Case of central nervous system inflammatory disease in late pregnancy. (14th March 2019)

• Record Type: Journal Article
• Authors: Isobe, Noriko; Baba, Toshikazu; Nakamura, Yuri; Shinoda, Koji; Watanabe, Mitsuru; Matsushita, Takuya; Kira, Jun‐ichi
• Other Names: Matsui Makoto guestEditor.
• Is Part Of: Clinical & experimental neuroimmunology. Volume 10(2019)Supplement 1
• Page Start: 54
• Page End: 58
• Publication Date: 2019-03-14
• Subjects: multiple sclerosis -- neuro‐Behҫet's disease -- neuroinflammation -- pregnancy; 616.80479
• DOI: 10.1111/cen3.12503
• Languages: English
• ISSNs: 1759-1961

Abstract

Abstract: Background: During pregnancy, dynamic changes occur not only in coagulation, but also in immune responses. We report a case of a patient who developed an inflammatory disease in the central nervous system during late pregnancy and was challenging to diagnose. Case presentation: A 27‐year‐old woman experienced dysarthria during pregnancy at approximately 33 gestational weeks. From the 38th week of pregnancy, she developed general fatigue, clumsiness of the left hand and numbness of the right side of the body. After delivery of her child at 41 weeks' gestation, she was moved to the neurology ward for further investigation. She showed limb ataxia of the left extremities and sensory disturbance on the right side of the body, including the face. Magnetic resonance imaging detected multiple gadolinium‐enhanced lesions at the brainstem and cerebrum. High‐dose intravenous methylprednisolone pulse therapy was effective, but her symptoms still remained, including palatal myoclonus. Diagnosing this patient was challenging, but clinically isolated syndrome or multiple sclerosis and neuro‐Behҫet's disease were the main candidates. Conclusions: We present a case of a pregnant woman who developed brain inflammatory lesions with unknown etiology. Longitudinal follow up is mandatory for diagnosis with careful tapering of oral prednisolone.