Paraneoplastic limbic encephalitis associated with mixed olfactory neuroblastoma and craniopharyngioma: A case report and literature review
- PMID: 29901583
- PMCID: PMC6024189
- DOI: 10.1097/MD.0000000000010932
Paraneoplastic limbic encephalitis associated with mixed olfactory neuroblastoma and craniopharyngioma: A case report and literature review
Erratum in
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Paraneoplastic limbic encephalitis associated with mixed olfactory neuroblastoma and craniopharyngioma: A case report and literature review: Erratum.Medicine (Baltimore). 2018 Jul;97(28):e11575. doi: 10.1097/MD.0000000000011575. Medicine (Baltimore). 2018. PMID: 29995829 Free PMC article. No abstract available.
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.
Conflict of interest statement
The authors have no funding and conflicts of interest to disclose .
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