RESUMEN
Congenital pseudarthrosis of the clavicle (CPC) is a rare disorder diagnosed at birth or early childhood presenting with a painless, non-tender mass on the clavicle. Its etiology is unknown, caused by failure of fusion of the medial and lateral ossification centers of the clavicle. Left-sided CPC is rare and linked to other pathological abnormalities. Bilateral involvement is extremely rare and it is seen in association with other congenital malformations. A full-term newborn baby girl was examined after a complicated emergency cesarean section delivery. Upon initial pediatric examination, there was suspicion of bilateral clavicle fracture with no limitation of movement and equal moro reflex bilateral. Plain radiographs of the clavicle revealed a suspected bilateral fracture of the clavicle. At the two-month follow-up, X-rays were taken to assess the clavicle fractures showing persistent bilateral clavicle deformities and there was no interval callus formation which confirmed the diagnosis of bilateral CPC and excluded the presence of the fracture. Bilateral pseudarthrosis of the clavicle is a rare entity, and surgical correction is not required unless the patient develops symptoms of limitations of movement or for aesthetic causes.
RESUMEN
Femoral intertrochanteric fractures can be occult and not visible on plain radiographs, even when there is a high clinical suspicion. This case study reports an occult intertrochanteric fracture that was diagnosed using a bone scan rather than an MRI or CT scan. A 91-year-old woman arrived at the emergency room with a complaint of left hip pain after slipping at home. Clinical examination revealed tenderness, mild swelling, limited range of motion, and an inability to bear weight. Radiographs and CT scans of the hip and pelvis showed no evidence of a fracture. An MRI was planned, but the patient's agitation resulted in improper images. Consequently, a bone scan identified an ill-defined focal area with slightly increased activity, consistent with an intertrochanteric femur fracture. In such challenging scenarios, bone scans can still serve as an alternative diagnostic tool, aiding in clinical decision-making.
RESUMEN
A proliferating trichilemmal tumor (PTT) is a rare, benign, exophytic tumor originating from the isthmus region of the outer root sheath of the hair follicle. Clinically, PTTs manifest as isolated, exophytic, firm nodules that have the potential to ulcerate. These tumors may occasionally originate from a pre-existing trichilemmal cyst, or they can emerge spontaneously. Most exclusively these lesions are seen on the scalp. However, rarely these tumors can be found in other anatomical areas. Our patient had a protruding mass in her shoulder for 20 years, and this is a rare site for the occurrence of these lesions; it could be the first case to document such a site, as far as we found in the literature. The mainstay treatment of the PTT is surgical excision of the tumor, assessing the histological margins to ensure sufficient resection was made, close monitoring, and follow-up with the patient.
RESUMEN
Septic arthritis (SA) is a type of joint inflammation caused by an infection. It is an orthopedic emergency that requires immediate treatment to avoid serious complications such as joint destruction, osteomyelitis, and sepsis. We present a case of bilateral knee SA in a seven-month-old female who presented to our emergency department with left knee SA, followed by right knee SA one month later.
RESUMEN
Giant cell tumor of tendon sheath (GCTTS) is a benign proliferative disorder of the synovial joints and tendon sheaths that typically manifests as a painless, firm, localized, and slow-growing mass. Commonly seen among women in the third to fifth decades, GCTTS can be diagnosed clinically; however, histopathological confirmation is required. The tumor is primarily removed surgically. Recurrence after excision is possible and occurs in up to 45% of cases.