3
Med J Malaysia Vol 74 No 1 February 2019 87 SUMMARY Large intracranial tumour may present only with psychiatric symptoms without any neurological deficits. Delay in surgical treatment may significantly affect the quality of life in these patients. We report a case of a young engineering student who was diagnosed as treatment-resistant depression without initial neuroimaging study. Further neuroimaging studies revealed he has a large falcine meningioma. His psychiatric symptoms resolved following surgical resection of the tumour. We emphasized the importance of initial neuroimaging study in young patients presenting with psychiatric symptoms. INTRODUCTION Intracranial tumours commonly present with neurological signs and symptoms related to mass effect. However, some patients may present with psychiatric symptoms only especially when a slow growing tumour is located in the frontal lobe. The incidence of psychiatric symptoms in patients with brain tumours has been reported as high as 50 to 78%. 1,2 Here we report a case of a young patient with falcine meningioma who was diagnosed and treated as depression for 10 years without initial neuroimaging study and nearly undergo for electroconvulsive therapy. CASE REPORT The patient is a 33-year-old man who presented with progressive behavioural changes, poor memory and social isolation over the past ten years. He had twice dropped out from engineering course in two different colleges due to his illness and was treated for depression at private clinic for nine years. His symptoms worsened since the last one year, where he spent most of his time on the bed with poor oral intake and poor self-care. He was then taken to a private hospital and treated as a case of major depressive disorder. He was prescribed with Olanzapine and Desvenlafaxine. No initial neuroimaging study was performed during the years. There was no history of chronic headache or any symptoms that was suggestive of raised intracranial pressure or motor- sensory deficits all the while. Subsequently, he was referred to the Psychiatry Team for electroconvulsive therapy in view of failed medical therapy. Computed tomography (CT) scan of the brain was arranged and scan revealed a large falcine meningioma. Following that he was referred to the Neurosurgical Team for further management. On examination, he was conscious but blunted looking and appeared lethargic. He was slow in response including his speech but was still able to follow simple two steps commands. Pupils were 3mm bilaterally and reactive to light. Fundoscopy examination revealed bilateral papilledema. There was no cranial nerve dysfunction. His lower limbs power was 4/5, hypertonia and hypereflexia. Assessment of higher mental functions was not performed due to general slowness of his response. Magnetic resonance imaging (MRI) of the brain demonstrated a well circumscribed falcine meningioma measuring about 7cm X 7.5cm X 7.5cm. There was no involvement of the superior sagittal sinus (Figure 1). Patient was started on steroid therapy and antiepileptic prior to surgical intervention. He underwent bifrontal craniotomy and excision of tumour (Simpson 2). Intraoperatively, the meningioma was firm with multiple arterial feeders from the falx. Tumour was devascularised medially from the falx, centrally debulked and excised. Histopathological finding was consistent with Meningioma (WHO grade 1). Postoperatively he had transient worsening of frontal lobe syndrome as he uttered rude words and disinhibition. However, these symptoms subsided after three days. The subsequent recovery period was uneventful, and he started to mobilise in the ward. At post-operative one week, he appeared cheerful with normal speech, and communicated well with his mother and the hospital staff. The power in his lower limbs also improved to 5/5 one week after the surgery. The anti-depressant and anti-psychotic medications were then ceased at post-operative two weeks. Neurology examination at postoperative three-month revealed his memory was improving with no other neurological deficits. There was no longer appearance of any of his pre-operative neuropsychiatric symptoms and was able to use telecommunication device. At one year follow up, his higher mental function was intact and started farming works for living. Figure 2 showed the one-year postoperative MRI of the brain with no recurrence. DISCUSSION Meningioma is a slow growing tumour and it can grow to considerable size before symptoms become apparent. 3 Commonly the manifesting symptoms are due to the Large falcine meningioma presented as treatment- resistant depression: A case report Sim Sze Kiat, MSurg 1,2 , Khairul Aizad Bin Adzman, MD 2 , Lim Swee San, MSurg 2 , Albert Wong Sii Hieng, FRACS 2 1 Department of Surgery, Faculty of Medicine & Health Sciences, Universiti Malaysia Sarawak, Sarawak Malaysia, 2 Department of Neurosurgery, Sarawak General Hospital, Sarawak, Malaysia CASE REPORT This article was accepted: 25 November 2018 Corresponding Author: Dr Sim Sze Kiat Email: [email protected]

Large falcine meningioma presented as treatment-resistant ...e-mjm.org/2019/v74n1/large-falcine-meningioma.pdf · Intracranial tumours commonly present with neurological signs and

  • Upload
    others

  • View
    1

  • Download
    0

Embed Size (px)

Citation preview

Page 1: Large falcine meningioma presented as treatment-resistant ...e-mjm.org/2019/v74n1/large-falcine-meningioma.pdf · Intracranial tumours commonly present with neurological signs and

Med J Malaysia Vol 74 No 1 February 2019 87

SUMMARYLarge intracranial tumour may present only with psychiatricsymptoms without any neurological deficits. Delay insurgical treatment may significantly affect the quality of lifein these patients. We report a case of a young engineeringstudent who was diagnosed as treatment-resistantdepression without initial neuroimaging study. Furtherneuroimaging studies revealed he has a large falcinemeningioma. His psychiatric symptoms resolved followingsurgical resection of the tumour. We emphasized theimportance of initial neuroimaging study in young patientspresenting with psychiatric symptoms.

INTRODUCTIONIntracranial tumours commonly present with neurologicalsigns and symptoms related to mass effect. However, somepatients may present with psychiatric symptoms onlyespecially when a slow growing tumour is located in thefrontal lobe. The incidence of psychiatric symptoms inpatients with brain tumours has been reported as high as 50to 78%.1,2 Here we report a case of a young patient withfalcine meningioma who was diagnosed and treated asdepression for 10 years without initial neuroimaging studyand nearly undergo for electroconvulsive therapy.

CASE REPORTThe patient is a 33-year-old man who presented withprogressive behavioural changes, poor memory and socialisolation over the past ten years. He had twice dropped outfrom engineering course in two different colleges due to hisillness and was treated for depression at private clinic for nineyears. His symptoms worsened since the last one year, wherehe spent most of his time on the bed with poor oral intakeand poor self-care. He was then taken to a private hospitaland treated as a case of major depressive disorder. He wasprescribed with Olanzapine and Desvenlafaxine. No initialneuroimaging study was performed during the years. Therewas no history of chronic headache or any symptoms thatwas suggestive of raised intracranial pressure or motor-sensory deficits all the while. Subsequently, he was referred tothe Psychiatry Team for electroconvulsive therapy in view offailed medical therapy. Computed tomography (CT) scan ofthe brain was arranged and scan revealed a large falcinemeningioma. Following that he was referred to theNeurosurgical Team for further management.

On examination, he was conscious but blunted looking andappeared lethargic. He was slow in response including hisspeech but was still able to follow simple two stepscommands. Pupils were 3mm bilaterally and reactive to light.Fundoscopy examination revealed bilateral papilledema.There was no cranial nerve dysfunction. His lower limbspower was 4/5, hypertonia and hypereflexia. Assessment ofhigher mental functions was not performed due to generalslowness of his response.

Magnetic resonance imaging (MRI) of the braindemonstrated a well circumscribed falcine meningiomameasuring about 7cm X 7.5cm X 7.5cm. There was noinvolvement of the superior sagittal sinus (Figure 1).

Patient was started on steroid therapy and antiepileptic priorto surgical intervention. He underwent bifrontal craniotomyand excision of tumour (Simpson 2). Intraoperatively, themeningioma was firm with multiple arterial feeders from thefalx. Tumour was devascularised medially from the falx,centrally debulked and excised. Histopathological findingwas consistent with Meningioma (WHO grade 1).

Postoperatively he had transient worsening of frontal lobesyndrome as he uttered rude words and disinhibition.However, these symptoms subsided after three days. Thesubsequent recovery period was uneventful, and he started tomobilise in the ward. At post-operative one week, heappeared cheerful with normal speech, and communicatedwell with his mother and the hospital staff. The power in hislower limbs also improved to 5/5 one week after the surgery.The anti-depressant and anti-psychotic medications werethen ceased at post-operative two weeks. Neurologyexamination at postoperative three-month revealed hismemory was improving with no other neurological deficits.There was no longer appearance of any of his pre-operativeneuropsychiatric symptoms and was able to usetelecommunication device. At one year follow up, his highermental function was intact and started farming works forliving. Figure 2 showed the one-year postoperative MRI of thebrain with no recurrence.

DISCUSSIONMeningioma is a slow growing tumour and it can grow toconsiderable size before symptoms become apparent.3

Commonly the manifesting symptoms are due to the

Large falcine meningioma presented as treatment-resistant depression: A case report

Sim Sze Kiat, MSurg1,2, Khairul Aizad Bin Adzman, MD2, Lim Swee San, MSurg2, Albert Wong Sii Hieng, FRACS2

1Department of Surgery, Faculty of Medicine & Health Sciences, Universiti Malaysia Sarawak, Sarawak Malaysia, 2Departmentof Neurosurgery, Sarawak General Hospital, Sarawak, Malaysia

CASE REPORT

This article was accepted: 25 November 2018Corresponding Author: Dr Sim Sze KiatEmail: [email protected]

17-Large00100R1_3-PRIMARY.qxd 2/27/19 2:36 PM Page 87

Page 2: Large falcine meningioma presented as treatment-resistant ...e-mjm.org/2019/v74n1/large-falcine-meningioma.pdf · Intracranial tumours commonly present with neurological signs and

Case Report

88 Med J Malaysia Vol 74 No 1 February 2019

compression of the adjacent structures, direct invasion, orreactive changes in adjacent brain tissue, and obstruction ofcerebrospinal fluid pathways, cortical veins, or major venoussinuses. In addition, the presentation of meningiomadepends on the location of occurrence also in the brain.Symptoms mimicking psychiatric disorder might be the onlymanifestation if the meningioma is located in the frontallobe as in our case. Study revealed 21% of meningiomapatients in the 4th decade of life presented with psychiatricpresentations with no neurological symptoms.1

Neuroimaging study is still not a routine investigation forpsychiatric patients in general, despite the wide availabilityand accessibility of imaging facilities nowadays. Also, there isno consensus yet in the use of neuroimaging as a routinestudy in patients with newly diagnosed psychiatric disorder.

Few authors recommend that psychiatrists should be awareof focal neurological signs caused by left temporal lobe inschizophrenic patients, and neuroimaging should beperformed to psychiatric patients with atypical presentation,such as auditoric hallucinations, visual hallucinations or

peduncular hallucinations. Neuroimaging is also suggestedfor established psychiatric patients with new psychiatricsymptoms or neurobehavioral changes.2

On the other hand, some authors do not recommend the useof neuroimaging in patients who present with typicalpsychosis or first episode of psychosis.4 The NICE guideline5

does not recommend the use of structural neuroimagingtechniques (either MRI or CT scanning) as a routine part ofthe initial investigations for the management of first-episodepsychosis in view of the limited evidence base to supportroutine scanning.

In our case, this young patient had been diagnosed as havingdepression mainly based on clinical presentation and wasstarted on anti-depressant. No neuroimaging was done whenthe first diagnosis was made, or throughout the course ofdepression treatment for 10 years. And he was referred forelectroconvulsive therapy for treatment-resistant depression.It is important to emphasize that accuracy of the firstdiagnosis is crucial for the quality of life of the patients.Ignoring the possibility of having intracranial lesion had

Fig. 1: Preoperative MRI showed a large homogenously contrast enhanced falcine meningioma measured about 7 cm x 7.5 cm x 7.5 cm.(a) axial view; (b) coronal view.

Fig. 1: Postoperative MRI at one year follow-up showed no recurrence of tumour. (a) axial view; (b) sagittal view; (c) coronal view.

17-Large00100R1_3-PRIMARY.qxd 2/27/19 2:36 PM Page 88

Page 3: Large falcine meningioma presented as treatment-resistant ...e-mjm.org/2019/v74n1/large-falcine-meningioma.pdf · Intracranial tumours commonly present with neurological signs and

Large falcine meningioma presented as treatment-resistant depression: A case report

Med J Malaysia Vol 74 No 1 February 2019 89

caused the tumour to progress and at the same time it wasthought that his psychiatric disorder was not responsive tomedical therapy. If the neuroimaging has been performedearlier for this patient, he would not have had the need toundergo unnecessary treatment, letting the primary diseaseto progress further and losing his opportunity to become anengineer.

CONCLUSIONWe suggest that neuroimaging, at least a plain CT scan of thebrain, to be done in young patients presenting withpsychiatric symptoms, specifically mood disorder or frontallobe syndromes before any diagnosis of psychiatric disorder ismade in view of the possible negative impact to the quality oflife of the patient

REFERENCES1. Moise D, Madhusoodanan S. Psychiatric symptoms associated with brain

tumours: a clinical enigma. CNS Spectr 2006; 11(1): 28-31.2. Madhusoodanan S, Danan D, Moise D. Psychiatric manifestation of brain

tumours: diagnostic implications. Expert Rev Neurother 2007; 7(4): 343-9. 3. Bondy M, Ligon BL. Epidemiology and etiology of intracranial

meningiomas: a review. J Neurooncol 1996; 29(3): 197-205.4. Khandanpour N, Hoggard N, Connolly DJ. The role of MRI and CT of the

brain in first episodes of psychosis. Clin Radiol 2013; 68(3): 245-50.5. National Institute for Health and Clinical Excellence. NICE technology

appraisal guidance No 136. Structural neuroimaging in first-episodepsychosis. [cited June 2018]. Available athttp://guidance.nice.org.uk/TA136/Guidance/ doc/English.

17-Large00100R1_3-PRIMARY.qxd 2/27/19 2:36 PM Page 89