Spontant epiduralt hæmatom hos en pædiatrisk patient med seglcellesygdom

Camilla Dall-Jepsen; Anne Zahrtmann Møller; Louise Tram; Theis Chang Grud Gielstrup; Pia Danstrup-Dinesen

doi:10.61409/V11230703

Spontant epiduralt hæmatom hos en pædiatrisk patient med seglcellesygdom

Translated title of the contribution: Spontaneous epidural haematoma in a paediatric patient with sickle cell disease

Camilla Dall-Jepsen^*
, Anne Zahrtmann Møller
, Louise Tram
, Theis Chang Grud Gielstrup
, Pia Danstrup-Dinesen

^*Corresponding author for this work

Research output: Contribution to journal › Journal article › Communication

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Abstract

Spontaneous epidural haematoma (SEDH) is a rare complication of sickle cell disease (SCD). To our knowledge, 38 cases of patients with SEDH associated with SCD have been reported in the literature. In this case report we describe the first Danish paediatric case with SCD and SEDH. The pathophysiology of this association is not fully understood, but skull bone infarction, haemopoietic marrow expansion or compromised blood flow due to hyper viscosity might contribute to this rare complication. In patients with SCD presenting with relevant symptoms, early imaging could be considered.

Translated title of the contribution	Spontaneous epidural haematoma in a paediatric patient with sickle cell disease
Original language	Danish
Article number	V11230703
Journal	Ugeskrift for Læger
Volume	186
Number of pages	3
ISSN	0041-5782
DOIs	https://doi.org/10.61409/V11230703
Publication status	Published - 11 Mar 2024

Bibliographical note

Published under Open Access CC-BY-NC-BD 4.0. https://creativecommons.org/licenses/by-nc-nd/4.0/.

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10.61409/V11230703Licence: CC BY-NC-ND 4.0

Dall-Jepsen et al. (2024). Spontaneous epidural haematoma in a paediatric patient with sickle cell diseaseFinal published version, 175 KBLicence: CC BY-NC-ND 4.0

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title = "Spontant epiduralt h{\ae}matom hos en p{\ae}diatrisk patient med seglcellesygdom",

abstract = "Spontaneous epidural haematoma (SEDH) is a rare complication of sickle cell disease (SCD). To our knowledge, 38 cases of patients with SEDH associated with SCD have been reported in the literature. In this case report we describe the first Danish paediatric case with SCD and SEDH. The pathophysiology of this association is not fully understood, but skull bone infarction, haemopoietic marrow expansion or compromised blood flow due to hyper viscosity might contribute to this rare complication. In patients with SCD presenting with relevant symptoms, early imaging could be considered.",

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note = "Published under Open Access CC-BY-NC-BD 4.0. https://creativecommons.org/licenses/by-nc-nd/4.0/.",

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T1 - Spontant epiduralt hæmatom hos en pædiatrisk patient med seglcellesygdom

AU - Dall-Jepsen, Camilla

AU - Møller, Anne Zahrtmann

AU - Tram, Louise

AU - Gielstrup, Theis Chang Grud

AU - Danstrup-Dinesen, Pia

N1 - Published under Open Access CC-BY-NC-BD 4.0. https://creativecommons.org/licenses/by-nc-nd/4.0/.

PY - 2024/3/11

Y1 - 2024/3/11

N2 - Spontaneous epidural haematoma (SEDH) is a rare complication of sickle cell disease (SCD). To our knowledge, 38 cases of patients with SEDH associated with SCD have been reported in the literature. In this case report we describe the first Danish paediatric case with SCD and SEDH. The pathophysiology of this association is not fully understood, but skull bone infarction, haemopoietic marrow expansion or compromised blood flow due to hyper viscosity might contribute to this rare complication. In patients with SCD presenting with relevant symptoms, early imaging could be considered.

AB - Spontaneous epidural haematoma (SEDH) is a rare complication of sickle cell disease (SCD). To our knowledge, 38 cases of patients with SEDH associated with SCD have been reported in the literature. In this case report we describe the first Danish paediatric case with SCD and SEDH. The pathophysiology of this association is not fully understood, but skull bone infarction, haemopoietic marrow expansion or compromised blood flow due to hyper viscosity might contribute to this rare complication. In patients with SCD presenting with relevant symptoms, early imaging could be considered.

KW - Humans

KW - Child

KW - Hematoma, Epidural, Cranial/complications

KW - Anemia, Sickle Cell/complications

KW - Head

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DO - 10.61409/V11230703

M3 - Tidsskriftartikel

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SN - 0041-5782

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JF - Ugeskrift for Læger

M1 - V11230703

ER -

Spontant epiduralt hæmatom hos en pædiatrisk patient med seglcellesygdom

Abstract

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