Sefcsik Victoria, Rodriguez Paulette, Makar Monica, Chun Magnus, Bahar Rayeheh, Kairamkonda Supriya, Kioka Mutsumi
Family Medicine Residency, 99th Medical Group, Nellis Air Force Base, Las Vegas, NV, 89191, USA.
Kirk Kerkorian School of Medicine, University of Nevada, Las Vegas, NV, 89154, USA.
BMC Neurol. 2025 Jul 30;25(1):308. doi: 10.1186/s12883-025-04337-8.
Anti-Dipeptidyl-peptidase-like protein-6 (DPPX) antibody-associated encephalitis is a rare autoimmune condition that affects the central and enteric nervous systems. It often presents with neuropsychiatric symptoms, cerebellar ataxia, and gastrointestinal dysmotility, though clinical manifestations can vary widely.
We report the case of a 38-year-old woman with psychiatric symptoms who developed severe cognitive impairment, seizures, and a profound weight loss of 100 pounds over one year. Her symptoms initially led to multiple psychiatric diagnoses and treatments, delaying recognition of the underlying autoimmune process. Ultimately, cerebrospinal fluid analysis revealed high-titer anti-DPPX antibodies (1:1000). Despite aggressive immunotherapy—including corticosteroids, plasmapheresis, IVIG, and rituximab—the patient’s condition deteriorated, and she died under hospice care.
This case expands the known clinical spectrum of anti-DPPX encephalitis by documenting the most extreme reported case of weight loss associated with the disease. The prodromal presentation with isolated weight loss underscores the diagnostic challenges when neuropsychiatric symptoms emerge late. Our case highlights the importance of maintaining clinical suspicion for autoimmune encephalitis in patients with unexplained weight loss and neurocognitive decline.
Profound, unexplained weight loss may be an early and under-recognized manifestation of anti-DPPX encephalitis. Early recognition and immunotherapy are critical, but the potential for rapid progression and relapse demands heightened clinical vigilance and further research into optimal treatment strategies.
The online version contains supplementary material available at 10.1186/s12883-025-04337-8.
抗二肽基肽酶样蛋白6(DPPX)抗体相关脑炎是一种罕见的自身免疫性疾病,可影响中枢和肠道神经系统。其临床表现通常包括神经精神症状、小脑共济失调和胃肠动力障碍,不过临床表现差异很大。
我们报告一例38岁有精神症状的女性病例,该患者出现严重认知障碍、癫痫发作,并在一年内体重剧减100磅。她的症状最初导致了多种精神科诊断和治疗,从而延误了对潜在自身免疫过程的识别。最终,脑脊液分析显示抗DPPX抗体高滴度(1:1000)。尽管进行了积极的免疫治疗,包括使用皮质类固醇、血浆置换、静脉注射免疫球蛋白和利妥昔单抗,但患者病情仍恶化,最终在临终关怀下死亡。
本病例记录了与该疾病相关的最极端的体重减轻病例,从而扩展了抗DPPX脑炎已知的临床谱。以单纯体重减轻为前驱表现突出了神经精神症状出现较晚时的诊断挑战。我们的病例强调了对不明原因体重减轻和神经认知功能下降的患者保持自身免疫性脑炎临床怀疑的重要性。
严重的、不明原因的体重减轻可能是抗DPPX脑炎早期且未被充分认识的表现。早期识别和免疫治疗至关重要,但疾病快速进展和复发的可能性要求提高临床警惕性,并进一步研究最佳治疗策略。
在线版本包含可在10.1186/s12883-025-04337-8获取的补充材料。