Severe progressive scoliosis due to huge subcutaneous cavernous hemangioma: A case report
- Yoji Ogura†1,
- Kota Watanabe†2,
- Naobumi Hosogane1,
- Takashi Tsuji1,
- Ken Ishii1,
- Masaya Nakamura1,
- Yoshiaki Toyama†1,
- Kazuhiro Chiba†1 and
- Morio Matsumoto†1Email author
© Ogura et al; licensee BioMed Central Ltd. 2011
Received: 22 December 2010
Accepted: 17 March 2011
Published: 17 March 2011
Cavernous hemangioma consists mainly of congenital vascular malformations present before birth and gradually increasing in size with skeletal growth. A small number of patients with cavernous hemangioma develop scoliosis, and surgical treatment for the scoliosis in such cases has not been reported to date. Here we report a 12-year-old male patient with severe progressive scoliosis due to a huge subcutaneous cavernous hemangioma, who underwent posterior correction and fusion surgery. Upon referral to our department, radiographs revealed a scoliosis of 85° at T6-L1 and a kyphosis of 58° at T4-T10. CT and MR images revealed a huge hemangioma extending from the subcutaneous region to the paraspinal muscles and the retroperitoneal space and invading the spinal canal. Posterior correction and fusion surgery using pedicle screws between T2 and L3 were performed. Massive hemorrhage from the hemangioma occurred during the surgery, with intraoperative blood loss reaching 2800 ml. The scoliosis was corrected to 59°, and the kyphosis to 45° after surgery. Seven hours after surgery, the patient suffered from hypovolemic shock and disseminated intravascular coagulation due to postoperative hemorrhage from the hemangioma. The patient developed sensory and conduction aphasia caused by cerebral hypoxia during the shock on the day of the surgery. At present, two years after the surgery, although the patient has completely recovered from the aphasia. This case illustrates that, in correction surgery for scoliosis due to huge subcutaneous cavernous hemangioma, intraoperative and postoperative intensive care for hemodynamics should be performed, since massive hemorrhage can occur during the postoperative period as well as the intraoperative period.
Cavernous hemangioma consists mainly of congenital vascular malformations, which is present before birth and gradually increasing in size with skeletal growth. The vertebral body is one of the most commonly recognized sites of cavernous hemangioma, and found incidentally on radiological imaging[1, 2]. While many cases of hemangioma are asymptomatic, others present with pain or spinal deformity, and those located within the spinal canal may present with neurological disorders. There are several reports of scoliosis secondary to cavernous hemangioma originating in the vertebral body [3–6], and one of scoliosis secondary to a subcutaneous cavernous hemangioma. However, to our knowledge, there are no reports of surgical treatment for these conditions. Here we report a case of scoliosis caused by a huge subcutaneous cavernous hemangioma that was surgically treated.
The diagnosis of severe progressive scoliosis associated with cavernous hemangioma was made. Prior to the surgery, we decided against the use of radiotherapy, which may reduce the size of the tumor or blood circulation through it, because irradiation of the spine can lead to pseudoarthrosis. In planning the surgery, an anterior approach was considered first, since the hemangioma was mainly located on the concave side of the curve. However, we abandoned this idea because damage to the hemangioma during disc removal or screw placement would have required us to manage the hemorrhage from inside the narrow thoracic cage, which might not have been successful. Although bleeding from hemangioma was inevitable if we used the posterior approach, we had the option of stopping the bleeding by the tamponade effect of closing the wound. Therefore, we used the posterior approach for correction surgery and fusion with pedicle screws at T2-L3.
To our knowledge, there has been only one report of scoliosis caused by an enlarging subcutaneous cavernous hemangioma, which was reported by Lozman et al. The case was that of a 13-year-old boy with a scoliosis of 55°. Although surgical removal of the hemangioma was attempted, the procedure was halted after only a biopsy was completed, due to massive hemorrhage. Treatment using a Milwaukee brace was then undertaken, and fortunately, the patient showed no progression of the scoliosis for 15 months of follow-up . Because cavernous hemangiomas invading the spinal epidural space are often seen in Klippel-Trenaunay syndrome, we initially suspected an association with this disease. However, since port wine stain (cutaneous hemangiomas), varicosities, and hypertrophy of the affected limbs are characteristics of Klippel-Trenaunay syndrome, but were not seen in the present case, we have reported this case as solely a cavernous hemangioma. In general, asymptomatic cavernous hemangioma is not an indication for surgery, since uncontrollable hemorrhage can occur during the operation . Some reports have described treating hemangiomas with vascular embolization or radiotherapy, concluding that enlargement or relapse of the hemangiomas could be controlled without surgery [3, 5–7, 9]. Asumu et al. reported a patient with scoliosis caused by cavernous hemangioma originating in the vertebral body. The Cobb angle of the curve was 35°, and the patient was treated by vascular embolization, without exacerbation of the neurologic symptoms or an increase in the Cobb angle, yielding a favorable result. The authors concluded that vascular embolization may be a useful option when a single vasa vasorum is identifiable . Bucknill also reported a favorable result with ligation of the vasa vasorum followed by radiotherapy combined with posterior fusion .
In our present case of a 12-year-old boy with scoliosis of 85 degrees, posterior correction and fusion surgery were considered necessary, because significant progression of the deformity was recognized despite thorough brace treatment. Preoperative vascular embolization, which is reported to be effective, was not performed for the following reasons. Preoperative contrast-enhanced CT showed only a slight enhancement in part of the tumor, and no enlarged feeding arteries were visible. These are rare findings for hemangioma. We speculated that the blood flow inside the sinusoid was so slow that contrast-enhanced CT could not provide a clear image of the tumor, and expected that we would not be successful in identifying feeding arteries by angiography either. Although preoperative radiotherapy could have reduced the vascularity of the hemangioma, it was not performed because of the increased risk of pseudarthrosis following irradiation. Local radiotherapy also might have reduced the size or blood circulation of the tumor near the operated area. However, to reduce bleeding during correction and fusion surgery of the spinal column, even local radiotherapy would have had to be directed close to the spine, increasing the risk of pseudoarthrosis. Therefore, we decided against its use.
During the surgery, the posterior correction and fusion were performed without removing the hemangioma, since massive hemorrhage associated with removal of the tumor was predicted. As was expected preoperatively, massive hemorrhage from the hemangioma occurred following a breach of the tumor pseudocapsule, and hemostasis was difficult to achieve. However, the intraoperative hemorrhage was reduced to some extent by the cautious subperiosteal detachment of the soft tissues from the posterior bony elements, which prevented damage to the hemangioma. At the time of wound closure, the absence of massive hemorrhage was confirmed. Nevertheless, the patient suddenly entered a state of hypovolemic shock after the administration of diazepam 7 hours postoperatively. We suspect that the reduced circulating blood volume due to the intraoperative massive hemorrhage depleted the blood inside the hemangioma, which reduced the hemorrhage from the hemangioma by the end of the surgery. However, the postoperative blood and fluid transfusion increased the circulating blood volume, causing the reperfusion of the hemangioma, which resulted in hemorrhage from hemangioma and unstable hemodynamics. Since the patient's hemodynamics were stable according to the arterial line monitor, we underestimated the hemorrhage inside the wound and did not pay sufficient attention to the hemoglobin concentration. To monitor the postoperative hemorrhage status more accurately, we should have checked the hemoglobin concentration and coagulation factor levels more frequently, even though the hemodynamics were stable. The disseminated intravascular coagulation that developed one day after surgery was thought to be caused, at least in part, by the large amount of hemorrhage and consumption of coagulation factors inside the huge hemangioma. Transfusion of whole blood and fresh frozen plasma should have been performed earlier to prevent hypovolemic shock. The reasons for the delayed blood transfusion were, first, we overestimated the hemoglobin level and underestimated the postoperative hemorrhage inside the wound. Moreover, we tried to manage the loss of circulating blood volume with autologous blood collected perioperatively. Although this episode of shock may have caused the cerebral hypoxia, the early resuscitation and youth of the patient may have contributed to his gradual recovery from aphasia.
In the surgical treatment of progressive scoliosis in patients with huge cavernous hemangioma, preoperative embolization should be considered if dominant feeding arteries are recognized on contrast CT or angiography. The use of radiotherapy, which is reported to be effective in reducing hemangioma size, should be considered carefully, since it may increase the risk of pseudoarthrosis. Because a large hemorrhage can occur during the postoperative period as well as intraoperatively, careful perioperative attention should be paid to such patients' hemodynamics by using arterial and central venous line monitoring. Transfusions of whole-blood and/or fresh frozen plasma at volumes that could prevent postoperative hypovolemic shock and coagulopathy should be considered.
Written informed consent was obtained from the parents of the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review from the Editor-in-Chief of this journal
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