|Year : 2019 | Volume
| Issue : 11 | Page : 3726-3735
The spectrum of malignancies presenting with neurological manifestations: A prospective observational study
Dhruv Batra1, Hardeep S Malhotra1, Ravindra K Garg1, Kiran P Malhotra2, Neeraj Kumar1, Madan L Brahma Bhatt3, Rajesh Verma1, Praveen K Sharma1, Imran Rizvi1
1 Department of Neurology, King George Medical University, Lucknow, Uttar Pradesh, India
2 Department of Pathology, RML Institute of Medical Sciences, Lucknow, Uttar Pradesh, India
3 Department of Radiation Oncology, King George Medical University, Lucknow, Uttar Pradesh, India
|Date of Submission||28-Jun-2019|
|Date of Decision||22-Aug-2019|
|Date of Acceptance||30-Sep-2019|
|Date of Web Publication||15-Nov-2019|
Dr. Ravindra K Garg
Department of Neurology, King George Medical University, Lucknow, Uttar Pradesh - 226 003
Source of Support: None, Conflict of Interest: None
Introduction: A neurological consultation is needed in nearly 45% of patients suffering from cancer. The present study was planned to evaluate the clinical, radiological and histopathological spectrum of patients with an underlying malignancy and presenting with a neurological complaint. Materials and Methods: We prospectively evaluated all patients provisionally diagnosed either with a primary or secondary malignancy of the brain on the basis of clinical, radiological and/or histopathological features. Results: A total of 155 patients were enrolled from a total of 4893 admissions done from January 2015 to July 2016. The common presenting symptoms were headache, back pain and paraparesis. Around 26% of patients presented with an altered sensorium, 19.4% with seizures and 21% had at least one cranial nerve involvement. The most common site of involvement was the brain noted in 49.7% of patients. Primary malignancies constituted 78 cases (50.7%) while secondary malignancies included 77 cases (49.3%). Magnetic resonance imaging (MRI) revealed 92 (59.4%) intra-axial lesions and 59 (38.1%) extra-axial lesions, with five cases having both. The most common diagnoses were intra-cerebral metastases and glioblastoma (intra-axial), and vertebral metastases and meningioma (extra-axial). Histopathological confirmation was obtained in 59 patients (38.1%) with 12 primary and 47 secondary lesions. Ten (6.45%) patients had an unknown primary with secondary metastases. The three most common histopathologically confirmed diagnoses were adenocarcinoma lung, plasma cell dyscrasia and adenocarcinoma prostate. Conclusion: Primary neurological consultations with an unknown primary are common hence a high index of suspicion can prevent an inadvertent delay in the diagnosis and appropriate treatment of a malignant lesion. Developing a neuro-oncology register may help us in gaining more insight into such situations.
Keywords: Carcinoma lung, central nervous system, glioblastoma multiforme, metastasis, neuro-oncology
|How to cite this article:|
Batra D, Malhotra HS, Garg RK, Malhotra KP, Kumar N, Brahma Bhatt ML, Verma R, Sharma PK, Rizvi I. The spectrum of malignancies presenting with neurological manifestations: A prospective observational study. J Family Med Prim Care 2019;8:3726-35
|How to cite this URL:|
Batra D, Malhotra HS, Garg RK, Malhotra KP, Kumar N, Brahma Bhatt ML, Verma R, Sharma PK, Rizvi I. The spectrum of malignancies presenting with neurological manifestations: A prospective observational study. J Family Med Prim Care [serial online] 2019 [cited 2019 Dec 11];8:3726-35. Available from: http://www.jfmpc.com/text.asp?2019/8/11/3726/270920
One of the most frequent and debilitating complications of cancer is the involvement of the nervous system, with nearly 45% of these patients requiring evaluation of a neurological problem. Neurological complications are the most common reason for emergency admissions of patients with cancer as well as the most common and primary reason for admission, besides chemotherapy administration. Most studies dealing with this subject have been conducted in oncology settings, with analysis of the neurological referrals that may result in an under-reporting of neurological manifestations in cancer patients. It has been reported that approximately 15% of the patient population in an oncology centre was seen by a neurologist., The National Cancer Registry in India was set up in 1981 and as late as 2009 there was no mention of a neuro-oncology society., This is in contrast to the Netherlands, where a neuro-oncology register (NOR) was established nearly three decades ago and in the USA where a law was passed in 2004 making the reporting of nervous system tumours compulsory at a national level., It has been observed that nearly one-third of patients seek neurological consultation for brain metastasis without any prior malignancy., The clinical presentations in such patients may vary from subtle hypoactive delirium to quadriparesis and any delay in diagnosis may be catastrophic.,
The objective of our research was to study the clinical, radiological and histopathological spectrum of patients presenting with a neurological complaint to a neurology specialist, as the first manifestation of an underlying malignancy.
[TAG:2]Materials and Methods[/TAG:2]
This was a prospective observational study conducted in the Department of Neurology, King George's Medical University, Lucknow, from January 2015 to July 2016. This study was approved by the Institutional Ethics Committee (IEC). Written informed consent was obtained from each subject or their legal guardian, prior to enrolment.
All patients provisionally diagnosed with either primary or secondary malignancies, based on clinical, radiological and/or histopathological features, were included in the study.
All patients below the age of 18 years or with a diagnosed malignancy were excluded.
All included patients underwent a detailed clinical evaluation followed by imaging relevant to each case. All enrolled patients were subjected to routine blood tests. Patients with suspected metastases underwent further work up directed at finding the primary site of origin. This included a detailed urological and gynaecological examination, contrast-enhanced computed tomography (CECT) of the chest/abdomen (as indicated), radionuclide scan, FDG-PET, estimation of tumour markers (such as prostate-specific antigen, carcino-embryonic antigen and alpha-fetoprotein), serum immunoelectrophoresis and histopathological confirmation (as feasible) with the biopsy of the relevant tissue.
Brain/spine magnetic resonance imaging (MRI) was performed on a Sigma Excite 1.5 Tesla scanner (General Electric Medical Systems, Milwaukee, WI, USA). An experienced neuroradiologist blindly reviewed the MRI scans in terms of lesion characteristics on different sequences, perilesional oedema, contrast-enhancement, necrosis and mass effect.
Histopathology slides, whenever available, were examined independently by an expert neuro/oncopathologist and in relevant cases, immunohistochemistry staining was also performed.
Primary malignancies were provisionally diagnosed based on findings from their characteristic imaging while metastases were diagnosed on the basis of typical MRI findings of circumscribed contrast-enhancing lesions with disproportionate perilesional oedema and mass effect along with evidence of malignancy at another site. These cases were diagnosed as 'definite' or 'histopathologically proven' cases [Figure 1].
|Figure 1: Parasagittal T2W sequence of MRI of the brain (a) shows mixed intensity space occupying lesions involving the right frontoparietal and subcortical areas with moderate to severe perilesional edema, with relatively homogeneous GAD enhancement (b). Axial contrast-enhanced CT of the thorax (c) depicts an ill-defined heterogeneously enhancing soft tissue in the posterior segment of the right upper lobe with spiculated margins suggestive of a neoplastic etiology. Smear of CT-guided aspirated material (d) shows a papillaroid cluster and singly lying cells with moderate sized, round to oval hyperchromatic nuclei, and moderate amount of amphophilic cytoplasm with few mucin vacuoles (arrows), suggestive of a non-small cell lung carcinoma. (May Grunwald Giemsa, x200)|
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'Probable' or 'imaging' diagnoses of primary nervous system malignancies were based on neuroradiological features when the biopsy was not possible. The lesions were classified as extra-axial if they had a majority of these imaging features (cerebrospinal fluid cleft between brain and lesion, vessels interposed between brain and lesion, cortex between mass and oedematous white matter, dura (meninges) between (epidural) mass and brain). The rest were classified as intra-axial.
The origin of secondary malignancies were diagnosed as 'probable' or termed 'imaging diagnosis' if one of the following was noted: an abnormal CT scan (chest or abdomen), bone scan or positron emission tomography (PET) scan, suggesting the primary site of origin for nervous system metastasis, and the systemic workup being otherwise unremarkable and histopathological diagnosis were not possible. Presumptive diagnoses made after imaging were revised if a biopsy was possible and histopathological confirmation was obtained.
Based on the final diagnosis, patients were referred to the team of neurosurgery, radiation oncology and surgical oncology for further management.
The statistical analysis was performed using the Statistical Package for Social Sciences, Version 16.0 for Windows (SPSS, Chicago, IL). Statistical significance was defined at a P value of <0.05 and wherever analysis was done it was a 2-tailed analysis. Categorical variables were expressed as percentages while continuous variables were expressed as mean ± SD. Chi-square test was used to compare proportions; independent sample t-test/ANOVA was used to compare means.
There were a total of 4893 admissions to the department of neurology, of which 155 patients were enrolled.
The mean age of the patients was 47.19 ± 17.08 years with 87 (56%) male patients. The mean duration of the presentation was 134.17 ± 24.90 days. Headache (47.7%) was the most common symptom followed by back pain (29.7%). The most common motor symptom was paraparesis (27.7%) followed by hemiparesis (21.1%). Sensory loss in one form or the other was noticed in 40.6% of the patients. Patients were graded on their disability based on the Modified Barthel Index (MBI) with a score of ≤12 (severe) in 39 patients (25.2%) and >12 in 116 patients (74.8%). The baseline characteristics of the cohort have been detailed in [Table 1].
The most common site involving the neuraxis was the brain (49.7%) followed by the spinal cord (29.0%). Nearly 24% of the patients had multiple sites of involvement along the neuraxis as well as multiple lesions within the same site. Primary malignancies were seen in 78 cases (50.7%) while secondary malignancies were noted in 77 cases (49.3%). MRI revealed intra-axial involvement in 92 (59.4%) cases and extra-axial involvement in 59 (38.1%) cases with 5 cases having both intra- as well as extra-axial involvement. Histopathological confirmation following biopsy could be obtained in 59 patients (38.1%) [Table 2].
The mean age was 46.94 ± 17.09 years with 55.8% of patients being male and the rest female. The primary malignancy group constituted 45.5% of these patients while 54.5% fell into the secondary malignancies group. Fifty (64.9%) of these lesions were intra-axial and 24 patients (31.2%) had extra-axial lesion; 3 patients (3.9%) had both type of lesions. Histopathological confirmation could be achieved in 26 patients (33.7%) with the most common malignancy being adenocarcinoma lung.
The mean age was similar to the 'brain' group (46.96 ± 17.81 years) with 60% males and 40% females. Twenty (44.4%) patients had a primary malignancy and 25 (55.6%) patients were classified in the secondary malignancies group. In contrast to the 'brain' group, extra-axial lesions were found to be in a higher proportion (73.3%) as compared to intra-axial lesions (20.0%). However, in 16 patients (35.6%), the diagnosis could be confirmed histopathologically.
Two patients had brachial plexus involvement while the rest (21 patients) had involvement of the lumbosacral plexus. The mean age was higher as compared to the brain and spinal cord lesions (51.87 ± 14.93 years) with 60.9% females and 39.1% males. Secondary malignancies were also higher in this group (60.9%) as compared to the primary ones (39.1%). Twelve of these lesions were proven by histopathology.
Five patients were males (83.3%) and one female (16.7%). Histopathology revealed two of these having a primary involvement (neurofibroma and adenoid cystic carcinoma) and the rest of them having multiple myeloma with chronic inflammatory demyelinating polyneuropathy (CIDP).
Primary versus Secondary malignancies
The mean age of patients with secondary malignancies (55.05 ± 13.05 years) was significantly higher (P-value <0.001, 95% CI: - 20.644 -10.991) than those with primary involvement (39.23 ± 17.06 years). Severe disability (MBI ≤12) at the time of admission was seen in 32 patients (41.0%) with secondary malignancies, as against 7 patients (9.1%) with a primary malignancy.
On MRI scanning the primary group had 44% intra-axial and 56% extra-axial lesions, whereas in the secondary group extra-axial involvement was proportionally higher (62.5% extra-axial and 32.5% intra-axial). Moreover, 5% of patients in the secondary group had both intra-axial and extra-axial involvement.
The most common imaging diagnosis in the primary group was glioma/glioblastoma multiforme (16), followed closely by meningioma (13). In the secondary group, the most common imaging diagnosis was multiple intracranial metastases (27) followed by multiple vertebral metastases (26). A single intracranial metastatic lesion was seen in eight patients. Histopathological confirmation rate was higher in the secondary group (i.e. 57.7% versus 18.2% in the primary group).
In patients with primary brain tumours, a total of 12 definite histopathologically confirmed diagnoses were obtained. Two patients who presented with myasthenia gravis had a thymoma on chest CT and another two who had a solitary plasmacytoma in the cervical vertebral lamina and spinous process were also included in this list.
The most common histopathological diagnosis in the secondary malignancies group was adenocarcinoma lung and multiple myeloma (ten patients each). Overall, the lung was the most common tissue of primary origin of metastases (15; 10 adenocarcinomas, 3 NSCLC, 2 bronchoalveolar) followed by plasma cells and the prostate. Other prominent diagnoses included adenocarcinoma breast, adenocarcinoma prostate and poorly/undifferentiated carcinoma. The details of diagnoses are listed in [Table 3]. Ten (6.45%) patients remained undiagnosed [Table 4].
Headache, hemiparesis, seizures, speech abnormality, altered sensorium and vomiting (P < 0.001) were seen in a considerably higher proportion in the intra-axial group whereas back pain, pain radiating to a limb, paraparesis and sensory loss (P < 0.001) were seen more frequently in the extra-axial group.
Out of a total of 4893 patients admitted, 155 patients were enrolled and evaluated during the study period of 2 years. The mean duration of symptoms prior to diagnosis in our study was around 4 months; patients with spinal cord compression showed a shorter duration at a median of 2 months (range 5 days to 2 years). Headache, back pain, and paraparesis were the most common presenting features. The brain was the most common site of involvement. Primary malignancies accounted for nearly 51% of cases with the remaining cases being secondary malignancies. The age of patients with secondary malignancies was significantly higher than of those belonging to the primary group. About 60% of cases were found to be intra-axial on MRI scanning, the rest being extra-axial. The most common imaging diagnosis was glioblastoma multiforme (primary malignancies group) and multiple intracranial metastases (secondary malignancies group). Histopathological confirmation was obtained in almost one-third of cases with the most common diagnoses being adenocarcinoma lung and multiple myeloma. The most common primary tissue of origin of metastases was the lung.
Clouston et al. in their study found headache, back pain and altered sensorium to be the most common symptoms in cancer patients having neurological complications. In addition to these, we found weakness (paraparesis, hemiparesis, quadriparesis and monoparesis) to be one of the leading initial manifestations of systemic malignancy. They also reported that 33% of patients with cancer, presenting with undiagnosed back pain, harbour an epidural metastasis. Rodichok et al. and Ruff and Lanska, however, reported a higher incidence of epidural metastases in cancer patients with back pain (57% and 43%, respectively)., In our study, 43.5% of patients presenting with back pain were diagnosed having extra-axial lesions. Le chevalier et al. reported 58% of their patients presenting with motor deficits. The high incidence of motor weakness in patients with a malignancy suggests that most primary care physicians tend to treat pain as a trivial symptom and patients are referred late to a specialised centre.
In our study, we noted that a high number of patients with malignancy presented with seizures (19.4%). This result was far more than reported by Gilbert and Grossman (4%) and Clouston et al. (4.5%). A higher incidence of seizure in our patient population may be due to the fact that patients with seizures were more likely to be referred to a neurology facility for further management vis-à-vis to a non-neurological setting.,, We also found sphincter disturbances (bowel or bladder) in a higher proportion of patients (34.8%) as opposed to 2.1% (Clouston et al.); a disproportionately high incidence of sphincter involvement (96%) has also been reported from Pakistan.,
The most common site of malignancies overall was the brain (49.7%; primary and secondary included). A large proportion of patients had involvements of multiple sites, either vertebral or intracranial or both (23.9%), indicating the advanced stage at which first manifestations of malignancy were presented to us. Gilbert et al. reported epidural spinal compression in a marginally higher number of patients than the brain (primary and metastases) followed by plexus involvement. Kori et al. reported 0.43% of patients with malignancies having brachial plexopathy. Jaeckel reported nearly 15% of patients with malignancies initially presented with lumbosacral plexopathy. A peripheral nervous system including peripheral nerves may be involved in 1.6%–17% of patients with malignancies., Clouston et al. reported 18.6% of patients with brain metastasis (including skull base metastases). This demonstrates the glaring difference between the presentation of malignancies in neurology versus oncology settings.
Even though our cohort was younger, those with secondary malignancies were in the higher age group (55 versus 40 years). Based on the age at the presentation, the geriatric group (≥65 years) is more likely to present with delirium, neurocognitive deficits, stroke and movement disorders while the non-geriatric group (<65 years) more often presents with headache, seizures and cranial nerve involvement (especially visual disturbances). One must always be aware of hypoactive delirium that may mask as depression in this vulnerable geriatric population. Non-thyroid, urologic, skin and gastrointestinal malignancies have been reported to be significantly higher in the geriatric group while ovarian and haematological malignancies are common in the non-geriatric age group. These findings can help in planning the battery of investigations, prioritizing one over the other, as appropriate.
Imaging revealed a higher number of intra-axial lesions (59.4%) as compared to extra-axial (38.1%) with the most common imaging diagnosis in the intra-axial group being intracranial metastases and glioblastoma multiforme amongst primary tumours. Vertebral metastases among secondary malignancies and meningioma among primary tumours were the most common imaging diagnosis in the extra-axial group. Le Chevalier et al. noted multiple metastases in the brain in two-thirds of patients in their series. Approximately 10–15% of autopsies reveal intracranial metastatic lesions signifying their asymptomatic seeding in brain parenchyma. Kohler et al., however, reported glioblastoma as the most common malignant and meningioma as the most common non-malignant tumour in adults. A Chinese study also noted that multiple metastases account for nearly three-fourths of the total brain metastases. A study from Pakistan, in an oncology setting reported 59.3% of patients having brain metastases with nearly 60% of them having multiple metastases. The reason for the higher proportion of multiple intracranial metastases (84%) in our and other studies seems to be the better detection rate as a result of MRI and increased survival with better management modalities.
It has been reported that 15–50% of patients with metastases end up with an undiagnosed primary despite an extensive work-up., We could not find primary site of malignancy in 1 in 10 cases (6.4%) which were labelled carcinoma with unknown primary [Table 5]. Ante-mortem histopathological confirmation could be achieved in 38.1% of our patients. A higher histopathological confirmation rate; 60% and 44.2% have been reported by Merchut and Le Chevalier et al., respectively., With recent advances in imaging, different groups have studied the predictive value of whole body CT, positron-emission CT (PET-CT), and PET-MRI in their respective settings; they recommend initial use of these techniques to increase the yield of cancer detection.,, Overall, PET-CT appears to be a reasonable choice depending on the availability and cost constraints, especially in patients presenting with solitary lesions.
The neuro-oncology register in the Netherlands reported lung, breast and prostate as the most common sites of primary cancer (in that order) causing metastases. Merchut reported lung as the most common primary followed by gastrointestinal tumours. Le Chevalier et al. found melanoma to be the second after lung cancer. Jin et al. reported an unknown primary followed by gastrointestinal tumours as the second and third most common tumours after lung. Van de Pol et al. reported an unknown primary and breast as the second and third most common sites, respectively. Barnholtz et al. reported melanoma and renal carcinoma as the next common sources of metastases in that order after lung. Our finding falls in line with the reported literature.
Surprisingly, in our study, plasma cell dyscrasias (22%; 10: multiple myeloma, 2: solitary plasmacytoma) was the second most common diagnosis followed by adenocarcinoma prostate in the third place (9%). This is a novel finding as earlier series have reported a minuscule proportion (approximately 1%) of their patients having myeloma (9 out of 855; 77 out of 7004)., A higher index of suspicion for plasma cell dyscrasias must be kept while evaluating patients with suspected metastases. Nerve conduction studies in these patients, might unmask the underlying radiculo-neuropathy, especially in the elderly age group.
We did not find a high number of carcinoma breast patients (four patients), being a neurology referral facility, as compared to those reported in the literature. Hovestadt et al. reported that patients with breast cancer have a high referral index, almost twice as that of lung cancer for complications. If we compare the age-standardized incidence rates of breast cancer per 100,000 population, India (25.8) has a significantly lower incidence when compared with the world average (43.1) and other parts of the world such as Europe (69.9), Canada (79.8), European Union (80.3) and Northern America (91.6).
There were a few limitations to our study. Based on the evaluation protocol, only admitted patients were considered for inclusion in this study; owing to the low socio-economic profile of a majority of patients the complete battery of investigations planned as per protocol could not be completed. Post-mortem analysis is not done at our centre whereby patients with an undiagnosed primary could not be evaluated further.
Regarding neurological consultations with an unknown primary, organ-specific targeted efforts based on clinical evaluation for systemic localisation must be directed at diagnosing the primary. PET-CT may come handy in such situations. Besides providing an overview of malignancies primarily presenting with a neurological symptom, our study calls for a concerted effort in making a neuro-oncology register to aid early detection and timely initiation of therapy.
The authors acknowledge the support and cooperation of their patients and support staff of the concerned departments in conducting this study. It also acknowledges the Uttar Pradesh Government's pledge to bear the expenses of poor patients with malignancies and treat them free of cost.
Financial support and sponsorship
Funding was not involved in the conduct of this study.
Conflicts of interest
The authors declare that there are no financial and personal relationships with other people or organizations that could inappropriately influence (bias) their work.
| References|| |
Gilbert MR, Grossman SA. Incidence and nature of neurologic problems in patients with solid tumours. Am J Med 1986;81:951-4.
Posner JB. Neuro-oncology: An overview. In: Ongerboer de Visser BW, Bosch DA, van Woerkom-Eykenboom WHM, editors. Neuro-Oncology: Clinical and Experimental Aspects. Boston: Martinus Nijhoff; 1979. p. 1-11.
Clouston PD, DeAngelis LM, Posner JB. The spectrum of neurological disease in patients with systemic cancer. Ann Neurol 1992;31:268-73.
Indian Council of Medical Research. National Cancer Registry Programme (Indian Council of Medical Research). Available from: http://www.ncrpindia.org
. [Last assessed on 2018 Jan 17].
Lassouw GM, Twijnstra A, Schouten LJ, Van de Pol M. The neuro-oncology register. Neuroepidemiology 1993;11:261-6.
Kohler BA, Ward E, McCarthy BJ, Schymura MJ, Ries LA, Eheman C, et al
. Annual report to the nation on the status of cancer, 1975-2007, featuring tumors of the brain and other nervous system. J Natl Cancer Inst 2011;103:714-36.
Dhopesh VP, Yagnik PM. Brain metastasis: Analysis of patients without known cancer. South Med J 1985;78:171-2.
Zimm S, Wampler GL, Stablein D, Hazra T, Young HF. Intracerebral metastases in solid-tumor patients: Natural history and results of treatment. Cancer 1981;48:384-94.
Giglio P, Gilbert MR. Neurologic complications of cancer and its treatment. Curr Oncol Rep 2010;12:50-9.
Mendez JS, DeAngelis LM. Metastatic complications of cancer involving the central and peripheral nervous systems. Neurol Clin 2018;36:579-98.
Gilbert RW, Kim JH, Posner JB. Epidural spinal cord compression from metastatic tumor: Diagnosis and treatment. Ann Neurol 1978;3:40-51.
Ruff RL, Lanska DJ. Epidural metastases in prospectively evaluated veterans with cancer and back pain. Cancer 1989;63:2234-41. [Erratum appears in Cancer 1990;66:935].
Rodichok LD, Harper GR, Ruckdeschel JC, Price A, Roberson G, Barron KD, et al
. Early diagnosis of spinal epidural metastases. Am J Med 1981;70:1181-8.
Le Chevalier T, Smith FP, Caille P, Constans JP, Rouesse JG. Sites of primary malignancies in patients presenting with cerebral metastases. A review of 120 cases. Cancer 1985;56:880-2.
Sharfuddin AA, Fatima H, Jilani SM, Mozaffar FH, Mozaffar T. The spectrum of neurological complications in Pakistani patients with malignancies. J Pak Med Assoc 2008;58:160-4.
Kori SH, Foley KM, Posner JB. Brachial plexus lesions in patients with cancer: 100 cases. Neurology 1981;31:45-50.
Jaeckle KA. Neurologic Manifestations of neoplastic and radiation-induced plexopathies. Semin Neurol 2010;30:254-62.
Croft PB, Wilkinson M. The incidence of carcinomatous neuromyopathy in patients with various types of carcinoma. Brain 1965;88:427-34.
Currie S, Henson RA, Morgan HG, Poole AJ. The incidence of the non-metastatic neurological syndromes of obscure origin in the reticuloses. Brain 1970;93:629-40.
Cacho-Díaz B, Lorenzana-Mendoza NA, Reyes-Soto G, Ávila-Funes JA, Navarrete-Reyes AP. Neurologic manifestations of elderly patients with cancer. Aging Clin Exp Res 2019;31:201-7.
Khasraw M, Posner JB. Neurological complications of systemic cancer. Lancet Neurol 2010;9:1214-27.
Jin J, Zhou X, Liang X, Huang R, Chu Z, Jiang J, et al
. A study of patients with brain metastases as the initial manifestation of their systemic cancer in a Chinese population. J Neurooncol 2011;103:649-55.
Chee CP, Byrnes DP. Cases of brain metastasis presenting as the first sign of systemic cancer. Singapore Med J 1988;29:252-6.
Merchut MP. Brain metastases from undiagnosed systemic neoplasms. Arch Intern Med 1989;149:1076-80.
Koç ZP, Kara PÖ, Daǧtekin A. Detection of unknown primary tumor in patients presented with brain metastasis by F-18 fluorodeoxyglucose positron emission tomography/computed tomography. CNS Oncol 2018;7:CNS12.
White MD, Agarwal N, Tonetti DA. The utility of whole body imaging in the evaluation of solitary brain tumors. World Neurosurg 2019;126:e1206-10.
Mayerhoefer ME, Prosch H, Beer L, Tamandl D, Beyer T, Hoeller C, et al
. PET/MRI versus PET/CT in oncology: A prospective single-center study of 330 examinations focusing on implications for patient management and cost considerations. Eur J Nucl Med Mol Imaging 2019. doi: 10.1007/s00259-01904452-y.[Epub ahead of print].
Polyzoidis KS, Miliaras G, Pavlidis N. Brain metastasis of unknown primary: A diagnostic and therapeutic dilemma. Cancer Treat Rev 2005;31:247-55.
van de Pol M, van Aalst VC, Wilmink JT, Twijnstra A. Brain metastases from an unknown primary tumour: Which diagnostic procedures are indicated? J Neurol Neurosurg Psychiatry 1996;61:321-3.
Barnholtz-Sloan JS, Sloan AE, Davis FG, Vigneau FD, Lai P, Sawaya RE. Incidence proportions of brain metastases in patients diagnosed (1973 to 2001) in the metropolitan detroit cancer surveillance system. J Clin Oncol 2004;22:2865-72.
Hovestadt A, van Woerkom CM, Vecht J. Frequency of neurological disease in a cancer hospital. Eur J Cancer 1990;26:765-6.
Ferlay J, Soerjomataram I, Ervik M, Dikshit R, Eser S, Mathers C, et al
. GLOBOCAN 2012 v1.0, Cancer Incidence and Mortality Worldwide: IARC CancerBase No. 11 [Internet]. Lyon, France: International Agency for Research on Cancer; 2013. Available from: http://globocan.iarc.fr
. [Last accessed on 2018 Jan 16].
[Table 1], [Table 2], [Table 3], [Table 4], [Table 5]