Literature DB >> 15926783

Single enhancing computerized tomography-detected lesion in immunocompetent patients.

Ravindra Kumar Garg1.   

Abstract

Single enhancing computerized tomography (CT)-documented lesions may occur in several infectious and neoplastic diseases of the central nervous system and are the most common radiological abnormality seen in patients with acute-onset seizures in India and many other developing countries. Similar CT-documented lesions have also been reported in the developed world where these lesions are often considered to be caused by neoplasms or tuberculoma. Histopathological studies in India and even in some developed countries revealed that neurocysticercosis (NCC) is the most likely cause of these lesions provided they fulfill a rigid set of clinical and radiological criteria. Single cysticercus granuloma measures less than 20 mm in diameter, may be associated with cerebral edema not severe enough to produce midline shift, and occur in patients with seizures, normal neurological status, and no evidence of active systemic disease. When these lesions resolve spontaneously, either disappearing or changing into a calcified nodule, the diagnosis of NCC is very likely. The second most common cause of these CT-detected lesions is tuberculoma; in patients with these lesions similar clinical and neuroimaging features are also present. Few authors believe that in poor and developing countries, where both tuberculosis and NCC are common, it is difficult to differentiate between tuberculoma and a single cysticercal granuloma. The most interesting feature of these solitary enhancing lesions is their spontaneous disappearance within weeks or months. Some lesions "heal" by becoming calcified. These patients require only antiepileptic therapy, and this medication may be withdrawn safely after the lesion has resolved on CT scanning. In several studies provision of anticysticercal drugs has been attempted, but because of conflicting results, their role in the management of these single lesions is uncertain. Neurosurgeons have a very limited role to play. In very rare situations, if the lesion increases in size and if focal neurological deficits manifest or seizures are uncontrolled, a brain biopsy sample may be required and histopathological evaluation performed to establish the correct diagnosis.

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Year:  2002        PMID: 15926783     DOI: 10.3171/foc.2002.12.6.5

Source DB:  PubMed          Journal:  Neurosurg Focus        ISSN: 1092-0684            Impact factor:   4.047


  6 in total

1.  Predictors of Lesion Calcification in Patients with Solitary Cysticercus Granuloma and New-Onset Seizures.

Authors:  Lalit Mahajan; Hardeep Singh Malhotra; Ravindra Kumar Garg; Neeraj Kumar; Praveen Kumar Sharma; Rajesh Verma; Imran Rizvi
Journal:  Am J Trop Med Hyg       Date:  2016-07-18       Impact factor: 2.345

2.  Natural course of typical and atypical parenchymal solitary cysticercus granuloma of the brain: a 3-year prospective clinico-radiological study.

Authors:  Neeraj Kumar; Ravindra Kumar Garg; Hardeep Singh Malhotra; Rakesh Kumar Gupta; Rajesh Verma; Praveen Kumar Sharma
Journal:  Neuroradiol J       Date:  2015-12-11

3.  A rare cause of temporal lobe ring-enhancing lesion.

Authors:  Biplab Das; Manoj Kumar Goyal; Manish Modi; Vivek Lal; Sahil Mehta; Anu Gupta; Chirag Ahuja
Journal:  Neurol Clin Pract       Date:  2015-12

Review 4.  Immunological and molecular diagnosis of cysticercosis.

Authors:  Silvia Rodriguez; Patricia Wilkins; Pierre Dorny
Journal:  Pathog Glob Health       Date:  2012-09       Impact factor: 2.894

5.  Ring-enhancing lesions in the brain: a diagnostic dilemma.

Authors:  Guruprasada Shetty; Kadke Shreedhara Avabratha; Boodyar Sanjeev Rai
Journal:  Iran J Child Neurol       Date:  2014

6.  Disseminated cysticercosis in an immunocompetent individual.

Authors:  Kothai Gnanamoorthy; Prasanna Karthik Suthakaran
Journal:  Ann Afr Med       Date:  2019 Jan-Mar
  6 in total

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