Abstract
BACKGROUNDFactor XI deficiency, also known as hemophilia C, is a rare inherited bleeding disorder that may leave routine coagulation parameters within normal range. Depending on the mutation subtype, prolonged activated partial thromboplastin time may occasionally be found. The disease has an autosomal transmission, with an estimated prevalence in the general population of approximately 1 in 1 million. Heterozygosis accounts for partial deficits, but the tendency to bleed is unrelated to the measured activity of factor XI. Diagnosis usually follows unexpected hemorrhages occurring spontaneously or after trauma or surgical procedures.OBSERVATIONSFew cases have been reported in the neurosurgical literature, all occurring spontaneously or after head trauma. Owing to its subtle features, the true incidence of the disease is probably underestimated. The authors report a case of a patient with previously undiagnosed factor XI deficiency who underwent uncomplicated resection of a fourth-ventricle papilloma and experienced delayed, severe hemorrhagic complications.LESSONSThe known association between choroid plexus tumors and intracranial bleeding raised differential diagnosis issues. This report may serve to help to investigate delayed hemorrhages after cranial surgery.
Highlights
Factor XI deficiency, known as hemophilia C, is a rare inherited bleeding disorder that may leave routine coagulation parameters within normal range
We report a case of undiagnosed Factor XI (FXI) deficiency that manifested with delayed, severe hemorrhages after uncomplicated resection of a fourth-ventricle tumor
Observations To our knowledge, this is the first description of a post-craniotomy hemorrhage related to FXI deficiency
Summary
Factor XI deficiency, known as hemophilia C, is a rare inherited bleeding disorder that may leave routine coagulation parameters within normal range. Factor XI (FXI) deficiency, known as Rosenthal syndrome or hemophilia C, is a rare, inherited bleeding disorder with a prevalence in the general population of approximately 1 in 1 million.[1] Higher frequency has been found in some populations, such as Ashkenazi Jews and Iraqi Jews, who have a heterozygosis rate of 9%.2. The suspicion is usually raised by unexpected bleeding occurring spontaneously or after trauma or surgical procedures.[1] Few cases have been reported in the neurosurgical literature, all related to spontaneous hemorrhages and only sporadically to trauma.[6,7,8,9,10,11,12,13,14] An association between FXI deficiency and intracranial hemorrhages after craniotomy procedures has not been documented so far. We report a case of undiagnosed FXI deficiency that manifested with delayed, severe hemorrhages after uncomplicated resection of a fourth-ventricle tumor
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