scholarly journals EXTENSIVELY DISSEMINATED CYSTICERCOSIS – CASE REPORT AND REVIEW OF LITERATURE

2020 ◽  
pp. 68-69
Author(s):  
Navdeep Kaur ◽  
Narinder Kaur ◽  
Harvinder Singh Chhabra ◽  
Ravinder Kaur

Cysticercosis is a known disease of the developing world and accounts for the majority of epilepsy cases in these nations. The disseminated form represents a rare presentation of the disease with neurocysticercosis being the most common. Patients may present with neurological complaints of seizures only with no clinical manifestations of muscular pseudohypertrophy or palpable subcutaneous nodules usually found in disseminated form falsely localizing disease to the central nervous system. This case report highlights the fact that despite its rarity a high index of suspicion for disseminated form should be kept in mind in endemic areas and warrants routine screening of all patients for multi-organ involvement who present with multiple lesions in brain parenchyma.

2021 ◽  
pp. 44-45
Author(s):  
Piyush Modi ◽  
Rajeev Kumar Singh ◽  
K.S Shahi ◽  
Prateek Shakya

Neurocysticercosis is the most common parasitic infection of the central nervous system worldwide. However , cysticercosis affecting the spine is considered extremely rare. We report one case of spinal cysticercosis with review of literature.


2017 ◽  
Vol 03 (03) ◽  
pp. 178-180
Author(s):  
Rama Badyal ◽  
Rakesh Vasishta ◽  
Devi Patra ◽  
Pravin Salunke ◽  
Amey Savardekar ◽  
...  

2017 ◽  
Vol 31 (2) ◽  
pp. 248-252
Author(s):  
Alfonso Pacheco-Hernandez ◽  
Jorque Aquino-Matus ◽  
Willem Guillermo Calderon-Miranda ◽  
Jean Carlos Pinto-Angarita ◽  
Ronsangela Ramirez-Barranco ◽  
...  

Abstract Actinomycosis infection is a slow progressing disease, in which involvment of the central nervous system by Actinomyces israelii is uncommon (less than 5%). Clinical picture is non-specific and is often misdiagnosed with neoplasia; some clinical clues my arise suspicion. The case of a 59 year-old female is reported who presented headache and focal neurologic signs and in whom a out-of the hospital diagnosis of a neuroepitelial dysembryoplastic tumor was made; nonetheless after careful interview and physical exploration, a spectroscopy magnetic resonance of the brain and hystopathological description of the lesion was made and yielded the definitive diagnosis of intracranial actinomyces infection. Treatment and progression were uneventful.


2018 ◽  
Vol 52 (1) ◽  
pp. 102-106 ◽  
Author(s):  
Andrea Stabile ◽  
Vincenzo Di Lazzaro ◽  
Cesare Colosimo ◽  
Fabrizio Piazza ◽  
Carlo Ferrarese ◽  
...  

2021 ◽  
Vol In Press (In Press) ◽  
Author(s):  
Manizhe Ataee Kachuei

: Primary inflammatory pseudotumor of the central nervous system is extremely rare. These lesions may be intra-axial, extra-axial, or a mix of them. We report a case of intracranial inflammatory pseudotumor involving both brain parenchyma and dura.


2018 ◽  
Vol 2018 ◽  
pp. 1-3 ◽  
Author(s):  
Rita Martins ◽  
Carlos Casimiro ◽  
Ana Valverde ◽  
Jose Campillo

We herein report a rare case of a 25-year-old immunocompetent male patient with disseminated tuberculosis of central nervous system (CNS), first presenting as multiple cerebral lesions with no meningeal involvement. Subsequent diagnostic workup disclosed extensive peritoneal involvement. A broad differential diagnosis was considered, including neoplastic and infectious diseases. The diagnosis was confirmed with positive PCR result for Mycobacterium tuberculosis in the biopsied mesenteric tissue. The patient was started on tuberculostatic regimen with favorable outcome. No acquired or hereditary immunodeficiency was documented. Disseminated tuberculosis in immunocompetent individuals is extremely rare. Genetic susceptibility factors have been reported in individuals with extensive forms of the disease and a high index of suspicion is required, as observed in our case.


2021 ◽  
Vol 21 ◽  
pp. S437-S438
Author(s):  
Carine Ribeiro Franzon ◽  
Andressa Oliveira Martin Wagner ◽  
Annelise Correa Wengerkievicz Lopes ◽  
Douglas Gebauer Bona ◽  
Talita Bertazzo Schmitz

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