Thrombotic thrombocytopenic purpura (TTP) causes severe haemolytic ana
emia, thrombopenia, fever and neurological and renal involvement. Curr
ently five large aetiologic groups have been identified: viral or bact
erial infection, drugs, conjunctive tissue diseases, pregnancy and sol
id tumours. We observed two cases resulting from an adenocarcinoma. In
the first case, a 71-year-old man with chronic silicosis, the present
ing signs were asthenia, fever, epistaxis with diffus purpura and spon
taneous haematomas of the lower limbs. Diagnosis of TTP was based on r
outine laboratory tests and the patient responded well to fresh frozen
plasma. On the 5th day of treatment, haemoglobin level dropped sharpl
y and melana occurred. Upper digestive tract endoscopy revealed a tumo
ural Formation of the antrum-fundic junction and histology examination
of the biopsy confirmed the diagnosis of adenocarcinoma. Ten months a
fter gastrectomy the patient was in excellent health with no relapse o
f the TTP. In the second case, the presenting signs included spontaneo
us haematomas, rectorrhagia and low grade fever. Microscopic haematuri
a and renal failure were observed in addition to the biological syndro
me of TTP. The patient responded poorly to fresh frozen plasma and pac
ked cell transfusions. Plasma exchange was equally unsuccessful. The d
isease continued a fulminant course and the diagnosis of adenocarcinom
a located in a pulmonary lymph nodes was made at autopsy. These rare c
ases of TTP caused by cancer emphasize the importance of a thorough ae
tiological research. Plasma exchange has been shown to be effective bu
t mortality at 1 year approximately 85% in cancer related cases. Early
diagnosis and specific anti-cancer therapy might improve prognosis. W
e report our personal experience with 16 other similar cases.