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1.
Vascular ; 22(3): 161-6, 2014 Jun.
Article in English | MEDLINE | ID: mdl-23493279

ABSTRACT

Subclavian artery aneurysm is a rare but serious disease due to the risk of thrombosis, embolization, rupture and compression of adjacent structures. Treatment consists of surgical and endovascular techniques. Up to now few long-term follow-up results have been reported. In our study the results from 15 patients treated for subclavian artery aneurysms were evaluated. Eleven patients underwent open surgical reconstruction, four patients were treated endovascularly. After a mean follow-up period of 77 months (83 months for the open surgical group, 38 months for the endovascular group), 10 of 11 open surgical reconstructions and all primarily implanted stent grafts were patent. Secondary intervention was necessary in two patients. Thirty-day mortality for both treatment groups was 0%. Subclavian artery aneurysm-related symptoms disappeared in six out of 10 patients after the treatment. Long-term outcomes with good technical results, patency rates and low periprocedural morbidity could be shown in both treatment groups.


Subject(s)
Aneurysm, False/surgery , Blood Vessel Prosthesis Implantation , Endovascular Procedures , Postoperative Complications/surgery , Aneurysm, False/diagnosis , Aneurysm, False/mortality , Austria/epidemiology , Blood Vessel Prosthesis Implantation/adverse effects , Blood Vessel Prosthesis Implantation/methods , Disease Management , Endovascular Procedures/adverse effects , Endovascular Procedures/methods , Female , Follow-Up Studies , Humans , Male , Middle Aged , Reoperation , Risk Assessment , Stents , Subclavian Artery/pathology , Subclavian Artery/physiopathology , Subclavian Artery/surgery , Survival Analysis , Treatment Outcome , Vascular Patency
2.
J Autoimmun ; 39(4): 441-50, 2012 Dec.
Article in English | MEDLINE | ID: mdl-22901435

ABSTRACT

Atherosclerosis is a multifactorial chronic inflammatory disease characterized by the presence of T-cells, macrophages, and dendritic cells in the arterial intima. Classical risk factors lead to over-expression of stress proteins, especially heat shock protein 60 (HSP60). HSP60 on the surface of arterial endothelial cells (ECs) then becomes a target for pre-existing adaptive anti-HSP60 immunity resulting in infiltration of the intima by mononuclear cells. In the present study, T-cells derived from early, clinically still inapparent human atherosclerotic lesions were analyzed phenotypically and for their reactivity against HSP60 and HSP60-derived peptides. HSP60 was detected in ECs and CD40- and HLA Class II-positive cells within the intima. Effector memory CD4(+) T-cells producing high amounts of interferon-γ and low levels of interleukin-4 were the dominant subpopulation. T-cells derived from late lesions displayed a more restricted T-cell receptor repertoire to HSP60-derived peptides than those isolated from early lesions. Increased levels of soluble HSP60 and circulating anti-human HSP60 autoantibodies were found in donors with late but not early lesions. This is the first functional study of T-cells derived from early human atherosclerotic lesions that supports the previously proposed concept that HSP60-reactive T-cells initiate atherosclerosis by recognition of atherogenic HSP60 epitopes.


Subject(s)
Atherosclerosis/immunology , Autoantibodies/immunology , CD4-Positive T-Lymphocytes/immunology , Chaperonin 60/immunology , Endothelial Cells/immunology , Atherosclerosis/blood , Atherosclerosis/genetics , Atherosclerosis/pathology , Autoantibodies/blood , Autoantibodies/genetics , Autopsy , CD4-Positive T-Lymphocytes/metabolism , CD4-Positive T-Lymphocytes/pathology , CD40 Antigens/genetics , CD40 Antigens/immunology , Chaperonin 60/blood , Chaperonin 60/genetics , Endothelial Cells/metabolism , Endothelial Cells/pathology , Endothelium, Vascular/immunology , Endothelium, Vascular/metabolism , Endothelium, Vascular/pathology , Female , Gene Expression/immunology , Histocompatibility Antigens Class II/genetics , Histocompatibility Antigens Class II/immunology , Humans , Immunologic Memory , Interferon-gamma/genetics , Interferon-gamma/immunology , Interleukin-4/genetics , Interleukin-4/immunology , Male , Middle Aged , Peptides/genetics , Peptides/immunology , Signal Transduction , Time Factors , Tunica Intima/immunology , Tunica Intima/metabolism , Tunica Intima/pathology
3.
Aesthetic Plast Surg ; 36(5): 1128-33, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22810556

ABSTRACT

BACKGROUND: Long-term aesthetic results after reduction mammaplasty remain an important issue for evaluating the success of different techniques. Superior pedicled techniques are reported to maintain a better breast projection with less bottoming-out of the inferior mammary pole than inferior pedicled techniques. METHODS: The outcomes of 18 patients who had undergone the superior pedicled technique described by Pitanguy and 16 patients operated on using the inferior pedicled technique by Robbins were compared. RESULTS: The mean follow-up period was 49 months in the Pitanguy group and 35 months in the Robbins group. The distance between the inframammary crease and the inferior margin of the nipple-areola complex (NAC) showed a mean elongation of 3.3 cm (80.5 %) after the superior pedicled Pitanguy technique and 3.9 cm (92.9 %) after the inferior pedicled Robbins technique (p = 0.077). Using postoperative photographs, the overall aesthetic result after Pitanguy's technique was judged significantly better than the result after Robbins' technique (p = 0.002). CONCLUSIONS: Distinct postoperative elongation of the inferior mammary pole length must be considered in the preoperative marking for inferior and superior pedicled reduction mammaplasty. Guide values for the elongation can be used for planning unilateral adjustment reduction mammaplasty. To avoid bottoming-out of the inferior mammary pole, the NAC should be located at the level of the inframammary crease and the distance between the inframammary crease and the inferior border of the NAC should not exceed 4-4.5 cm. The definite position of the NAC should be decided after final shaping of the reduced breast toward the end of the operation. LEVEL OF EVIDENCE III: This journal requires that authors assign a level of evidence to each article.


Subject(s)
Mammaplasty/methods , Adult , Female , Follow-Up Studies , Humans , Retrospective Studies , Time Factors , Treatment Outcome
4.
Curr Microbiol ; 64(3): 271-5, 2012 Mar.
Article in English | MEDLINE | ID: mdl-22173653

ABSTRACT

Candida albicans is one of the most frequent causes of fungal infections in humans. Significant correlation between candiduria and invasive candidiasis has previously been described. The existing diagnostic methods are often time-consuming, cost-intensive and lack in sensitivity and specificity. In this study, the profile of low-molecular weight volatile compounds in the headspace of C. albicans-urine suspensions of four different fungal cell concentrations compared to nutrient media and urine without C. albicans was determined using proton-transfer reaction mass spectrometry (PTR-MS). At fungal counts of ≥1.5 × 10(5) colony forming units (CFU)/ml signals at 45, 47 and 73 atomic mass units (amu) highly significantly increased. At fungal counts of <1.5 × 10(5) CFU/ml signals at 47 and 73 amu also increased, but only at 45 amu a statistically significant increase was seen. Time course alterations of signal intensities dependent on different cell concentrations and after addition of Sabouraud nutrient solution were analysed. Recommendations for measurement conditions are given. Our study is the first to describe headspace profiling of C. albicans-urine suspensions of different fungal cell concentrations. PTR-MS represents a promising approach to rapid, highly sensitive and non-invasive clinical diagnostics allowing qualitative and quantitative analysis.


Subject(s)
Candida albicans/chemistry , Candida albicans/metabolism , Mass Spectrometry/methods , Metabolome , Mycology/methods , Volatile Organic Compounds/analysis , Candida albicans/isolation & purification , Colony Count, Microbial , Humans , Urine/microbiology
5.
Int J Colorectal Dis ; 25(10): 1231-42, 2010 Oct.
Article in English | MEDLINE | ID: mdl-20563874

ABSTRACT

PURPOSE: The epithelial lining of the anorectum still raises discussions concerning the levels of transition between the various zones and leads to an incomplete understanding of the immmunoprofile of rectal carcinoma. Since the expression of cytokeratins depends on the epithelial cell-type and the parahox-gene CDX2 is important for the development of the colorectal epithelium, we investigated different cytokeratins and CDX2 in the anorectum of human prenatal stages and in adult normal and neoplastic anorecta. MATERIALS AND METHODS: The differentiation and spatiotemporal distribution of the epithelial zones were examined in 33 human embryos and fetuses, in a 2-year-old child and four adults. In comparison, 17 specimens of ultralow rectal adenocarcinoma and 4 specimens of anal carcinoma were investigated. Monoclonal antibodies were directed against cytokeratin (CK) 18, 20, 7 and 14 and CDX2. RESULTS: Due to the cytokeratin profile and to CDX2 expression, the different anorectal zones could already be differentiated in human prenatal life. We showed that anorectal epithelial differentiation including the squamous epithelia ran in a craniocaudal direction, and that the anorectal zone was a transitional zone between rectal zone and anal transitional zone where CK 7, 18, 20 and CDX2 are simultaneously expressed. All cases of rectal adenocarcinoma showed positivity for CK 18, 20 and CDX2, and three also labelled for CK 7, whereas CK 14 was only expressed in the cases of anal carcinoma. CONCLUSIONS: Our results elucidate the connection between the prenatal pattern and the origin of the different types of anorectal carcinoma.


Subject(s)
Anal Canal/growth & development , Epithelial Cells/cytology , Epithelium/pathology , Rectum/growth & development , Adult , Anal Canal/embryology , Anus Neoplasms/pathology , CDX2 Transcription Factor , Child, Preschool , Epithelium/embryology , Fetus/cytology , Homeodomain Proteins , Humans , Rectal Neoplasms/pathology , Rectum/embryology
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