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考登综合征与勒米特-迪克洛病之间的关联:一例罕见遗传性错构瘤病的病例报告。

Association between Cowden syndrome and Lhermitte-Duclos disease: A case report of an uncommon Genetic Hamartomatous Disorder.

作者信息

Aggari Hanane El, Nasri Siham, Zohra Ahsayen Fatima, Aichouni Narjisse, Kamaoui Imane, Skiker Imane

机构信息

Department of Radiology, Mohammed VI University Hospital, Oujda, Morocco.

Faculty of Medicine and Pharmacy, Mohammed 1st University, Oujda, Morocco.

出版信息

Radiol Case Rep. 2023 Jun 6;18(8):2763-2767. doi: 10.1016/j.radcr.2023.05.013. eCollection 2023 Aug.

Abstract

The dysplastic gangliocytoma of the cerebellum, also known as Lhermitte-Duclos disease, is an uncommon hamartomatous lesion in the posterior fossa with some distinctive neuroradiological characteristics. It can happen in combination with Cowden syndrome or sporadically. Cowden disease, or multiple hamartoma-neoplasia syndrome, is a rare autosomal dominant condition which is characterized by mucocutaneous lesions and systemic malignancies. We present a case of Lhermitte-Duclos disease and Cowden disease occurring in adult patients. The clinical and radiological features as well as the management approaches of this unusual disease complex are addressed.

摘要

小脑发育异常性神经节细胞瘤,又称Lhermitte-Duclos病,是后颅窝一种罕见的错构瘤性病变,具有一些独特的神经放射学特征。它可与考登综合征合并发生或散在发生。考登病,即多发性错构瘤-肿瘤综合征,是一种罕见的常染色体显性遗传病,其特征为皮肤黏膜病变和全身性恶性肿瘤。我们报告一例发生于成年患者的Lhermitte-Duclos病和考登病。本文探讨了这种不寻常疾病组合的临床和放射学特征以及治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8cf0/10250148/f6b4a2e2b303/gr1.jpg

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