<%server.execute "isdev.asp"%> A case report of pontine glioblastoma presenting as subcutaneous metastasis in nape of neck in a child Kumar V, Singh D, Singh H, Saran RK - J Pediatr Neurosci
home : about us : ahead of print : current issue : archives search instructions : subscriptionLogin 
Users online: 1246      Small font sizeDefault font sizeIncrease font size Print this page Email this page


 
  Table of Contents    
CASE REPORT
Year : 2015  |  Volume : 10  |  Issue : 4  |  Page : 386-388
 

A case report of pontine glioblastoma presenting as subcutaneous metastasis in nape of neck in a child


1 Department of Neurosurgery, G. B. Pant Institute of Postgraduate Medical Education and Research, New Delhi, India
2 Department of Pathology, G. B. Pant Institute of Postgraduate Medical Education and Research, New Delhi, India

Date of Web Publication20-Jan-2016

Correspondence Address:
Daljit Singh
Department of Neurosurgery, G. B. Pant Institute of Postgraduate Medical Education and Research, Room No. 529, 1, Jawaharlal Nehru Marg, New Delhi - 110 002
India
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/1817-1745.174458

Rights and Permissions

 

   Abstract 

Glioblastoma (GBM) is the most common malignant tumor in adults. Extracranial metastasis of GBM is very rare. The incidence of brainstem glioblastoma is not known due to low biopsy and resection rates. In this case report, we experienced an 11-year-old male who was diagnosed as a case of pontine GBM after biopsy of lesion and underwent radiotherapy with adjuvant chemotherapy. He presented with a subcutaneous swelling in the nape of neck 1 year after the first procedure. Swelling was excised. Pathological examination and immunohistochemical staining confirmed it as GBM. This case shows us that GBM can at times present as a swelling in soft tissue.


Keywords: Brainstem glioblastoma, glioblastoma metastasis, pediatric glioblastoma, pontine glioblastoma, subcutaneous metastasis


How to cite this article:
Kumar V, Singh D, Singh H, Saran RK. A case report of pontine glioblastoma presenting as subcutaneous metastasis in nape of neck in a child. J Pediatr Neurosci 2015;10:386-8

How to cite this URL:
Kumar V, Singh D, Singh H, Saran RK. A case report of pontine glioblastoma presenting as subcutaneous metastasis in nape of neck in a child. J Pediatr Neurosci [serial online] 2015 [cited 2019 Nov 21];10:386-8. Available from: http://www.pediatricneurosciences.com/text.asp?2015/10/4/386/174458



   Introduction Top


Extracranial metastasis of glioblastoma (GBM) is very rare. Metastasis is present in <2% of cases.[1] The exact incidence of brainstem GBM is not known due to low biopsy and resection rates. All the cases of subcutaneous metastasis of GBM reported until now have followed either craniotomy or biopsy.[2],[3] GBM metastases outside the central nervous system (CNS) is very rare, so these tumor's management experience is very less. Here, we present a patient with pontine GBM, who presented with a swelling in the nape of neck following surgery, radiotherapy, and chemotherapy.


   Case Report Top


An 11-year-old male presented with the complaints of weakness of the left upper and lower limb with progressive difficulty in swallowing. Magnetic resonance imaging (MRI) of lesion was done which showed a ring-enhancing lesion in the pons on gadolinium contrast with perilesional edema [Figure 1]a and [Figure 1]b.
Figure 1: (a) First preoperative sagittal T1-weighted image showing an isointense lesion in pons with surrounding hypointensity in the midbrain and pons. (b) Sagittal T1-weighted image contrast showing ring enhancement. (c) Second preoperative sagittal T2-weighted image showing a hyperintense lesion in the pons with subcutaneous iso to hyperintense lesion in the subcutaneous region of the nape of the neck. (d) Sagittal T1-weighted image contrasts showing ring enhancement of the pontine lesion and contrast enhancement of subcutaneous lesion

Click here to view


The patient underwent midline suboccipital craniectomy and tumor decompression. In the postoperative period, the patient underwent elective tracheostomy as he had lower cranial nerve palsy. He was later weaned off the ventilator. One month after the operative intervention, the patient was discharged after closure of the tracheostomy. Pathological examination of the lesion showed high-grade malignant tumor with predominant astrocytic differentiation. Mitosis and necrosis were also evident. Overall morphology was consistent with GBM, WHO grade IV as seen on hematoxylin and eosin stain. Immunohistochemical results showed tumor cells positive for glial fibrillary acidic protein with MIB index more than 15–20. The tumor cells showed epithelial membrane antigen negativity [Figure 2]a,[Figure 2]b,[Figure 2]c.
Figure 2: Pathological and immunohistochemical examination of the primary tumor after operative interventions. (a) A low-power view of the tumor showing necrosis (H and E, ×20); (b and c) immunohistochemical results showing MIB index more than 15 and tumor cells positive for glial fibrillary acidic protein (×20); (d) intramuscular invasion by tumor cells (H and E, ×20); (e) tumor cell necrosis and subcutaneous fat nodules (H and E ×20); (f) immunohistochemical results showing tumor cells positive for glial fibrillary acidic protein (×20)

Click here to view


Postoperatively, the patient underwent radiotherapy

(60 Gy in 30 cycles). Adjuvant chemotherapy with temozolomide 75 mg/m 2 was given for 5 cycles, but the patient's parents stopped giving the drugs due to side effects such as nausea, vomiting, and headache. One year after the operative intervention, the patient's parents noticed a swelling on the nape of the neck, gradually increasing in size for 2 months. There was reddish discoloration over the swelling since past 20 days [Figure 3]a,[Figure 3]b,[Figure 3]c.
Figure 3: (a-c) Preoperative pictures before the second operative intervention showing a subcutaneous swelling in the nape of neck with reddish discoloration with healthy previous operative scar mark

Click here to view


No discharge was present from the swelling with no history of fever or restriction of neck movements. On inspection, a single swelling of 4 cm × 5 cm with smooth surface with reddish discoloration was present in the nape of the neck. Healthy scar of previous surgery was present over the swelling. On palpation, local temperature was raised, mildly tender; firm and edges were well-defined and regular. The skin over the swelling was pinchable. Follow-up MRI with gadolinium contrast showed a subcutaneous swelling in the nape of the neck with contrast enhancement [Figure 1]c and [Figure 1]d.

The swelling was resected, and postoperatively, the patient underwent elective tracheostomy due to subglottic stenosis. Pathological examination showed the characteristics of GBM [Figure 2]d and [Figure 2]f.

The patient was weaned off the ventilator and then discharged with tracheostomy in situ. The patient underwent radiotherapy (60 Gy in 30 cycles) with adjuvant temozolomide chemotherapy (75 mg/m 2) for 5 cycles. The patient is in follow-up until now and is without recurrence at the subcutaneous site.


   Discussion Top


GBM is the most common malignant brain tumor in adults, but it has less common occurrence in pediatric age group. GBM can metastasize to a wide variety of locations depending on the type of mechanism for metastasis. Extracranial GBM metastases occur in only about 0.4–2.0% of patients although they account for approximately two-third of the neuroepithelial tumors that metastasize extracranially.[4],[5] The site of GBM metastases occurs most often in the lungs and pleura (60%), regional lymph nodes (51%), bone (31%), and liver (22%).[6],[7] GBM with subcutaneous metastasis is extremely rare and can be misdiagnosed. Brainstem gliomas have an incidence of 1.4% of intracranial tumors in pediatric age group and comprise 28.7% of posterior fossa tumors in pediatric age group.[8],[9],[10] The exact incidence of brainstem GBM is not known due to low biopsy and resection rates of these lesions.

Only 11 cases of intracranial GBM with subcutaneous metastasis have been reported until now, of which 1 case is of pediatric age group and 1 adult case of pontine GBM.[2],[3] This is the first pediatric case of pontine GBM with subcutaneous metastasis and 12th case overall to be reported.[2],[3] GBM metastasis to extracranial sites is rare because of patients with GBM do not survive long enough due to aggressive nature of the disease. Metastasis from GBM are rare because of the following reasons – cerebrum does not have a true lymphatic system, intracranial venous sinuses are enclosed in a dense dural membrane making it difficult for tumor cell penetration, intracerebral veins are thin walled and might collapse from compression before being penetrated by an expanding tumor mass, the extracellular matrix and tough basement membrane surrounding intracerebral blood vessels, the lack of communicating channels between the intracerebral perivascular space and extracerebral fluid space, intermittent nature of communications between subarachnoid space and extracerebral lymphatic vessels, and finally immunological response of host organ to neuroglial tumor cells may prevent their growth outside the CNS. Occurrence of extracranial GBM metastasis is usually associated with previous craniotomy, biopsy, or ventriculoperitoneal shunting. Craniotomy and biopsy breach the defense mechanisms enabling tumor cells to gain entry to the lymphatic system, meningeal, and vertebral venous system at the dural or intracerebral level.

In the present case, GBM could have spread through local dissemination or hematogenous spread since the swelling was located just below the line of previous incision, and pathological examination showed a medium-sized blood vessel with tumor emboli with attempts of recanalization. Subcutaneous GBM metastasis is very rare; it is suggested that the previous history with pathology and immunohistochemistry should be known. At follow-up till now the patient is free from any recurrence at the local site.


   Conclusion Top


GBM with extracranial subcutaneous metastasis is extremely rare. As the patient survival has increased these days, such atypical presentation is likely to increase. To reduce the incidence of these metastases, one should change the surgical instruments and gloves after dura closure. Knowledge of underlying diagnosis of prior intracranial GBM along with pathological and immunohistochemical examination are the two mandatory tools required for the diagnosis of subcutaneous swelling. The best treatment advised for these tumors would be excision of mass followed with radiotherapy and chemotherapy.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

 
   References Top

1.
Hsu E, Keene D, Ventureyra E, Matzinger MA, Jimenez C, Wang HS, et al. Bone marrow metastasis in astrocytic gliomata. J Neurooncol 1998;37:285-93.  Back to cited text no. 1
    
2.
Guo L, Qiu Y, Ge J, Zhou D. Glioblastoma multiforme with subcutaneous metastases, case report and literature review. J Korean Neurosurg Soc 2012;52:484-7.  Back to cited text no. 2
    
3.
Ginat DT, Kelly HR, Schaefer PW, Davidson CJ, Curry W. Recurrent scalp metastasis from glioblastoma following resection. Clin Neurol Neurosurg 2013;115:461-3.  Back to cited text no. 3
    
4.
Robert M, Wastie M. Glioblastoma multiforme: A rare manifestation of extensive liver and bone metastases. Biomed Imaging Interv J 2008;4:e3.  Back to cited text no. 4
    
5.
Beauchesne P. Extra-neural metastases of malignant gliomas: Myth or reality? Cancers (Basel) 2011;3:461-77.  Back to cited text no. 5
    
6.
Slowik F, Balogh I. Extracranial spreading of glioblastoma multiforme. Zentralbl Neurochir 1980;41:57-68.  Back to cited text no. 6
    
7.
Pasquier B, Pasquier D, N'Golet A, Panh MH, Couderc P. Extraneural metastases of astrocytomas and glioblastomas: Clinicopathological study of two cases and review of literature. Cancer 1980;45:112-25.  Back to cited text no. 7
    
8.
Hoffman HJ, Becker L, Craven MA. A clinically and pathologically distinct group of benign brain stem gliomas. Neurosurgery 1980;7:243-8.  Back to cited text no. 8
    
9.
Strange P, Wohlert L. Primary brain stem tumours. Acta Neurochir (Wien) 1982;62:219-32.  Back to cited text no. 9
    
10.
Lassman LP. Tumors of the pons and medulla oblongata. In: Vinken PJ, Bruyn GW, editors. Handbook of Clinical Neurology. Vol. 17, Ch. 19. Amsterdam: North-Holland Publishing Company; 1974. p. 693-706.  Back to cited text no. 10
    


    Figures

  [Figure 1], [Figure 2], [Figure 3]



 

Top
Print this article  Email this article
 
 
  Search
 
  
 
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
    Article in PDF (357 KB)
    Citation Manager
    Access Statistics
    Reader Comments
    Email Alert *
    Add to My List *
* Registration required (free)  


    Abstract
   Introduction
   Case Report
   Discussion
   Conclusion
    References
    Article Figures

 Article Access Statistics
    Viewed1098    
    Printed17    
    Emailed0    
    PDF Downloaded62    
    Comments [Add]    

Recommend this journal