Neurology India · 2020
Tumors masquerading as neurological diseases: A caution for clinicians in planning diagnosis and treatment.
СтатьяНазвание и аннотация: Перевод в очереди
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Vidhya Annapoorni C S, Retnaswami Chandra Sadanandavalli, Mailankody Pooja, Katragadda Pavan, Pillai Sivakumar Krishna, Rangarajan Anush, Padmanabha Hansashree, Pendharkar Hima
Аннотация
INTRODUCTION: Neurological diseases can be due to direct diseases of the central nervous system (CNS) or peripheral nervous system (PNS) or be a bystander syndrome of systemic diseases. Treatment options depend on the cause. Toxic, metabolic and nutritional, and immune-mediated consequences of clinically occult neoplasms produce a spectrum of neurological diseases, recognition of which has therapeutic and prognostic importance.
PATIENTS AND METHODS: Children, as well as adults who presented to the authors in the last 5 years with neurological diseases and later their diseases could be diagnosed or attributed to neoplasms which were occult, were included for the study.
OBSERVATION: 28 patients were seen by the authors in the last 5 years with neurological manifestation and hidden tumor. Maximum incidence was in the age of above 60 years followed by the age group of 21-40 years. The commonest neurological presentation was muscle and nerve in adults and seizure in children.
DISCUSSION: Short duration, rapid progression, severe weight loss, and poor response to treatment given for nontumor associated neurological syndrome are the red flags which point to the diagnosis.
CONCLUSION: Seizures and psychosis formed the commonest features in children, muscle and nerve in adults. Short duration, rapid progression, and resistance to treatment are the markers for possible underlying neoplasm.
PATIENTS AND METHODS: Children, as well as adults who presented to the authors in the last 5 years with neurological diseases and later their diseases could be diagnosed or attributed to neoplasms which were occult, were included for the study.
OBSERVATION: 28 patients were seen by the authors in the last 5 years with neurological manifestation and hidden tumor. Maximum incidence was in the age of above 60 years followed by the age group of 21-40 years. The commonest neurological presentation was muscle and nerve in adults and seizure in children.
DISCUSSION: Short duration, rapid progression, severe weight loss, and poor response to treatment given for nontumor associated neurological syndrome are the red flags which point to the diagnosis.
CONCLUSION: Seizures and psychosis formed the commonest features in children, muscle and nerve in adults. Short duration, rapid progression, and resistance to treatment are the markers for possible underlying neoplasm.
Предметные рубрики MeSH
AdenomaAdolescentAdultAnti-N-Methyl-D-Aspartate Receptor EncephalitisAtaxiaCarcinomaChildDementiaDiagnosis, DifferentialDiagnostic ErrorsFemaleGanglioneuromaHumansHypokalemic Periodic ParalysisLipomaLymphoma, Non-HodgkinMERRF SyndromeMaleMiddle AgedMyoclonic Epilepsy, JuvenileNeoplasmsNervous System DiseasesNeuroblastomaOpsoclonus-Myoclonus SyndromeOvarian NeoplasmsPOEMS SyndromePancreatic NeoplasmsParaneoplastic Syndromes, Nervous SystemParathyroid NeoplasmsParkinsonian DisordersPlasmacytomaPolymyositisStomach NeoplasmsSubacute Combined DegenerationTeratomaThymus NeoplasmsYoung Adult