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Chir Main ; 30(2): 127-9, 2011 Apr.
Article in French | MEDLINE | ID: mdl-21334949

ABSTRACT

Primary vascular tumours of bone are rare. Haemangiomas occur as incidental findings in the skull or in the spine. A solitary haemangioma of the hand skeleton is rare and difficult in radiological and histological differential diagnosis. We report a case of a 23 year-old patient presenting with a capillary hemangioma of the left second finger of few months duration for which he underwent amputation. Postoperative evolution was good and showed no recurrence. We discuss this through observation and a review of the literature including the different clinical, radiological and pathological diagnostic problems associated with an unusual site for vascular proliferation.


Subject(s)
Bone Neoplasms/surgery , Fingers/pathology , Fingers/surgery , Hemangioma, Capillary/surgery , Adult , Bone Neoplasms/diagnosis , Diagnosis, Differential , Fingers/diagnostic imaging , Hemangioma, Capillary/diagnosis , Humans , Male , Radiography , Rare Diseases , Treatment Outcome
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