Our investigation sought to describe a patient who exhibited refractory prosthetic joint infection (PJI) coupled with debilitating peripheral arterial disease, necessitating the extreme measure of hip disarticulation (HD). This HD procedure, though not the first for PJI, represents a novel presentation of profound infection burden and severe vascular disease, proving recalcitrant to all prior interventions.
An elderly patient with a past history of left total hip arthroplasty, PJI, and severe peripheral arterial disease, experienced a minimally invasive hemiarthroplasty procedure and was released with few complications, as we document here. In the run-up to this significant surgical operation, diverse surgical revisions and antibiotic treatment plans were applied. The patient's attempt at revascularization, aimed at resolving the occlusion stemming from peripheral arterial disease, ended in failure, resulting in a necrotic wound at the surgical site. Necrotic tissue irrigation and debridement proved ineffective, leading to the decision, with the patient's agreement, to perform hyperbaric oxygen therapy (HD) due to concerns about cellulitis.
A highly specialized procedure, hemipelvectomy (HD), accounts for a minuscule proportion of lower limb amputations, typically 1-3%, and is employed only for exceptionally severe conditions like infection, ischemia, or trauma. The 5-year mortality rate and complication rates have reached the concerning levels of 55% and 60%, respectively, as reported. In spite of these statistical measurements, the case of this patient demonstrates a situation where the early identification of potential problems related to HD prevented further negative results. From this case study, we maintain that HD treatment represents a sound approach for patients with severe peripheral arterial disease who have failed revascularization and have previously undergone moderate treatment. Despite the limited data on high-definition imaging and the diverse range of comorbid conditions present, a more in-depth investigation of outcomes is required.
The HD amputation procedure, a rare intervention in lower limb amputations, accounts for only a small fraction (1-3%) of the total. It is utilized exclusively for the most harmful conditions, including infections, ischemia, and trauma. Reported complication and five-year mortality rates reached a staggering 60% and 55%, respectively. While these rates were present, the patient's case exemplifies a situation where prompt recognition of HD indications mitigated further negative results. This case study suggests high-dose therapy as a plausible treatment option for patients exhibiting severe peripheral arterial disease, following the failure of revascularization and prior moderate therapies. Despite the limited scope of data pertaining to high-definition imagery and diverse comorbid conditions, additional analysis of outcomes is imperative.
Amongst hereditary rickets, X-linked hypophosphatemic rachitis (XLHR) is the most prevalent cause, leading to long bone deformities that necessitate repeated corrective surgical procedures. see more Furthermore, adult XLHR patients are frequently reported to experience a high incidence of fractures. We report a case of mechanical axis correction treatment for a femoral neck stress fracture in a patient with XLHR. No prior studies, as documented in the literature, described a combined technique for valgus correction and cephalomedullary nail fixation.
The outpatient clinic received a visit from a 47-year-old male patient with XLHR who was experiencing extreme pain in his left hip. Left proximal femoral varus deformity and a stress fracture of the femoral neck were revealed by the X-ray examination. Due to a month's duration of pain without radiographic signs of healing, a cephalomedullary nail was implemented to achieve correction of the proximal femoral varus deformity and fixation of the cervical neck fracture. see more After eight months, radiographs clearly showed healing of the femoral neck stress fracture and the proximal femoral osteotomy, which was directly correlated with the alleviation of hip pain.
Case reports describing the fixation of femoral neck fractures in adults with coxa vara were identified via a thorough review of the existing literature. Stress fractures in the femoral neck can be a manifestation of coxa vara or XLHR. In this investigation, the surgical procedure for a rare stress fracture of the femoral neck in a XLHR patient with coxa vara was demonstrated. Deformity correction, coupled with fracture fixation via a femoral cephalomedullary nail, resulted in the desired outcomes of pain relief and bone healing. The method of correcting coxa vara and implanting a cephalomedullary nail in a patient is illustrated.
A search of the literature was performed to locate any case reports documenting the fixation of femoral neck fractures occurring in adults due to coxa vara. Femoral neck stress fractures are a consequence of both coxa vara and XLHR. In this study, the surgical technique to address a rare femoral neck stress fracture in a patient with XLHR and coxa vara was presented. Deformity correction, in conjunction with fracture fixation using a femoral cephalomedullary nail, proved efficacious in achieving pain relief and bone healing. The procedure of correcting deformities and inserting cephalomedullary nails in coxa vara patients is demonstrated.
Locally aggressive, expansile, and benign, aneurysmal bone cysts (ABCs) are characterized by fluid-filled cysts, often located at the metaphyseal extremities of long bones. Infrequent manifestations and atypical etiologies are hallmarks of these conditions, which frequently impact children and young adults. En bloc resection, curettage, bone graft or substitute augmentation, instrumentation, sclerosing agents, arterial embolization, and adjuvant radiotherapy are among the treatment modalities available.
A case of ABC, a rare condition, is highlighted in this report, involving a 13-year-old male patient. The patient reported severe right hip pain and an inability to walk subsequent to a trivial fall during play, and exhibited a proximal femoral pathological fracture. Following an open biopsy curettage, modified hydroxyapatite granules were implanted, along with internal fixation using a pediatric dynamic hip screw and a four-hole plate for the subtrochanteric fracture, yielding a favorable result.
A standardized management protocol is absent due to the distinct nature of these cases; curettage, coupled with bone grafts or substitutes, and internal fixation of any accompanying pathologic fractures, consistently results in bony union and favorable clinical outcomes.
The absence of a standardized approach to management stems from the unique characteristics of these instances; curettage combined with bone grafts or bone substitutes, and concurrent internal fixation of associated pathologic fractures, results in robust bony union with favorable clinical results.
Periprosthetic osteolysis (PPO), a significant complication arising after total hip replacement, necessitates swift intervention to impede its expansion into adjacent tissues and ultimately aim for the restoration of hip function. The patient's experience with PPOL treatment presented a particularly demanding and challenging situation, which we now describe.
This case study details a 75-year-old patient diagnosed with PPOL 14 years after undergoing a primary total hip arthroplasty, with the condition progressing to affect the soft tissues and pelvic region. Throughout the course of treatment, the synovial fluid aspirate from the left hip joint displayed a consistently elevated neutrophil-dominant cell count, while microbiological cultures proved negative. Due to substantial bone deterioration and the patient's general condition, no additional surgical procedures were considered necessary, and a plan for future action remains unclear.
The management of severe PPOL is frequently a complex undertaking, as surgical remedies yielding a good long-term outlook are scarce. Suspected osteolytic processes necessitate immediate intervention to forestall the escalation of associated complications.
The difficulty in managing severe PPOL stems from the limited surgical choices that lead to promising long-term results. Treatment of a suspected osteolytic process is urgently needed to prevent the escalation of any complications arising from it.
Individuals with mitral valve prolapse (MVP) face the risk of developing ventricular arrhythmias, characterized by a progression from premature ventricular contractions to non-sustained, more intricate ventricular tachycardia, and potentially progressing to sustained, life-threatening cases. Studies on sudden deaths in young adults, as determined by post-mortem examinations, indicate that MVP is present in approximately 4% to 7% of cases. In conclusion, erratic mitral valve prolapse (MVP) has been found to be an often overlooked source of sudden cardiac death, resulting in a renewed interest in the study of this association. Frequent or complex ventricular arrhythmias, observed in a select group of patients diagnosed with arrhythmic MVP, are found in the absence of any additional arrhythmic factors, and often accompanied by mitral valve prolapse (MVP), either with or without mitral annular disjunction. A complete understanding of their co-existence within the framework of modern management and prognosis is yet to be achieved. In light of recent consensus statements, the conflicting literature regarding arrhythmic mitral valve prolapse (MVP) prompts a comprehensive review of the diagnostic procedures, prognostic assessments, and targeted therapies for MVP-related ventricular arrhythmias. see more Recent data on left ventricular remodeling, which makes the simultaneous presence of mitral valve prolapse and ventricular arrhythmias more intricate, is also summarized by us. Predicting sudden cardiac death risk related to MVP-associated ventricular arrhythmias is intricate, given the dearth of evidence and its reliance on often inadequate, retrospective data collection. In order to build a more dependable predictive model, we sought to list potential risk factors identified in relevant seminal reports, requiring additional prospective data.