The patient was referred to our Hospital with a 6-month history of a painless swelling on the right thigh, associated with march disturbance. Upon physical examination, a firm mass was palpable on the anterior surface of the thigh. The patient denies traumatic events, weight loss or other associated signs/symptoms.
Antero-posterior and lateral plain radiography revealed an excentric lesion (7cm) on the distal antero-lateral femoral diaphysis, with spiculated periosteal reaction (fig.1).
On T1 –weighted MRI (fig.2) and FS T2–weighted MRI (fig.3) the distal antero-lateral femoral diaphysis showed a cortical lesion, measuring 6, 8x4, 6x2cm. This lesion presented peripheral high signal intensity on FS T2–weighted MRI. Central smaller foci of lower intensity were observed on both sequences. There was no intramedullary invasion. There were no skip lesions.
On CT scan (fig.4) there was calcified matrix extending into a low attenuation heterogeneous mass. There was an image suggestive of spiculated periosteal reaction. There was no evidence of intramedullary invasion.
The histological examination showed a low-grade neoplastic proliferation area, consistent with a superficial osteosarcoma (OS), according to clinical and radiological features. Histopathologic findings of surgical specimen (14 cm of distal femur) have confirmed to be a low-grade parosteal osteosarcoma.
Surface OS constitute 4-10% of all osteosarcomas and have been subdivided in parosteal, periosteal and high grade surface OS.
Parosteal OS is the most common type of surface OS, accounting for 5% of all OS cases. It is seen in patients in their 3rd to 4th decades, with a female predominance. The tumor usually occurs in the metaphyses of long bones, characteristically affecting the posterior aspect of the distal femur. These lesions have an excellent prognosis. The classic appearance is a lobulated and exophytic mass adjacent to the bone, with central dense ossification, sharply delineated from the peripheral soft tissues, and cortical thickening. There is often a cleavage plane separating the tumor and adjacent normal cortex (string sign) that corresponds histologically to the periosteum interposed. The lesion arises on the outer fibrous layer of the periosteum, virtually never provoking a periosteal reaction. At MRI the ossified tumour is predominantly low in signal intensity on both T1- and T2-weighted images, similar to the appearance of the cortex. When the lesion is predominantly high in T2 signal intensity, the tumor is more likely to be of high grade.[1][2][3]
Periosteal OS has a peak incidence during the 2nd decade of life. These tumors show a strong predilection to arise in the diaphysis. These lesions are intermediate to high-grade and prognosis is usually worse than parosteal OS. Common radiological findings include a broad-based soft tissue mass, cortical thickening and extrinsic scalloping of the cortex, with periosteal reaction, often extended perpendicularly from the inner cortex. Hyperintensity on T2-weighted MRI and low attenuation on CT image are consistent with its cartilaginous component. In fact, histopathologically, the tumour is predominantly chondroid matrix with moderate cellularity, and reveals a large amount of cartilage matrix undergoing calcification, with areas of moderately differentiated osteoblastic osteosarcoma (osteoid formation). Invasion into the medullary canal is considered rare and needs to be distinguished from areas thought to represent reactive changes. This point is very important in directing the extent of surgical resection [1][2][3].
High-grade surface OS is rare and commonly involves metaphyses and diaphysis of long bones, especially femur. The prognosis is similar to that of conventional OS. High-grade surface OS presents dense ossification, bone destruction and periosteal reaction in the majority of cases. This tumour is often difficult to distinguish from periosteal OS. However, it usually surrounds a much higher percentage of bone circumference and is more likely to invade the medullary canal [1][2][3].
Parosteal Osteosarcoma
Based on the provided X-ray, MRI, and CT images of the lower limb, a significant mass is observed in the anterior soft tissue area of the right thigh. The main characteristics are as follows:
Combined with the patient's medical history (62-year-old female, 6 months of painless swelling, no obvious history of trauma or weight loss) and the imaging characteristics, the following diagnoses are considered:
In summary, taking into consideration the patient's age, sex, a gradually enlarging painless mass, and imaging findings of dense ossification with exophytic growth, along with a relatively clear boundary between the lesion and the cortex, the most likely diagnosis is:
Parosteal Osteosarcoma.
For a definitive diagnosis, a pathological biopsy is recommended to further clarify the histological grade and specific characteristics of the tumor.
Treatment Strategy:
Rehabilitation and Exercise Prescription:
A gradual rehabilitation program after treatment (especially surgery) is crucial. The following is recommended:
Guided by the FITT-VP principle (frequency, intensity, time, type, progression, and individualization), it is suggested to start with training three to four times per week at a tolerable or light-to-moderate intensity for about 20-30 minutes each time, and then gradually increase the duration and intensity as rehabilitation progresses. If the patient has reduced bone density or lower cardiopulmonary function, initial loads should be decreased, and close communication with the primary physician and rehabilitation specialist is essential. Periodic imaging follow-up is also recommended.
This report provides a reference medical analysis and should not replace a face-to-face consultation or the advice of a professional medical institution. Specific treatment regimens should be formulated by the patient in consultation with specialist physicians, taking into account individual circumstances.
Parosteal Osteosarcoma