Secondary jaw aneurysmal bone cyst (<scp>JABC</scp>) – a possible misnomer? A review of literature on secondary <scp>JABC</scp>s, their pathogenesis and oncogenesis

Arora, Saryu; Paul, Samrity; Arora, Sunil; Kapoor, Varun

doi:10.1111/jop.12132

Cited by 14 publications

(15 citation statements)

References 39 publications

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“…This varies remarkably varies from Triantafillidou et al research (50%) ( 1 ). Arora et al ( 49 ) reported a result of 14.8% secondary ABC. Besides, Sun et al reported an incidence of secondary JABCs of 76.5% with a detailed presentation of 17 JABC patients, which indicted that most secondary JABCs are lesions where the primary disease has been completely overlapped with aneurysmal change ( 50 , 51 ).…”

Section: Discussionmentioning

confidence: 96%

Clinicopathology and Recurrence Analysis of 44 Jaw Aneurysmal Bone Cyst Cases: A Literature Review

2021

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In the past half-century, considerable attention has been paid to oral and maxillofacial skeletal cyst, however, aneurysmal bone cyst (ABC), unlike other common bone diseases, still contours numerous unanswered questions in terms of classification, etiology and pathological mechanism. The purpose of this article was to evaluate the proportion of primary ABC and secondary ABC, and to assess the recurrence of ABC and related factors. A methodical search of Embase, MEDLINE, Cochrane Library, Web of Science was conducted for well-documented jaw aneurysmal bone cyst (JABC) cases. One hundred thirty-one articles were identified after database searching and 31 of them were included in our study for further research with 44 JABC cases. All the articles were analyzed by two separate authors. About 25% of the reported jaw aneurysmal bone cyst was secondary. Both the pathological classification and surgical treatment had a significant influence on recurrence rate (P = 0.0082, P = 0.0022), while patients' age or radiographic features rarely affected prognosis. Jaw aneurysmal bone cysts can present variable clinical and histological presentations. Recurrence may be attributed to omittance of underlying potential blood supply or conservative surgical protocol.

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Section: Discussionmentioning

confidence: 96%

Clinicopathology and Recurrence Analysis of 44 Jaw Aneurysmal Bone Cyst Cases: A Literature Review

2021

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“…Aneurysmal bone cyst secondary to giant cell tumor mostly occurs in patients of 20 to 40 years [12]. Recent studies suggest that secondary aneurysmal bone cysts may be related to factors such as hyperemia and dilatation of the vascular bed [13] or induced vascular bed caused by arteriovenous malformation of primary lesions [14]. Patients often present with intermittent pain, soft tissue mass, limited joint activity, etc.…”

Section: Discussionmentioning

confidence: 99%

Huge aneurysmal bone cyst secondary to giant cell tumor of the hand phalanx: a case report and related literature

Gan

Shi

et al. 2020

BMC Cancer

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Background: Aneurysmal bone cyst (ABC) secondary to Giant Cell Tumor of bone (GCT) is a rare lesion, of which the incidence is about 0.011 to 0.053 per 100,000 every year. There are only a few previous case reports, and most of them occur in the spine, long bones or flat bones. Case presentation: We report one case of a patient who complained of "progressive enlargement of the mass on right-hand fifth finger for 5 years with ulceration for 6 months". After the imaging examination in our hospital, it was diagnosed as a "huge bone tumor on the proximal phalanx of the right-hand fifth finger", then wide excision and amputation of the fifth finger were made. The pathological examination diagnosed the mass as aneurysmal bone cyst secondary to giant cell tumor, 13 × 8 × 6 cm 3 , with no local infiltration observed. No recurrence and metastasis occurred 18 months after the operation, and the patient recovered well. Conclusion: In this report, we discuss the etiology, diagnosis, differentiation, and management of Aneurysmal bone Cyst secondary to Giant Cell Tumor of bone, and review previous case studies.

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“… 8 The origin of secondary ABC is probably attributed to trauma or to a local vascular abnormality in a pre-existing bone lesion. 4 , 5 It is proposed that there is an initial focal myxoid change in the stroma of JOF followed by hemorrhage and amassing of osteoclastic giant cells which leads to gradual expansion and formation of a cyst. 7 Another proposed notion states that intercellular edema in the primary bone lesion with loose unsupported stroma might initiate microcyst formation, into which blood is pooled under hemodynamic pressure via rupture of blood vessels, leading to secondary ABC formation.…”

Section: Discussionmentioning

confidence: 99%

“…In the jaws, the incidence of secondary ABC is reported to be 14.8% and frequently associated with ossifying fibromas. 4 , 5 The fact that JOF associated with secondary ABC cases presents with greater aggressive growth potential and higher recurrence rate adds to its clinical significance. 6 In view of that, the present report describes a case of recurrent PsJOF with secondary ABC in a young patient along with a comprehensive review of similar published case reports in the English literature.…”

Section: Introductionmentioning

confidence: 99%

Recurrent Juvenile Psammomatoid Ossifying Fibroma with Secondary Aneurysmal Bone Cyst of the Maxilla: A Case Report and Review of Literature

Sarode

Ingale³

et al. 2018

Clinics and Practice

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Juvenile ossifying fibroma is a benign fibro-osseous lesion commonly affecting the extra-gnathic craniofacial skeleton of the young individuals. The psammomatoid and trabecular variants are its two histopathological subtypes having distinctive clinico-pathological characteristics. Secondary aneurysmal bone cysts are frequently reported to arise in the pre-existing fibro-osseous lesions but rarely reported in the psammmomatoid variant of the juvenile ossifying fibroma. Such hybrid lesions, especially massive in size, tend to exhibit a greater aggressive growth potential and higher recurrence rate and mandate complete surgical removal of the lesion along with a long-term follow-up. The objective of this case report was to present a rare incident of recurrent psammomatoid ossifying fibroma associated with a secondary aneurysmal bone cyst in the maxillary jaw bone of a young patient and review the similar published reports in the English literature.

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Secondary jaw aneurysmal bone cyst (JABC) – a possible misnomer? A review of literature on secondary JABCs, their pathogenesis and oncogenesis

Cited by 14 publications

References 39 publications

Clinicopathology and Recurrence Analysis of 44 Jaw Aneurysmal Bone Cyst Cases: A Literature Review

Clinicopathology and Recurrence Analysis of 44 Jaw Aneurysmal Bone Cyst Cases: A Literature Review

Huge aneurysmal bone cyst secondary to giant cell tumor of the hand phalanx: a case report and related literature

Recurrent Juvenile Psammomatoid Ossifying Fibroma with Secondary Aneurysmal Bone Cyst of the Maxilla: A Case Report and Review of Literature

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