Literature DB >> 21275564

Chronic spontaneous diploic hematoma.

José González-Tortosa1, Javier Ros de San Pedro, Guillermo Parrilla, Belen Ferri-Ñiguez, Juan F Martínez-Lage.   

Abstract

The authors report the case of a 23-year-old woman with café-au-lait spots and axillary and inguinal freckling who presented with a diploic chronic spontaneous hematoma of the left parietal bone. To the authors' knowledge, this case represents the first description of a diploic hematoma in a patient with stigmata of neurofibromatosis Type 1 unrelated to head trauma. Plain skull radiography showed an osteolytic lesion with well-circumscribed margins, corresponding to the hematoma, together with exuberant perilesional vascular markings. Angiography demonstrated an incidental aneurysm of the left supraclinoidal internal carotid artery and an unusual cortical venous drainage toward the diploic vessels. The blood flow of these vessels on the right hemicranium was sluggish and exhibited enlarged diploic venous lacunas. The authors hypothesize that the hematoma was formed by both an abnormal venous drainage toward the diploic vascular net, together with a vasculopathy that caused stenosis and obstruction of the normal drainage pathways from these vessels.

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Year:  2011        PMID: 21275564     DOI: 10.3171/2010.12.JNS101589

Source DB:  PubMed          Journal:  J Neurosurg        ISSN: 0022-3085            Impact factor:   5.115


  1 in total

1.  Neurofibromatosis type 1 is not associated with subarachnoid haemorrhage.

Authors:  Arttu Kurtelius; Roope A Kallionpää; Jukka Huttunen; Terhi J Huttunen; Katariina Helin; Timo Koivisto; Juhana Frösen; Mikael von Und Zu Fraunberg; Sirkku Peltonen; Juha Peltonen; Juha E Jääskeläinen; Antti E Lindgren
Journal:  PLoS One       Date:  2017-06-02       Impact factor: 3.240

  1 in total

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