除了3枚。术后高钙血症持续存在,患者死亡。尸检时,显微镜检查显示疾病已转移至肺和肺门淋巴结。肝脏有大量转移灶;肝脏含有大量iPTH。这些研究结果表明:(1)颈部静脉及甲状旁腺外肿瘤流出血液的静脉插管有助于识别和定位iPTH的产生;(2)原发性良性甲状旁腺功能亢进在癌症患者中并不少见及其共存情况必须得到认识;(3)胸腔转移性或原发性癌症患者上腔静脉中可能发现血清iPTH水平升高;(4)甲状旁腺功能亢进可能是家族性多发性内分泌综合征的首个提示。