Japanese Journal of Clinical Immunology
Online ISSN : 1349-7413
Print ISSN : 0911-4300
ISSN-L : 0911-4300
A case of systemic lupus erythematosus complicated with marked intestinal edema and paralytic ileus
Kenji KamiuchiHajime SanoAkira HashiramotoYufuko TakahashiHideki OnoderaYutaka KobayashiKunio YanagidaHaruki KatoMotoharu Kondo
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JOURNAL FREE ACCESS

1998 Volume 21 Issue 1 Pages 48-56

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Abstract
A 43-years-old female was admitted to our hospital because of facial erythema and photosensitivity in 1983 and was diagnosed as systemic lupus erythematosus (SLE). She was treated with betamethazone 2.5mg/day as an outpatient. Abdominal pain and diarrhea were developed in September, 1995. So she was admitted to our hospital and diagnosed as having paralytic ileus. Ultrasonography showed marked intestinal edema. Forbidden oral intake and given antibiotics, she was satisfactorily improved in a few days, but the symptoms got worse soon. We forbad oral intake again. We performed a pulse therapy with 1g of methylprednisolone and increased a dose of betamethasone 2.5 to 4.0mg/day, but the symptoms were not improved. Since October 6th, serum ceatinine level (s-CRE) increased to 8.1mg/dl at October, 20th. We suspected the worsening of SLE nephropathy or drug-induced nephropathy, so we stopped a medication of pravastatin and used 50 mg/day of azathioprine. Moreover, we did a pulse therapy of methylprednisolone and a plasmapheresis. By these treatments, s-CRE level returned to normal range and paralytic ileus was completely improved.
The cause of hypercreatininemia was suspected to be rhabdomyolysis due to pravastatin. The main cause of paralytic ileus with intestinal edema was suspected to be vascular disturbance of superior mesenteric arteries.
We consider that pulse therapy and plasmapheresis are useful for a patient of SLE with marked intestinal edema and paralytic ileus.
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© The Japan Society for Clinical Immunology
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