Nunes M L, da Costa J C, Severini M H
Division of Neurology, Sö Lucas Hospital, Porto Alegre, RS, Brazil.
Pediatr Neurol. 1995 Jul;13(1):80-2. doi: 10.1016/0887-8994(95)00085-t.
Bilateral occipital calcifications associated with epilepsy and sometimes with celiac disease have been described previously. A boy with bilateral frontal and occipital diffuse calcifications accompanied by failure to thrive, nephrogenic diabetes insipidus, developmental delay and seizures, but without celiac disease is presented. Follow-up at 3 years of age disclosed neurodevelopmental delay, height and weight less than expected for age, and seizures controlled with carbamazepine. The uncommon association of these features and the early onset of symptoms is discussed. Although bilateral occipital calcifications share some clinical features with bilateral fronto-occipital calcifications, it is arguable whether the two are on a spectrum of a single disease or represent separate entities.
先前已有双侧枕叶钙化与癫痫相关,有时还与乳糜泻相关的描述。本文报告一名患有双侧额叶和枕叶弥漫性钙化的男孩,伴有生长发育迟缓、肾性尿崩症、发育延迟和癫痫发作,但无乳糜泻。3岁时的随访显示存在神经发育延迟、身高和体重低于预期年龄,癫痫发作通过卡马西平得到控制。讨论了这些特征的罕见关联以及症状的早期出现。尽管双侧枕叶钙化与双侧额枕叶钙化有一些共同的临床特征,但这两者是单一疾病的不同表现还是代表不同的实体仍存在争议。