Spontaneous iliopsoas muscle hematoma secondary to disseminated intravascular coagulation caused by nafamostat mesilate allergy: a case study

被引:1
|
作者
Nezu, Kunihisa [1 ]
Yoshioka, Takashi [2 ]
Katayama, Hiromichi [1 ]
Fukushi, Taro [3 ]
Kyan, Atsushi [1 ]
机构
[1] Shirakawa Kosei Gen Hosp, Dept Urol, Shirakawa, Japan
[2] Fukushima Med Univ, Ctr Innovat Res Communities & Clin Excellence CiR, 1 Hikarigaoka, Fukushima, Fukushima 9601295, Japan
[3] Tohoku Univ Hosp, Div Blood Purificat, Sendai, Miyagi, Japan
关键词
Spontaneous iliopsoas muscle hematoma; Nafamostat mesilate; Hemodialysis; Disseminated intravascular coagulation; SPONTANEOUS RETROPERITONEAL HEMORRHAGE; LUMBAR ARTERY; PROCALCITONIN; EMBOLIZATION; PATIENT;
D O I
10.1186/s41100-019-0207-x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background A spontaneous iliopsoas muscle hematoma is relatively rare and often associated with abnormal coagulation. Nafamostat mesilate is an anticoagulant agent that is sometimes used to treat hemodialysis patients at high risk of bleeding. Although severe drug allergy caused by nafamostat mesilate was previously reported, spontaneous iliopsoas muscle hematoma secondary to disseminated intravascular coagulation caused by nafamostat mesilate allergy has not yet been reported. Case presentation Severe nafamostat mesilate allergy occurred in a 78-year-old male patient with a 2-year history of hemodialysis. During hospitalization, disseminated intravascular coagulation occurred followed by a progressive iliopsoas muscle hematoma a few days later. Emergent transarterial lumbar artery embolization was successfully performed. Conclusion For dialysis patients, a detailed medical history including repeated nafamostat mesilate use and considering an allergy to nafamostat mesilate in differential diagnosis are critical. In addition to early diagnosis, when an iliopsoas hematoma occurs, early intravascular treatment is important.
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页数:6
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