Validating the management paradigm for pediatric spinal aneurysmal bone cysts to optimize long-term outcomes: an institutional experience

2020 ◽  
Vol 36 (11) ◽  
pp. 2775-2782 ◽  
Author(s):  
Victor M. Lu ◽  
Kendall A. Snyder ◽  
Edward S. Ahn ◽  
David J. Daniels
2006 ◽  
Vol 192 (4) ◽  
pp. 492-495 ◽  
Author(s):  
Adora Fou ◽  
Freya R. Schnabel ◽  
Diane Hamele-Bena ◽  
Xiao-Jun Wei ◽  
Bin Cheng ◽  
...  

2014 ◽  
Vol 121 (3) ◽  
pp. 541-548 ◽  
Author(s):  
Liang Wu ◽  
Tao Yang ◽  
Xiaofeng Deng ◽  
Chenlong Yang ◽  
Jingyi Fang ◽  
...  

2012 ◽  
Vol 9 (3) ◽  
pp. 305-315 ◽  
Author(s):  
Georgios Zenonos ◽  
Osama Jamil ◽  
Lance S. Governale ◽  
Sarah Jernigan ◽  
Daniel Hedequist ◽  
...  

Object Spinal aneurysmal bone cysts (ABCs) constitute a rare and clinically challenging disease, primarily affecting the pediatric population. Information regarding the management of spinal ABCs remains sparse. In this study the authors review their experience with spinal ABCs at Children's Hospital Boston. Methods The medical records of all patients treated surgically for primary spinal ABCs between January 1998 and July 2010 were retrospectively reviewed. Results Fourteen cases were identified (6 males and 8 females, ages 5–19 years old). The ABCs were located throughout the spine, with an equal number in the thoracic and lumbar spine, and rarely in the cervical spine. The majority of patients presented with back pain, but neurological deficits and spinal deformity were common. A variety of radiographic techniques were used to establish the diagnosis, including needle biopsy. Preoperative selective arterial embolization was performed in 7 cases (50%), and the majority of cases required spinal instrumentation along with resection. Mean follow-up was 55.9 months (range 15–154 months) after initial intervention. Two ABCs recurred (14%), at 9 months and 8 years after incomplete initial resection, and the patients underwent reoperation. Complete resection was ultimately achieved in all cases. All patients were asymptomatic and neurologically intact at their last follow-up evaluation, and showed no evidence of deformity or recurrence on imaging. Conclusions Computed tomography and MR imaging are adequate for an initial evaluation of spinal ABCs, although solid variants can present a diagnostic challenge. Given the high rates of recurrence with residual disease, complete obliteration of the lesion should be the goal of treatment. Preoperative embolization is often performed, although in the authors' opinion the degree of bleeding tends not to support its routine use. Long-term follow-up is warranted as recurrences can occur years after initial intervention. However, gross-total excision in conjunction with spinal stabilization, as needed, usually provides cure of the ABC and excellent long-term spinal alignment.


2018 ◽  
Vol 29 (05) ◽  
pp. 412-416
Author(s):  
Riccardo Coletta ◽  
Bashar Aldeiri ◽  
Antonino Morabito

Aim The aim of this study was to report our initial experience using spiral intestinal lengthening and tailoring (SILT) technique in selected cases of short bowel syndrome (SBS). Materials and Methods We analyzed all cases of SBS underwent SILT in our unit since the introduction of the procedure in 2012. We retrospectively analyzed patients' demographics, pre- and postprocedure bowel length, surgical complications, and postoperative parenteral nutrition (PN) requirements. Data were compared using independent samples, Mann–Whitney's U-test. Results Five children with SBS underwent SILT between 2012 and 2017. Median age at procedure was 8.3 months (4.5–16). Preoperative small bowel length measured a median of 22 cm (17.5–50) with a median diameter of 4 cm (3.5–4.6). SILT allowed a median increase in length of 56% (10–15 cm; p = 0.03) and tailoring of the dilated segment providing a reduction in diameter of 50% (4.3–2.1 cm; p = 0.01). No major complications related to SILT were encountered and none of the children required further surgical intervention following a median follow-up of 26 months (14.5–41). Interestingly, we observed a significant reduction of PN requirement at 6 months (p = 0.008) associated with liver function preservation during the follow-up period. Conclusion In our experience, SILT is a promising adjunct in the surgical management of SBS. It can be used to tailor and lengthen mildly dilated segments of the bowel where other procedures are technically challenging, with a view to reduce the risk of intestinal failure associated liver disease and thereby improving chances for quality survival. Further studies are needed to investigate long-term outcomes of SILT in pediatric SBS.


Author(s):  
Rohan Savoor ◽  
Timothy L. Sita ◽  
Nader S. Dahdaleh ◽  
Irene Helenowski ◽  
John A. Kalapurakal ◽  
...  

2009 ◽  
Vol 18 (6) ◽  
pp. 375-380 ◽  
Author(s):  
Harvey L. George ◽  
Puthanveettil Nithin Unnikrishnan ◽  
Neeraj K. Garg ◽  
Jayanth Sundar Sampath ◽  
Alf Bass ◽  
...  

2002 ◽  
Vol 25 (4) ◽  
pp. 282-290 ◽  
Author(s):  
Piergiorgio Falappa ◽  
Fausto M. Fassari ◽  
Arturo Fanelli ◽  
Elisabetta Genovese ◽  
Elio Ascani ◽  
...  

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