|Year : 2016 | Volume
| Issue : 4 | Page : 364-366
Idiopathic bilateral chronic subdural hematoma with left internal carotid artery infarct in a 3 months infant: A rare case report
Mahesh Kumar, Krishan Yadav, Saurabh Kumar Verma, Vikas Maheshwari
Department of Neurosurgery, Command Hospital (SC), Wanwadi, Pune, Maharashtra, India
|Date of Web Publication||3-Feb-2017|
Department of Neurosurgery, Command Hospital (SC) and AFMC, Ward No. 16, Wanwadi, Pune - 411 040, Maharashtra
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Spontaneous chronic subdural hematoma (CSH) in infants is extremely rare. A very limited number of cases are known and reported in literature. The clinical presentation can be myriad varying from asymptomatic cases to gross neurological deficits. We report a case of a 3-month-old child who presented to us with repeated episodes of focal seizures of the left upper and lower limb of 1 month duration. Subsequent imaging revealed bilateral CSH (right > left) with left internal carotid artery infarct and midline shift to left by 8 mm. The child improved following burr hole evacuation of the right-sided CSH. The management of such case and a brief review of literature are discussed.
Keywords: Burr hole, chronic subdural hematoma, focal seizures
|How to cite this article:|
Kumar M, Yadav K, Verma SK, Maheshwari V. Idiopathic bilateral chronic subdural hematoma with left internal carotid artery infarct in a 3 months infant: A rare case report. J Pediatr Neurosci 2016;11:364-6
|How to cite this URL:|
Kumar M, Yadav K, Verma SK, Maheshwari V. Idiopathic bilateral chronic subdural hematoma with left internal carotid artery infarct in a 3 months infant: A rare case report. J Pediatr Neurosci [serial online] 2016 [cited 2021 Aug 4];11:364-6. Available from: https://www.pediatricneurosciences.com/text.asp?2016/11/4/364/199466
| Introduction|| |
Chronic subdural hematoma (CSH) in neonates and infants is very rare. Limited cases have been reported in literature. Commonly associated factors include trauma during pregnancy, maternal coagulopathy, intrauterine infections, use of anticoagulants, metabolic disorders, etc.
However, spontaneous CSH without known etiology is extremely rare. Unrecognized in-utero trauma and a complex interaction of intracranial and intrauterine pressures seem to be a convincing explanation for such cases. Subtle degree of birth asphyxia could also be a possible etiological factor. We present a rare case of CSH in which etiology remained unknown.
| Case Report|| |
A 3-month-old female infant firstborn of nonconsanguineous marriage presented with recurrent episodes of focal seizures of the left upper and left lower limb. She was put on tablet phenobarbitone (according to her body weight) by a pediatrician, but the seizures remained uncontrolled.
The antenatal history was insignificant, and there was no history suggestive of birth trauma. However, the child did not cry immediately following birth.
There was no evidence of neonatal sepsis, however social, motor, and language developmental milestones of the child were delayed.
Physical examination revealed head circumference 40 cm and anterior fontanelle open and not tense. There was no apparent cranial nerve paresis. On gross examination, the power and bulk of all limbs were normal.
Preliminary investigations revealed a low hemoglobin concentration (11 g/dl), normal complete blood count picture, normal platelet counts, normal prothrombin time, and a normal partial thromboplastin time.
Magnetic resonance imaging (MRI) brain showed bilateral CSH (right > left) with mass effect to left of 8 mm and left fronto tempero parietal area of encephalomalacia suggestive of the left internal carotid artery (ICA) territory chronic infarct [Figure 1].
|Figure 1: Preoperative magnetic resonance imaging - chronic subdural hematoma in bilateral frontoparietal region with mass eff ect toward left and underlying cortical infarct in the left frontotemporoparietal area|
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Sodium valproate was added to the previous treatment to control the seizures. Bleeding and clotting parameters were repeated.
As mass effect was towards the right with focal seizures of left upper and lower limb, a decision taken to evacuate right-sided subdural haematoma.
The child was taken up for surgery under general anesthesia.
Right sided frontal and parietal burr holes were done and 80cc altered colored blood drained out.
Postoperatively, the child recovered well; subsequently, seizures were controlled on the single antiepileptic drug.
Follow-up MRI after 6 months [Figure 2] showed complete resolution of CSH with encephalomalacia changes in the left ICA territory.
|Figure 2: Postoperative magnetic resonance imaging after 6 months with complete resolution of chronic subdural hematoma with underlying left cortical infarct|
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| Discussion|| |
Spontaneous CSH without known etiology is an extremely rare presentation in infants.
There are only five case reports in the literature which have described this entity in newborn babies.,,,,
The diagnosis is established only after excluding known causes of CSH in infants, most common being birth trauma, hemorrhagic diathesis, and metabolic disorders.,
Various possible etiological factors can be hypothesized for the development of such entity in infants.
Unrecognized in-utero trauma and a complex interaction of intracranial and intrauterine pressures seem to be the most convincing explanation for such cases.,,,
Evidence of these factors coming into play is further stressed by associated cortical infarcts and atrophy in our case.
Although cerebral infarction has been reported in neonates with traumatic acute subdural hematoma, its association with infantile CSH has not been described.
Occlusion of major vessels does occur in head injury leading to cortical infarction.
The occlusion may follow rupture of the vessel, deranged microcirculation, or arterial dissection.
Cerebral atrophy of the ipsilateral hemisphere after acute subdural hematoma (SDH) has been reported in infants.
Other factors associated with the development of idiopathic CSH in infants include sudden resolution of infantile hydrocephalus in cases with intermittent aqueductal stenosis and hydrocephalus, maternal use of anticoagulants, parental history of coagulopathy, cryptic vascular malformations, subtle bleeding diathesis, asymptomatic intrauterine infections, premature closure of fetal foramen ovale causing cardiac and hepatic decompensation with increase in central venous pressure, and secondary coagulopathy  and associated arachnoid and neuroepithelial cysts.,
Our case is unique in the sense that no exact etiological factors proved, unrecognized in-utero trauma and a complex interaction of intracranial and intrauterine pressures seem to be the most convincing explanation in our case.
The clinical presentation of infantile CSH varies from asymptomatic cases to infants with gross neurological deficits. The presentation could be subtle manifesting as only anemia to the extent of seizures.
Infantile CSHs are often managed successfully with simple burr hole evacuation and drainage. Other surgical options include craniotomy with excision of membrane and subdural peritoneal shunt in recurrent cases.
| Conclusion|| |
CSH in infants is most commonly due to nonaccidental trauma, while acute SDH in neonates is most commonly due to birth-related trauma.
In contrast, idiopathic CSH in neonates is a rare entity. Unrecognized in-utero trauma seems to be the most common causative factor in such cases.
Review of literature suggests that etiology in these cases is multifactorial, although the final common pathway is tearing of veins and accumulation of blood in subdural space. These infants must be thoroughly investigated to rule out known causative factors.
Prognosis is generally fair in these cases, provided early management is ensured.
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Conflicts of interest
There are no conflicts of interest.
| References|| |
Atluru VL, Kumar IR. Intrauterine chronic subdural hematoma with postoperative tension pneumocephalus. Pediatr Neurol 1987;3:306-9.
Breningstall GN, Patterson RJ. Intrauterine subdural hematoma. Pediatr Radiol 2000;30:630-1.
Diaz A, Taha S, Vinikoff L, Andriamamonjy C, Leriche B, Bintner M. Chronic subdural hematoma in utero
. Case report with literature review. Neurochirurgie 1998;44:124-6.
Gunn TR, Mok PM, Becroft DM. Subdural hemorrhage in utero
. Pediatrics 1985;76:605-10.
Hadzikaric N, Al-Habib H, Al-Ahmad I. Idiopathic chronic subdural hematoma in the newborn. Childs Nerv Syst 2006;22:740-2.
Kumar R, Mahapatra AK. Head injury in children. In: Mahapatra AK, Kamal R, editors. Head Injury. 3rd
ed. New Delhi: Modern Publisher; 2005. p. 253-70.
Miura T, Tanaka H, Yoshinari M, Tokunaga A, Koto S, Saito K, et al.
A case of scurvy with subdural hematoma. Rinsho Ketsueki 1982;23:1235-40.
Franklin J, Belkin R, Howieson J, Gallo A. Posterior fossa chronic subdural hematoma in the neonate. AJNR Am J Neuroradiol 1986;7:1099-100.
Tomita H, Ito U, Tone O, Masaoka H, Tominaga B. Atrophy and maldevelopment of the ipsilateral cerebral hemisphere after acute subdural hematoma in infants. Surg Neurol 1994;42:498-504.
Robinson MJ, Cameron MD, Smith MF, Ayers AB. Fetal subdural haemorrhages presenting as hydrocephalus. Br Med J 1980;281:35.
Cheung PY, Obaid L, Rajani H. Spontaneous subdural haemorrhage in newborn babies. Lancet 2004;363:2001-2.
Hanigan WC, Ali MB, Cusack TJ, Miller TC, Shah JJ. Diagnosis of subdural hemorrhage in utero
. Case report. J Neurosurg 1985;63:977-9.
Parsch CS, Krauss J, Hofmann E, Meixensberger J, Roosen K. Arachnoid cysts associated with subdural hematomas and hygromas: Analysis of 16 cases, long-term follow-up, and review of the literature. Neurosurgery 1997;40:483-90.
Matsuyama T, Aoyama N, Sakaki T. A rare case of middle fossa neuroepithelial cyst accompanied by chronic subdural hematoma. No Shinkei Geka 1993;21:931-3.
Misra M, Salazar JL, Bloom DM. Subdural-peritoneal shunt: Treatment for bilateral chronic subdural hematoma. Surg Neurol 1996;46:378-83.
[Figure 1], [Figure 2]