The interdural hematoma: A subtype of convexity subdural/dural hematoma with specific radioanatomical characteristics

Author:

Kiss-Bodolay Daniel1,Papadimitriou Kyriakos2,Hedjoudje Abderrahmane3,Duc Christophe4,Vargas Maria Isabel5,Kiss Jozsef Zoltan6,Schaller Karl1,Fournier Jean-Yves2

Affiliation:

1. Department of Neurosurgery, University Hospital of Geneva, Geneva, Switzerland

2. Department of Neurosurgery, Sion Hospital, Sion, Switzerland

3. Department of Radiology, Sion Hospital, Sion, Switzerland

4. Department of Pathology, Sion Hospital, Sion, Switzerland

5. Department of Neuroradiology, University Hospital of Geneva, Geneva University Hospital, Geneva, Switzerland

6. Department of Fundamental Neurosciences, Faculty of Medicine, University of Geneva, Geneva, Switzerland.

Abstract

Background: Rare cases of biconvex hematomas splitting the convexity dura mater were reported and denominated interdural hematoma (IDH). Due to their rarity, little is known about their radiological characteristics, and in most cases, their invasive management with craniotomy and dural membrane excision is unnecessary. Case Description: We report here a case of single burr-hole endoscopic evacuation of an IDH and its complete resolution after the 6-month follow-up imaging. The literature review reveals 11 reported cases of IDH. Most of them are male and the mean age is 65 years (range 51–90). Most of the reported IDHs were misdiagnosed as epidural hematoma or meningioma, and therefore, they have been managed invasively through craniotomy with dural excision. Diagnosis of the interdural nature was confirmed macroscopically during surgery in all cases and histology was reported for 6 cases. Image analysis found a double dural beak sign and biconvex shape on coronal planes, subarachnoid space enlargement at the collection extremities, and irregular thick inner wall as common radiological aspects of the IDH. Conclusion: IDH is a rarely reported and often misdiagnosed dural hematoma subtype. Its invasive treatment through craniotomy is likely related to its unknown radiological characteristics. We review and raise awareness about potentially unique radiological anatomy that could avoid unnecessary invasive treatment. Moreover, we report the first case of endoscopically evacuated IDH with long-term follow-up imaging showing complete resolution.

Publisher

Scientific Scholar

Subject

Neurology (clinical),Surgery

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