A 37-year-old Caucasian man was referred to our department from an external hospital because of severe abdominal pain of unclear aetiology.
The patient suffered from Friedreich's ataxia.1 2 His most recent transthoracic echocardiography, performed on the day of admission, showed a dilated cardiomyopathy, impaired left ventricular function with an ejection fraction of 30% and a pulmonary artery pressure of 55 mm Hg; all findings were unchanged from previous examinations.
At that time, he lived alone in a residential home and was mobile using a wheelchair.
On arrival at our emergency department, the patient was somnolent and disoriented.
His axillary body temperature was 35.7 °C and his arterial blood pressure 125/89 mm Hg, with a pulse rate of 84 rhythmic beats/min.
He complained of an increasing, diffuse abdominal pain during the whole day, combined with absence of appetite and vomiting on a single occasion.
His daily medication was perindopril 2.5 mg, torasemide 7.5 mg and esomeprazole 40 mg.
On physical examination, we found a tender abdomen with painful epigastric palpation.
Normal bowel sounds were auscultated in the upper right and lower left quadrants.
The renal bed was free of pain on palpation.
On cardiac auscultation, a 2/6 systolic murmur was audible.
Lung auscultation showed normal respiration.
Laboratory findings were slightly elevated C reactive protein (CRP) of 16 mg/l (normal: <5 mg/l), elevated troponin-T-hs of 0.070 µg/l (normal: <0.014 µg/l) and highly elevated pro-B-type natriuretic peptide of 7382 pg/ml (normal: <63 pg/ml).
Kidney function parameters were in the upper normal range, with creatinine of 100 µmol/l and a calculated glomerular filtration rate of 73 ml/min.
Blood count revealed leucocytosis of 15.6×109/litre.
Regarding thyroid function, thyroid-stimulating hormone, f-T3 and f-T4 were in the reference range.
Urine analysis showed no pathology.
In abdominal sonography, all organs were normal, especially the kidneys.
No free fluid was detected (figure 1).
As the severe pain persisted all night, despite analgesia with paracetamol 1 g, metamizole 1 g and pethidine 75 µg, a contrast-enhanced abdominal CT was performed revealing infarction of the right kidney, which appeared as a hypodense area although kidney arteries and veins were assessed as open (figures 2 and ​3).
Cardiac dysfunction is the most frequent cause of death in patients affected by Friedreich's ataxia, most commonly from congestive heart failure or arrhythmia.
Renal artery embolism is not a rare event in these patients.
However, other non-abdominal viscous causes of severe diffuse abdominal pain such as porphyria, familial Mediterranean fever, diabetic ketoacidosis, tocopherol deficiency also had to be excluded.
The negative cardiolipin test excluded tabetic crises.
No evidence for pre-existing porphyria was encountered for example, quantitative determination of δ-aminolevulinic acid, porphobilinogen and porphyrin in 24-h urine was negative.
Further genetic diagnosis regarding, for example, clotting disorder, was also not conclusive.
Hypovitaminosis was not present.
The patient had no endocrinopathies, for example, no diabetes and no evidence for hypothyreosis or hyperthyreosis.
The patient was hospitalised without delay at the department of nephrology.
Immediate anticoagulation with heparin was initiated and later replaced by lifelong oral anticoagulation with phenprocoumon.
During 11 days of hospitalisation, no complications occurred.
Kidney function parameters remained normal.
Transoesophageal echocardiography on the fifth day showed no cardiac thrombus and no patent foramen ovale.
Deep vein thrombosis was excluded with duplex sonography.
Anticardiolipin antibody testing and genetic testing regarding clotting disorders were both negative.
Urine tests revealed no evidence of porphyria.
During hospitalisation the patient remained stable regarding cardiological function, while diuretics were adjusted according to the fluid balance.
The patient had already been treated with levofloxacin for pneumonic infection prior to hospitalisation.
The antibiotic treatment was continued because of increasing inflammatory parameters in the further course of disease.
A CRP increase of up to 200 mg/l was interpreted as an inflammatory response to renal infarction.
By discharge, laboratory parameters were significantly decreased.