Yuasa H, Tokito S, Nakagaki H, Kitamura K
Department of Neurosurgery, Kagoshima Municipal Hospital, Japan.
Neurol Med Chir (Tokyo). 1990 Dec;30(13):1016-9. doi: 10.2176/nmc.30.1016.
The authors report four cases of familial pituitary adenomas from two unrelated families. No clinical or biochemical evidence of multiple endocrine neoplasia, type I (MEN-I) was demonstrated. Detailed study of the family trees disclosed no other family members affected by MEN-I. Familial occurrence of pituitary adenomas unassociated with MEN-I is rare.
作者报告了来自两个无亲缘关系家庭的4例家族性垂体腺瘤病例。未发现多发性内分泌腺瘤病I型(MEN-I)的临床或生化证据。对家族谱系的详细研究未发现其他受MEN-I影响的家庭成员。与MEN-I无关的垂体腺瘤家族性发生情况罕见。