MNJ (Malang Neurology Journal)
Vol. 12 No. 2 (2026): July

OVERLAPPING PONTINE SYNDROME SYMPTOMATOLOGY: A RUPTURED CEREBELLAR PEDUNCLE ARTERIOVENOUS MALFORMATION

Abrar, Muhammad Nabil (Unknown)
Danishara, Mahawikan Akmal (Unknown)
Putra, Gabriel Zefanya Handoko (Unknown)
Addimaysqi, Rafi (Unknown)
Adrianto, Yudhi (Unknown)



Article Info

Publish Date
01 Jul 2026

Abstract

Background: Localizing brainstem lesions depends on identifying specific clinical syndromes. In the pons, the commonly confused Millard-Gubler and Foville syndromes share similar features. Millard-Gubler syndrome arises from a ventral pontine lesion, causing ipsilateral CN VII and CN VI palsies with contralateral hemiparesis while preserving conjugate gaze. In contrast, Foville syndrome involves a dorsal pontine lesion and is distinguished by ipsilateral conjugate gaze palsy due to pontine gaze center involvement. Case Report:  This case describes a 56-year-old female patient with neurological deficits of crossed hemiparesis manifested by left-sided hemiparesis, hemihypesthesia and right-sided lower motor facial palsy, pathognomonic for a brainstem syndrome. Computed tomographic angiography (CTA) imaging revealed a cerebellar peduncle arteriovenous malformation (AVM) rupture with an intranidal aneurysm related to the brainstem syndrome. The anatomical lesion and clinical manifestations are considerably consistent with the definitions of Millard-Gubler and Foville syndrome. Upon DSA, the intranidal aneurysm was spontaneously thrombosed, leading to a decision to leave the AVM without intervention. Discussion: The clinical manifestations of ventrocaudal pontine lesions include Millard-Gubler and  Foville syndromes. In this patient, involvement of the ventrocaudal and dorsomedial pons affected the abducens nucleus, facial colliculus, and corticospinal tract, producing overlapping Millard-Gubler and Foville features. Unlike typical ischemic or hemorrhagic pontine syndromes, this presentation resulted from secondary pontine hemorrhage due to a ruptured cerebellar peduncle AVM. Spontaneous thrombosis of the AVM nidus further created a therapeutic dilemma given its poorly defined natural history. Conclusion: This case illustrates that classic brainstem syndromes may arise from rare structural causes such as AVMs and highlights spontaneous thrombosis as a rare event complicating management. Recognition of atypical etiologies and the use of comprehensive neuroimaging are essential for accurate diagnosis and identification of potentially treatable vascular lesions.

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Journal Info

Abbrev

MNJ

Publisher

Subject

Neuroscience

Description

Malang Neurology Journal is a peer-reviewed and open access journal that focuses on promoting neurological sciences generated from basic neurosciences and clinical neurology. This journal publishes original articles, reviews, and also interesting case reports. Brief communications containing short ...