Aneurysmal bone cyst

Aneurysmal bone cyst (ABC) is a non-cancerous bone tumor composed of multiple varying sizes of spaces in a bone which are filled with blood.[1][4] The term is a misnomer, as the lesion is neither an aneurysm nor a cyst.[5] It generally presents with pain and swelling in the affected bone.[1] Pressure on neighbouring tissues may cause compression effects such as neurological symptoms.[1]

Aneurysmal bone cyst
Other namesNot recommended: Giant cell reparative granuloma of small bone, giant cell lesion of small bones[1]
A. X-ray: osteolytic lesion in tibia near knee. B/C/D/E. MRI with E showing fluid levels.
SpecialtyOrthopedics[1]
SymptomsPain, swelling, pressure related neurological symptoms[1]
CausesUnknown[1]
Diagnostic methodMedical imaging: CT scan, X-ray, MRI, bone scan.[1]
Differential diagnosisTelangiectatic osteosarcoma[1]
TreatmentSurgery[2]
Prognosis20-70% recur after curettage.[1]
FrequencyRare,[3] ~0.15 cases per one million per year.[1] 80% age <20 years.[1] M=F[1]

The cause is unknown.[1] Diagnosis involves medical imaging.[1] CT scan and X-ray show lytic expansion lesions with clear borders.[1] MRI reveals fluid levels.[1]

Treatment is usually by curettage, bone grafting or surgically removing the part of bone.[2] 20–30% may recur, usually in the first couple of years after treatment, particularly in children.[2]

It is rare.[3] The incidence is around 0.15 cases per one million per year.[1] Aneurysmal bone cyst was first described by Jaffe and Lichtenstein in 1942.[5][6]

Signs and symptoms

The afflicted may have relatively small amounts of pain that will quickly increase in severity over a time period of 6–12 weeks. The skin temperature around the bone may increase, a bony swelling may be evident, and movement may be restricted in adjacent joints.[7]

Spinal lesions may cause quadriplegia and patients with skull lesions may have headaches.

Sites

Commonly affected sites are metaphyses of vertebra, flat bones, femur and tibia.[8] Approximate percentages by sites are as shown:

  • Skull and mandible (4%)
  • Spine (16%)
  • Clavicle and ribs (5%)
  • Upper extremity (21%)
  • Pelvis and sacrum (12%)
  • Femur (13%)
  • Lower leg (24%)
  • Foot (3%)

Causes

Aneurysmal bone cyst has been widely regarded a reactive process of uncertain cause since its initial description by Jaffe and Lichtenstein in 1942. Many hypotheses have been proposed to explain the cause and pathogenesis of aneurysmal bone cyst, and until very recently the most commonly accepted idea was that aneurysmal bone cyst was the consequence of an increased venous pressure and resultant dilation and rupture of the local vascular network. However, studies by Panoutsakopoulus et al. and Oliveira et al. uncovered the clonal neoplastic nature of aneurysmal bone cyst. Primary cause has been regarded arteriovenous fistula within bone.[9]

The lesion may arise de novo or may arise secondarily within a pre-existing bone tumor, because the abnormal bone causes changes in hemodynamics. An aneurysmal bone cyst can arise from a pre-existing chondroblastoma, a chondromyxoid fibroma, an osteoblastoma, a giant cell tumor, or fibrous dysplasia. A giant cell tumor is the most common cause, occurring in 19–39% of cases. Less frequently, it results from some malignant tumors, such as osteosarcoma, chondrosarcoma, and hemangioendothelioma.

Pathology

Micrograph of an aneurysmal bone cyst. H&E stain.

Histologically, they are classified in two variants.

  • The classic (or standard) form (95%) has blood filled clefts among bony trabeculae. Osteoid tissue is found in stromal matrix.
  • The solid form (5%) shows fibroblastic proliferation, osteoid production and degenerated calcifying fibromyxoid elements.

According to Buraczewski and Dabska, the development of the aneurysmal bone cyst follows three stages.[5]

StageDescription
Initial phase (I)Osteolysis without peculiar findings
Growth phase (II)
  • Rapid increase in size of osseous erosion
  • Enlargement of involved bone
  • Formation of shell around central part of lesion
Stabilization phase (III)Fully developed radiological pattern

They can also be associated with a TRE17/USP6 translocation.[10]

Aneurysmal bone cysts may be intraosseous, staying inside of the bone marrow. Or they may be extraosseous, developing on the surface of the bone, and extending into the marrow. A radiograph will reveal a soap bubble appearance.

Diagnosis

X-ray and CT scan show lytic expansion lesions with clear borders.[1] Expansion of cortex gives the lesion a balloon-like appearance. Larger lesions may appear septated.[11] MRI reveals fluid levels.[1] Bone scan shows outer radiotracer uptake, with a central dark area.[1][11]

Differential diagnosis

Following conditions are excluded before diagnosis can be confirmed:[12]

  • Unicameral bone cyst
  • Giant cell tumor
  • Telangiectatic osteosarcoma
  • Secondary aneurysmal bone cyst

Treatment

Curettage is performed on some people,[13] and is sufficient for inactive lesions. The recurrence rate with curettage is significant in active lesions, and marginal resection has been advised. Liquid nitrogen, phenol, methyl methacrylate are considered for use to kill cells at margins of resected cyst.[9]

Prognosis

20–70% recur after curettage.[1]

Epidemiology

It is rare.[3] The incidence is around 0.15 cases per one million per year.[1] 80% occur in people age less than 20 years.[1] It is second most common tumor of spine and most common benign tumor of pelvis in pediatric population.[9] Males and females are equally affected.[1]

Additional images

See also

References

  1. WHO Classification of Tumours Editorial Board, ed. (2020). "3. Bone tumours: simple bone cyst". Soft Tissue and Bone Tumours: WHO Classification of Tumours. Vol. 3 (5th ed.). Lyon (France): International Agency for Research on Cancer. pp. 437–439. ISBN 978-92-832-4503-2.
  2. "Bone tumours. What are Bone Tumours?". patient.info. Archived from the original on 24 April 2021. Retrieved 24 April 2021.
  3. Muratori, Francesco; Mondanelli, Nicola; Rizzo, Anna Rosa; Beltrami, Giovanni; Giannotti, Stefano; Capanna, Rodolfo; Campanacci, Domenico Andrea (10 November 2019). "Aneurysmal Bone Cyst: A Review of Management". Surgical Technology International. 35: 325–335. ISSN 1090-3941. PMID 31476792.
  4. Stevens, Kyle J.; Stevens, James A. (5 September 2020). "Aneurysmal Bone Cysts". StatPearls. StatPearls Publishing.
  5. Maroldi, Roberto (2005). Imaging in Treatment Planning for Sinonasal Diseases. Springer. pp. 114–116. ISBN 9783540266310.
  6. Tomasik, Patryk; Spindel, Jerzy; Miszczyk, Leszek; Chrobok, Adam; Koczy, Bogdan; Widuchowski, Jerzy; Mrozek, Tomasz; Matysiakiewicz, Jacek; Pilecki, Bolesław (September 2009). "Treatment and differential diagnosis of aneurysmal bone cyst based on our own experience". Ortopedia, Traumatologia, Rehabilitacja. 11 (5): 467–475. ISSN 1509-3492. PMID 19920289.
  7. Zadik, Yehuda; Aktaş Alper; Drucker Scott; Nitzan W Dorrit (2012). "Aneurysmal bone cyst of mandibular condyle: A case report and review of the literature". J Craniomaxillofac Surg. 40 (8): e243–8. doi:10.1016/j.jcms.2011.10.026. PMID 22118925.
  8. Rosai and Ackerman's surgical pathology, Volume 2, 9th ed. Mosby. 2004. p. 148. ISBN 9780323013420.
  9. Pediatric Orthopedics in Practice. Springer. 2007. pp. 151–155. ISBN 9783540699644.
  10. Ye Y, Pringle LM, Lau AW, et al. (June 2010). "TRE17/USP6 oncogene translocated in aneurysmal bone cyst induces matrix metalloproteinase production via activation of NF-kappaB". Oncogene. 29 (25): 3619–29. doi:10.1038/onc.2010.116. PMC 2892027. PMID 20418905.
  11. Davies, Arthur (2002). Who Manual Of Diagnostic Imaging: Radiographic Anatomy And Interpretation Of The Muskuloskeletal System, VOlume. World Health Organization. pp. 168–186. ISBN 9241545550.
  12. Differential Diagnosis in Surgical Pathology: Expert Consult - Online and Print, 2e. Elsevier Health Sciences. 2010. pp. 878–879. ISBN 9781416045809.
  13. Mankin HJ, Hornicek FJ, Ortiz-Cruz E, Villafuerte J, Gebhardt MC (September 2005). "Aneurysmal bone cyst: a review of 150 patients". J. Clin. Oncol. 23 (27): 6756–62. doi:10.1200/JCO.2005.15.255. PMID 16170183. Archived from the original on 2013-04-15.
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