Spontaneous Regression of Aneurysm Remnant after Incomplete Surgical Clipping in a Patient with Ruptured Cerebral Aneurysm

Article information

J Cerebrovasc Endovasc Neurosurg. 2016;18(4):402-406
Publication date (electronic) : 2016 December 31
doi : https://doi.org/10.7461/jcen.2016.18.4.402
Department of Neurosurgery, Hallym University Sacred Heart Hospital, Anyang, Korea.
Correspondence to In Bok Chang. Department of Neurosurgery, Hallym University Sacred Heart Hospital, 22 Gwanpyeong-ro 170beon-gil, Dongan-gu, Anyang 14068, Korea. Tel: 82-31-380-3771, Fax: 82-31-380-4118, nscib71@gmail.com
Received 2016 February 01; Revised 2016 June 20; Accepted 2016 November 15.

Abstract

Cases of spontaneous regression of cerebral aneurysm remnant after incomplete surgical clipping have been rarely reported. This paper reports the regression of an aneurysm remnant after incomplete surgical clipping during postsurgical follow-up. A 50-year-old male presented with subarachnoid hemorrhage because of rupture of an anterior communicating artery aneurysm. An emergency clipping of the aneurysm was performed. A cerebral angiography, which was performed two weeks postoperatively, revealed an aneurysm remnant. The patient refused additional treatment and was discharged without apparent neurological deficit. One-year follow up cerebral angiography demonstrated a partially regressed aneurysm remnant.

INTRODUCTION

Cerebral aneurysm remnants are major concerns after incomplete microsurgical clipping. The risk of regrowth and rupture of a remnant aneurysm warrants close follow-up with digital subtraction angiography (DSA) with additional endovascular coiling or surgical clipping if needed.1)5)6) To the best of my knowledge, cases of spontaneous regression of aneurysm remnant after surgical clipping have rarely been reported. Here in, we report a rare case of aneurysm remnant which regressed without additional treatment during the observation period.

CASE REPORT

A 50-year-old male presented with sudden headache. At presentation, his Glasgow coma scale was 14 and no lateralizing sign was found. Brain computed tomography (CT) showed a thick subarachnoid hemorrhage in the basal cistern and a hemorrhage on the left frontal lobe and both lateral ventricles. CT angiography revealed an aneurysm at the anterior communicating artery (ACoA). The patient underwent preoperative digital subtraction angiography, which demonstrated a wide necked and bilobulated aneurysm with maximal size of 5.2 mm arising from the left ACoA (Fig. 1). The morphology of the aneurysm in this patient was deemed not amenable to treatment with coil embolization. An emergency clipping of the ruptured ACoA aneurysm was performed. Left side pterional craniotomy was chosen for aneurysm dome avoidance and more favorable view of the aneurysm neck. Brain swelling was moderate and ventricular drain was inserted through Payne's point. Ruptured point of the aneurysm was obliterated by a bayonet type clip. Further dissection of the aneurysm and confirmation of distal tip of the clip was difficult due to the gradually swelling brain and tight adhesions with the surrounding tissues. The patient tolerated the surgery well and showed no neurologic deterioration after surgery. Transcranial Doppler ultrasonography revealed no evidence of vasospasm. The patient's mental status fully recovered with conservative management. Follow-up cerebral angiography, which was obtained on the fourteenth postoperative day showed remnant aneurysm behind the surgical clip (Fig. 2). We recommended repositioning of the clip, but the patient was reluctant to undergo a reoperation. The patient was discharged with no apparent neurological deficit. Follow-up cerebral angiography at 12 months postoperatively showed the remnant aneurysm had regressed almost completely (Fig. 3). A recommendation to monitor the remaining tiny aneurysm with DSA after 12 months was made.

Fig. 1

Brain computed tomography demonstrated subarachnoid hemorrhage in the basal cistern and a hematoma on the left frontal lobe. (A) Subsequent digital subtraction angiography revealed a ruptured anterior communicating artery aneurysm. (B) Left anteroposterior view. (C) 3D reconstruction.

Fig. 2

Digital subtraction angiography obtained two weeks after surgery showed remnant aneurysm behind the clip (arrow). (A) Left anterior oblique view. (B) 3D reconstruction.

Fig. 3

One-year follow-up cerebral angiography demonstrated regression of the remnant aneurysm, leaving a small saccular aneurysm (arrow). (A) Left anterior oblique view. (B) 3D reconstruction.

DISCUSSION

According to previous research, the incidence of residual aneurysm after endovascular or surgical treatment ranged from 3.5% to 13%.1)4)5)6)8)11)12)14) The persistence of aneurysm remnants after surgical clipping may result from technical or anatomic difficulties at the time of surgery, slippage of a successfully placed clip, or regrowth of an aneurysmal sac from an incompletely excluded neck.15)16)17)19)20) Although the natural history of remnant aneurysms after surgical treatment has not been fully described, several studies have reported that aneurysm remnants were associated with persistent risk of rebleeding.12)13)15)16) Aneurysm remnants may also grow over time and can later produce symptoms by compressing neighboring structures.1)5)6)8)11) The reported incidence of enlargement and rebleeding rate in incompletely clipped aneurysms were 2.5-3.8% and 1.9-3.8, respectively.3)7) Although rare, cases of spontaneous obliteration of aneurysm remnant after surgical clipping of ruptured cerebral aneurysm have been reported.2)9)18) The incidence of aneurysm remnant was 3.8% in a series of 715 aneurysms that were managed using microsurgical techniques. Of 28 aneurysm remnants, 5 aneurysms disappeared in follow-up angiography.7) Most of the aneurysms that spontaneously disappeared had small diameters (less than 4 mm).

Several mechanisms and dynamic parameters related to spontaneous thrombosis of intracranial aneurysms have been suggested10); including 1) stasis of blood in the aneurysm sac, 2) a ratio of aneurysm sac volume to orifice area than 28:1 (mm3:mm2), 3) stagnation of blood in a large aneurysm, 4) endothelial injury due to turbulent blood flow, and 5) stasis of contrast material in the aneurysm sac. Hamilton and Dold proposed that hypotension, severe vasospasm, use of antifibrinolytic agents, giant aneurysm, and local injury to the arterial wall were associated with spontaneous obliteration of aneurysm in the ruptured aneurysms.9) Tan et al. reported a case of growth and spontaneous regression of a remnant aneurysm after incomplete surgical clipping of a ruptured middle cerebral artery aneurysm.18) In this case, the authors suggested that the sudden regression of the remnant aneurysm could be explained by the fact that endothelial repair exceeded endothelial destruction. They also suggested that thrombogenesis within the aneurysmal sac may have obliterated the aneurysm.

CT or magnetic resonance image may be helpful in documenting thrombus formation in the aneurysm sac. However, difficulties may be encountered in identifying the thrombus in a clipped aneurysm because of clip artifact. In our case, the patient had no medical factors such as dehydration or medical disease to accelerate thrombus formation within the aneurysm. Furthermore, the size of the aneurysm remnant was neither large or giant nor small (less than 4 mm). Although the exact mechanism involved in regression of aneurysm is unclear in our case, we speculated that the intraoperative manipulation may have led to endothelial injury that resulted in thrombus formation by platelet deposition and aggregation. In addition, vascular remodeling and stagnated blood flow within the aneurysm induced by the resulting vertically narrowed aneurysm neck after the incomplete clipping may have facilitated the formation of the thrombus.

At present, there is no reliable method to predict whether an aneurysm remnant will spontaneously regress or grow over time. Consequently, close follow-up with angiographic imaging is required in patients with incompletely clipped aneurysm, even in cases with spontaneously regressed aneurysm due to the possibility of recanalization in the future.

CONCLUSION

A case of spontaneous regression of cerebral aneurysm remnant after incomplete surgical clipping was reported. Close follow-up with angiographic imaging is required in incompletely clipped case.

Notes

Disclosure: The authors report no conflict of interest concerning the materials or methods in this study or the fundings specified in this paper.

References

1. Bavinzski G, Talazoglu V, Killer M, Gruber A, Richling B, al-Shameri R. Coiling of recurrent and residual cerebral aneurysms after unsuccessful clipping. Minim Invasive Neurosurg 1999;3. 42(1):22–26. 10228935.
2. Choi CY, Han SR, Yee GT, Lee CH. Spontaneous regression of an unruptured and non-giant intracranial aneurysm. J Korean Neurosurg Soc 2012;9. 52(3):243–245. 23115669.
3. David CA, Vishteh AG, Spetzler RF, Lemole M, Lawton MT, Partovi S. Late angiographic follow-up review of surgically treated aneurysms. J Neurosurg 1999;9. 91(3):396–401. 10470813.
4. Deshmukh VR, Kakarla UK, Figueiredo EG, Zabramski JM, Spetzler RF. Long-term clinical and angiographic follow-up of unclippable wrapped intracranial aneurysms. Neurosurgery 2006;3. 58(3):434–442. discussion 434-42. 16528182.
5. Drake CG, Friedman AH, Peerless SJ. Failed aneurysm surgery. Reoperation in 115 cases. J Neurosurg 1984;11. 61(5):848–856. 6491730.
6. Ebina K, Suzuki M, Andoh A, Saitoh K, Iwabuchi T. Recurrence of cerebral aneurysm after initial neck clipping. Neurosurgery 1982;12. 11(6):764–768. 7162566.
7. Feuerberg I, Lindquist C, Lindqvist M, Steiner L. Natural history of postoperative aneurysm rests. J Neurosurg 1987;1. 66(1):30–34. 3783256.
8. Giannotta SL, Litofsky NS. Reoperative management of intracranial aneurysms. J Neurosurg 1995;9. 83(3):387–393. 7666212.
9. Hamilton MG, Dold ON. Spontaneous disappearance of an intracranial aneurysm after subarachnoid hemorrhage. Can J Neurol Sci 1992;8. 19(3):389–391. 1393850.
10. Jayakumar PN, Ravishankar S, Balasubramaya KS, Chavan R, Goyal G. Disappearing saccular intracranial aneurysms: do they really disappear? Interv Neurol 2007;9. 13(3):247–254.
11. Johnston SC, Dowd CF, Higashida RT, Lawton MT, Duckwiler GR, Gress DR, et al. Predictors of rehemorrhage after treatment of ruptured intracranial aneurysms: the Cerebral Aneurysm Rerupture After Treatment (CARAT) study. Stroke 2008;1. 39(1):120–125. 18048860.
12. Kang HS, Han MH, Kwon BJ, Jung SI, Oh CW, Han DH, et al. Postoperative 3D angiography in intracranial aneurysms. AJNR Am J Neuroradiol 2004;10. 25(9):1463–1469. 15502122.
13. Le Roux PD, Elliott JP, Eskridge JM, Cohen W, Winn HR. Risks and benefits of diagnostic angiography after aneurysm surgery: a retrospective analysis of 597 studies. Neurosurgery 1998;6. 42(6):1248–1254. discussion 1254-5. 9632182.
14. Lee JH, Kim SJ, Cha J, Kim HJ, Lee DH, Choi CG, et al. Postoperative multidetector computed tomography angiography after aneurysm clipping: comparison with digital subtraction angiography. J Comput Assist Tomogr 2005;Jan-Feb. 29(1):20–25. 15665677.
15. Lin T, Fox AJ, Drake CG. Regrowth of aneurysm sacs from residual neck following aneurysm clipping. J Neurosurg 1989;4. 70(4):556–560. 2926496.
16. Rabinstein AA, Nichols DA. Endovascular coil embolization of cerebral aneurysm remnants after incomplete surgical obliteration. Stroke 2002;7. 33(7):1809–1815. 12105358.
17. Sindou M, Acevedo JC, Turjman F. Aneurysmal remnants after microsurgical clipping: classification and results from a prospective angiographic study (in a consecutive series of 305 operated intracranial aneurysms). Acta Neurochir (Wien) 1998;140(11):1153–1159. 9870061.
18. Tan CB, Rodesh G, Lasjaunias P. Growth and spontaneous regression of a middle cerebral artery aneurysm after surgical clipping. Interv Neuroradiol 2001;6. 7(2):147–151. 20663342.
19. Thielen KR, Nichols DA, Fulgham JR, Piepgras DG. Endovascular treatment of cerebral aneurysms following incomplete clipping. J Neurosurg 1997;8. 87(2):184–189. 9254080.
20. Thornton J, Bashir Q, Aletich VA, Debrun GM, Ausman JI, Charbel FT. What percentage of surgically clipped intracranial aneurysms have residual necks? Neurosurgery 2000;6. 46(6):1294–1298. discussion 1298-300. 10834634.

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Fig. 1

Brain computed tomography demonstrated subarachnoid hemorrhage in the basal cistern and a hematoma on the left frontal lobe. (A) Subsequent digital subtraction angiography revealed a ruptured anterior communicating artery aneurysm. (B) Left anteroposterior view. (C) 3D reconstruction.

Fig. 2

Digital subtraction angiography obtained two weeks after surgery showed remnant aneurysm behind the clip (arrow). (A) Left anterior oblique view. (B) 3D reconstruction.

Fig. 3

One-year follow-up cerebral angiography demonstrated regression of the remnant aneurysm, leaving a small saccular aneurysm (arrow). (A) Left anterior oblique view. (B) 3D reconstruction.