Aneurysmal bone cyst primary. About eight pediatric cases: Radiological aspects and review of the literature
Meryem Boubbou, Karima Atarraf, Lamiae Chater, Abderrahmane Afifi, Siham Tizniti
Received: 07 Oct 2012 - Accepted: 06 May 2013 - Published: 28 Jul 2013
Domain: Clinical medicine
Keywords: Bone cyst, aneurysm, osteolytic lesion
©Meryem Boubbou et al. Pan African Medical Journal (ISSN: 1937-8688). This is an Open Access article distributed under the terms of the Creative Commons Attribution International 4.0 License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Cite this article: Meryem Boubbou et al. Aneurysmal bone cyst primary. About eight pediatric cases: Radiological aspects and review of the literature. Pan African Medical Journal. 2013;15:111. [doi: 10.11604/pamj.2013.15.111.2117]
Available online at: https://www.panafrican-med-journal.com/content/article/15/111/full
Aneurysmal bone cyst primary. About eight pediatric cases: Radiological aspects and review of the literature
Aneurysmal bone cyst primary. About eight pediatric cases: radiological aspects and review of the literature
Meryem Boubbou1,&, Karima Atarraf2, Lamiae Chater2, Abderrahmane Afifi2, Siham Tizniti1
1Department of Radiology, CHU Hassan II, Fez, Morrocco, 2Department of Pediatric Surgey, CHU Hassan II, Fez, Morrocco
Meryem Boubbou, Lot Oued El Makhazine, S4, N° 2, 60000, Oujda, Morocco
The aneurysmal bone cyst is a pseudotumoral lesion that can take several aspects. This is a rare lesion representing 1% of bone tumors. It appears usually during the first 30 years of life. The pathogenesis is that of a process of "dysplasia/hyperplasia" favored by a deficiency circulatory and hemorrhage within the lesion and the phenomena of osteoclasis. The objective of this work is to illustrate with analysis the specific forms and atypical aneurysmal bone cyst which often pose a diagnostic challenge requiring radiological investigation with histological confirmation. We report eight cases pediatric of aneurysmal cysts collected over a period of 3 years, 3 boys and 5 girls. All patients had standard radiographs. MRI was performed in three patients. The diagnosis was confirmed histologically. The atypia has been in the seat: fibula (1 case), metaphyseal (2 cases), diaphyseal (4 cases) and metatarsal (1 case). The aneurysmal bone cyst is a rare benign tumor with predilection affecting the metaphysis of long bones. Atypical forms even fewer are dominated by the atypical seat.
Aneurysmal bone cysts (ABC) are nonneoplastic expansile lesions that may exist as a primary bone cyst or as a secondary lesion arising from other osseous conditions such as giant cell tumors or unicameral bone cysts . The peak age of occurrence is in the second decade of life; approximately 80% occur within the first two decades.
The long bones (especially the tibia and femur) and vertebrae are the most common sites. However, aneurysmal bone cysts may occur in any bone. The male to female ratio is 1 to 1.3. Pain is the most common clinical symptom at presentation. Local swelling may develop as the lesion increases in size. Occasionally, the patient may present with a pathologic fracture within the aneurismal bone cyst where the cortex is compromised. Major radiographic features include dilated or aneurysmal cystic expansion of the involved bone with no significant matrix mineralization. The lesion tends to affect the metaphyses of long bones and the dorsal elements of the vertebrae. Sclerotic rims with periosteal new bone formation are common. The radiographic differential diagnosis includes unicameral bone cysts, giant cell tumors, osteosarcoma, and osteoblastoma (in vertebral lesions). The diagnosis must be based on histopathologic evidence . Local recurrence rate after classic surgical procedures (curettage and grafting) is about 11.8%-30.8%  The purpose of this article is to show some unusual atypical head of pathology and a review of the literature.
Patients: From 2008 to 2011, eight patients were treated for ABCs of long and flat bones at Hassan II Hospital by means chirurgical. The following data were collected retrospectively by one author (K.A): patient age, sex, symptoms, osseous location, and type of treatment, treatment outcome, pathologic findings, and complications.
ABC Typing and Staging: All patients had undergone initial conventional radiography. Three of them had an MRI. Surgical biopsy with histologic examination was performed for all patients for confirmed diagnostic.
Imaging: In radiography, the appearance was typical with the presence of a lesion lytic fan, responsible for a thinning of the cortex compared associated with thin walls intra-lesional (Figure 1, Figure 2, Figure 3). In MRI, the lesion is of heterogeneous signal containing a liquid level, with partitions sometimes taking the contrast (Figure 4, Figure 5, Figure 6).
Treatment procedure: Treatment consists mainly of surgical treatment which currently represents the treatment of choice. In most large series, the percentage of local recurrence after curettage Conventional is approximately 20%. In our series, all patients were operated without recurrence described so far.
Eight patients (3 boys and 5 girls) were treated. Mean age at presentation was 10.3 years (range, 3-15 years). Symptoms at presentation included pain (8 patients) and pathologic fracture (four patients). Osseous locations were the proximal femur in one patient, proximal tibia in one, distal tibia in one, distal fibula in one, diaphyseal humerus in three, and metatarsal in one. All our patients were operated on. The surgical procedure consisted of curettage with bone replacement and plugging. The postoperative course was uneventful with almost complete radiographic healing (Figure 7).
ABCs represent approximately 1% -2% of all primary bone lesions that are sampled for biopsy , with a slight female preponderance, a male-to-female ratio of 1 - 1.04 and a median patient age of 13 years in large studies [5, 6]. In the present study, the median age was 9.6 years at presentation.
ABCs are most commonly found in the metaphysis of long tubular bones [5,7-9]. Many theories have been postulated as to the etiology of these lesions, such as dynamic vascular changes within a newly formed part of the immature skeleton, with the possibility of some cases arising from preexisting bone lesions. This vascular change causes increased venous pressure, dilated vascular beds or thrombosis, or an arteriovenous fistula. The engorged vascular bed can lead to rapid resorption of spongy bone and erosion of cortical bone [6, 8, 9].
Essadki et al  hypothesize that ABCs are caused by the opposed direction of periosteal and medullary blood circulation. ABCs pass through different stages of development as part of their natural progression. The first stage consists of an early osteolytic lesion. The lesion then progresses into a mature characteristic cyst that eventually evolves into a late or calcified stage. Progression of ABCs is variable. They may have aggressive growth or grow slowly. They eventually mature and rarely undergo spontaneous regression [6, 11, 12].
CT can be helpful in the differentiation of ABCs from unicameral bone cysts when showing fluid-fluid levels within the cystic cavity, a finding nonspecific to but suggestive of ABC. Magnetic resonance imaging findings may also be highly suggestive of an ABC when a segmented, expansile, multiseptated lesion with fluid-fluid levels is demonstrated. Bone scintigraphy with technetium 99m typically shows a photon-deficient area with a rim of increased uptake [6, 8].
The high recurrence rate of ABCs indicates the need for new therapeutic modalities. Surgical treatment consists of excision of the lesion by means of curettage-with or without packing of bone chips-or en bloc resection. About 70% of ABCs show spontaneous ossification after intracapsular curettage. Marginal extracapsular excision is the treatment of choice, especially for recurrent lesions. Treatment of secondary lesions is directed against the underlying primary lesion . Vergel De Dios et al  reported a 20% recurrence rate after curettage with or without bone grafting, usually within the first 2 postoperative years.
A local recurrence rate of 20% after curettage alone was reported by Campanacci et al . The recurrence rate is increased in patients with a mitotic index greater than 7, patients who undergo curettage treatment alone (although repeat curettage usually provides a lasting cure), younger patients (<15 years old), patients with smaller lesions (<5 cm in diameter), and patients who have undergone surgery within 2 years. Patient sex, preoperative duration of symptoms, and lesion location do not seem to affect recurrence rate .
Always think of an aneurysmal bone cyst to a tumor metaphyseal front fan 20. Should always seek a traumatic background and never forget to seek an underlying lesion (secondary ABC).
The authors declare no competing interests.
All the authors have equally contributed to the write up of this manuscript and have read and approved the final version of the manuscript.
Figure 1: Radiograph showing an osteolytic lesion of the head of the fibula associated with intralesional few thin walls
Figure 2: Radiograph showing an osteolytic lesion well demarcated from the lower end of the tibia containing the partitions associated with a spiral fracture
Figure 3: radiograph showslesion osteolytic very limited of the upper end of tibia
Figure 4: radiography (A) showing an osteolytic lesion oval metaphyseal tibial very limited. Cuts MRI sagittal T1-weighted (B), coronal T2 (C) and T1 post contrast (D) and axial T2 FATSAT (E) showing the partitions after intralesional contrast enhanced liquid level typical of an aneurysmal cyst
Figure 5: radiography (A) showing a multiloculated osteolytic lesion metatarsal very limited. Cuts sagittal T1-weighted MRI (B), axial T2 (C) and FAT SAT T1 after contrast (D) showing an enhancement of intralesional walls with liquid level
Figure 6: radiography (A) showing a lesion osteolytic multiloculated diaphyseal humeral fracture very limited. Cuts MRI T2 sagittal (B) Coronal T1 Fat Sat after contrast (C) showing a cystic lesion fractured in the center with peripheral enhancement. The child received surgical treatment (D)
Figure 7: radiography (A) showing a lesion osteolytic multiloculated diaphyseal humeral very limited. The child was given a plug-curettage (B). Images C and D showing a lesion osteolytic multiloculated diaphyseal humeral fracture very limited. The child received a pinning (D)
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