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Cognitive evaluation following the evolution of brain myofibroblastic tumor in the adolescence: a case study report

Avaliação cognitiva após a evolução do tumor miofibroblástico cerebral na adolescência: relato de estudo de caso

ABSTRACT

Objective

To report the case of a teenager (12 years old) diagnosed with a brain tumor in the right frontal-parietal region emphasizing the main characteristics observed in neuropsychological examinations.

Methods

In the pre-surgical evaluation, the patient presented behavioral alterations, including deficits in verbal comprehension, perceptual organization, working memory, processing speed, and slight alterations regarding constructive praxis.

Results

A reevaluation after two years surgery revealed significant improvement in verbal and perceptual comprehension and constructive praxis while remaining a slight change in processing speed. These results suggest that the tumor’s surgical resection produced significant improvements in the patient’s neurocognitive context, especially in executive functions. This study also indicates that Neuropsychological evaluation are useful for pre- and post- surgical evaluation of cognitive functioning and its evolution.

Conclusion

Brain tumor causes cognitive and behavioral changes and its resection can result in improvements in the patient’s quality of life.

Cognition; brain tumor; adolescence; neuropsychological evaluation

RESUMO

Objetivo

Relatar o caso de uma adolescente (12 anos de idade) diagnosticada com tumor cerebral na região frontoparietal direita, enfatizando as principais características observadas em exames neuropsicológicos.

Métodos

Na avaliação pré-cirúrgica, a paciente apresentou alterações comportamentais, incluindo déficits na compreensão verbal, organização perceptual, memória de trabalho, velocidade de processamento e pequenas alterações na praxia construtiva.

Resultados

Uma reavaliação dois anos após a cirurgia revelou melhora significativa na compreensão verbal e perceptiva e na práxis construtiva, permanecendo uma ligeira alteração na velocidade de processamento. Esses resultados sugerem que a ressecção cirúrgica do tumor produziu melhoras significativas no contexto neurocognitivo da paciente, sobretudo nas funções executivas. Este estudo também indica que a avaliação neuropsicológica é útil para avaliação pré e pós-cirúrgica do funcionamento cognitivo e sua evolução.

Conclusão

O tumor cerebral causa alterações cognitivas e comportamentais e a sua ressecção pode resultar em melhorias na qualidade de vida do paciente.

Cognição; tumor cerebral; adolescência; avaliação neuropsicológica

INTRODUCTION

Tumors of the central nervous system (CNS) in adolescence significantly impact morbidity and mortality and often follow cognitive and behavioral changes. Neuropsychological evaluation (NPE) is an instrument used to assess cognitive changes 11. Ostrom QT, Gittleman H, Truitt G, Boscia A, Kruchko C, Barnholtz-Sloan JS. CBTRUS Statistical Report: Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2011-2015. Neuro Oncol. 2018;20(suppl_4):iv1–iv86. severity and plan rehabilitation. CNS tumors are more prevalent in individuals aged 0-14 years; mean annual incidence rate adjusted by age is 5.65 per 100,000 inhabitants 11. Ostrom QT, Gittleman H, Truitt G, Boscia A, Kruchko C, Barnholtz-Sloan JS. CBTRUS Statistical Report: Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2011-2015. Neuro Oncol. 2018;20(suppl_4):iv1–iv86. , 22. Linabery AM, Ross JA. Trends in childhood cancer incidence in the U.S. (1992-2004). Cancer. 2008;112(2):416-32. . The inflammatory myofibroblastic tumor (IMT) is also described as inflammatory pseudotumor or plasma cell granuloma, among the benign or low malignancy potential lesions. IMT is a rare neoplasm composed of myofibroblastic fusiform cells, usually accompanied by an inflammatory infiltrate of plasma cells, lymphocytes, and eosinophils 33. Vardhan KH. Inflammatory Myofibroblastic Tumor of Central Nervous System: A Case Report. J Neuropathol Exp Neurol.2015;3(6):3. , 44. Singhal N, Agarwal V, Chawla A, Tangri R. Central Nervous System Inflammatory Myofibroblastic Tumor Masquerading as Chronic Suppurative Otitis Media. J Pediatr Neurosci. 2017;12(2):188-91. and occurs mainly in soft tissues and the viscera of children and young adults 33. Vardhan KH. Inflammatory Myofibroblastic Tumor of Central Nervous System: A Case Report. J Neuropathol Exp Neurol.2015;3(6):3. , 55. Lai LM, McCarville MB, Kirby P, Kao SC, Moritani T, Clark E, et al. Shedding light on inflammatory pseudotumor in children: spotlight on inflammatory myofibroblastic tumor. Pediatr Radiol. 2015;45(12):1738-52. . CNS tumors, in general, are capable of producing signs and symptoms through local invasion, compression of adjacent structures, and increased intracranial pressure. In children and adolescents, these manifestations can be unspecific 66. Wilne SH, Dineen RA, Dommett RM, Chu TPC, Walker DA. Identifying brain tumours in children and young adults. BMJ. 2013;347:f5844. . In 7% of the cases of adolescents with IMT, deficits in behavioral and school performance may occur 77. Wilne S, Collier J, Kennedy C, Koller K, Grundy R, Walker D. Presentation of childhood CNS tumours: a systematic review and meta-analysis. Lancet Oncol. 2007;8(8):685-95. . Also, children treated for low-grade CNS tumors present an increased risk for impairment of neurobehavioral function 88. Ris MD, Beebe DW, Armstrong FD, et al. Cognitive and Adaptive Outcome in Extracerebellar Low-Grade Brain Tumors in Children: A Report From the Children’s Oncology Group. J Clin Oncol. 2008;26(29):4765-70. .

Neuropsychological evaluation in CNS tumors can contribute to the early diagnosis of these conditions, decisively influencing the evolution and prognosis 99. Madhusoodanan S, Ting MB, Farah T, Ugur U. Psychiatric aspects of brain tumors: A review. World J Psychiatry. 2015;5(3):273-85. . In the following case, we describe social behavior and cognition changes in a 12-year-old patient diagnosed with IMT. We sought to describe the main neuropsychological alterations in the preoperative and postoperative periods and the case’s evolutionary outcome.

CASE REPORT

Identification and history of the disease

ALS, 12 years old, female, an elementary school in progress. The first consultation occurred in 2018 with the family’s main complaint of challenging behavior and the presence of signs of disinhibition, motor stereotypes, and saccadic eye movements.

The patient had a history of motor, cognitive, and socio-affective development within the expected standards until seven years old when she started to decrease school performance and psychomotor retardation. The condition evolved with progressive irritability, difficulty concentrating, and the onset of obsessive-compulsive symptoms.

After three years, she began to present episodes of frequent and brief changes in the level of consciousness, associated with paroxysmal vertigo and paresthesia in the left upper limb. Magnetic resonance imaging demonstrated brain tumor (BT) in the right frontal-parietal region. Three months later surgical resection of the lesion was performed ( Figure 1 ) and the subsequent anatomopathological study revealed an IMT-CNS.

Figure 1
Axial Tomography the level where the cystic lesion is first visible (red arrow/rectangle), particularly the parietal (A) and right frontal lobe (B). The coronal slice (C) depicts the area after surgical removal.

Preoperative evolution

According to the relative’s report, the patient developed mood dysphoria, decreased will and general disinterest, evidenced mainly in the academic context, and aggravated the behavior opposing the norms. In the following months, she presented a substantial reduction of appetite and weight loss, about 6.0 kg in 2 months. There was also alternation of the saccadic ocular movements, body rocking stereotypes, and frequent difficulties in performing daily life activities. Subsequently, there was an increase of the oppositional behavior and adoption of a defiant attitude, evidenced by the non-acceptance of rules, intentional speech with words of low slang and disinhibition, manifested in various contexts, in addition to a sharp drop in school performance and frequent school occurrences.

Initial neuropsychological examination

During the pre-surgical evaluation (December 2018), the patient presented a non-collaborative attitude (she needed encouragement to perform the requested activities) and was uninhibited; the speech focused on sexual issues, irritable mood, unstable affection, hypobulia and absence of morbidity judgment.

The Wechsler Intelligence Scale for Children (4th Edition – WISC-IV) was applied and reading in the first and second evaluation was medium (see Table 1 ). There were changes in the factorial indices: verbal comprehension with difficulties in interpreting complex sentences and texts; perceptual organization with scores below the predicted for the age; working memory with scores lower than expected for immediate, short-term and working memory; processing speed with a score below the predicted for her age. In the Rey Auditory-Verbal Learning Test (RAVLT), a lower than average score was observed in most test components (see Table 1 ).

Table 1
Results of the neuropsychological evaluation in 2018 and 2020

Rey Complex Figure Test was also applied, with an average result in the copy of a complex geometric figure = 36 (PC = 90) and above the average in visual memory = 9,5 (PC = 50), reading in copy was upper-middle and reading in memory was medium. Similar results were seen in the Benton Visual Retention Test (BVRT). However, there were slight difficulties in carrying out activities involving constructive praxis, visual-spatial orientation and fine motor skills (see Table 1 ).

Cognitive reassessment (post-surgery)

Eighteen months after the first neuropsychological evaluation, the patient, now 14 years old, was reevaluated, and there were significant improvements in behavior and cognitive performance. The evaluation took place in five sessions of approximately 90 minutes each.

In the evaluation with WISC-IV, a change in the intelligence quotient (IQ) was obtained ( Table 1 ). In the factorial rates: presented good verbal comprehension; perceptual organization with scores slightly below the predicted for the age; working memory with scores lower than expected for immediate, short-term and working memory; processing speed with a score below the predicted for her age. In the RAVLT, scores within the average were observed in most test components ( Table 1 ).

The Rey Complex Figure Test, with below-average results in copying a complex geometric figure = 30 (PC = 20) and visual memory = 25 (PC = 40), reading in copy was lower and reading in memory was medium. Results within the average and superior to those of the first evaluation were observed in the BVRT ( Table 1 ). Better dexterity was observed in carrying out activities that involved constructive praxis, visual-spatial orientation and fine motor skills, compared to the previous assessment.

In the WISC-IV and RAVLT tests, there was a compromise in activities related to interpreting complex phrases and texts, perceptual organization, immediate memory, short-term memory, working memory and processing speed. The Rey Complex Figure and BVRT tests were also applied, in which there was some compromise in the activities related to constructive praxis, visual-spatial orientation, perceptual organization and fine motor skills.

DISCUSSION

Individuals with CNS tumors often live with impairments resulting from the injury itself or its treatment, with cognitive dysfunction being the most frequent complication as a long term outcome 1010. Correa DD. Neurocognitive Function in Brain Tumors. Curr Neurol Neurosci Rep. 2010;10(3):232-9. . Cognitive changes resulting from brain injuries can be assessed through ANP, helping to understand the impact of the injury and associated treatment on performing activities of daily living and managing possible changes in mood or personality 1111. Noll KR, Bradshaw ME, Rexer J, Wefel JS. Neuropsychological Practice in the Oncology Setting. Arch Clin Neuropsychol. 2018;33(3):344-53. .

Changes in cognitive functions and neuropsychiatric impairment, in the context of intracranial neoplasms, may affect from 51% to 78% of cases 1212. Schlesinger B. Mental Changes in Intracranial Tumors and Related Problems. Part I. p. 240-263. Stereotact Funct Neurosurg. 1949;10(4):240-63. , 1313. Keschner M. Mental symptoms associated with brain tumor: a study of 530 verified cases. JAMA. 1938;110(10):714. . Specifically, in the context of low-grade brain tumors, it is already documented that the presence of the tumor itself contributes as a primary factor for cognitive dysfunction 1010. Correa DD. Neurocognitive Function in Brain Tumors. Curr Neurol Neurosci Rep. 2010;10(3):232-9. . In patients with frontal or temporal tumors, before treatment, 90% of the patients presented impairments in at least one area of cognitive functioning 1414. Tucha O, Smely C, Preier M, Lange KW. Cognitive Deficits before Treatment among Patients with Brain Tumors. Neurosurgery. 2000;47(2):324-34. . Brain tumors in the pediatric population, cognitive impairment is observed in functions such as language and non-linguistic skills, attention, working memory and processing speed 1111. Noll KR, Bradshaw ME, Rexer J, Wefel JS. Neuropsychological Practice in the Oncology Setting. Arch Clin Neuropsychol. 2018;33(3):344-53. . Memory is significantly impaired in tumors located in the third ventricle and thalamus region’s temporal and frontal lobes. Executive dysfunctions are frequently observed in primary tumors located in the frontal lobe or regions with frontal connections as well as changes in the speed of information processing and working memory 1515. Da Silva MC, Miotto EC, De Lucia MCS, De Aguiar PHP. Investigação neuropsicológica pré-operatória em pacientes com glioma de baixo grau. JBNC. 2018;18(3):35-9. .

A meta-analysis assessed the association between psychiatric symptoms and tumor location. It was observed that specific locations, e.g., frontal and temporal areas, were more likely to be affected, leading to personality changes 1616. Madhusoodanan S, Opler MG, Moise D, Gordon J, Danan DM, Sinha A, et al. Brain tumor location and psychiatric symptoms: is there any association? A meta-analysis of published case studies. Expert Rev Neurother. 2010;10(10):1529-36. . Such associations have long been described, as well as changes in mood/affection 1313. Keschner M. Mental symptoms associated with brain tumor: a study of 530 verified cases. JAMA. 1938;110(10):714. , 1717. Strauss I. Mental symptoms in cases of tumor of the frontal lobe. Arch Neurol Psychiatry. 1935;33(5):986-1005. . What is described in the literature is true in this case, with the patient’s significant behavioral changes and the presence of frontal involvement.

From the neurobiological point of view, the changes presented are associated to the disconnection of limbic-frontal pathways, related to social cognition, affecting different modalities, such as decision making, inhibitory control, the intensity of the experience of immediate gratification 1818. Salzman CD, Fusi S. Emotion, Cognition, and Mental State Representation in Amygdala and Prefrontal Cortex. Annu Rev Neurosci. 2010;33(1):173-202. , 1919. Banks SJ, Eddy KT, Angstadt M, Nathan PJ, Phan KL. Amygdala-frontal connectivity during emotion regulation. Soc Cogn Affect Neurosci. 2007;2(4):303-12. . In adolescence, the disconnection of the frontal limbic circuits can be correlated with substance abuse and compulsion behavior, academic performance failure, and changes in sexual behavior 2020. Rosenbloom MH, Schmahmann JD, Price BH. The Functional Neuroanatomy of Decision-Making. J Neuropsychiatry Clin Neurosci. 2012;24(3):266-77. .

Parietal lesions may be associated with changes in visual-spatial representations. One of the most commonly impaired functions in patients with parietal lesions is constructive praxis 2121. Gainotti G, Trojano L. Constructional apraxia. In: Vallar G, Coslett HB (Eds.). Handbook of Clinical Neurology. Philadelphia: Elsevier; 2018. p. 331-48. . The occurrence of constructive apraxia (CA) has long been considered a typical sign of parietal lobe injury 2222. R.N.DeJ. The Parietal Lobes. Neurology. 1954;4(5):402. , 2323. Mayer-Gross W. Some Observations on Apraxia. Proceedings of the Royal Society of Medicine. 1935;28(9):1203-12. . In the first evaluation, although it was not observed below the expected result in the tests of the Rey Complex Figure and BVRT, the finding of difficulties in performing activities involving constructive praxis, visual orientation, perceptual organization, and fine motor skills may be justified by parietal involvement of the lesion.

The factors related to the presence of a brain tumor are related to the lesion’s with behavioral and cognitive damage. The proposed treatments, such as surgical resection, are also determinant in the impact on these aspects 2424. Shen C, Bao WM, Yang BJ, Xie R, Cao XY, Luan SH, et al. Cognitive deficits in patients with brain tumor. Chin Med J. 2012;125(14):2610-7. . A systematic review of the literature evaluating neurocognitive deficits secondary to the treatment of primary cranial tumors showed deficits in working memory, processing speed, “visual search,” “planning and forecasting” and “general attention” 2525. Gehrke AK, Baisley MC, Sonck ALB, Wronski SL, Feuerstein M. Neurocognitive deficits following primary brain tumor treatment: systematic review of a decade of comparative studies. J Neurooncol. 2013;115(2):135-42. , which could be observed in the present case. Interestingly 1717. Strauss I. Mental symptoms in cases of tumor of the frontal lobe. Arch Neurol Psychiatry. 1935;33(5):986-1005. , cognitive reassessment performed 34 months after surgery showed significant improvement in several cognitive domains, such as written language interpretation, short- and long-term memory, and mood improvement (less irritability), behaving calmly and collaboratively during the sessions. Despite favorable evolution, some cognitive functions, such as processing speed, constructive praxis, and visual-spatial orientation, remained significantly impaired.

An inflammatory myofibroblastic tumor can increase aggressive behavior and as tumor sequelae can be involved in various parts of the risk, including clinical manifestations of inflammatory symptoms 2626. Dong Y, Zahid KR, Han Y, Hu P, Zhang D. Treatment of Pediatric Inflammatory Myofibroblastic Tumor: The Experience from China Children’s Medical Center. Children (Basel). 2022;9(3):307. .

Romero-Garcia et al . conducted a survey with 17 young people with a brain tumor, glioma 2727. Romero-Garcia R, Owen M, McDonald A, Woodberry E, Assem M, Coelho P, et al. Assessment of neuropsychological function in brain tumor treatment: a comparison of traditional neuropsychological assessment with app-based cognitive screening. Acta Neurochir (Wien). 2022;164(8):2021-34. . After performing a neuropsychological assessment performed before and after the operation. In this type of problem, there is an early improvement after the intervention.

CONCLUSION

The brain tumor caused changes in the patient’s cognitive and behavioral sphere, being these closely related to the location of the lesion and the findings in the NPE. Tumor resection resulted in improvements in various cognitive and behavioral domains. Besides, the performance of a multidisciplinary follow-up with a psycho-educationalist, a psychologist of Behavioral Cognitive Therapy approach (TCC), the neurologist and the neurosurgeon physician certainly contributed to the significant improvement of the picture initially presented.

ACKNOWLEDGMENTS

We thank all those who allowed this study to be carried out successfully.

REFERENCES

  • 1
    Ostrom QT, Gittleman H, Truitt G, Boscia A, Kruchko C, Barnholtz-Sloan JS. CBTRUS Statistical Report: Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2011-2015. Neuro Oncol. 2018;20(suppl_4):iv1–iv86.
  • 2
    Linabery AM, Ross JA. Trends in childhood cancer incidence in the U.S. (1992-2004). Cancer. 2008;112(2):416-32.
  • 3
    Vardhan KH. Inflammatory Myofibroblastic Tumor of Central Nervous System: A Case Report. J Neuropathol Exp Neurol.2015;3(6):3.
  • 4
    Singhal N, Agarwal V, Chawla A, Tangri R. Central Nervous System Inflammatory Myofibroblastic Tumor Masquerading as Chronic Suppurative Otitis Media. J Pediatr Neurosci. 2017;12(2):188-91.
  • 5
    Lai LM, McCarville MB, Kirby P, Kao SC, Moritani T, Clark E, et al. Shedding light on inflammatory pseudotumor in children: spotlight on inflammatory myofibroblastic tumor. Pediatr Radiol. 2015;45(12):1738-52.
  • 6
    Wilne SH, Dineen RA, Dommett RM, Chu TPC, Walker DA. Identifying brain tumours in children and young adults. BMJ. 2013;347:f5844.
  • 7
    Wilne S, Collier J, Kennedy C, Koller K, Grundy R, Walker D. Presentation of childhood CNS tumours: a systematic review and meta-analysis. Lancet Oncol. 2007;8(8):685-95.
  • 8
    Ris MD, Beebe DW, Armstrong FD, et al. Cognitive and Adaptive Outcome in Extracerebellar Low-Grade Brain Tumors in Children: A Report From the Children’s Oncology Group. J Clin Oncol. 2008;26(29):4765-70.
  • 9
    Madhusoodanan S, Ting MB, Farah T, Ugur U. Psychiatric aspects of brain tumors: A review. World J Psychiatry. 2015;5(3):273-85.
  • 10
    Correa DD. Neurocognitive Function in Brain Tumors. Curr Neurol Neurosci Rep. 2010;10(3):232-9.
  • 11
    Noll KR, Bradshaw ME, Rexer J, Wefel JS. Neuropsychological Practice in the Oncology Setting. Arch Clin Neuropsychol. 2018;33(3):344-53.
  • 12
    Schlesinger B. Mental Changes in Intracranial Tumors and Related Problems. Part I. p. 240-263. Stereotact Funct Neurosurg. 1949;10(4):240-63.
  • 13
    Keschner M. Mental symptoms associated with brain tumor: a study of 530 verified cases. JAMA. 1938;110(10):714.
  • 14
    Tucha O, Smely C, Preier M, Lange KW. Cognitive Deficits before Treatment among Patients with Brain Tumors. Neurosurgery. 2000;47(2):324-34.
  • 15
    Da Silva MC, Miotto EC, De Lucia MCS, De Aguiar PHP. Investigação neuropsicológica pré-operatória em pacientes com glioma de baixo grau. JBNC. 2018;18(3):35-9.
  • 16
    Madhusoodanan S, Opler MG, Moise D, Gordon J, Danan DM, Sinha A, et al. Brain tumor location and psychiatric symptoms: is there any association? A meta-analysis of published case studies. Expert Rev Neurother. 2010;10(10):1529-36.
  • 17
    Strauss I. Mental symptoms in cases of tumor of the frontal lobe. Arch Neurol Psychiatry. 1935;33(5):986-1005.
  • 18
    Salzman CD, Fusi S. Emotion, Cognition, and Mental State Representation in Amygdala and Prefrontal Cortex. Annu Rev Neurosci. 2010;33(1):173-202.
  • 19
    Banks SJ, Eddy KT, Angstadt M, Nathan PJ, Phan KL. Amygdala-frontal connectivity during emotion regulation. Soc Cogn Affect Neurosci. 2007;2(4):303-12.
  • 20
    Rosenbloom MH, Schmahmann JD, Price BH. The Functional Neuroanatomy of Decision-Making. J Neuropsychiatry Clin Neurosci. 2012;24(3):266-77.
  • 21
    Gainotti G, Trojano L. Constructional apraxia. In: Vallar G, Coslett HB (Eds.). Handbook of Clinical Neurology. Philadelphia: Elsevier; 2018. p. 331-48.
  • 22
    R.N.DeJ. The Parietal Lobes. Neurology. 1954;4(5):402.
  • 23
    Mayer-Gross W. Some Observations on Apraxia. Proceedings of the Royal Society of Medicine. 1935;28(9):1203-12.
  • 24
    Shen C, Bao WM, Yang BJ, Xie R, Cao XY, Luan SH, et al. Cognitive deficits in patients with brain tumor. Chin Med J. 2012;125(14):2610-7.
  • 25
    Gehrke AK, Baisley MC, Sonck ALB, Wronski SL, Feuerstein M. Neurocognitive deficits following primary brain tumor treatment: systematic review of a decade of comparative studies. J Neurooncol. 2013;115(2):135-42.
  • 26
    Dong Y, Zahid KR, Han Y, Hu P, Zhang D. Treatment of Pediatric Inflammatory Myofibroblastic Tumor: The Experience from China Children’s Medical Center. Children (Basel). 2022;9(3):307.
  • 27
    Romero-Garcia R, Owen M, McDonald A, Woodberry E, Assem M, Coelho P, et al. Assessment of neuropsychological function in brain tumor treatment: a comparison of traditional neuropsychological assessment with app-based cognitive screening. Acta Neurochir (Wien). 2022;164(8):2021-34.

Publication Dates

  • Publication in this collection
    24 Oct 2022
  • Date of issue
    Jul-Sep 2022

History

  • Received
    7 Mar 2022
  • Accepted
    8 June 2022
Instituto de Psiquiatria da Universidade Federal do Rio de Janeiro Av. Venceslau Brás, 71 Fundos, 22295-140 Rio de Janeiro - RJ Brasil, Tel./Fax: (55 21) 3873-5510 - Rio de Janeiro - RJ - Brazil
E-mail: editora@ipub.ufrj.br