Interest of targeted computed tomography guided by scintigraphy in the diagnosis of an osteoid osteoma of the talus: A surgical case report.

INTRODUCTION AND IMPORTANCE: Osteoid osteoma is a benign primary bone tumor with a predilection for the long bones and vertebrae, presenting a unique challenge when occurring in rare locations such as the talus, accounting for 5 to 8 % of cases. Early imaging struggles to detect its nidus, leading to diagnostic delays, especially when atypical symptoms and previous trauma complicate clinical presentations. This case report illustrates the diagnostic challenges and emphasizes the importance of targeted computed tomography (CT) guided by scintigraphy in diagnosing osteoid osteoma of the talus. CASE PRESENTATION: A 23-year-old male presented with chronic left ankle pain spanning three years, with a history of previous trauma. Initial evaluations including standard radiology and magnetic resonance imaging (MRI) suggested algodystrophy of the talus and tenosynovitis, but failed to identify the osteoma. Persistent pain led to further investigation with bone scintigraphy, revealing hyperfixation indicative of partial algodystrophy. Targeted CT scans focused on the scintigraphy-identified area ultimately revealed an osteoid osteoma's nidus, enabling successful surgical intervention and symptomatic relief. DISCUSSION: The diagnosis of osteoid osteoma in the talus is frequently delayed due to its atypical presentation and rare occurrence. Traditional imaging techniques may overlook the tumor's nidus, underscoring the necessity for targeted diagnostic approaches. This case demonstrates the value of integrating scintigraphy with targeted CT to enhance early diagnosis and treatment planning, contrasting with the limited diagnostic yield of MRI and underscoring CT's superiority for nidus detection. CONCLUSION: Osteoid osteoma of the talus poses significant diagnostic challenges. This case report highlights the utility of scintigraphy-guided targeted CT in identifying the nidus and facilitating prompt surgical management, advocating for a multidisciplinary approach to atypical ankle pain, especially in patients with a history of trauma.

Floating patella: Ipsilateral and simultaneous rupture of the quadriceps and patellar tendons in a young individual (a surgical case report).

INTRODUCTION AND IMPORTANCE: The phenomenon of a floating patella or ipsilateral bifocal rupture of the extensor apparatus is an extremely rare injury, with few cases reported in the literature. The aim of this case study is to report an unprecedented event: the simultaneous trans-tendinous rupture of both quadriceps and patellar tendons in a young adult without predisposing factors, emphasizing the need for awareness in diagnosis and management, and suggesting a new avenue for research in prevention and rehabilitation. CASE PRESENTATION: We report the case of a 35-year-old patient with no significant medical history, who experienced this injury following a sudden start in a sprint without prior warm-up. The clinical examination revealed a swollen, painful knee with active extension deficit, patellar ascent, and a sub patellar hiatus. Magnetic Resonance Imaging (MRI) confirmed a trans-tendinous rupture of both the patellar and quadriceps tendons. CLINICAL DISCUSSION: Tendon repair was performed using end-to-end sutures and a figure-8 reinforcement with the semitendinosus tendon, along with gracilis plastie to strengthen the patellar tendon repair. This methodological approach is discussed in the context of its effectiveness and potential implications for future surgical management of similar injuries. CONCLUSION: After a 12-month follow-up, the patient exhibited highly satisfactory results, resuming both professional and sporting activities. To our knowledge, this is the first published case of a trans-tendinous rupture of the extensor apparatus tendons. This observation serves as a reference in understanding the mechanism and surgical management of such lesions, emphasizing the need for further research and clinical vigilance in similar cases.

Juxta articular myxoma of the foot: An exceptional entity.

INTRODUCTION: Myxoma, a benign and uncommon tumor, is primarily characterized by undifferentiated spindle cells and a myxoid matrix with muscular infiltration. While the intramuscular form is predominant, the juxta-articular variant is rare, especially in the foot. Juxta-articular myxomas had a heightened risk of recurrence post-surgical excision, emphasizing the need for effective management strategies. CASE PRESENTATION: We report the first description in the literature of a myxoma in the foot with bone invasion in a 59-year-old male with a ten-month history of a progressively enlarging antero-internal swelling near the base of the first metatarsal in the left foot. Clinical examination and imaging revealed erosive changes in the bone, prompting excision-curettage. Histopathological examination confirmed the presence of a juxta-articular myxoma, an exceptionally rare localization. The patient exhibited satisfactory outcomes at the 13-month follow-up. DISCUSSION: Myxomas, primarily occurring around the knee, are infrequently found in the foot, with juxta-articular presentation being exceptionally rare. Traumatic causes and osteoarthritis are debated etiopathogenic factors. Radiologically, bone involvement is atypical, and magnetic resonance imaging aids in diagnosis. Treatment involves surgical excision, often requiring additional procedures. Juxta-articular myxomas, despite sharing characteristics with intramuscular myxomas, are distinguished by location and a higher recurrence rate. CONCLUSION: This case contributes to the limited literature on myxomas localized in the foot, particularly with bone invasion. Histological diagnosis is crucial, and surgery is the mainstay of treatment despite the substantial recurrence risk. This report underscores the importance of vigilance in managing myxomas, especially in rare anatomical presentations, and advocates for ongoing research to enhance understanding and therapeutic approaches.

Irreducible posterolateral knee dislocation: Diagnostic challenges and management (a surgical case report).

INTRODUCTION AND IMPORTANCE: Posterolateral knee dislocations are rare, complex injuries predominantly resulting from high-energy trauma. They present significant diagnostic and therapeutic challenges, crucial for maintaining long-term knee function and stability. CASE PRESENTATION: We report the case of Mr. Y.G., a 34-year-old male who suffered a left knee posterolateral dislocation due to a motorcycle accident. Clinical examination and imaging revealed a valgus deformity, swelling, ecchymosis, and a persistent medial joint line groove. The injury was classified based on NEYRET et al. criteria and 2008 SOFCOT standards. Surgical intervention involved repairing medial structures and applying a femoro-tibial external fixator. Radiographic and MRI findings confirmed a complete capsuloligamentous rupture and chondral injury of the lateral condyle. CLINICAL DISCUSSION: This case exemplifies the critical need for rapid radiological evaluation and tailored surgical interventions in managing posterolateral knee dislocations. It also demonstrates the effectiveness of using established classification systems for treatment planning and prognostic prediction. CONCLUSION: Timely and suitable management is essential for successfully treating posterolateral knee dislocations. Utilizing recognized classification systems plays a key role in guiding management decisions and improving patient outcomes, ensuring optimal recovery and knee functionality.

A rare occurrence of a giant synovial sarcoma in the plantar region of the foot: A case report.

Introduction and Significance. Synovial sarcoma, accounting for 7-8 % of malignant sarcomas, typically manifests in adulthood, but it is noteworthy that adolescents and children make up 30 % of reported cases. Contrary to its name, this malignancy often originates from multipotent stem cells rather than the synovium. This report highlights a rare case involving a 23-year-old male with a localized synovial sarcoma in the plantar region, underscoring the importance of recognizing radiological signs for an accurate diagnosis. CASE PRESENTATION: A 23-year-old male, a chronic smoker, presented with a 5-year history of a mass on the plantar region of the right foot. Following an excision biopsy, the tumor recurred after two years, significantly impacting mobility. Radiological imaging revealed a cloud-like soft tissue mass. Surgical biopsy confirmed biphasic synovial sarcoma. A multidisciplinary consultation guided the decision for transtibial amputation and adjuvant chemotherapy. Postoperatively, the patient experienced a superficial infection, effectively treated, with subsequent positive outcomes and successful prosthetic adaptation. DISCUSSION: Synovial sarcoma, a rare and aggressive soft tissue malignancy, predominantly affects young individuals and often develops peri-articularly, presenting diagnostic challenges. Imaging modalities, particularly MRI, play a pivotal role in diagnosis, showcasing characteristic features. The primary treatment involves surgical intervention, with chemotherapy and radiotherapy contributing to local control. Despite advancements, recurrence rates remain significant, necessitating vigilant follow-up. CONCLUSION: Synovial sarcoma of the extremities is characterized by insidious progression and a high metastatic risk. MRI, while nonspecific, is indispensable for diagnostic orientation, later confirmed through histological examination. Surgery remains the mainstay therapy, with radiotherapy and chemotherapy contributing to enhanced local control. The awareness of this rare malignancy and its diagnostic and therapeutic nuances is crucial for optimal patient management and outcomes.

A remarkable and aggressive aneurysmal bone cyst ravaging the femoral shaft, advancing to lung metastases: An extremely rare case.

INTRODUCTION AND IMPORTANCE: Aneurysmal bone cysts (ABCs) are relatively uncommon tumor-like lesions that require careful management. Reporting such cases is crucial to highlight the importance of understanding the physiopathology and treatment options associated with ABCs. Literature-based writing emphasizes the significance of reporting cases like the one presented here. The aneurysmal bone cyst, classified as a Tumor Rich in Giant Cells according to the latest World Health Organization (WHO) classification of soft tissue and bone tumors, has posed several hypotheses and challenge. This aggressive form and rare localization of this lesion necessitates thorough discussions regarding its management. CASE PRESENTATION: We present a compelling case of a 37-year-old patient, without any specific pathological history, with a giant diaphyseal aneurysmal bone cyst located in the right femur. Remarkably, the lesion had been progressing for a decade, leading to extensive destruction of the entire femoral diaphysis despite undergoing previous surgical interventions. The patient's unique circumstances highlight the unpredictable behavior and destructive potential of aneurysmal bone cysts in rare anatomical locations. DISCUSSION AND CONCLUSION: This case underscores the need for a comprehensive understanding of aneurysmal bone cysts and their management. The utilization of denosumab, an inhibitor of the RANK/RANKL system, as a medical treatment in conjunction with surgery resulted in a favorable therapeutic response, including a reduction in tumor mass. The current WHO classification, recognizing ABCs as Tumors Rich in Giant Cells, consolidates previous hypotheses and enables the development of new therapeutic protocols. The integration of surgery and medical treatment holds promise for improving outcomes in patients with aneurysmal bone cysts. In conclusion, advancements in understanding the physiopathology and treatment options are crucial for developing effective therapeutic protocols to these aggressive forms of ABCs.

Intra-articular lipoma arborescens of the knee: A report of two cases with bilateral localization.

INTRODUCTION: Lipoma arborescens is a very rare pseudo-tumoral lesion of unknown etiology, characterized by lipomatous infiltration of subsynovial stroma, bilateral involvement is exceptional, only eight cases are reported in the literature. PRESENTATION OF CASE: We report the very rare case of two men presented at our department with complaints of swelling of both knees and intermittent joint effusion, Surgical biopsy revealed Lipoma arborescens in both cases. Open total synovectomy was performed. Follow-up evaluation showed no signs of recurrence. DISCUSSION AND CONCLUSION: Lipoma arborescens is a rare entity, the unilateral form affecting the knee is the most common, with a predilection for suprapellar recess. Magnetic resonance imaging (MRI) is the examination of choice showing multiple villous proliferation of the synovium and fat-like cells, with a fatty signal on all sequences. Treatment by open or arthroscopic synovectomy offers the best outcomes.

Unusual localization of glomus tumor of the knee.

Glomus tumor is an uncommon benign neuromyoarterial tumor. The extradigital location at the knee is unusual. Ignorance of this disease characterized by atypical clinical signs and the absence of specific imaging are responsible for a significant diagnostic delay in these forms localized in the knee. Complete resection of the tumor results in an immediate resolution of the pain. We report three rare locations of glomus tumor in the knee with an exceptional location in the quadriceps tendon and discuss epidemiological, diagnostic and therapeutic aspects of these tumors.