Tan Tze-Ching, Ho Luen-Cheung
Department of Neurosurgery, Queen Elizabeth Hospital, Kowloon, Hong Kong.
J Clin Neurosci. 2007 Aug;14(8):801-5. doi: 10.1016/j.jocn.2006.06.007. Epub 2007 May 7.
Lhermitte-Duclos disease or dysplastic gangliocytoma of the cerebellum, is a rare cerebellar lesion, which can cause mass effects in the posterior fossa. It may occur sporadically, or in association with Cowden syndrome. Cowden syndrome or multiple hamartoma-neoplasia syndrome, is an uncommon autosomal dominant condition characterized by mucocutaneous lesions and systemic malignancies. We report two patients with Lhermitte-Duclos disease and associated Cowden syndrome. The clinical, radiological and histopathological features and management strategies of this rare disease complex are discussed.
Lhermitte-Duclos病或小脑发育异常性神经节细胞瘤是一种罕见的小脑病变,可在后颅窝产生占位效应。它可能散发性出现,或与考登综合征相关。考登综合征或多发性错构瘤-肿瘤综合征是一种罕见的常染色体显性疾病,其特征为皮肤黏膜病变和全身性恶性肿瘤。我们报告了两名患有Lhermitte-Duclos病及相关考登综合征的患者。本文讨论了这种罕见疾病复合体的临床、放射学和组织病理学特征及治疗策略。