Diagnosis and conservative treatment of a rare case of femoral intraosseous arteriovenous malformation in a patient with polyostotic fibrous dysplasia: A case report

Abstract

Pure intraosseous arteriovenous malformation (AVM) in a limb bone is extremely rare. Furthermore, there is currently insufficient information on the diagnostic and therapeutic strategies for pure intraosseous AVMs. We herein report a case of pure intraosseous AVM of the proximal femur occurring in a patient with polyostotic fibrous dysplasia. The patient was a 39-year-old woman who presented with pain in the right thigh. Plain radiographs and computed tomography scans revealed a medullary lytic lesion with expansion and thinning of the bone cortex in the right proximal femur, mimicking a primary bone tumor. Magnetic resonance imaging (MRI) examination revealed intramedullary signal voids and feeding arteries arising from the deep femoral artery. A non-surgical approach using embolization and denosumab achieved satisfactory results, which included complete obliteration of the AVM, increased cortical thickness of the right proximal femur, and attenuation of the high-turnover bone metabolism 1 year later. Careful review of MRI images is crucial for distinguishing between bone tumors and intraosseous AVM, which exhibit signal voids and feeding arteries, in order to avoid unnecessary interventions such as bone biopsy or surgery.

Introduction

The International Society for the Study of Vascular Anomalies (ISSVA) classifies vascular anomalies into vascular tumors and vascular malformations, according to the biological classification proposed by Mulliken and Glowacki (1,2). Arteriovenous malformations (AVMs) are high-flow vascular malformations in which well-formed arterial and venous elements communicate directly, rather than through a normal capillary network. Although the majority of AVMs occur in soft tissues, osseous involvement is occasionally encountered, with symptoms such as pain, mass effects with pulsation, swelling of the extremity, skin ulceration, bone overgrowth, bone destruction, and heart failure (3,4).

Intraosseous AVMs, which are relatively rare, predominantly occur in craniofacial bones, such as the mandible and maxilla (5,6). Pure intraosseous AVMs that do not involve soft tissue are extremely rare (3,4). Although several intraosseous AVMs have been described in the spine or long bones (7–14), little is known on the diagnostic and therapeutic strategies for pure intraosseous AVMs. It is crucial for physicians, particularly orthopedic oncologists, to understand the clinical characteristics of pure intraosseous AVMs in order to distinguish them from primary or metastatic bone tumors. We herein present a case of pure intraosseous AVM of the proximal femur in a patient with polyostotic fibrous dysplasia, which was treated by embolization and denosumab, and discuss the diagnostic characteristics and therapeutic approach.

Case report

A 37-year-old woman was referred to the Hirosaki University Hospital (Hirosaki, Japan) on December, 2014 with a 1-year history of pain in the left thigh while walking. The patient's medical history included a diagnosis of polyostotic fibrous dysplasia (poly-FD) when she was in her 20s at another hospital, without endocrinopathy or skin pigmentation. Plain radiographs and computed tomography (CT) examination revealed a central, longitudinal, medullary lytic lesion of the left proximal femur, with expansion and thinning of the bone cortex (Fig. 1A and B). An intramedullary lytic lesion and endosteal scalloping were also observed in the right proximal femur. There were multiple intramedullary lesions with a ground-glass appearance and lytic lesions throughout the bilateral femora and pelvis. Magnetic resonance imaging (MRI) revealed a lesion in the left proximal femur that exhibited a homogeneous intermediate signal on T1-weighted images and hyperintensity on the T2-weighted images (Fig. 1C and D). In the right proximal femur, an intramedullary hypointense lesion was identified on both T1- and T2-weighted images. An impending fracture of the left femur was diagnosed, resulting from a secondary cyst formation of the FD, and intramedullary nailing of the left femur was performed. The patient had an uneventful recovery after surgery. At the 1-year follow-up on December, 2015, she remained asymptomatic, without progressive changes in the right lower extremity on plain radiographs, and was scheduled for routine orthopedic follow-up at another hospital.

Figure 1.

Initial imaging findings in a 37-year-old patient with polyostotic fibrous dysplasia. (A) Plain radiograph (anteroposterior view) and (B) coronal plain CT revealed a central, longitudinal, medullary lytic lesion in the left proximal femur with expansion and thinning of the bone cortex. In the right proximal femur, an intramedullary lytic lesion and endosteal scalloping were also observed. Coronal MRI revealed a lesion with a (C) homogeneous intermediate signal on T1-weighted images and (D) a hyperintense signal on T2-weighted images in the left proximal femur. In the right proximal femur, an intramedullary hypointense lesion (arrowheads) was observed on both T1- and T2-weighted images. CT, computed tomography; MRI, magnetic resonance imaging.

The patient visited our hospital again at the age of 39 years on November, 2016, with a 5-month history of right thigh pain while walking. Plain radiographs and CT scans revealed worsening of the findings compared with those 2 years earlier, consisting of a central, longitudinal medullary lytic lesion with expansion and thinning of the bone cortex (Fig. 2A-C). There was a mild disruption of the intertrochanteric posterior bone cortex (Fig. 2D), but there were no soft tissue masses or periosteal reaction. MRI revealed an extended intramedullary hypointense lesion on both T1- and T2-weighted images (Fig. 3A and B). The fat-suppressed post-contrast T1-weighted MRI revealed heterogeneous enhancement around the intramedullary hypointense lesion (Fig. 3C). There were no soft tissue masses near the right proximal femur. An impending fracture of the right femur was diagnosed, resulting from progression of the FD. Intramedullary nailing of the right femur was attempted, but the operation was discontinued due to rapid profuse bleeding after drilling the greater trochanter. The hemorrhage was controlled by filling the drill hole with bone wax. A review of the preoperative MRI revealed several feeding arteries arising from the deep femoral artery that were responsible for the intramedullary hypointense signal (signal void; Fig. 3D and E). Contrast-enhanced CT and 3-dimensional CT images obtained on the day after the discontinued surgery revealed marked intramedullary enhancement of the proximal femoral lesion and multiple hypertrophied perforating arteries arising from the deep femoral artery (Fig. 4A-C). Selective angiography of the deep femoral artery demonstrated multiple hypertrophied perforating arteries penetrating the femoral cortex, as well as early formation of the nidus and venous sac within the medullary cavity of the femur (Fig. 4D and E). These findings indicated that the proximal femoral lesion was an intraosseous AVM.

Figure 2.

Imaging findings when the same patient presented again 2 years later with a 5-month history of right thigh pain. Plain radiographs of the (A) anteroposterior and (B) lateral view and (C) plain coronal computed tomography (CT) revealed marked worsening in the changes of the right proximal femur compared with those from 2 years earlier, consisting of a central longitudinally medullary lytic lesion with expansion and thinning of the bone cortex. (D) Plain axial CT revealed slight disruption of the intertrochanteric posterior bone cortex, but no soft tissue mass or periosteal reaction were identified.

Figure 3.

Magnetic resonance imaging (MRI) findings of the patient at the same time as Fig. 2. Coronal MRI revealed an extended intramedullary hypointense lesion both on (A) T1- and (B) T2-weighted images. (C-E) Coronal fat-suppressed post-contrast T1-weighted MRI revealed heterogeneous enhancement around the intramedullary hypointense lesion, as well as several feeding arteries (arrowheads) arising from the deep femoral artery.

Figure 4.

Contrast-enhanced computed tomography (CT) and selective angiography of the patient in Figs. 2 and 3 after discontinued surgery for intramedullary nailing of the right femur. Post-contrast (A) axial and (B) coronal CT and (C) 3-dimensional CT images revealed marked intramedullary enhancement of the right proximal femoral lesion, as well as multiple hypertrophied perforating arteries arising from the deep femoral artery. (D and E) Digital subtraction angiography images revealed multiple hypertrophied perforating arteries penetrating through the femoral cortex and early formation of the nidus and venous sac within the medullary cavity of the femur. (F and G) Digital subtraction images after the third embolization demonstrated that the venous sac had been completely obliterated by the transvenous coil embolization.

Therapeutic embolization was then performed for a total of 3 times (on days 2, 9 and 21 after the initial surgery). In the first and second embolizations, transarterial n-butyl-2- cyanoacrylate (NBCA) injections were performed. In the third embolization, a small venous sac remaining within the medullary cavity was completely obliterated by transvenous coil embolization (Fig. 4F and G). The patient was able to stand and walk with full weight-bearing without pain on the day after the final embolization, but she was advised to walk with crutches with load restriction on the right lower extremity and to avoid activities that would increase the risk of pathological fracture for 3 months after the embolization. In addition, biochemical measurements, including serum total alkaline phosphatase (ALP), bone alkaline phosphatase (BAP), calcium, phosphate and urine N-terminal cross-linked telopeptide of type I collagen (NTX), indicated high bone turnover rate (Table I). Therefore, subcutaneous injections of 60 mg denosumab (Pralia^®; once every 6 months) with oral activated vitamin D and calcium were initiated. One year after the embolization, the patient remained asymptomatic, and the right proximal femur exhibited increased cortical thickness on plain radiographs and CT images (Fig. 5A-D). No intramedullary signal void was detected on MRI (Fig. 5E-G). Biochemical tests before and after treatment revealed attenuation of the high-turnover bone metabolism (Table I). The bone mineral density (BMD) of the lumbar spine (L2-L4) on dual-energy-X-ray absorptiometry was also increased on December, 2017 after 1 year treatment.

Table I.

Changes in biochemical measurements and lumbar spine (L2-L4) BMD before and after denosumab administration.

Measurement time point	Serum ALP (normal range, 115–359 U/l)	Serum BAP (normal range, 2.9–14.5 U/l)	Serum calcium corrected for albumin level (normal range, 8.7–10.3 mg/dl)	Serum phosphate (normal range, 2.5–4.7 mg/dl)	Urine NTX/Cr (reference range, 9.3–54.3 nMBCE/mMCr)	BMD (g/cm2)
Pretreatment	627	66.6	9.3	3.4	440.5	1.253
Post-treatment (1 week)	524	57.2	8.8	1.9	89.4
Post-treatment (1 year)	187	13.3	9.4	2.7	15.1	1.459

The total serum calcium was normalized to the albumin level. BMD, bone mineral density; ALP, total serum alkaline phosphatase; BAP, bone alkaline phosphatase; NTX, N-terminal cross-linked telopeptide of type I collagen; Cr, creatinine.

Figure 5.

Imaging findings of the patient 1 year after embolization and denosumab treatment. Plain radiographs on (A) anteroposterior and (B) lateral view, as well as plain (C) coronal and (D) axial CT, revealed increased cortical thickness of the right proximal femur. Coronal MRI did not show an intramedullary signal void on (E) T1-, (F) T2-, or (G) fat-suppressed post-contrast T1-weighted images. CT, computed tomography; MRI, magnetic resonance imaging.

Discussion

The present case demonstrated that careful imaging review is crucial for distinguishing bone tumors from intraosseous AVMs, which are characterized by signal void and the presence of feeding arteries on MRI. Denosumab treatment also achieved a satisfactory result, including increased cortical thickness of the right proximal femur and attenuation of high-turnover bone metabolism. To the best of our knowledge, this is the first report of pure intraosseous AVM occurring in combination with poly-FD.

MRI examination in this case clearly demonstrated intramedullary signal voids and feeding arteries in a pure intraosseous AVM of a limb bone. MRI is an extremely important modality for assessing vascular tumors and malformations, and the presence of signal void is a hallmark MRI finding in AVMs (15–17). In previous reports (7–14), intramedullary lesions exclusively displayed a hypointense or isointense signal on T1-weighted images and a hyperintense signal on T2-weighted images, without signal voids. However, in the present case, MRI demonstrated intramedullary signal voids and feeding arteries, indicating a high-flow malformation. Although the signal voids were misinterpreted as solid fibrous tissues on initial diagnosis, contrast-enhanced CT pointed towards the correct diagnosis, as it revealed marked intramedullary enhancement and hypertrophied surrounding arteries. Therefore, careful imaging review is warranted to avoid unnecessary bone biopsies and surgeries that may cause excessive bleeding.

In this case, complete obliteration of the intraosseous AVM was achieved by transarterial NBCA injections and transvenous coil embolization. The management of patients with AVM includes conservative treatment, transcatheter embolization, sclerotherapy, surgical resection, or a combination of these methods. Conservative treatment is recommended for asymptomatic or mildly impaired patients, as incomplete treatment may stimulate more aggressive growth (17). Transcatheter embolization is recommended for symptomatic, impaired patients with extensive high-flow lesions, either preoperatively or as a first-line therapeutic strategy, when surgical resection carries a significant risk of postoperative morbidity (5,6). In addition, sclerotherapy may be applied preoperatively or as a definitive treatment in selected patients (18). Do et al reported good results of ethanol embolotherapy for extremity AVM involving bone (3). Complete surgical resection is recommended when the AVM is small and located in a surgically accessible area.

In the present case, denosumab achieved increased cortical thickness of the proximal femur and attenuated the high-turnover bone metabolism. Pathological fracture was a concern in this case, due to the low blood supply post-embolization and the high-turnover bone metabolism. Although surgical treatment is usually recommended for FD of the lower limbs causing pain and deformity (19), good results were achieved with denosumab, which rapidly decreased the serum ALP, BAP and urine NTX levels (Table I). Several previous studies reported that intravenous pamidoronate or oral alendronate markedly relieved bone pain, improved radiological findings, increased bone density and decreased bone turnover in children or adults with poly-FD (20,21). Ganda and Seibel reported that denosumab induced a rapid biochemical response and alleviated bone pain in two poly-FD patients in whom the efficacy of prior long-term bisphosphonate therapy was unsatisfactory (22). In the present case, we hypothesized that the increased cortical thickness of the proximal femur 1 year after embolization was the result of improved bone metabolism by denosumab, as well as of the spontaneous bone remodeling after the complete obliteration of the AVM.

In conclusion, we herein report a case of pure intraosseous AVM of the proximal femur in a patient with poly-FD. Non-surgical treatment by embolization and denosumab achieved a satisfactory result, which included complete obliteration of the AVM, increased cortical thickness of the proximal femur, and improvement of the high-turnover bone metabolism 1 year after embolization. Careful imaging review is crucial for distinguishing between bone tumors and intraosseous AVMs, which is characterized by the presence of signal voids and feeding arteries on MRI, in order to avoid unnecessary bone biopsy or surgery.

Glossary

Abbreviations

AVM

arteriovenous malformation

poly-FD

polyostotic fibrous dysplasia

Funding

No funding was received.

Availability of data and materials

All the data analyzed in this case are available from the corresponding author on reasonable request.

Authors' contributions

SO, MY, YI participated in the treatment of the patient including pharmacotherapy and surgery. FT performed arterial embolization on the patient. All the authors have read and approved the final version of this manuscript.

Ethics approval and consent to participate

Not applicable.

Patient consent for publication

We received patient consent for the publication of the case details and any associated laboratory data and images.

Competing interests

The authors declare that they have no competing interests.