Aneurysmal bone cyst of the rib: a case report
© Yasaroglu et al.; licensee Cases Network Ltd. 2009
Received: 9 March 2008
Accepted: 22 January 2009
Published: 9 September 2009
An aneurysmal bone cyst is a benign, but expansile tumor like lesion that generally occurs in the long bones including the vertebral column. An aneurysmal bone cyst arising from the rib, especially in the elderly, is extremely rare.
We report a 58-year-old Turkish woman with an aneurysmal bone cyst of the right 3rd rib treated with chest wall resection. The pathologic findings confirmed the diagnosis of aneurysmal bone cyst. The patient has been followed up for 5 years with no evidence of recurrence.
En bloc resection can be curative and provide good results for this rare type of chest wall tumor.
Aneurysmal bone cyst (ABC) was first reported by Jaffe and colleagues in 1942. They used this term to describe the "blow out" radiographic appearance and blood filled contents of the cystic spaces . ABC is a non-neoplastic bone tumor that occurs predominantly in children and young adults, mainly involving the long bones and the vertebrae . ABC occurring as a primary rib tumor is unusual, especially in the elderly -. We report a case of ABC of the right 3rd rib treated with chest wall resection.
A 58-year-old Turkish woman was admitted to our hospital complaining of pain from a swelling on the right side of her chest for the previous 4 years. She had no history of trauma and her past medical history was unremarkable. Physical examination revealed a 10 cm × 7 cm tender palpable mass in the midaxillary line with otherwise normal findings.
Primary rib neoplasms are uncommon. They comprise 5% to 7% of all primary bone tumors [2, 4]. ABC presenting as a primary rib tumor is very rare. It is a benign, progressive tumor that comprises 1.3% of all primary bone tumors . It may involve any bone, mostly the spine and the long bones but localization in the ribs is unusual [2, 3]. ABC has been observed in every rib except the lower three . The age of our patient is unusual for ABC since it is extremely rare in the elderly. Approximately 80% of ABC occurs in patients who are younger than age 20. There is no race or sex predominance .
ABC is not a true cyst or aneurysm . The etiology is unknown but circulatory disturbance due to arteriovenous malformation is widely accepted [2, 5, 6]. Grossly, the lesion consists of a paper-thin cortex and multiple blood filled cavities. Microscopically, the patient had a primary ABC with no additional bone tumor. The lesion should be designated as a primary ABC if it has a uniform histological pattern or as a secondary ABC if the lesion contains another bone tumor such as fibrous dysplasia, non-ossifying fibroma, osteoblastoma or chondromyxoid fibroma . The patient was symptomatic with complaints of pain and swelling. About 29% of reported cases have been found incidentally by a routine chest X-ray. Dyspnea, paraplegia and pathologic fractures are less frequent symptoms .
The typical radiographic appearance of ABC is that of an eccentric, lytic, "blow out" type of lesion, demarcated by a thin shell of subperiosteal new bone [1, 6]. There is often expansion into the adjacent soft tissues. Computed tomography and magnetic resonance imaging (MRI) are useful in the diagnosis of ABC. We evaluated the patient with CT scans. The appearance of multiple cavernous spaces filled with fluid levels on CT scans was suggestive of ABC. The expansion of ABC into the adjacent intercostal muscle indicated an aggressive stage. However, it should be emphasized that the radiographic appearance is not sufficiently specific to establish a definitive diagnosis. Radiological differential diagnosis should include: giant cell tumor, plasmocytoma, chondromyxoid fibroma, chondrosarcoma, fibrous dysplasia, and metastasis .
Once the lesion is diagnosed, treatment should be initiated as soon as possible since local extension and rapid growth can cause pathologic fractures, paralysis due to spinal cord compression, compression of the vital organs and malignant transformation [4, 6]. The current methods of treatment include curettage bone grafting, curettage and cryosurgery, radiation, or en bloc resection . The treatment of choice is complete excision of the rib involvement of ABC. Other treatment modalities result in a higher recurrence rate . FNAC and radiological evaluation suggested a benign pathology in our patient. The lesion was resected along with adjacent ribs to avoid recurrence. Complete resection offers the best chance for cure in both benign and malignant lesions of the chest wall. Incomplete resection of ABC may result in rapid recurrence [6, 7]. Reconstruction with double-layered Prolene mesh (Ethicon) provides good functional results. No further treatment was required in our patient and she was healthy with no recurrence observed after 5 years of follow up.
ABC is a rare, benign pathology, which should be considered in the differential diagnosis of chest wall tumors. Complete surgical excision can be the best treatment for cure.
Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
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