| 저자 |
Hong Joon Kim1, Mi Yeon Jung1, Eun A Lee1, Yu Ah Hong1, Jin Wan Park2,Gang Jee Ko1, Heui Jung Pyo1, Young Joo Kwon1 |
| 초록 |
Encapsulating peritoneal sclerosis (EPS) is a rare
complication in peritoneal dialysis (PD) with high mortality.
Spontaneous
bacterial peritonitis (SBP) in EPS is rare, and the treatment
of that has not been elucidated. We reported two
cases with SBP in EPS that developed after hemodialysis
(HD) transfer.
Case I. 55-year-old female was transferred due to
abdominal pain and distension. 5 years ago, she was
switched to
HD because of frequent PD peritonitis, and the diagnosis
of EPS was made by abdominal CT scan. Her
paracentesis
showed SG 1.036, WBC 16,000/㎣ (PMN 95%), protein 5.6
g/dl, LDH 8,032 IU/L, amylase 113 U/L, ADA 105.4 IU/L,
and Enterococcus facium was cultured in peritoneal fluid.
During antibiotics treatment, surgical drainage was tried
three times, but she died due to malnutrition and sepsis by
antibiotics associated-colitis after 5 months.
Case II. 64-year-old male visited our hospital because of
fever, abdominal pain and distension. He was switched to
HD because of pleural effusion 14 months ago. He was
diagnosed as EPS 5 months ago, and had been treated by
steroid and tamoxifen. His paracentesis showed SG 1.027,
WBC 1,706/mm3 (PMN 75%), protein 3.39 g/dl, LDH 342
IU/L, amylase 69 U/L, ADA 17.31 IU/L, and Klebsiella
pneumonia was cultured in peritoneal fluid. After 40 days
of
antibiotics treatment, surgical laparotomy and adhesiolysis
was done. He discharged after two months, and has been
well-being status until now.
Conclusion: SBP in EPS is one of the very rare
complications in PD, and shows poor response to
antibiotics treatment.
We think the combination with adequate surgical
intervention and antibiotics is required in the treatment of
SBP in
EPS. |