Thurner Lorenz, Melivadze Ketevani, Matschke Jakob, Topalidis Theodoros, Bachhuber Armin, Speicher Tilman, Rosar Florian, Reischl Udo, Tränkenschuh Wolfgang, Friesenhahn-Ochs Bettina, Fries Peter, Becker Sören L, Fleser Octavian
Department of Internal Medicine I, Saarland University Medical School, Homburg/Saar, Germany.
Institute of Neuropathology, University Medical Center Hamburg-Eppendorf, Hamburg, Hamburg, Germany.
Front Immunol. 2024 Dec 4;15:1462310. doi: 10.3389/fimmu.2024.1462310. eCollection 2024.
We report here on a patient with concomitant indolent lymphoma who showed a rapid progressive deterioration of his general condition and emerging neurological symptoms. The combination of severe B symptoms with hypermetabolic involvement of the adrenal glands and multiple central nervous system (CNS) lesions initially suggested a malignant disease. However, when the patient presented to us with biopsy results from one of the CNS lesions, the biopsy revealed granulomatous inflammation but no evidence of malignancy. This case illustrates the difficulties and challenges of diagnosing in a timely manner , an ultra rare infectious disease in Europe.
我们在此报告一例伴有惰性淋巴瘤的患者,该患者出现全身状况迅速进行性恶化并伴有新发神经症状。严重的B症状、肾上腺的高代谢受累以及多个中枢神经系统(CNS)病变的组合最初提示为恶性疾病。然而,当该患者带着其中一个CNS病变的活检结果前来我们这里时,活检显示为肉芽肿性炎症,未发现恶性证据。该病例说明了及时诊断欧洲一种极为罕见的传染病的困难和挑战。