A Case of Diabetic Ketoacidosis Associated with Guillain-Barre Syndrome
-
- Kanemasa Yusuke
- Center for Diabetes and Endocrinology, Tazuke Kofukai Medical Research Institute Kitano Hospital, Japan
-
- Hamamoto Yoshiyuki
- Center for Diabetes and Endocrinology, Tazuke Kofukai Medical Research Institute Kitano Hospital, Japan
-
- Iwasaki Yorihiro
- Center for Diabetes and Endocrinology, Tazuke Kofukai Medical Research Institute Kitano Hospital, Japan
-
- Kawasaki Yukiko
- Center for Diabetes and Endocrinology, Tazuke Kofukai Medical Research Institute Kitano Hospital, Japan
-
- Honjo Sachiko
- Center for Diabetes and Endocrinology, Tazuke Kofukai Medical Research Institute Kitano Hospital, Japan
-
- Ikeda Hiroki
- Center for Diabetes and Endocrinology, Tazuke Kofukai Medical Research Institute Kitano Hospital, Japan
-
- Wada Yoshiharu
- Center for Diabetes and Endocrinology, Tazuke Kofukai Medical Research Institute Kitano Hospital, Japan
-
- Koshiyama Hiroyuki
- Center for Diabetes and Endocrinology, Tazuke Kofukai Medical Research Institute Kitano Hospital, Japan
この論文をさがす
抄録
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.<br>
収録刊行物
-
- Internal Medicine
-
Internal Medicine 50 (19), 2201-2205, 2011
一般社団法人 日本内科学会
- Tweet
詳細情報 詳細情報について
-
- CRID
- 1390282679846786176
-
- NII論文ID
- 130001087904
-
- ISSN
- 13497235
- 09182918
-
- 本文言語コード
- en
-
- データソース種別
-
- JaLC
- Crossref
- CiNii Articles
-
- 抄録ライセンスフラグ
- 使用不可