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垂体腺瘤的家族性发病(作者译)

[Familial occurrence of pituitary adenoma (author's transl)].

作者信息

Himuro H, Kobayashi E, Kono H, Jinbo M, Kitamura K

出版信息

No Shinkei Geka. 1976 Apr;4(4):371-7.

PMID:944879
Abstract

The familial occurrence of brain tumors are exceedingly rare except in cases with phacomatosis. We encountered pituitary adenomas in two sisters of a family, so far presenting no evidence of multiple endocrine adenomatosis (MEA). Case 1, K. O. a 26-year-old woman was admitted to our Hospital on September 10, 1970 with visual acuity and field disturbance, irregular menstruation and acromegaly. Neurological examination: Her visual acuity was Vd 0.6 and Vs 0.3, visual field was bitemporal hemianopsia, and ther was papilledema bilaterally. She had left exophthalmos and left abducens palsy. Roentgenogram of the skull, brain scanning, cerebral angiogram, pneumoencephalogram suggested the presence of a pituitary tumor. On Sep. 17, 1970, through a left frontotemporal craniotomy the tumor was removed subtotally. The pathological diagnosis was pituitary adenoma (chromophobe). Case 2, M. T. a 31-year-old woman, sister of case 1, was admitted to the Hospital on September 19, 1973, with mild headache, left visual field disturbance and amenorrhea. She had a child, and a past history of pulmonary tbc. Neurological examination: Her visual acuity was Vd 1.2 and Vs 0.03, and visual field of the right eye was temporal lower quandrant anopsia. There was optic nerve atrophy in the left eye. Plain X-ray craniogram, brain scanning, cerebral angiogram and pheumoencephalogram suggested the presence of a pituitary tumor. On Sep. 28, 1973, a right frontal craniotomy was performed. The tumor tissue with capsule was removed subtotally. The pathological diagnosis was pituitary adenoma (mixed type). In the literatures about familial brain tumors with histological diagnosis, glioma and glioblastoma are common, meningioma is relatively rare. Pituitary adenoma with no evidence of MEA is exceedingly rare. The two sisters presented in this paper, have no evidence of hyperparathyroidism, pancreas adenoma and peptic ulcer. So, we consider, at present, these cases should not be field in MEA.

摘要

除了在患有错构瘤病的病例中,脑肿瘤的家族性发病极为罕见。我们在一个家族的两姐妹中发现了垂体腺瘤,目前尚无多发性内分泌腺瘤病(MEA)的证据。病例1,K.O.,一名26岁女性,于1970年9月10日因视力和视野障碍、月经不规律及肢端肥大症入住我院。神经学检查:她的视力右眼为0.6,左眼为0.3,视野为双颞侧偏盲,双侧有视乳头水肿。她有左眼突眼和左侧展神经麻痹。头颅X线片、脑部扫描、脑血管造影、气脑造影提示存在垂体肿瘤。1970年9月17日,通过左额颞开颅术部分切除肿瘤。病理诊断为垂体腺瘤(嫌色细胞型)。病例2,M.T.,一名31岁女性,病例1的妹妹,于1973年9月19日因轻度头痛、左眼视野障碍和闭经入住我院。她育有一子女,有肺结核病史。神经学检查:她的视力右眼为1.2,左眼为0.03,右眼视野为颞下象限盲。左眼有视神经萎缩。头颅平片、脑部扫描、脑血管造影和气脑造影提示存在垂体肿瘤。1973年9月28日,进行了右额开颅术。完整切除有包膜的肿瘤组织。病理诊断为垂体腺瘤(混合型)。在有组织学诊断的家族性脑肿瘤文献中,胶质瘤和胶质母细胞瘤常见,脑膜瘤相对少见。无MEA证据的垂体腺瘤极为罕见。本文报道的两姐妹无甲状旁腺功能亢进、胰腺腺瘤和消化性溃疡的证据。所以,我们认为,目前这些病例不应归为MEA。

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