A. Shwaiki et al., Acquired inhibitor to factor VIII in small cell lung cancer: a case reportand review of the literature, ANN HEMATOL, 80(2), 2001, pp. 124-126
Acquired hemophilia (antibodies or inhibitors to factor VIII) is the most c
ommon acquired disease affecting clotting factors. It has been described in
association with autoimmune disease, malignancy, dermatologic disorders, i
n the postpartum period, and with drug interactions. Factor VIII inhibitors
have been previously described with lung cancer, three with squamous cell
and one with adenocarcinoma. A 54-year-old woman presented with weight loss
and shoulder pain. A chest X-ray revealed a right hilar mass, confirmed by
computed tomography (CT) scan and biopsy revealed small cell lung cancer.
Coagulation panel prior to bronchoscopy showed an increased partial thrombo
plastin time (aPTT). The presence of factor VIII inhibitor was demonstrated
at 5 Bethesda units. The patient was treated with fresh frozen plasma twic
e for hemorrhagic episodes, and six cycles of chemotherapy were begun with
carboplatin and etoposide 16. Eight months after the diagnosis, her aPTT wa
s normal and the factor VIII inhibitor titer was undetectable. This is the
first case report of small cell lung cancer and acquired hemophilia. A caus
al relationship between the malignancy and the presence of factor VIII inhi
bitors is suggested by the response to therapy.