Sathish Kumar Krishnan, Vijaya Sivalingam Ramalingam, Melissa Johnson
{"title":"Rapid Paralysis and Hidden Malignancy: Acute Motor Axonal Neuropathy Revealing Pleomorphic Liposarcoma.","authors":"Sathish Kumar Krishnan, Vijaya Sivalingam Ramalingam, Melissa Johnson","doi":"10.12890/2025_005481","DOIUrl":null,"url":null,"abstract":"<p><p>Guillain-Barré syndrome is an immune-mediated neuropathy characterised by acute-onset of symmetric, ascending motor weakness and areflexia. Acute motor axonal neuropathy, a severe axonal variant, is distinguished by direct axonal injury and poor functional recovery. Although infections are recognised triggers for Guillain-Barré syndrome, it is notable that up to half of cases occur without a preceding infectious event, suggesting that other factors such as underlying malignancy may contribute to disease onset. We present a rare and fatal case of acute motor axonal neuropathy in a 70-year-old woman, who was ultimately found to have an underlying pleomorphic liposarcoma. The patient presented with one week of progressive weakness, fatigue and encephalopathy. She required urgent mechanical ventilation due to respiratory failure; imaging identified multiple bilateral pulmonary nodules. Neurologic evaluation confirmed acute motor axonal neuropathy through nerve conduction studies and cerebrospinal fluid analysis, which showed albuminocytologic dissociation and positive anti-GM1 IgG antibodies. Despite standard treatment with intravenous immunoglobulin, the patient experienced no neurological recovery. Further imaging revealed a large pelvic mass, that was not present on a scan performed two months earlier. A biopsy confirmed pleomorphic liposarcoma, a rare and aggressive soft tissue sarcoma. Paraneoplastic panel testing was negative for onconeural antibodies, yet the clinical context raised suspicion for an immune-mediated, tumour-associated neuropathy. Clinicians should maintain a high level of suspicion of underlying malignancy in patients with Guillain-Barré syndrome, especially in the absence of preceding infection and with rapid neurological decline.</p><p><strong>Learning points: </strong>Although infection is a well-established trigger for Guillain-Barré syndrome, patients presenting with Guillain-Barré syndrome may also have an increased risk of underlying malignancy.Clinicians should remain vigilant for the possibility of occult malignancy in patients hospitalised with Guillain-Barré syndrome, especially in those without a preceding infectious event.</p>","PeriodicalId":11908,"journal":{"name":"European journal of case reports in internal medicine","volume":"12 6","pages":"005481"},"PeriodicalIF":0.0000,"publicationDate":"2025-05-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12151569/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European journal of case reports in internal medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.12890/2025_005481","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
Abstract
Guillain-Barré syndrome is an immune-mediated neuropathy characterised by acute-onset of symmetric, ascending motor weakness and areflexia. Acute motor axonal neuropathy, a severe axonal variant, is distinguished by direct axonal injury and poor functional recovery. Although infections are recognised triggers for Guillain-Barré syndrome, it is notable that up to half of cases occur without a preceding infectious event, suggesting that other factors such as underlying malignancy may contribute to disease onset. We present a rare and fatal case of acute motor axonal neuropathy in a 70-year-old woman, who was ultimately found to have an underlying pleomorphic liposarcoma. The patient presented with one week of progressive weakness, fatigue and encephalopathy. She required urgent mechanical ventilation due to respiratory failure; imaging identified multiple bilateral pulmonary nodules. Neurologic evaluation confirmed acute motor axonal neuropathy through nerve conduction studies and cerebrospinal fluid analysis, which showed albuminocytologic dissociation and positive anti-GM1 IgG antibodies. Despite standard treatment with intravenous immunoglobulin, the patient experienced no neurological recovery. Further imaging revealed a large pelvic mass, that was not present on a scan performed two months earlier. A biopsy confirmed pleomorphic liposarcoma, a rare and aggressive soft tissue sarcoma. Paraneoplastic panel testing was negative for onconeural antibodies, yet the clinical context raised suspicion for an immune-mediated, tumour-associated neuropathy. Clinicians should maintain a high level of suspicion of underlying malignancy in patients with Guillain-Barré syndrome, especially in the absence of preceding infection and with rapid neurological decline.
Learning points: Although infection is a well-established trigger for Guillain-Barré syndrome, patients presenting with Guillain-Barré syndrome may also have an increased risk of underlying malignancy.Clinicians should remain vigilant for the possibility of occult malignancy in patients hospitalised with Guillain-Barré syndrome, especially in those without a preceding infectious event.
期刊介绍:
The European Journal of Case Reports in Internal Medicine is an official journal of the European Federation of Internal Medicine (EFIM), representing 35 national societies from 33 European countries. The Journal''s mission is to promote the best medical practice and innovation in the field of acute and general medicine. It also provides a forum for internal medicine doctors where they can share new approaches with the aim of improving diagnostic and clinical skills in this field. EJCRIM welcomes high-quality case reports describing unusual or complex cases that an internist may encounter in everyday practice. The cases should either demonstrate the appropriateness of a diagnostic/therapeutic approach, describe a new procedure or maneuver, or show unusual manifestations of a disease or unexpected reactions. The Journal only accepts and publishes those case reports whose learning points provide new insight and/or contribute to advancing medical knowledge both in terms of diagnostics and therapeutic approaches. Case reports of medical errors, therefore, are also welcome as long as they provide innovative measures on how to prevent them in the current practice (Instructive Errors). The Journal may also consider brief and reasoned reports on issues relevant to the practice of Internal Medicine, as well as Abstracts submitted to the scientific meetings of acknowledged medical societies.