Diffusion magnetic resonance imaging diagnostic relevance in pyogenic ventriculitis with an atypical presentation: a case report
© Marinelli et al.; licensee BioMed Central Ltd. 2014
Received: 7 October 2013
Accepted: 7 March 2014
Published: 14 March 2014
Pyogenic ventriculitis is a rare and severe cerebral infection characterized by the presence of suppurative fluid in the cerebral ventricles. It is a life-threatening condition and may present with an aspecific neurological picture. Brain imaging techniques usually demonstrate intraventricular debris and pus, but negative imaging along with a misleading clinical picture may delay the diagnosis.
The described patient underwent a number of surgical procedures and eventually developed an unusual clinical picture characterized by psychomotor slowing, facial dyskinesias and myoclonic jerks without complaint of headache and in absence of meningeal irritation signs or focal neurological deficits. Cerebrospinal fluid cultural examination showed methicillin-resistant Staphylococcus aureus and vancomycin treatment lead to a complete recovery. Brain computed tomography scan was normal, while only diffusion magnetic resonance imaging sequences were able to define the presence of purulent material within the brain lateral ventriculi.
The present case underlines the importance of taking into account the diagnosis of pyogenic ventriculitis even when the neurological picture does not match the suspect of a central nervous system infection. Moreover, brain computed tomography scan and standard magnetic resonance imaging sequences may be unable to confirm the diagnosis, whereas diffusion-weighted sequences prove a unique role in diagnosing cerebral pyogenic ventriculitis.
Pyogenic ventriculitis (also called ventricular empyema or pyocephalus) is a rare and severe cerebral infection characterized by the presence of suppurative fluid in the cerebral ventricles. The clinical picture is usually characterized by headache, vomiting, impaired consciousness with fever and meningeal signs . Although a life threatening condition requiring the earliest diagnosis, symptoms and signs of pyogenic ventriculitis may sometimes be subtle and aspecific . Among a large number of bacteria responsible for nosocomial infections, methicillin resistant Staphylococcus aureus (MRSA) was detected in many patients with pyogenic ventriculitis [2, 3]. The possible mechanisms of infection of the ventricular system include hematogenous spread to the subependyma of the choroid plexus, diffusion by contiguity from a brain abscess or direct implantation secondary to trauma or surgical procedure . Brain imaging techniques can demonstrate intraventricular debris and pus, representing the most common signs of ventriculitis [3–5]; other findings may include hydrocephalus and periventricular magnetic resonance abnormalities reflecting inflammatory changes .
We report a patient with pyogenic ventriculitis with an atypical neurological presentation, in whom the diffusion magnetic resonance imaging (MRI) findings were crucial for the diagnosis.
The reported patient had pyogenic ventriculitis due to infection by MRSA. The most important features of his clinical history were the background of malignancy and the repeated complications of surgery leading to an unusually high number of abdominal surgical procedures. It is conceivable that all this has delayed the healing process allowing the MRSA to infect the surgical wound and eventually disseminate, in a patient whose clinical status was impaired by nephropathy and other diseases. Moreover, an additional role may have been played by the corticosteroid therapy, which could on one side have facilitated the spreading of MRSA into the central nervous system by lowering the patient’s immunological defenses, on the other be responsible for the absence of signs of meningeal irritation and the peculiar clinical picture. The clinical manifestations of pyogenic ventriculitis are often aspecific, since consciousness impairment may hide other symptoms, and neurological focal deficits are hardly found when there are no abscesses or other lesions involving the brain. Our patient presented with a complex and atypical neurological picture, mainly characterized by motor symptoms and behavioral abnormalities, but with no evidence of meningeal irritation, headache or focal deficits (considering “focal” those neurological signs of symptoms suggesting a lesion of a specific structure within the neurological system). Neuroimaging had a critical role in the diagnosis. CT scan was quite unremarkable and only the diffusion MRI sequences could clearly indicate the presence of purulent material within the ventricles. Recent studies have emphasized the importance of diffusion sequences in the diagnosis of pyogenic ventriculitis [2–4]. Indeed, the relatively high viscosity, hypercellularity and binding of water to macromolecules have been suggested as explanations for the restricted water diffusion observed in the purulent material . Conversely, FLAIR sequences are considered useful in detecting periventricular high signal and ependymal enhancement . Mild ventricular enlargement and increased periventricular signal were also detected in our patient, but specificity of these findings was obviously low.
In conclusion our patient underscores the unique role of MR diffusion sequences to detect purulent material inside the ventricles, thus warranting the diagnosis of pyogenic ventriculitis; this is even more true when the pathological process is limited. Moreover, the clinical features of this case point out that the diagnosis of pyogenic ventriculitis should be considered also when signs of meningeal irritation are poor or even absent. In fact, the clinical evidence pointing to an acute infection of the brain may be lacking, and a misleading neurological picture with mainly motor and behavioral manifestations may occur. Finally, it should be underlined that ventricular infection may follow an hematogenic route, in absence of a brain abscess, trauma or a surgical procedure.
Written informed consent was obtained from the patient for publication of this Case Report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
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