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Paraneoplastic limbic encephalitis associated with mixed olfactory neuroblastoma and craniopharyngioma: A case report and literature review. | LitMetric

AI Article Synopsis

  • Paraneoplastic limbic encephalitis (PLE) is a rare nervous system disorder linked to cancers, presenting with symptoms like cognitive dysfunction and seizures.
  • A case study detailed a 35-year-old man with PLE related to a unique tumor combination of olfactory neuroblastoma (ONB) and craniopharyngioma, who underwent successful surgery and treatment.
  • Post-surgery, the patient’s neurological symptoms improved significantly, and there were no signs of tumor recurrence after 4 years, highlighting the unusual tumor's impact and the association with anti-Hu antibodies.

Article Abstract

Rationale: Paraneoplastic limbic encephalitis (PLE) is a rare disorder of the nervous system associated with malignant disease. It has a subacute onset with the following symptoms: cognitive dysfunction, seizures, irritability, hallucinations, and short-term memory loss. Herein, we report the case of a 35-year-old man with PLE, an olfactory neuroblastoma (ONB) admixed with craniopharyngioma, and serum anti-Hu antibodies.

Patient Concerns: The patient presented with generalized seizures, short-term memory loss, and a polypoid mass located high in the nasal cavity.

Interventions: He underwent surgical resection of the tumor and postoperative chemoradiotherapy with concurrent intra-arterial cisplatin administration.

Diagnosis: Pathological examination indicated an ONB admixed with craniopharyngioma.

Outcomes: The patient's neurological symptoms gradually diminished after surgery. No evidence of recurrence was observed during a 4-year follow-up.

Lessons: We reported a histologically unusual heterogeneous tumor that comprised ONB and craniopharyngioma. This is the first reported case of PLE with anti-Hu antibodies possibly associated with ONB admixed with craniopharyngioma.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6024189PMC
http://dx.doi.org/10.1097/MD.0000000000010932DOI Listing

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