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1.
Bone Joint J ; 100-B(3): 370-377, 2018 03 01.
Article in English | MEDLINE | ID: mdl-29589498

ABSTRACT

Aims: The use of a noninvasive growing endoprosthesis in the management of primary bone tumours in children is well established. However, the efficacy of such a prosthesis in those requiring a revision procedure has yet to be established. The aim of this series was to present our results using extendable prostheses for the revision of previous endoprostheses. Patients and Methods: All patients who had a noninvasive growing endoprosthesis inserted at the time of a revision procedure were identified from our database. A total of 21 patients (seven female patients, 14 male) with a mean age of 20.4 years (10 to 41) at the time of revision were included. The indications for revision were mechanical failure, trauma or infection with a residual leg-length discrepancy. The mean follow-up was 70 months (17 to 128). The mean shortening prior to revision was 44 mm (10 to 100). Lengthening was performed in all but one patient with a mean lengthening of 51 mm (5 to 140). Results: The mean residual leg length discrepancy at final follow-up of 15 mm (1 to 35). Two patients developed a deep periprosthetic infection, of whom one required amputation to eradicate the infection; the other required two-stage revision. Implant survival according to Henderson criteria was 86% at two years and 72% at five years. When considering revision for any cause (including revision of the growing prosthesis to a non-growing prosthesis), revision-free implant survival was 75% at two years, but reduced to 55% at five years. Conclusion: Our experience indicates that revision surgery using a noninvasive growing endoprosthesis is a successful option for improving leg length discrepancy and should be considered in patients with significant leg-length discrepancy requiring a revision procedure. Cite this article: Bone Joint J 2018;100-B:370-7.


Subject(s)
Bone Neoplasms/surgery , Leg , Prostheses and Implants , Prosthesis Implantation/methods , Adolescent , Adult , Amputation, Surgical , Child , Female , Humans , Leg Length Inequality , Male , Postoperative Complications , Prospective Studies , Prosthesis Design , Reoperation , Treatment Outcome
2.
Case Rep Med ; 2017: 2923696, 2017.
Article in English | MEDLINE | ID: mdl-28194180

ABSTRACT

Purpose. Anterior screw fixation has become a popular surgical treatment method for instable odontoid fractures. Screw loosening and migration are a rare, severe complication following anterior odontoid fixation, which can lead to esophagus perforation and requires revision operation. Methods. We report a case of screw loosening and migration after anterior odontoid fixation, which perforated the esophagus and was excreted without complications in a 78-year-old male patient. Results. A ventral dislocated anterior screw perforated through the esophagus after eight years after implantation and was excreted through the gastrointestinal (GI) tract. At a 6-month follow-up after the event the patient was asymptomatic. Conclusion. Extrusion via the GI tract is not safe enough to be considered as a treatment option for loosened screws. Some improvements could be implemented to prevent such an incident. Furthermore, this case is a fine example that recent preoperative imaging is mandatory before revision surgery for screw loosening.

3.
Bone Joint J ; 98-B(12): 1697-1703, 2016 Dec.
Article in English | MEDLINE | ID: mdl-27909134

ABSTRACT

AIMS: Extendible endoprostheses have been available for more than 30 years and have become more sophisticated with time. The latest generation is 'non-invasive' and can be lengthened with an external magnetic force. Early results have shown a worryingly high rate of complications such as infection. This study investigates the incidence of complications and the need for further surgery in a cohort of patients with a non-invasive growing endoprosthesis. PATIENTS AND METHODS: Between 2003 and June 2014, 50 children (51 prostheses) had a non-invasive growing prosthesis implanted for a primary bone sarcoma. The minimum follow-up was 24 months for those who survived. Their mean age was 10.4 years (6 to 14). The incidence of complications and further surgery was documented. RESULTS: The mean follow-up was 64 months (20 to 145). The overall survivorship of the patients was 84% at three years and 70% at five years. Revision-free survival was 81.7% at three years and 61.6% at five years with competing risk analysis. Deep infection occurred in 19.6% of implants at a mean of 12.5 months (0 to 55). Other complications were a failure of the lengthening mechanism in five prostheses (9.8%) and breakage of the implant in two (3.9%). Overall, there were 53 additional operations (0 to 5 per patient). A total of seven patients (14%) underwent amputation, three for local recurrence and four for infection. Their mean limb length discrepancy was 4.3 mm (0 to 25) and mean Musculoskeletal Tumor Society Score functional score was 26.5 (18 to 30) at the final follow-up. CONCLUSIONS: When compared with previously published early results, this mid-term series has shown continued good functional outcomes and compensation for leg-length discrepancy. Infection is still the most common complication: post-operative wound healing problems, central line infection and proximal tibial location are the main risk factors. Cite this article: Bone Joint J 2016;98-B:1697-1703.


Subject(s)
Bone Lengthening/instrumentation , Bone Neoplasms/surgery , Prostheses and Implants , Prosthesis Implantation/adverse effects , Sarcoma/surgery , Adolescent , Age Distribution , Bone Lengthening/methods , Bone Neoplasms/pathology , Child , Child, Preschool , Female , Follow-Up Studies , Humans , Kaplan-Meier Estimate , Male , Periprosthetic Fractures/etiology , Prostheses and Implants/adverse effects , Prosthesis Design , Prosthesis Failure , Prosthesis Implantation/methods , Prosthesis-Related Infections/etiology , Reoperation/methods , Sarcoma/pathology , Sex Distribution
4.
Sci Rep ; 6: 33551, 2016 Sep 26.
Article in English | MEDLINE | ID: mdl-27666393

ABSTRACT

Sclerostin has been proposed as a potent inhibitor of bone formation. Sclerostin antibodies are under clinical development to treat osteoporosis and metastatic bone disease. Serum sclerostin level is elevated in multiple myeloma, an osteolytic malignancy, where it might serve as predictive marker for the use of sclerostin-directed antibodies. As renal cell carcinoma (RCC) patients often present with osteolytic metastases, we aimed to investigate serum sclerostin levels in RCC patients. Our study included 53 RCC patients (19 with bone metastases, 25 with visceral metastases and 9 with localized disease) and 53 age- and gender-matched non-osteoporotic controls. Frozen serum samples were subjected to sclerostin quantitative sandwich ELISA. The mean serum sclerostin levels of RCC patients and controls were 45.8 pmol/l and 45.1 pmol/l, respectively (p = 0.86). Analysis of variance showed no difference between the subgroups of RCC patients with regard to visceral or bone metastases or localized disease (p = 0.22). There was no significant association between eGFR (estimated glomerular filtration rate) and serum sclerostin levels in RCC patients (r = 0.05; p = 0.74) and controls (r = 0.06; p = 0.68). Our results indicate that serum sclerostin levels appear not to be a valuable biomarker to assess the occurrence of bone metastases in RCC patients.

5.
Pathologe ; 34(2): 155-8, 2013 Mar.
Article in German | MEDLINE | ID: mdl-23483315

ABSTRACT

Esophageal duplications are congenital abnormalities of the foregut. We present the case of a 33-year-old woman suffering from progressive dysphagia who had surgery for esophageal duplication. The following three criteria define the cystic lesion: an intimate attachment to the esophageal wall, the presence of a smooth muscle coat and a mucosal lining consisting of squamous and/or ciliated respiratory epithelium. Diverticula, bronchogenic cysts and cystic neoplasms have to be considered in the differential diagnosis. Congenital cystic esophageal duplication is a rare cause of dysphagia in adulthood.


Subject(s)
Deglutition Disorders/pathology , Esophageal Cyst/congenital , Esophageal Cyst/pathology , Esophagus/abnormalities , Adult , Deglutition Disorders/surgery , Diagnosis, Differential , Disease Progression , Esophageal Cyst/surgery , Esophageal Stenosis/congenital , Esophageal Stenosis/pathology , Esophageal Stenosis/surgery , Esophagoscopy , Esophagus/surgery , Female , Humans , Surgical Stapling , Thoracoscopy , Tomography, X-Ray Computed
6.
Pathologe ; 33(1): 61-4, 2012 Feb.
Article in German | MEDLINE | ID: mdl-22293791

ABSTRACT

Granular cell tumors are peripheral neuroectodermal tumors. Within the gastrointestinal tract, they have to be differentiated from gastrointestinal stromal tumors (GIST). We present the case of a 61-year-old patient who was diagnosed with a granular cell tumor of the stomach. The tumor cells showed transmural infiltration form the mucosa into the adipose tissue of the lesser curvature. The tumor cells were diffusely positive for S100-protein and negative for KIT, CD34 und SMA. The MIB1-proliferation index was below 2%. Granular cell tumors rarely occur within the gastrointestinal tract. Oesophagus and colon are most commonly affected. Diagnostic criteria and differential diagnosis of this peculiar lesion are thoroughly discussed.


Subject(s)
Granular Cell Tumor/pathology , Stomach Neoplasms/pathology , Biomarkers, Tumor/analysis , Biomarkers, Tumor/genetics , Cell Proliferation , Cell Transformation, Neoplastic/pathology , Diagnosis, Differential , Gastrointestinal Stromal Tumors/genetics , Gastrointestinal Stromal Tumors/pathology , Gastrointestinal Stromal Tumors/surgery , Gastroscopy , Granular Cell Tumor/genetics , Granular Cell Tumor/surgery , Humans , Laparoscopy , Liver/pathology , Liver/surgery , Liver Neoplasms/genetics , Liver Neoplasms/pathology , Liver Neoplasms/secondary , Liver Neoplasms/surgery , Male , Middle Aged , Neoplasm Invasiveness , Neoplasm Staging , Stomach/pathology , Stomach/surgery , Stomach Neoplasms/genetics , Stomach Neoplasms/surgery
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