CC BY-NC-ND 4.0 · Indian Journal of Neurosurgery 2022; 11(01): 099-100
DOI: 10.1055/s-0039-3401389
Letter to the Editor

Spontaneous Delayed Hematoma at Operative Site in a Child with Anaplastic Ependymoma: A Rare Case

Sumit Bansal
1   Department of Neurosurgery, All India Institute of Medical Sciences, Bhubaneswar, Orissa, India
,
Ayusman Satapathy
1   Department of Neurosurgery, All India Institute of Medical Sciences, Bhubaneswar, Orissa, India
,
Suvendu Purkait
1   Department of Neurosurgery, All India Institute of Medical Sciences, Bhubaneswar, Orissa, India
,
Rabi Narayan Sahu
1   Department of Neurosurgery, All India Institute of Medical Sciences, Bhubaneswar, Orissa, India
› Author Affiliations
Funding None.
 

Intratumoral hemorrhage is a known phenomenon, especially in high-grade brain tumors.[1] Delayed hematoma formation after tumor excision is rare and rarely reported. Hemorrhage into posterior fossa tumor is reported in preoperative, intraoperative,[2] or postoperative period. Contributing factors may be reverse herniation due to overdraining ventriculoperitoneal shunt, high altitude flight used for travelling before tumor surgery,[3] hemorrhage in residual tumor, neomembrane formation associated with dural substitute used to repair the dural defect after suboccipital craniectomy[4] (fragile vessels associated with nonmembranes have been proposed as the source of hemorrhage), or local trauma to the operative site.

Authors are reporting a rare case in which spontaneous delayed hematoma formation was present after excision of posterior fossa anaplastic ependymoma in a young child.

A 9-year-old boy was brought to our department with features of raised intra cranial pressure (ICP). Noncontrast computed tomography (NCCT) head showed midline posterior fossa tumor with hydrocephalus ([Fig. 1A]). MRI brain was suggestive of fourth ventricular tumor with heterogeneous enhancement ([Fig. 1B-D]). VP shunt followed by near total excision of tumor was done. Tumor was greyish red, moderately vascular, firm, multilobulated, and had both solid and cystic components and firmly adhered to the floor of fourth ventricle, so a thin sheet of tumor was left attached to it. Postoperative NCCT Head was satisfactory ([Fig. 1E]). Later, patient was discharged in satisfactory condition. Histopathology was suggestive of anaplastic ependymoma, MIB-1 labeling index—30 to 35% (WHO Grade III; [Fig. 2]).

Zoom Image
Fig. 1 (A) NCCT head showing solid cystic partially calcified midline posterior fossa tumor with upstream hydrocephalus. MRI brain (contrast) showing contrast-enhancing tumor: axial (B), coronal (C), and sagittal (D) images. Postoperative NCCT head showing good operative cavity with no hematoma (E). (F) On second admission, NCCT head showing operative cavity hematoma. (G) MRI brain (contrast) showing no residual tumor with operative site hematoma. (H) NCCT Head showing resolved posterior fossa hematoma. MRI, magnetic resonance imaging; NCCT, noncontrast computed tomography.
Zoom Image
Fig. 2 (A) Tumor showing predominant pseudorosette arrangement of cells with foci of necrosis (H&E × 100). (B) Tumor cells showing relatively uniform round to oval nuclei with granular chromatin. Frequent mitotic activity is also noted (H&E × 400). (C) Tumor cells showing cytoplasmic dot-like immunopositivity for EMA (× 400). (D) Tumor cells showing high MIB-1 labeling index indicating high proliferative activity (× 400). EMA, epithelial membrane antigen; H&E, hematoxylin and eosin.

About 35 days after tumor surgery, patient came with recurrent vomiting and headache. NCCT Head showed operative site hematoma with intraventricular extension ([Fig. 1F]). MRI brain with contrast showed no residual tumor with resolving hematoma at operative site ([Fig. 1G]). NCCT Head at the time of discharge showed resolved operative site hematoma ([Fig. 1H]). Later, patient discharged and he is under regular follow-up.

In our case, delayed hematoma formation at operative site may be due to neoangiogenesis at the tumor bed because thin sheet of tumor was left behind attached to the floor of fourth ventricle. However, further studies are required to confirm our observation.


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Conflict of Interest

None declared.

  • References

  • 1 Nutt SH, Patchell RA. Intracranial hemorrhage associated with primary and secondary tumors. Neurosurg Clin N Am 1992; 3 (03) 591-599
  • 2 Fukai J, Uematsu Y, Shintani A, Nakai K, Itakura T. Intraoperative hemorrhage in medulloblastoma: a case report and review of the literature. Childs Nerv Syst 2002; 18 (06/07) 356-360
  • 3 Mahdavi A, Baradaran N, Nejat F, El Khashab M, Monajemzadeh M. Sudden deterioration due to intra-tumoral hemorrhage of ependymoma of the fourth ventricle in a child during a flight: a case report. J Med Case Rep 2010; 4: 143
  • 4 Nixon KT, Hudgins PA, Davis PC, O'Brien MS, Hudgins RJ, Hoffman Jr JC. Delayed intracranial hemorrhage in children after suboccipital craniectomy. Am J Roentgenol 1994; 163 (04) 897-900

Address for correspondence

Sumit Bansal, MCh
Department of Neurosurgery, All India Institute of Medical Sciences
Room No. 419, Bhubaneswar, Orissa 751019
India   

Publication History

Article published online:
29 January 2020

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  • References

  • 1 Nutt SH, Patchell RA. Intracranial hemorrhage associated with primary and secondary tumors. Neurosurg Clin N Am 1992; 3 (03) 591-599
  • 2 Fukai J, Uematsu Y, Shintani A, Nakai K, Itakura T. Intraoperative hemorrhage in medulloblastoma: a case report and review of the literature. Childs Nerv Syst 2002; 18 (06/07) 356-360
  • 3 Mahdavi A, Baradaran N, Nejat F, El Khashab M, Monajemzadeh M. Sudden deterioration due to intra-tumoral hemorrhage of ependymoma of the fourth ventricle in a child during a flight: a case report. J Med Case Rep 2010; 4: 143
  • 4 Nixon KT, Hudgins PA, Davis PC, O'Brien MS, Hudgins RJ, Hoffman Jr JC. Delayed intracranial hemorrhage in children after suboccipital craniectomy. Am J Roentgenol 1994; 163 (04) 897-900

Zoom Image
Fig. 1 (A) NCCT head showing solid cystic partially calcified midline posterior fossa tumor with upstream hydrocephalus. MRI brain (contrast) showing contrast-enhancing tumor: axial (B), coronal (C), and sagittal (D) images. Postoperative NCCT head showing good operative cavity with no hematoma (E). (F) On second admission, NCCT head showing operative cavity hematoma. (G) MRI brain (contrast) showing no residual tumor with operative site hematoma. (H) NCCT Head showing resolved posterior fossa hematoma. MRI, magnetic resonance imaging; NCCT, noncontrast computed tomography.
Zoom Image
Fig. 2 (A) Tumor showing predominant pseudorosette arrangement of cells with foci of necrosis (H&E × 100). (B) Tumor cells showing relatively uniform round to oval nuclei with granular chromatin. Frequent mitotic activity is also noted (H&E × 400). (C) Tumor cells showing cytoplasmic dot-like immunopositivity for EMA (× 400). (D) Tumor cells showing high MIB-1 labeling index indicating high proliferative activity (× 400). EMA, epithelial membrane antigen; H&E, hematoxylin and eosin.