Mick G J, McCormick K L, Wakimoto H
Department of Pediatrics, SUNY Health Science Center, 750 East Adams Street, NY 13210.
Eur J Pediatr. 1991 Jan;150(3):154-7. doi: 10.1007/BF01963555.
A 6-month-old female is described who presented with severe idiopathic macromastia. The breast enlargement began at 2 months of age and progressed such that subtotal mastectomies were necessary at 23 months. Extensive hormonal evaluation prior to surgery revealed no evidence of estrogenization or precocious puberty. There was no galactorrhea. A breast biopsy showed immature mammary tissue. In vitro analysis of the patient's serum using a mouse mammary thymidine incorporation assay revealed similar mitogenic activity in the patient's serum compared to adult controls. Post surgical follow up of this patient, 3.5 years later, has revealed no breast enlargement, precocious sexual development, or growth acceleration. Of interest, however, she has manifested an idiopathic degenerative neurologic condition characterized by psychomotor delay, ataxia, and seizures. Remarkably, hormone studies at age 5.5 years showed an exaggerated gonadotrophin response to intravenous gonadotrophin releasing hormone and prepubertal estrogen levels. While this case may represent an extraordinary example of idiopathic premature thelarche, the severe nature of this infant's macromastia in association with neurologic dysfunction and increased gonadotrophins suggests that central nervous system factors were etiologic.
本文描述了一名6个月大的女性,她患有严重的特发性巨乳症。乳房增大始于2个月大时,并持续发展,以至于在23个月大时需要进行次全乳房切除术。手术前进行的广泛激素评估未发现雌激素化或性早熟的证据。无溢乳现象。乳房活检显示乳腺组织不成熟。使用小鼠乳腺胸苷掺入试验对患者血清进行的体外分析显示,与成年对照组相比,患者血清中的促有丝分裂活性相似。该患者术后3.5年的随访显示,没有乳房增大、性早熟或生长加速的情况。然而,有趣的是,她出现了一种特发性退行性神经疾病,其特征为精神运动发育迟缓、共济失调和癫痫发作。值得注意的是,5.5岁时的激素研究显示,促性腺激素对静脉注射促性腺激素释放激素的反应过度,且雌激素水平处于青春期前。虽然该病例可能是特发性早熟乳房发育的一个特殊例子,但该婴儿巨乳症的严重程度与神经功能障碍和促性腺激素增加表明中枢神经系统因素是病因。