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Keywords = Raritan Bay

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24 pages, 5836 KB  
Article
Mitigation of Channel Shoaling at a Sheltered Inlet Subject to Flood Gate Operations
by Laura Lemke, Matthew S. Janssen and Jon K. Miller
J. Mar. Sci. Eng. 2020, 8(11), 865; https://doi.org/10.3390/jmse8110865 - 31 Oct 2020
Cited by 4 | Viewed by 2731
Abstract
A comprehensive case study of Keansburg Inlet (New Jersey, USA) is presented with the objective of evaluating inlet management alternatives and assessing the influence of an operational flood gate on channel shoaling. The goal of the research is determining the most effective strategy [...] Read more.
A comprehensive case study of Keansburg Inlet (New Jersey, USA) is presented with the objective of evaluating inlet management alternatives and assessing the influence of an operational flood gate on channel shoaling. The goal of the research is determining the most effective strategy for minimizing the frequency of maintenance dredging. This study compares the effectiveness of (1) traditional structural solutions; (2) modified dredging templates; and (3) assesses the influence of the flood gate operations during conditions representative of a typical year. Alternative analysis is completed using a coupled hydrodynamic–wave model (Delft3D-Flexible Mesh (FM)) with Real Time Control to simulate morphological changes. The model was calibrated and evaluated using collected field data. Water levels are reproduced within 6% of the spring tide range with lag times less than 20 min. The model results and observations suggest sediment transport is dominated by wave action with pronounced variations in dominant wave direction. The results indicate that changes to the operational dredging, or what the authors have termed broadly as “adaptive dredging techniques”, appear to deliver the most promising improvement. Model results suggest that the current operational procedures of the flood gate do not significantly alter the channel infilling rates and patterns during typical (i.e., non-extreme event) conditions. Full article
(This article belongs to the Section Coastal Engineering)
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9 pages, 199 KB  
Review
New Horizons from Novel Therapies in Malignant Pleural Mesothelioma
by Mutlay Sayan, Swati Mamidanna, Mehmet Fuat Eren, Vasudev Daliparty, Teuta Zoto Mustafayev, Carl Nelson, Nisha Ohri, Salma K. Jabbour, Aslihan Guven Mert and Banu Atalar
Adv. Respir. Med. 2020, 88(4), 343-351; https://doi.org/10.5603/ARM.a2020.0103 - 15 Jul 2020
Cited by 1 | Viewed by 1133
Abstract
Malignant pleural mesothelioma (MPM) is a relatively rare, but highly lethal cancer of the pleural mesothelial cells. Its pathoge-nesis is integrally linked to asbestos exposure. In spite of recent developments providing a more detailed understanding of the pathogenesis, the outcomes continue to be [...] Read more.
Malignant pleural mesothelioma (MPM) is a relatively rare, but highly lethal cancer of the pleural mesothelial cells. Its pathoge-nesis is integrally linked to asbestos exposure. In spite of recent developments providing a more detailed understanding of the pathogenesis, the outcomes continue to be poor. To date, trimodality therapy involving surgery coupled with chemotherapy and/or radiotherapy remains the standard of therapy. The development of resistance of the tumor cells to radiation and several che-motherapeutic agents poses even greater challenges in the management of this cancer. Ionizing radiation damages cancer cell DNA and aids in therapeutic response, but it also activates cell survival signaling pathways that helps the tumor cells to overcome radiation-induced cytotoxicity. A careful evaluation of the biology involved in mesothelioma with an emphasis on the workings of pro-survival signaling pathways might offer some guidance for treatment options. This review focuses on the existing treatment options for MPM, novel treatment approaches based on recent studies combining the use of inhibitors which target different pro-survival pathways, and radiotherapy to optimize treatment. Full article
9 pages, 1412 KB  
Article
The Impact of Everolimus and Radiation Therapy on Pulmonary Fibrosis
by Mehmet Fuat Eren, Ayfer Ay Eren, Mutlay Sayan, Birsen Yücel, Şahende Elagöz, Yıldıray Özgüven, Irina Vergalasova, Ahmet Altun, Saadettin Kılıçkap, Vasudev Malik Daliparty and Nuran Beşe
Medicina 2020, 56(7), 348; https://doi.org/10.3390/medicina56070348 - 13 Jul 2020
Cited by 5 | Viewed by 3463
Abstract
Background and objectives: Everolimus (EVE) is a mammalian target of the rapamycin (mTOR) inhibitor that is widely used in cancer patients. Pulmonary toxicity, usually manifesting as interstitial pneumonitis, is a serious adverse effect of this drug. Radiation therapy, which is often administered in [...] Read more.
Background and objectives: Everolimus (EVE) is a mammalian target of the rapamycin (mTOR) inhibitor that is widely used in cancer patients. Pulmonary toxicity, usually manifesting as interstitial pneumonitis, is a serious adverse effect of this drug. Radiation therapy, which is often administered in conjunction with chemotherapy for synergistic effects, also causes pulmonary fibrosis. In view of pulmonary damage development in these two forms of cancer treatment, we have examined the effect of EVE administration individually, in combination with radiation given in varying sequences, and its relation to the extent of pulmonary damage. Materials and Methods: We performed an experimental study in albino rats, which were randomized into five groups: (1) control group, (2) EVE alone, (3) EVE 22 h after radiation, (4) EVE 2 h after irradiation, and (5) only radiation. Sixteen weeks after thoracic irradiation, rat lung tissue samples were examined under light microscopy, and the extent of pulmonary damage was estimated. After this, we calculated median fibrosis scores in each group. Results: The highest fibrosis score was noted in Group 4. Among the five groups, the control group had a significantly lower median fibrosis score compared to the others. When the median fibrosis score of the group that received concurrent EVE with radiation therapy (RT) (Group 4) was compared with that of the control group, the difference was statistically significant (p = 0.0022). However, no significant differences were achieved among the study groups that received EVE only or RT only, whether concurrently or sequentially (p > 0.05). Conclusion: EVE is an effective treatment option for the management of several malignancies and is often combined with other therapies, such as radiation, for a more efficient response. However, an increased risk of pulmonary fibrosis should also be anticipated when these two modalities are combined, as they both can cause pulmonary damage, especially when administered concurrently. Full article
(This article belongs to the Section Oncology)
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2 pages, 574 KB  
Case Report
Thoracic Actinomycosis: A Rare Occurrence
by Waqas Jehangir, Bhumesh Vaidya, Souad Enakuaa, Nazar Raoof, John R. Middleton and Abdalla Yousif
Infect. Dis. Rep. 2016, 8(1), 5963; https://doi.org/10.4081/idr.2016.5963 - 21 Mar 2016
Cited by 7 | Viewed by 893
Abstract
Actinomyces israelii is a branching anaerobic bacilli microorganism that can be identified as normal flora throughout various portions of the human alimentary canal. It is crucial to establish a diagnosis as treatment will vary depending on the clinical form of the disease. We [...] Read more.
Actinomyces israelii is a branching anaerobic bacilli microorganism that can be identified as normal flora throughout various portions of the human alimentary canal. It is crucial to establish a diagnosis as treatment will vary depending on the clinical form of the disease. We report a case of a 78-year-old man who initially presented with an acute onset of respiratory distress displayed contrast leakage on computed tomography from the site of a previously inserted esophageal stent for an unsuccessful surgical repair of an esophageal rupture. In addition to the contrast leakage, the presence of a bronchopulmonary fistula imaging prompted the need for further investigation. Our patient was empirically treated with antibiotics and obtained blood cultures, which returned positive A. israelii. Full article
3 pages, 616 KB  
Case Report
A Rare Case of Myelodysplastic Syndrome with Refractory Thrombocytopenia
by Waqas Jehangir, John Webb, Shilpi Singh, Sabrina Arshed, Shuvendu Sen and Abdalla Yousif
Hematol. Rep. 2015, 7(3), 5897; https://doi.org/10.4081/hr.2015.5897 - 23 Sep 2015
Viewed by 764
Abstract
Myelodysplastic syndromes (MDS) represent a variety of clonal abnormalities, possibly preleukemic and display numerous phenotypic manifestations. Specific mutations carry high morbidity and mortality rates due to cell line dysplasia. MDS commonly presents with symptoms related to anemia, and approximately two-thirds will develop thrombocytopenia, [...] Read more.
Myelodysplastic syndromes (MDS) represent a variety of clonal abnormalities, possibly preleukemic and display numerous phenotypic manifestations. Specific mutations carry high morbidity and mortality rates due to cell line dysplasia. MDS commonly presents with symptoms related to anemia, and approximately two-thirds will develop thrombocytopenia, a rare, but potentially lethal complication that increases complexity in treatment and morbidity, and may be due to unique genetic mutations leading to refractory thrombocytopenia, ultimately leading to an overall reduction in survival. Careful identification and monitoring of this patient subdivision can significantly reduce morbidity and mortality, and potential identification of specific gene mutations and advances in treatment options will hopefully provide guidance on detecting at-risk patients in the future. We present a case of a man with MDS-U (karyotype 46, XY, del (20) (q11.2q13.3) (20) with no detected JAK2 V617F mutation), who in despite of appropriate evidenced based treatment, continued to exhibit refractory thrombocytopenia. Full article
147 KB  
Article
Unusually Large Cellular Schwannoma of the Foot
by Warren A. Pasternack and Deborah J. Winter-Reiken
J. Am. Podiatr. Med. Assoc. 2005, 95(2), 157-160; https://doi.org/10.7547/0950157 - 1 Mar 2005
Cited by 13 | Viewed by 30
Abstract
This article presents a case of an unusually large cellular schwannoma of the foot. This uncommon lesion of the lower extremity is described with regard to clinical appearance, radiologic evaluation (including magnetic resonance imaging), histologic characteristics, and intraoperative findings. Full article
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