Vertebral haemangioma (VH) being called benign tumour is a vascular malformation, usually asymptomatic, but can on rare occasions cause pain and bone fractures [1] . The extraosseous soft-tissue component can extend into the epidural space causing compression of the spinal cord and nerve roots. Because of the rarity of aggressive VH, diagnosis and treatment protocols for these cases remain controversial and problematic [2] . In this study, we report a 59-year-old woman case of T12 aggressive and symptomatic type IV VH with neurologic deficit, treated successfully until 6 months by Ethanol embolization, posterior decompression and fixation followed by postoperative radiotherapy. The evolution was in particular marked by the disappearance of pain.

The case is a 59-year-old woman without past medical history. She was presented with mechanical back pain after falling from standing height. Physical examination revealed weight at 61 kg, height at 157 cm. Loss of lumbar lordosis, thoracolumbar pain pressure, contractures of the paravertebral muscles, back pain caused by the mobilization of the spine. Low patellar reflexes, and muscle testing was at 4/5 for relievers.

Plain radiographs of the thoracolumbar spine showed L1 and L2 benign vertebral fractures with grid appear- ance at T12 vertebra (Figure 1). MRI revealed T12 intensity signal on T1 and T2 with ductal extension, com- patible with aggressive vertebral angioma (Figure 2 and Figure 3).

At blood analysis, speed sedimentation was at 14 mm/1hour, CRP at 2.7 mg/l, normal electrophorese of pro- tein, alcaline phosphate at 70 IU/l, calcium and pshosphorus at 2.23 mmol/l and 1.19 mmol/l respectively. Vita- min D at 8.90 ug/l then 31 ng/ml, after correction. At osteodensitometry, we found −2.6 T-Score at lumbar spine, −2.3 at femoral neack and −1.8 in total femoral head. T-score was −3.5 at forearm. Parathormon value was at 45 pg.

Patient was treated successfully for 6 months by ethanol embolization, with posterior decompression (lamin- ectomy and fixation), followed by radiotherapy sessions. After the 6 months of treatment, Thoraco-Lumbar MRI didn’t found canal extension signal (Figure 4). Pain, neurological also disappeared and the clinical examination did not objectified signs for neurological deficit.

Virchow first described VH in 1867, and Perman presented its first radiological description in 1926. Despite their common and usually benign occurrence, 11% of spines lesions at autopsy, vertebral hemangiomas can occasionally behave as aggressive tumours [3] .

The diagnosis is usually made at middle and late middle age, frequently in the thoracic spine, followed by the lumbar spine. HVs are devided into four histologically categories: capillary, cavernous, arteriovenous or venour. Symptomatic VHs account for 0.9% - 1.2% of cases, presenting with pain and neurologic compromise due to vertebral fracture and compression of nerve root or dual sac [4] . The tumour growth can produce compression, acute hemorrhage into the epidural space or spine cord ischemia because of hemodynamic effects [5] .

Radiologically, they are characterised by the vertical striation and/or palisade pattern in the vertebral bodies. In addition, CT can demonstrate sparse vertebral trabeculae separated by fatty stroma. MRI examinations show high signals on both T1 and T2 images. The prognosis of VH lesions remains unclear. The presence of low signals on T1 weighted MRI and high signals on T2 images, the presence of soft tissue stroma between the osseous trabeculae on CT images, the presence of epidural tissue and evidence of cortical erosion are all radiological features of aggressiveness [6] . In our case, symptomatic lesion showed sign of aggressiveness on MRI examination.

There are three categories and seven types of VHs, according to Tomita’s surgical classification of spinal tumours [7] : in the first category, the hemangioma is limited to vertebral body (type I), with pedicule extension (type II), body-lamina extension (type III). In the second category, VH is extra-compartmental: spinal canal extension (type IV), paravertebral (type V), and adjacent vertebral extension (type VI). In the third category, the VHs are multiple.

The differential diagnosis includes infectious etiologies, metastatic lesions, primary malignancies of bone and soft tissue, abscess or osteomylitis [8] . However, the characteristics of radiographs findings and their chronicity significantly lowered the likehood of them.

Based on the patient’s symptoms and lesions, VH can be classified into four categories [9] , which treatment should be entirely depending:

I: Asymptomatic patients with no signs of aggressiveness; II: Symptomatic patients with no signs of aggressiveness; III: Asymptomatic patients with signs of aggressiveness; IV: Symptomatic patients with signs of aggressiveness.

Lei Dang and al. [10] suggested protocol for the diagnosis and management of aggressive vertebral heman- gioma with neurological deficit, based on the literature and their previous experience.

The observation is needed for type I. For type II, the radiotherapy is effective with rare complications at 30 - 40 Gy over 3 - 4 week period, and vertebroplasty can cure VH by obstructing the vessels of tumour. Type III of VH can need observation, but spinal radiosurgery is a reasonable choice. Reported treatment protocol for type IV is more diversiform. It includes radiotherapy, vertebroplasty, direct alcohol injection, embolization arteries, surgery, and a combination of these modalities. Successful results have been reported for each of these modalities. Our patient presented satisfied results after combined embolization, surgery and radiotherapy.

Although vertebral hemangiomas are asymptomatic benign lesions with good outlook, there are symptomatic and aggressive cases with rapid onset of neuroligical deficits. The clinicians have to be aware of this condition as a differential and the place of MRI in order to expedite diagnosis. The symptomatic based treatment algorithm is well described. Clinicians and surgeons can coordinate to better elucidate the optimal management of these relatively rare lesions.

The authors declare that they have no conflicts of interest concerning this article.

KawtarNassar,WafaeRachidi,SaadiaJanani,OuafaMkinsi, (2015) Type IV Aggressive and Symptomatic Vertebral Hemangioma. Open Journal of Rheumatology and Autoimmune Diseases,05,87-91. doi: 10.4236/ojra.2015.53014