تقرير
Morvan Syndrome Manifesting as Autoimmune Paraneoplastic Encephalitis Associated with Thymoma and Antivoltage Gated Potassium Channel (Leucine Rich, Glioma Inactivated 1) Antibody Detected using F 18 Fluorodeoxyglucose Positron Emission Tomography/Computed Tomography.
| العنوان: | Morvan Syndrome Manifesting as Autoimmune Paraneoplastic Encephalitis Associated with Thymoma and Antivoltage Gated Potassium Channel (Leucine Rich, Glioma Inactivated 1) Antibody Detected using F 18 Fluorodeoxyglucose Positron Emission Tomography/Computed Tomography. |
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| المؤلفون: | Kamaleshwaran KK; Department of Nuclear Medicine, PET/CT and Radionuclide Therapy, Kovai Medical Center and Hospital Limited, Coimbatore, Tamil Nadu, India., Senthilkumar E; Department of Neurology, Kovai Medical Center and Hospital Limited, Coimbatore, Tamil Nadu, India., Ramkumar E; Department of Nuclear Medicine, PET/CT and Radionuclide Therapy, Kovai Medical Center and Hospital Limited, Coimbatore, Tamil Nadu, India., Ruth R; Department of Nuclear Medicine, PET/CT and Radionuclide Therapy, Kovai Medical Center and Hospital Limited, Coimbatore, Tamil Nadu, India. |
| المصدر: | Indian journal of nuclear medicine : IJNM : the official journal of the Society of Nuclear Medicine, India [Indian J Nucl Med] 2022 Apr-Jun; Vol. 37 (2), pp. 166-168. Date of Electronic Publication: 2022 Jul 08. |
| نوع المنشور: | Case Reports |
| اللغة: | English |
| بيانات الدورية: | Publisher: Medknow Country of Publication: India NLM ID: 8901274 Publication Model: Print-Electronic Cited Medium: Print ISSN: 0972-3919 (Print) Linking ISSN: 09740244 NLM ISO Abbreviation: Indian J Nucl Med Subsets: PubMed not MEDLINE |
| أسماء مطبوعة: | Publication: 2008 : Mumbai : Medknow Original Publication: [Delhi] : Society of Nuclear Medicine, India |
| مستخلص: | Morvan's syndrome (MoS) is a rare, complex neurological disorder characterized by neuromyotonia, neuropsychiatric features, dysautonomia, and neuropathic pain. The majority of MoS cases have a paraneoplastic etiology, most commonly thymoma, usually occurring before the diagnosis of the underlying tumor and showing improvement following surgery. We present a case of 60-year-old patient presenting with suspicious of MoS and autoimmune encephalitis (AE), F-18 fluorodeoxyglucose positron emission tomography/computed tomography as single imaging modality detected and confirmed both AE and thymoma. Competing Interests: There are no conflicts of interest. (Copyright: © 2022 Indian Journal of Nuclear Medicine.) |
| References: | Neurol Neuroimmunol Neuroinflamm. 2017 May 11;4(4):e352. (PMID: 28567435) Brain Nerve. 2010 Apr;62(4):339-45. (PMID: 20420173) Clin Nucl Med. 2013 May;38(5):392-4. (PMID: 23486322) Brain. 2001 Dec;124(Pt 12):2417-26. (PMID: 11701596) Lancet Neurol. 2016 Sep;15(10):1009-10. (PMID: 27571149) Ann Neurol. 2012 Aug;72(2):241-55. (PMID: 22473710) Autoimmun Rev. 2016 Jan;15(1):82-92. (PMID: 26408958) Brain. 2004 Oct;127(Pt 10):2331-8. (PMID: 15361417) |
| فهرسة مساهمة: | Keywords: F-18 fluorodeoxyglucose positron emission tomography/computed tomography; Morvan syndrome; paraneoplastic autoimmune encephalitis; thymoma |
| تواريخ الأحداث: | Date Created: 20220819 Latest Revision: 20220820 |
| رمز التحديث: | 20240628 |
| مُعرف محوري في PubMed: | PMC9380793 |
| DOI: | 10.4103/ijnm.ijnm_155_21 |
| PMID: | 35982802 |
| قاعدة البيانات: | MEDLINE |
Full Text Finder | تدمد: | 0972-3919 |
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| DOI: | 10.4103/ijnm.ijnm_155_21 |