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A Dandy-Walker malformation associated with ganglioglioma

Wang, Lei-Ming1; Zhang, Meng1; Wang, Pei-Pei2; Zhou, Xin-Gang3; Piao, Yue-Shan1; Lu, De-Hong1

Section Editor(s): Lyu, Peng

doi: 10.1097/CM9.0000000000000457

1Department of Pathology, Xuanwu Hospital, Capital Medical University, Beijing 100053, China

2Department of Radiology, Xuanwu Hospital, Capital Medical University, Beijing 100053, China

3Department of Pathology, Beijing Ditan Hospital, Capital Medical University, Beijing 100015, China.

Correspondence to: Dr. De-Hong Lu, Department of Pathology, Xuanwu Hospital, Capital Medical University, 45# Changchun street, Xicheng District, Beijing 100053, ChinaE-Mail:

How to cite this article: Wang LM, Zhang M, Wang PP, Zhou XG, Piao YS, Lu DH. A Dandy-Walker malformation associated with ganglioglioma. Chin Med J 2019;00:00–00. doi: 10.1097/CM9.0000000000000457

Received 7 July, 2019

Online date: September 19, 2019

This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.

To the Editor: The Dandy-Walker malformation (DWM) is a rare congenital malformation involving the posterior fossa. Diagnosis of the DWM is based on a series of characteristic neuroimaging findings, which include complete or partial agenesis of the cerebellar vermis, cystic dilatation of the fourth ventricle, and enlarged posterior fossa.[1] Several malformation syndromes and cytogenetic abnormalities have been associated with the DWM. However, the co-existence of the DWM and neoplasms is rare.[2] There are rare reports of the co-existence of the DWM and ganglioglioma.

A 6-year-old boy was admitted to the hospital with complaints of headache for 3 months. He was free from dizziness, nausea, vomiting, or limb weakness. He had normal vision, muscular strength and muscular ton. The laboratory examination of this case showed the increases of C-reactive protein (21.7 mg/L), blood glucose (7.6 mmol/L), and the decrease of albumin (39.6 g/L), blood potassium (3.5 mmol/L), sodium (136.5 mmol/L) and phosphorus (1.4 mmol/L). Cerebrospinal fluid (CSF) cytology was unremarkable. Computed tomography (CT) and magnetic resonance imaging (MRI) findings were compatible with variant DWM. At the same time, a round soft tissue mass was seen above the sellar region, with uneven internal density. The upper part of the lesion reached the interphalangeal cistern, the boundary of which was not clearly demarcated near the right parahippocampal gyrus [Figure 1A–1H]. He underwent a puncture of the hypothalamus and tissue samples were sent for pathological examination.

Figure 1

Figure 1

Histopathological examination revealed the presence of ganglioglioma which was composed of proliferated glial cells [Figure 1I], mature and immature ganglion cells [Figure 1J], in conjunction with vascular proliferation. The tumor cells were positive for glial fibrillary acidic protein (GFAP) [Figure 1K], Olig-2, neuronal nuclear antigen (NeuN) and CD34 [Figure 1L], and negative for mutations in the v-raf murine sarcoma viral oncogenes homolog B1 (BRAF) V600E, p53, isocitrate dehydrogenase 1 (IDH1) R132H and Histone H3.3/H3.1 in the codon for lysine 27 (H3K27M). Antibodies were obtained from Beijing Zhongshan Golden Bridge Biotechnology Co., Ltd. (Beijing, China). Based on the radiological examination and pathological findings, the patient was diagnosed as DWM associated with ganglioglioma (World Health Organization grade I). Neurosurgeons recommended close observation and did not perform further tumor resection. Six months later, routine follow-up CT and MRI scans demonstrated that there was no significant change in the lesion. The headache symptom was successfully alleviated.

The DWM was first described by Dandy and Blackfan in 1914 and is the most common congenital malformation of the cerebellum, with an incidence of about one in 25,000 to 30,000 live births.[3] DWM can be seen on CT and MRI by the presence of elevated venous sinuses and torcular, high tentorial attachment, and an enlarged cystic posterior fossa. Sometimes, DWM needs to be distinguished from other diseases, such as Joubert syndrome, mega cisterna magna (MCM), Blake pouch cyst, isolated vermian hypoplasia, arachnoid cyst, or cerebellar hypoplasia. Approximately, 70% to 90% of patients have supratentorial hydrocephalus, which represents the most common complication of this malformation. Associated neoplasms can be nephroblastoma, tongue hamartoma and intracranial cavernous angioma.[4] However, the incidence of the DWM associated with central nervous system (CNS) glioma has not been reported. This case represents a rare report of ganglioglioma in a patient with the DWM.

The cause of DWM is unknown, but it is occasionally familial. The most convincing pathogenetic theory is a developmental arrest of the hindbrain before the third month. The etiology of DWM, including chromosomal abnormalities and single-gene disorders, is also heterogeneous. Mutations of the sonic hedgehog (Shh) signaling pathway genes, zinc finger protein 1 (ZIC1) and ZIC4, as well as fibroblast growth factor genes (FGF) 8 and FGF17 have been implicated in DWM.[5] In our present case, no other pathological molecular alterations, including BRAF V600E, were found by next generation sequencing.

Various treatment options are available for children with DWM, such as shunt placement, either ventriculoperitoneal, cystoperitoneal, or combined ventriculoperitoneal and cystoperitoneal shunt, membrane excision, and endoscopic procedures. Cystoperitoneal shunts are currently favored by many neurosurgeons. A prognosis, which is only moderately favorable, is difficult to formulate even when hydrocephalus is treated early and correctly. Some people have variant Dandy-Walker without showing any symptoms in their entire lives. However, some infants may have it in association with other syndromes, resulting in severe complications or death. The presence of comorbidities may heavily affect the prognosis and quality of patients’ life. Although the patient in our case was diagnosed with ganglioglioma, neurosurgeons recommended close observation and did not perform further tumor resection or adjuvant therapy. He is under regular follow-up and no progression of the lesions has been observed. The identification of such associations highlights the correlation of pathogenesis of both the DWM and ganglioglioma, which suggests a novel and yet unexplored mechanism of disease that could be the basis for future study.

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Declaration of patient consent

The authors certify that they have obtained the appropriate patient consent form. In the form, the parents of the patient have given their consent for his images and other clinical information to be reported in the journal. The parents of the patient understand that his name and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

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This work was supported by grants from the Beijing Excellent Talent Training Project Grant (No. 201600026833ZK07) and the Beijing Higher Education Young Elite Teacher Project (No. CIT&TCD201904091).

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Conflicts of interest


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1. Karande V, Andrade NN. Dandy-Walker syndrome with giant cell lesions and cherubism. Ann Maxillofac Surg 2018; 8:131–136. doi: 10.4103/ams.ams_34_16.
2. Stambolliu E, Ioakeim-Ioannidou M, Kontokostas K, Dakoutrou M, Kousoulis AA. The most common comorbidities in Dandy-Walker syndrome patients: a systematic review of case reports. J Child Neurol 2017; 32:886–902. doi: 10.1177/0883073817712589.
3. Baro V, Manara R, Denaro L, D’Avella D. Dandy-Walker malformation and syringomyelia: a rare association. Childs Nerv Syst 2018; 34:1401–1406. doi: 10.1007/s00381-018-3773-2.
4. Huguet I, Walker L, Karavitaki N, Byrne J, Grossman AB. Dandy-Walker malformation, papillary thyroid carcinoma, and SDHD-associated paraganglioma syndrome. J Clin Endocrinol Metab 2013; 98:4595–4596. doi: 10.1210/jc.2013-3015.
5. Yang CA, Chou IC, Cho DY, Lin CY, Huang HY, Ho YC, et al. Whole exome sequencing in Dandy-Walker variant with intellectual disability reveals an activating CIP2A mutation as novel genetic cause. Neurogenetics 2018; 19:157–163. doi: 10.1007/s10048-018-0548-6.
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