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  • 1
    In: Journal of Pediatric Surgery, Elsevier BV, Vol. 59, No. 3 ( 2024-03), p. 483-487
    Type of Medium: Online Resource
    ISSN: 0022-3468
    RVK:
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2024
    detail.hit.zdb_id: 2039299-0
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  • 2
    Online Resource
    Online Resource
    Ovid Technologies (Wolters Kluwer Health) ; 2016
    In:  Journal of Pediatric Hematology/Oncology Vol. 38, No. 4 ( 2016-05), p. e147-e150
    In: Journal of Pediatric Hematology/Oncology, Ovid Technologies (Wolters Kluwer Health), Vol. 38, No. 4 ( 2016-05), p. e147-e150
    Abstract: Wilms tumor is the most common renal malignancy of childhood. Because of the improvement in prognosis and the increase in survival rates, long-term consequences of the treatment for Wilms tumor are of greater concern. We investigated late renal effects of the treatment on 50 survivors of nonsyndromic unilateral Wilms tumor. After the second year since the cessation of treatment, the glomerular filtration rate (GFR), urinary protein excretion, urinary β2 microglobulin levels, and blood pressure as well as the general health status were assessed. Results were analyzed for correlation with clinical variables, chemotherapy, and radiotherapy as possible risk factors. At a median follow-up time of 8.8 years (mean=10.9; range, 2.3 to 35.4 y), none of the patients developed end-stage renal disease. Compensatory hypertrophy was observed in 68% of the cases. The median maximum bipolar length was significantly higher in patients diagnosed after the age of 36 months. Eleven (22%) and 2 (4%) of the 50 patients were hypertensive at the time of the diagnosis and the study, respectively. Similarly, median GFR values were significantly lower at the time of diagnosis, although at the time of the study, all patients had normal GFR values. With longer follow-up intervals, especially after 10 years, a significant decreasing trend in the GFR was observed ( P =0.002).
    Type of Medium: Online Resource
    ISSN: 1077-4114
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2016
    detail.hit.zdb_id: 2047125-7
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  • 3
    Online Resource
    Online Resource
    The Turkish Journal of Pediatrics ; 2019
    In:  The Turkish Journal of Pediatrics Vol. 61, No. 5 ( 2019), p. 760-
    In: The Turkish Journal of Pediatrics, The Turkish Journal of Pediatrics, Vol. 61, No. 5 ( 2019), p. 760-
    Type of Medium: Online Resource
    ISSN: 0041-4301
    Language: Unknown
    Publisher: The Turkish Journal of Pediatrics
    Publication Date: 2019
    detail.hit.zdb_id: 2120977-7
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  • 4
    Online Resource
    Online Resource
    Informa UK Limited ; 2018
    In:  Fetal and Pediatric Pathology Vol. 37, No. 4 ( 2018-07-04), p. 270-275
    In: Fetal and Pediatric Pathology, Informa UK Limited, Vol. 37, No. 4 ( 2018-07-04), p. 270-275
    Type of Medium: Online Resource
    ISSN: 1551-3815 , 1551-3823
    Language: English
    Publisher: Informa UK Limited
    Publication Date: 2018
    detail.hit.zdb_id: 2166926-0
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  • 5
    Online Resource
    Online Resource
    S. Karger AG ; 2015
    In:  Ophthalmologica Vol. 234, No. 4 ( 2015), p. 227-232
    In: Ophthalmologica, S. Karger AG, Vol. 234, No. 4 ( 2015), p. 227-232
    Abstract: 〈 b 〉 〈 i 〉 Background: 〈 /i 〉 〈 /b 〉 Studies conducted in recent years have reported promising results regarding the treatment of retinoblastoma with the intra-arterial use of melphalan. In the present study, we intended to report the results of intra-arterial chemotherapy with melphalan (IACT) in the treatment of newly diagnosed or relapsed-refractory retinoblastoma patients at the Department of Pediatric Oncology of Hacettepe University, Ankara, Turkey. 〈 b 〉 〈 i 〉 Materials and Methods: 〈 /i 〉 〈 /b 〉 This was a retrospective study of patients with intraocular retinoblastoma who were treated with IACT from December 2011 to May 2014. A total of 56 eyes of 46 consecutive patients (30 males and 16 females) were included in the study. Forty-four eyes received systemic chemotherapy upon diagnosis (systemic chemotherapy group, SCG), and 12 eyes were those of newly diagnosed patients (primary intra-arterial melphalan group, PIAG). The choice of the IACT dose was based on age. Tumor control and globe salvage with IACT were analyzed. Complete blood counts were examined 7 days after the IACT for systemic toxicity. Ocular toxicities such as proptosis, eyelid edema, ocular motility, and retinal and optic atrophy were assessed by an ocular oncologist with regular ophthalmologic examinations. 〈 b 〉 〈 i 〉 Results: 〈 /i 〉 〈 /b 〉 Enucleation was avoided overall in 66% (37/56) of the eyes, including 75% (9/12) in the PIAG and 64% (28/44) in the SCG patients. The 1-year enucleation-free survival rate was 56.7% at a median follow-up time of 11.9 months (range 0.27-27.6). IACT was administered in a total of 124 cycles (ranging from 1 to 7 cycles, mean 2.3). The responses were as follows: regression of the retinal tumor in 27 eyes and improvements in vitreous seeding in 5 of 15 eyes. The further treatment requirements after IACT were as follows: enucleation in 19 eyes (10 with vitreous seeding), radiotherapy in 3 eyes, systemic chemotherapy in 1 eye, and local therapy in 1 eye. No severe systemic side effects occurred. Transient swelling of the eyelids (22 patients), conjunctival chemosis (12 patients), upper eyelid ptosis (5 patients), redness over the frontal area (3 patients), limitation of ocular motility (3 patients) and mild proptosis (1 patient) were detected. Retinal pigment epithelial alterations (30 patients) and optic atrophy (3 patients) were seen in the late follow-up. 〈 b 〉 〈 i 〉 Conclusions: 〈 /i 〉 〈 /b 〉 Globe salvage and avoidance of radiotherapy may be achieved by IACT with limited toxicity. This treatment is efficient, repeatable and safe.
    Type of Medium: Online Resource
    ISSN: 0030-3755 , 1423-0267
    RVK:
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2015
    detail.hit.zdb_id: 1483531-9
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  • 6
    Online Resource
    Online Resource
    American Society of Clinical Oncology (ASCO) ; 2021
    In:  Journal of Clinical Oncology Vol. 39, No. 15_suppl ( 2021-05-20), p. e14042-e14042
    In: Journal of Clinical Oncology, American Society of Clinical Oncology (ASCO), Vol. 39, No. 15_suppl ( 2021-05-20), p. e14042-e14042
    Abstract: e14042 Background: Optic gliomas are the most common tumors of the optic pathway, comprising about 1% of all intracranial tumours. Here we present the clinical characteristics and the outcome of patients with optic glioma at our institution. Methods: Seventy two patients diagnosed and followed up at a pediatric cancer center in Ankara, Turkey between January 1, 2008 and December 31, 2020 were included in this analysis. The clinical features and outcome of patients were recorded from patient files and hospital information system retrospectively. Results: The median age at the time of diagnosis was 3.5 years (4-157 months), the female/male ratio was 1.3. Fourteen children (19%) were asymptomatic and tumors were detected with routine surveillance, and 58 (81%) had symptoms (the most common being proptosis in 16 patients (22%)). The most common site of optic glioma was the intraorbital region (31%). Fourty patients (55%) had neurofibromatosis type 1 (NF-1). Five patients had histopathological diagnoses; 3 pilomyxoid astrocytoma, 2 pilocytic astrocytoma. Children were treated if they had tumor progression on MRI and/or worsening visual acuity. Twenty seven (38%) children were observed without any therapy, 6 patients (8%) received radiation and chemotherapy, 4 patients (5%) received radiation only, and 35 patients (49%) received chemotherapy only. Treatment regimens for the 41 children who received chemotherapy included carboplatin/etoposide (17), cisplatin/etoposide (18), carboplatin/vincristine (5), and temozolomide (1). The 5-year progression-free survival (PFS) and overall survival (OS) were 64% and 90%, respectively with a 31 month median follow-up. The 5 year PFS was significantly lower in patients with optic tract-hypothalamic-chiasmatic involvement (34%) than orbital involvement (83%) (p=0.013). Five year PFS was significantly higher in patients with NF-1 (80%) than patients without NF-1(46%) (p=0.027) and significantly lower in patients diagnosed at 〈 3 years old (37%) (p=0.05). Five patients died of disease, and one died of infection after chemotherapy. Two patients treated with platin (1 carboplatin, 1 cisplatin) developed ototoxicity. One patient with NF-1 developed Moya-Moya disease. Two patients developed multiple pituitary hormone deficiencies and one patient developed precocious puberty during follow-up. No secondary malignancy was observed. Conclusions: The management of optic glioma remains challenging. Although the overall survival for children with this disease is excellent, progression of disease is frequent, particularly in those children without NF-1, younger children and non-orbital tumors. This study from Turkey showed comparable results with high-income countries. Further studies with longer follow-up periods are needed to find appropriate treatment strategies.
    Type of Medium: Online Resource
    ISSN: 0732-183X , 1527-7755
    RVK:
    RVK:
    Language: English
    Publisher: American Society of Clinical Oncology (ASCO)
    Publication Date: 2021
    detail.hit.zdb_id: 2005181-5
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  • 7
    In: Pediatric Pulmonology, Wiley, Vol. 42, No. 6 ( 2007-06), p. 565-567
    Type of Medium: Online Resource
    ISSN: 8755-6863 , 1099-0496
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2007
    detail.hit.zdb_id: 1491904-7
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  • 8
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2021
    In:  Skeletal Radiology Vol. 50, No. 10 ( 2021-10), p. 2023-2030
    In: Skeletal Radiology, Springer Science and Business Media LLC, Vol. 50, No. 10 ( 2021-10), p. 2023-2030
    Type of Medium: Online Resource
    ISSN: 0364-2348 , 1432-2161
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2021
    detail.hit.zdb_id: 1461957-X
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  • 9
    In: Nephron Clinical Practice, S. Karger AG, Vol. 100, No. 3 ( 2005-4-15), p. c86-c91
    Abstract: 〈 i 〉 Objective: 〈 /i 〉 To evaluate renal involvement in childhood lymphoma and define its prognostic effects. 〈 i 〉 Patients and Methods: 〈 /i 〉 One hundred and four patients with non-Hodgkin’s lymphoma and renal involvement on admission to a single center between 1972 and 2003 were evaluated retrospectively. Blood urea nitrogen, serum creatinine, uric acid, electrolytes, and lactate dehydrogenase levels, as well as urinalysis, were evaluated. One or more of the following imaging methods were performed: intravenous urogram, ultrasound, computed tomography, and magnetic resonance imaging. The χ 〈 sup 〉 2 〈 /sup 〉 test was used to compare the groups. The Kaplan-Meier survival method was used to calculate survival rates, and the log-rank test was used to compare groups with respect to survival. Survival rates were also compared in two different time periods (before 1991 and after 1991). 〈 i 〉 Results: 〈 /i 〉 There were 76 boys and 28 girls with a median age of 6 (0.9–16) years. The renal infiltration pattern was nodular in 62 patients (59.6%) and diffuse in 40 patients (38.5%). Two patients had tumoral masses that originated from their kidneys (1.9%). Renal involvement was bilateral in 75 patients (72.1%); the remaining 29 patients had unilateral involvement. The overall survival rate was 42.5% with a median follow-up of 64 months. The factors that had a statistically significant impact on survival were high creatinine (p = 0.00001) and blood urea nitrogen levels (p = 0.0001), the onset of tumor lysis syndrome (p = 0.01), and the need for dialysis (p = 0.009). The survival rate was higher in the time period after 1991 (p = 0.01). 〈 i 〉 Conclusion: 〈 /i 〉 Impaired renal function is a poor prognostic factor for non-Hodgkin’s lymphoma. Renal function should therefore be monitored closely. Renal dysfunction caused by direct tumoral involvement may complicate therapy and shorten survival.
    Type of Medium: Online Resource
    ISSN: 1660-2110
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2005
    detail.hit.zdb_id: 2098336-0
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  • 10
    In: Journal of Magnetic Resonance Imaging, Wiley, Vol. 55, No. 2 ( 2022-02), p. 594-607
    Abstract: Several functional imaging techniques, including monoexponential diffusion‐weighted imaging (m‐DWI), intravoxel incoherent motion (IVIM), and diffusion kurtosis (DK) imaging, have been used in differentiating benign and malignant musculoskeletal tumors. Combining all three techniques in the same study population may improve differentiation. Purpose To compare the diagnostic performance of m‐DWI, IVIM, and DK models and their combinations in differentiating benign and malignant musculoskeletal tumors. Study Type Prospective. Population Fifty patients with benign and malignant musculoskeletal tumors divided into nonmyxoid and nonchondroid and myxoid and/or chondroid subgroups. Field strength/Sequence A 1.5 T/ m‐DWI , IVIM, and DK single‐shot spin‐echo echo‐planar sequences. Assessment Minimum and volumetric values of apparent diffusion coefficient (ADC), pure molecular diffusion (D ivim ), pseudodiffusion (D*), perfusion fraction ( f ), diffusion coefficient for kurtosis model (D K ), and Kurtosis (K) were compared between all benign and malignant tumors. Subgroup analysis was also performed for nonmyxoid and nonchondroid and myxoid and/or chondroid tumors. Statistical tests Independent samples t‐test, Mann–Whitney U test, intraclass correlation coefficient, ROC analysis, and logistic regression analysis. A P value  〈  0.05 was considered statistically significant. Results ADC min , D ivim‐min , D* vol , D K‐min, K vol, and K min values showed statistically significant differences between all benign and malignant tumors and nonmyxoid and nonchondroid tumor subgroup. K min showed the highest diagnostic performance in differentiating benign and malignant tumors with AUCs of 0.760 for “all tumors” and 0.825 for the nonmyxoid and nonchondroid tumor subgroup. No significant differences were detected in m‐DWI‐, IVIM‐, and DK‐derived parameters for differentiating benign and malignant myxoid and/or chondroid tumors. Only three of 63 combinations of prediction models demonstrated a higher diagnostic performance than K min ; however, improvements were not significantly different. Data conclusion ADC min , D ivim‐min , D* vol , D K‐min , K vol , and K min values can be used to differentiate benign and malignant musculoskeletal tumors. Our findings suggest that the added value of multiparametric approach in such differentiation is not significant. Evidence Level 1 Technical Efficacy Stage 2
    Type of Medium: Online Resource
    ISSN: 1053-1807 , 1522-2586
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2022
    detail.hit.zdb_id: 1497154-9
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