Posterior spinal fusion for severe kyphosis in a child with Gaucher disease: a case report and review of the literature

doi:10.21203/rs.3.rs-2740012/v1

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Posterior spinal fusion for severe kyphosis in a child with Gaucher disease: a case report and review of the literature

https://doi.org/10.21203/rs.3.rs-2740012/v1

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Background The skeleton involvement is one of the most significant aspects of Gaucher disease (GD).However, the treatment for spinal involvement in GD among patients undergoing enzyme replacement therapy (ERT) is poorly characterized. We present a case of progressive kyphotic spinal deformity in a young child caused by vertebral involvement, which was managed by posterior spinal fusion without anterior spinal release under ERT.

Case presentation A 10-year-old boy presented progression kyphosis ( thoracic kyphotic angle of 113°) associated with type IIIb GD had undergoneposterior spinal fusion with segmental pedicle screw fixation (from T6-L3) and Ponte osteotomy. The patient went back to school without further brace protection. Proximal junctional kyphosis (PJK) was observed at 4 months postoperatively. Revision surgery was performed to prevent the neurological impairment. Additional posterior spinal fusion from T2–T6 and decompressive laminectomy was performed during the revision surgery. 2-year of follow-up showed no recurrence of PJK and solid fusion was achieved in the patient under ERT and brace protection.

Conclusions Posterior spinal fusion without anterior spinal release is a good treatment option for severe spinal deformity in patients with GD. However, the fusion level and reinforced fixation require careful consideration, revision surgeryand brace protection is needed as long as PJK was observed.

Gaucher disease

spinal deformities in children

posterior spinal approaches

proximal junctional kyphosis

case report

Gaucher disease (GD) was first reported in 1882 by a French dermatologist, Philippe Gaucher, in a patient with massive splenomegaly without leukemia. It is characterized by massive splenomegaly and thrombocytopenia due to the deficiency of the glucosidase enzyme^[1]. In the human glucocerebrosidase gene (chromosome 1q22)^[2], 250 mutations responsible for this enzymatic deficiency have been identified. Previous reports show that the four most common mutations observed in 90% of the disease alleles are N370S, 84GG, L444P, and IVS2 + 1^[3]. GD is divided into three types: chronic (type I, non-neurological), acute (type II, acute neuronopathic), and subacute (type III, chronic neuronopathic). Meanwhile, according to clinical manifestations of the subacute type, type III GD is classified as IIIa (progressive myoclonus and dementia), IIIb (horizontal gaze paralysis, short stature, suboptimal bodyweight, and prone to cardiopulmonary, liver, and bone complications), and IIIc (cardiac valve calcification)^{[4, 5]}.

Involvement of the skeleton is common in GD, which primarily causes pain, disability, and a reduced quality of life. In particular, spinal involvement in GD among patients undergoing enzyme replacement therapy (ERT) is poorly characterized. We present a case of progressive kyphotic spinal deformity in a young child (type IIIb) caused by vertebral involvement, which was managed only by posterior spinal fusion under ERT. To date, few studies have described the surgical correction of spinal deformities in patients with GD under ERT, while no treatment standards have been established.

A 10-year-old boy (weight, 23 kg; height, 123 cm; and body mass index, 13.33 kg/m²) was referred to us in 2019 with a diagnosis of type-III GD. Thrombocytopenia was detected in the patient and a β-glucocerebrosidase (GCase) level of 1.54 nmol/h.mg was detected. He had undergone splenectomy in 2012 and had been administered 1200 units of imiglucerase once every 2 weeks since 2015. He had no history of bone crisis, pathologic fractures, or osteomyelitis. Deterioration of the thoracic kyphosis (TK) was noted in July 2017, but no rigid bracing was used. Thereafter, the deformity increased rapidly, leading to a kyphosis of 113° in 2019 (Fig. 1A). Pain developed over the apex of his deformity, and he started to have difficulty in walking with lower extremity weakness (3+/5 − 4/5). Moreover, the boy suffered from moderate horizontal gaze palsy and sternum deformity. Genetic testing indicated heterogeneity for gene mutations c.1448T > C and c.1205A > G. There were no signs of pulmonary dysfunction or myelopathy. The patient had mild anemia with normal platelet counts and blood clotting. Radiographs were obtained, which revealed a Cobb angle of TK as 113°(Fig. 1A). Computed tomography (CT) and magnetic resonance imaging (MRI) revealed inflammation of the mesenteric lymph nodes and anterior wedging of vertebrae from T7 to T10 (data not shown). The patient was diagnosed as : Spinal kyphosis deformity, type IIIb GD and sternal lordosis.

After anesthesia was induced, the child was placed in the prone position without compression of the sternum. The spinous processes, lamina, and facet joints of the instrumented segments were exposed using the posterior midline approach. After the pedicle screws had been implanted from T6 to L3, Smith-Peterson osteotomies were performed at five levels (T8-L1). We used gentle posterior compression along the bilateral rods to allow controlled anterior lengthening. The surgical time was 180 min, and blood loss was 300 ml. Intraoperative monitoring with neurogenic or transcranial motor-evoked potentials were used during every procedure. Correction of the segmental kyphotic angle was achieved (70°) after the first surgery, yielding a 61% correction rate (TK, 43°; lumbar lordosis [LL],38°; pelvic incidence [PI], 45°; PI-LL: −7°, sagittal vertical axis [SVA], 39 mm).

The patient went back to school without further brace protection. He administered 1200 units of imiglucerase once every 2 weeks as before. However, proximal junctional kyphosis (PJK) was observed at 4 months postoperatively (PJA,55°). He felt very hard to lift his head in his daily life. Revision surgery was performed to prevent the neurological impairment. During the revision surgery, we found that the pedicle screws were intact. We initially placed the screws in T2–T5 and then removed the screws of T6, after which laminectomy was performed, and a domino linkage system was used to link the internal fixation (Fig. 2D; TK:60°, LL:45°, PI: 45°, PI-LL:0°, SVA:67 mm). The surgical time was 195 min, and blood loss was 200 ml. Neuromonitoring signals during the operation were stable.We tried to mobilize the boy on the following day and discharged him on the fourth day after the revision surgery. He used brace protection for 5 months and was followed up at 3 months, 5 months, and 2 years. X-rays were repeated at the 2-year follow-up, which showed no obvious recurrence of PJK and solid fusion was achieved (PJA,19°, TK:60°, LL:50°, PI: 45°, PI-LL:-5°, SVA:-30 mm).

Hematoxylin-eosin staining and immunohistochemistry analysis were performed for CD68 (M1-type macrophages) and CD206 (M2 type macrophages) in resected lamina of the patient and compared with those of a 14 year-old healthy boy (control). Increased expression of CD68 but lower expression of CD206 was observed in the cancellous bone of the patient (Fig. 4).

TK may develop in any patient with GD from previous vertebral fragility fractures due to low bone mass and infiltration of Gaucher cells ^{[6, 7]}. Such cases generally deteriorate progressively, and orthodontic treatment is often ineffective^{[8, 9]}. We found only nine cases in five reports from 1983 to 2021; the details of these nine cases are summarized in Table 1. There were six men and three women, with a mean age of 14.3 years (range, 10–31 years). Most patients presenting with back pain and lower extremity weakness, except two patients, had definite signs of neurological deficit, which could be explained by spinal cord compression. The combined strategy with anterior discectomy and posterior spinal fusion were used for most cases (7/9). Ruff et al. treated a 12-year-old girl with GD who had progressive kyphosis (Cobb angle, 65°) by staged anterior discectomy and T11 vertebrectomy with rib grafting, followed by posterior spinal fusion with segmental instrumentation of T8-L3^[10] and reported good outcomes Katz et al. reported a case of a 31-year-old man with kyphotic deformity at T12 with myelopathy and complete myelopgraphic block. Decompressive laminectomies over the apex of the deformity were performed; however, the patient died 7 weeks postoperatively from gastric hemorrhage^[11]. Wiesner et al. treated a 12-year-old boy with a collapse of three consecutive vertebral bodies (T7 − T9) and created a global kyphosis of 90°. Ventral decompression was performed, and fibular and rib grafts were used to support the ventral column; subsequently, the spine was stabilized by a TSRH-System from T5-L2^[12]. Mininder et al. reported four children and adolescents with GD who developed a TK angle of 70–120°; two of them were associated with neurologic compromise, which were managed by anterior spinal release in cases of spinal cord compromise at the apex of the kyphotic deformity^[7].

Table 1

Summary of Gaucher disease-associated spinal deformity cases corrected by surgery in the English literature
Report	Age(years)/Sex	Disease type	Presentation	Vertebrate Colllapse(site)	Complications	Treatment	Follow-up	Outcome
Ruff et al., 1984^[10]	12/F	Not available	Back pain	T11	Progressive kyphosis of 64°	Anterior discectomies and T11vertebrectomy, posterior spinal fusion of T8-L3	Not available	Good outcome and solid fusion
Katz et al., 1993^[11]	31/M	Not available	Back pain and lower extremity weekness	T12, L4	Cord compression, hemorrhage	Laminectomy	7 weeks	Died of gastric hemorrhage and bronchopneumonia
Katz et al., 1993^[11]	17/M	Not available	Back pain	T5, T7, T12, L1-5	Kyphoscoliosis, cord compression	Brace, laminectomy, spinal fusion	Not available	Not available
Kocher et al., 2000^[7]	18/M	Type I	lower extremity weekness and stumbling gait	T8-T12	Cord compression and edmea at the apex of the kyohosis	Anterior decompression and posterior fusion	5 years	Good outcome
	11/M	Type 3	Back pain and lower extremity weekness	Midthoracic spine	A thoracic kyphosis of ~ 120° and flattening of the cord	Anterior discectomies and fusion of T2-T11, posterior spinal fusion of T1-L3	19 months	solid fusion with normal strength and sensation
	13/M	Type 3	Back pain	T6 and T10	A thoracic kyphosis of 94°	Anterior discectomies and fusion of T8-L2, posterior spinal fusion of T5-L3	18 months	Mainrenance of correction and solid fusion
	15/F	Type 3	Back pain	T5 and T10	A thoracic kyphosis of 70° and slight cord impingement	Anterior discectomies and fusion of T8-T11, posterior spinal fusion of T2-L2	1 year	Good outcome and solid fusion
Wiesner et al., 2003^[12]	12/M	Type I	Back pain	T7-9	No complications	Ventral decompression with bone graft and fusion with TSRH(T5-L2)	5 years	Good outcome
Ito et al., 2017^[17]	10/F	Not available	lower extremity weekness	No collapse	kyphosis of 84° between T6 and L3	T3-L3 posterior fusion with T12 osteotomy and anterior fusion from T12-L3 with bone grafts	6 years	No progressive of kyphosis but suffered from fracture of limbs

Considering the spinal flexibility of the patient and the absence of spinal cord compression in our case, we decided to perform posterior fusion without anterior spinal release to the correction of severe kyphosis with segmental pedicle screw fixation and Ponte osteotomy. We performed corrective posterior fusion from T6 to L3 and achieved adequate correction after the first operation (TK angle decreased from 113° to 43°; Fig. 1B). The child returned to school after 1 month postoperatively without further bracing. However, the child experienced difficulties while lifting his head at 4 months postoperation and proximal junctional kyphosis (PJK angle [PJA], 55°) was detected without neurological impairment (Fig. 2D and Fig. 3A-C). CT and MRI revealed no obvious spinal cord compression owing to increased TK at the level of proximal adjacent fusion.

The overall incidence of PJK in pediatric and adolescent patients is estimated as 11%, with a range of 0–55%^{[13, 14]}, while in children with early-onset scoliosis, the prevalence of PJK is much higher (48.9%)^[15]. The upper instrumented vertebra with the highest PJK rate was T6-T7 in children with early-onset scoliosis ^[16] No standards on the selection of fusion levels and instrumentation by posterior fusion in previous studies have been suggested for patients with GD ^[17].We initially sought to preserve the T2–T6 interspinous ligament during the first surgery, although PJK developed soon after. According to the classification of PJK^[18], the type of PJK in this case was 1CN. Therefore, additional posterior spinal fusion from T2–T6 and decompressive laminectomy was performed during the revision surgery.

Histological and immunohistochemical evaluation of the resected vertebral lamina showed osseous manifestation of GD, with a positive reaction of histiocytes to CD68 and CD206 (Fig. 4). Our immunohistological staining analysis revealed a higher expression of CD68 (M1 type macrophages) but lower expression of CD206 (M2 type macrophages) in the cancellous bone of the patient than those of the healthy young 14-year-old boy. These results indicated that the infiltration of Gaucher cells may impair the M2 phenotype formation and promote the proinflammatory capacity of macrophages in these patients^{[19, 20]}.

Based on the present case, posterior spinal fusion without anterior spinal release is a good corrective option for severe spinal kyphosis in patients with GD undergoing ERT. However, the fusion level should be decided carefully because the infiltration of Gaucher cells in the patient’s vertebrate, and reinforced fixation is recommended to prevent PJK even under ERT. Revision surgery and brace protection were needed to prevent neurological involvement, as long as PJK was observed during follow-up.

GD: Gaucher disease; ERT: Enzyme replacement therapy; PJK: Proximal junctional kyphosis; TK: thoracic kyphosis; LL:Lumbar lordosis; PI: pelvic incidence, SVA: sagittal vertical axis, PJA: PJK angle

Ethics approval and consent to participate

This study was approved by the Institutional Review Board of Second Affiliated hospital of Zhejiang University, School of medicine.

Consent for publication

Written informed consent was obtained from the patient’s parents for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor of this journal.

Competing interests All authors declare that there is no conflict of interest for this work.

Funding

This study was financially supported by the National Natural Science Foundation of China (grant nos.82072481 and 81972096, Dr. Li) and the Natural Science Foundation of Zhejiang, China (grant no. LY20H060009, Dr. Zhao) for patient follow-up and data collection costs.

Authors’ contributions

All authors contributed to the treatment of this patient. Data collection was performed by JL and LWC. The first draft of the manuscript was written by TFZ. WYF and NZ was involved in the management of the patient. QXC and FCL revised previous versions of the manuscript. All authors read and approved the final manuscript.

Acknowledgements

N/A

Availability of data and materials

The data used and/or analyzed during the current study are available from the corresponding author on reasonable request.

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No competing interests reported.

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Posterior spinal fusion for severe kyphosis in a child with Gaucher disease: a case report and review of the literature

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