Kanemasa Yusuke, Hamamoto Yoshiyuki, Iwasaki Yorihiro, Kawasaki Yukiko, Honjo Sachiko, Ikeda Hiroki, Wada Yoshiharu, Koshiyama Hiroyuki
Center for Diabetes and Endocrinology, Tazuke Kofukai Medical Research Institute Kitano Hospital, Japan.
Intern Med. 2011;50(19):2201-5. doi: 10.2169/internalmedicine.50.5553. Epub 2011 Oct 1.
A 64-year-old woman was referred to our center presenting with thirst, malaise, and pain in both legs which occurred one week before admission. She was revealed to have hyperglycemia and diabetic ketoacidosis (DKA). After therapy for diabetic ketoacidosis was started, her blood glucose levels were improved, but urinary ketone body excretion persisted. Laboratory examination indicated a significant impairment of insulin secretion, although anti-GAD and anti-IA-2 antibody were not detected. After admission, she complained about weakness of lower extremities, which spread to her upper extremities. The diagnosis of Guillain-Barré syndrome (GBS) was made based on the nerve conduction study and cerebrospinal fluid analysis. The intravenous immunoglobulin therapy was started, and her muscle weakness showed gradual improvement. Although the possibility that GBS was casually accompanied with DKA could not be completely excluded, we considered that DKA triggered the development of GBS in this case. Although GBS is a rare condition, the present case suggests that GBS should be included in the differential diagnosis of DKA with its atypical course.
一名64岁女性因入院前一周出现口渴、全身不适及双腿疼痛而被转诊至我院。检查发现她患有高血糖和糖尿病酮症酸中毒(DKA)。在开始进行糖尿病酮症酸中毒治疗后,她的血糖水平有所改善,但尿酮体排泄持续存在。实验室检查显示胰岛素分泌严重受损,尽管未检测到抗谷氨酸脱羧酶(GAD)抗体和抗胰岛细胞抗体(IA-2)。入院后,她抱怨下肢无力,并蔓延至上肢。根据神经传导研究和脑脊液分析,诊断为吉兰-巴雷综合征(GBS)。开始静脉注射免疫球蛋白治疗后,她的肌肉无力逐渐改善。尽管不能完全排除GBS与DKA偶然并存的可能性,但我们认为在该病例中DKA引发了GBS的发生。虽然GBS是一种罕见疾病,但本病例提示,对于病程不典型的DKA,应将GBS纳入鉴别诊断。