The racemose form of brain cysticercosis arises from an intense proliferation of the bladder wall after the scolex part has degenerated. The proliferating zones are 2-3 times thicker than the remaining parts of the bladder and are characterized by a densely folded tegument and thick subtegumental and parenchymal layers. The tegument and subtegumental cells contain a large amount of acid mucosubstances with sulpho groups and hydrophilic lipids, and exhibit a high activity of alkaline and acid phosphatases. The parenchyma contains a large amount of glycogen. With the gradual aging of the bladder wall and with the first signs of autolysis, the enzymatic activity as well as the amounts of glycogen, neutral and acid mucosubstances, and proteins decrease, and the hydrophobic lipids prevail over the hydrophilic ones. The results obtained are important for the differential diagnostics of cestode larval stages in the human brain.
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J Neurosurg Case Lessons
October 2024
Department of Neurosurgery, Carilion Clinic, Virginia Tech Carilion School of Medicine, Roanoke, Virginia.
Background: Neurocysticercosis is a parasitic infection of the central nervous system caused by the helminth Taenia solium. Racemose neurocysticercosis is a rare form of the disease that specifically involves cerebrospinal fluid-filled spaces in the brain and carries a high rate of complications and mortality.
Observations: This report describes the case of a 37-year-old man who developed headaches and nausea, which were found to be secondary to racemose neurocysticercosis.
Cureus
August 2024
Critical Care, Basildon University Hospital, Basildon, GBR.
J Surg Case Rep
April 2024
Department of Neurosurgery, Hospital Nacional Edgardo Rebagliati Martins, EsSalud, Lima, Peru.
Racemose neurocysticercosis (RNC) is a malignant form of infection. It carries high mortality due to widespread intraparenchymal invasion, mass effect, and cyst rupture. Cerebellar RNC is unusual and constitutes a surgical challenge.
View Article and Find Full Text PDFBJR Case Rep
January 2024
Department of Radiodiagnosis, SGPGIMS, Lucknow 226014, India.
Neurocysticercosis (NCC) is a common parasitic condition of the central nervous system in certain parts of the world. The racemose variety of NCC is distinct from the commonly seen parenchymal form. It frequently infiltrates the basal cisterns and Sylvian fissures.
View Article and Find Full Text PDFPediatr Rheumatol Online J
June 2023
Pediatric Rheumatology Society of Iran, Tehran, Iran.
Background: Deficiency of adenosine deaminase 2 (DADA2) is an autosomal recessive autoinflammatory disease caused by mutations in the ADA2 gene. DADA2 has a broad spectrum of clinical presentations. Apart from systemic manifestations, we can categorize most of the signs and symptoms of DADA2 into the three groups of vasculitis, hematologic abnormalities, and immunologic dysregulations.
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