mixed connective tissue disease/muntah

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Safety and efficacy of iloprost for the treatment of ischaemic digits in paediatric connective tissue diseases.

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OBJECTIVE We analysed our experience with the use of iloprost for the treatment of critical ischaemic digits (ID) in children with connective tissue diseases (CTD) in order to assess its safety and efficacy. METHODS This was a retrospective analysis of paediatric patients with CTD who were treated

[A case of steroid psychosis caused by treatment for acute sensorineural hearing loss].

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A 36 y/o female presented with the chief complaint of diarrhea and vomiting which had lasted for four days, and with a family history of suicide. The first general examination showed severe dehydration with hyponatremia. After admission, she was diagnosed as having isolated adrenocorticotropic

[Chronic recurrent subileus due to Strongyloides stercoralis infection under immunosuppressive therapy].

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METHODS A 33-year-old woman from Laos was admitted due to recurrent vomiting and weight loss. Since one year, she was receiving immunosuppressive therapy (azathioprine 50 mg/d and methylprednisolone 18 mg/d) for a mixed connective tissue disease. Because of a drug induced Stevens-Johnson-Syndrome

[Gastroenterologic aspects of connective tissue diseases].

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The connective tissue disorders are a protean group of acquired diseases which have in common widespread immunologic and inflammatory alterations of connective tissue. The acquired connective tissue diseases generally include the following clinical entities: rheumatoid arthritis, systemic lupus

Spontaneous uterine perforation of pyometra presenting as acute abdomen.

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Pyometra is the accumulation of pus in the uterine cavity, and spontaneous perforation of pyometra resulting in generalized diffuse peritonitis is extremely uncommon. We report a rare case of diffuse peritonitis caused by spontaneous perforation of pyometra. A 66-year-old postmenopausal woman with

[Rare case of systemic lupus erythematosus with encapsulating peritoneal sclerosis during hemodialysis].

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A 57-year old male patient was admitted to our hospital because of severe vomiting and abdominal pain with massive ascites. He had been diagnosed as mixed connective tissue disease in 1997 and lupus nephritis ISN III (A/C) + V in 2003. Treatment was started with intravenous steroid pulse therapy

Clinical and upper gastrointestinal motility features in systemic sclerosis and related disorders.

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OBJECTIVE The aim of this study was to characterize the clinical and motility findings in 62 patients with systemic sclerosis or related disorders referred for evaluation of upper gastrointestinal (GI) symptoms. METHODS Methods included retrospective clinical record review and quantitation of

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