Kashiwagi S, Nishizaki T, Harada K, Ito H, Setoguchi M, Takahashi M, Ishihara T
Department of Neurosurgery, Yamaguchi University School of Medicine, Ube, Japan.
Childs Nerv Syst. 1998 Oct;14(10):602-5. doi: 10.1007/s003810050280.
Prolactin-secreting adenoma, which usually presents with amenorrhea and galactorrhea syndrome, is quite rarely diagnosed in the prepubertal age group. We reported a rare case of a prepubertal prolactin-secreting adenoma and discuss its clinical, radiological and histological features. An 8-year-old girl presented with headache, progressive visual deterioration and precocious puberty. The serum prolactin level was 57.8 ng/ml. Computerized tomography and magnetic resonance imaging revealed an invasive suprasellar tumor. The tumor was partially resected through an interhemispheric approach in a first operation, and residual tumor was resected through the right pterional approach in a second operation. The histological diagnosis was a prolactin-secreting adenoma with high cellular pleomorphism. The Ki-67 labeling index was 5.7%, indicating aggressive biological behavior. Postoperatively, the patient was prescribed bromocriptine as maintenance therapy, and the serum prolactin level became normalized. There is a tendency for diagnosis of a prepubertal prolactin-secreting adenoma to be delayed because there are no endocrinological manifestations. Therefore, the tumor tends to become larger and invasive. Although it is rarely experienced, a prolactin-secreting adenoma should be considered in the differential diagnosis of a large, invasive parasellar lesion in the prepubertal age group.
分泌催乳素的腺瘤通常表现为闭经和溢乳综合征,在青春期前年龄组中很少被诊断出来。我们报告了一例青春期前分泌催乳素腺瘤的罕见病例,并讨论其临床、放射学和组织学特征。一名8岁女孩出现头痛、进行性视力减退和性早熟。血清催乳素水平为57.8 ng/ml。计算机断层扫描和磁共振成像显示鞍上有侵袭性肿瘤。首次手术通过半球间入路部分切除肿瘤,第二次手术通过右侧翼点入路切除残留肿瘤。组织学诊断为具有高度细胞多形性的分泌催乳素腺瘤。Ki-67标记指数为5.7%,表明具有侵袭性生物学行为。术后,患者接受溴隐亭作为维持治疗,血清催乳素水平恢复正常。由于没有内分泌表现,青春期前分泌催乳素腺瘤的诊断往往会延迟。因此,肿瘤往往会变得更大且具有侵袭性。尽管很少遇到,但在青春期前年龄组中,分泌催乳素腺瘤应被考虑为鞍旁大的侵袭性病变鉴别诊断的一部分。