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Dive into the research topics where Katerina Tsirgogianni is active.

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Featured researches published by Katerina Tsirgogianni.


Annals of Translational Medicine | 2015

Lung abscess-etiology, diagnostic and treatment options

Ivan Kuhajda; Konstantinos Zarogoulidis; Katerina Tsirgogianni; Drosos Tsavlis; Ioannis Kioumis; Christoforos Kosmidis; Kosmas Tsakiridis; Andrew Mpakas; Paul Zarogoulidis; Athanasios Zissimopoulos; Dimitris Baloukas; Danijela Kuhajda

Lung abscess is a type of liquefactive necrosis of the lung tissue and formation of cavities (more than 2 cm) containing necrotic debris or fluid caused by microbial infection. It can be caused by aspiration, which may occur during altered consciousness and it usually causes a pus-filled cavity. Moreover, alcoholism is the most common condition predisposing to lung abscesses. Lung abscess is considered primary (60%) when it results from existing lung parenchymal process and is termed secondary when it complicates another process, e.g., vascular emboli or follows rupture of extrapulmonary abscess into lung. There are several imaging techniques which can identify the material inside the thorax such as computerized tomography (CT) scan of the thorax and ultrasound of the thorax. Broad spectrum antibiotic to cover mixed flora is the mainstay of treatment. Pulmonary physiotherapy and postural drainage are also important. Surgical procedures are required in selective patients for drainage or pulmonary resection. In the current review we will present all current information from diagnosis to treatment.


Journal of Cancer | 2015

Defining the role of tyrosine kinase inhibitors in early stage non-small cell lung cancer

Sofia Lampaki; George Lazaridis; Konstantinos Zarogoulidis; Ioannis Kioumis; Antonis Papaiwannou; Katerina Tsirgogianni; Anastasia Karavergou; Theodora Tsiouda; Vasilis Karavasilis; Lonny Yarmus; Kaid Darwiche; Lutz Freitag; Antonios Sakkas; Angeliki Kantzeli; Sofia Baka; Wolfgang Hohenforst-Schmidt; Paul Zarogoulidis

Historical, the non-small cell lung cancer (NSCLC) was as a united disease entity and the chemotherapy to the metastatic cancer had limited results. Recent studies for the metastatic non-small cell lung cancer led to the ascertainment that the NSCLC does not constitute exclusively a disease entity, but different neoplasms guided from different molecular paths, different biological behavior and at extension requires different confrontation. Thus the new direction for the therapeutic approach of NSCLC is henceforth the most individualized approach based on the activated molecular paths of tumor. Distinct subtypes of NSCLC are driven by a specific genetic alteration, like EGFR, ALK, ROS1 or BRAF mutations, and these genetic alterations are sensitized to the inhibition of specific oncogenic pathways. The benefit from the use of tyrosine kinase inhibitors in patients with EGFR mutations it was confirmed by six randomized studies of phase III that investigated the role of gefitinib, erlotinib and afatinib. In these studies the response rates vary in the impressive percentages from 55% to 86% and were connected with a remarkable median progression free survival of approximately 8 to 13 months, and with better quality of life compared to that of chemotherapy. In early stages NSCLC is needed the individualization of systemic treatment in order to reduce toxicity that is observed in the classic chemotherapy and to impact outcome. The role of EGFR TKIs has been evaluated in the adjuvant chemotherapy in early stage resected NSCLC. The data from these studies suggest that adjuvant TKI therapy might not increase the overall survival, but delay the recurrences. Prospective trials restricted to EGFR or ALK driven NSCLC subsets potentially offering the opportunity for a definitive answer in early disease adjuvant setting (ALCHEMIST) or as induction treatment before stage III chemo-radiotherapy (RTOG 1210/Alliance 31101), are ongoing. Ongoing prospective trials may offer the opportunity for a definitive answer of the role of tyrosine kinase inhibitors in induction treatment before chemo-radiotherapy or in early disease adjuvant therapy.


OncoTargets and Therapy | 2015

EGFR-TKIs in adjuvant treatment of lung cancer: to give or not to give?

Aleksandar Milovancev; Vladimir Stojsic; Bojan Zaric; Tomi Kovacevic; Tatjana Sarcev; Branislav Perin; Konstantinos Zarogoulidis; Katerina Tsirgogianni; Lutz Freitag; Kaid Darwiche; Drosos Tsavlis; Athanasios Zissimopoulos; Grigoris Stratakos; Paul Zarogoulidis

Epidermal growth factor receptor-tyrosine-kinase inhibitors (EGFR-TKIs) brought a significant revolution in the treatment of non-small-cell lung cancer (NSCLC). In a short period of time, EGFR-TKIs became the standard of treatment for mutation-positive, advanced stage non-squamous NSCLC. In recent years, second- and third-generation EGFR-TKIs are emerging, further widening the clinical use. However, the question of EGFR-TKIs efficiency in the treatment of early stage NSCLC still remains open. Early clinical trials failed to approve the use of EGFR-TKIs in adjuvant setting. The majority of these early trials were performed in unselected NSCLC populations and without standardized biomarker identification. One should certainly not rely solely on these results and dismiss the use of EGFR-TKIs as adjuvant therapy. Many important questions are still unanswered. Most important issues such as stage heterogeneity (IA–IIIA), timing (after or concomitantly with chemotherapy), and type of administration (monotherapy or combination) need to be answered in near future. Adjuvant TKIs in the treatment of lung cancer might offer significant number of advancements. Having in mind the significant duration of response observed in advance disease setting, there could be place for prolongation of response in adjuvant setting potentially, leading to improvement in survival. TKIs could offer less-toxic adjuvant treatment with better efficiency than chemotherapy. However, there is a chronic lack of randomized controlled trials in this field, leading to inability to draw any scientifically sound conclusion with regard to the adjuvant treatment. For now, the use of EGFR-TKIs outside clinical trial setting is not recommended. The purpose of this review is to evaluate current and available data.


Journal of Cancer | 2015

Could Somatostatin Enhance the Outcomes of Chemotherapeutic Treatment in SCLC

Kalliopi Domvri; Dimitrios Bougiouklis; Paul Zarogoulidis; Konstantinos Porpodis; Manolis Xristoforidis; Alexandra Liaka; Ellada Eleutheriadou; Sofia Lampaki; George Lazaridis; John Organtzis; George Kyriazis; Wolfgang Hohenforst-Schmidt; Katerina Tsirgogianni; Vasilis Karavasilis; Sofia Baka; Kaid Darwiche; Lutz Freitag; Georgia Trakada; Konstantinos Zarogoulidis

Purpose: Somatostatin is a peptide with a potent and broad antisecretory action, which makes it an invaluable drug target for the pharmacological management of pituitary adenomas and neuroendocrine tumors. Furthermore, somatostatin (SST) receptors (SSTR1, 2A and B, 3, 4 and 5) belong to the G protein coupled receptor family and are overexpressed in tumors. Since, human small-cell lung cancer overexpresses somatostatin receptors (STTR), they could be legitimate targets for treating SCLC.The aim of this study was the evaluation of cytotoxicity of somatostatin in combination with several anticancer drugs in HTB-175 cell line (Small Cell Lung Cancer Cell line that expresses neuron specific enolase). Methods: Docetaxel, Paclitaxel, Carboplatin, Cisplatin, Etoposide, Gemzar, Navelbine, Fluorouracil, Farmorubicin are the chemotherapeutic drugs that we used for the combination before and after adding somatostatin in SCLC cell culture. HTB-175 cell line was purchased from ATCC LGC Standards.At indicated time-point, 48h after the combination, cell viability and apoptosis were measured with Annexin V staining by flow cytometry. Results: Flow cytometry showed that Docetaxel, Paclitaxel, Gemzar and Cisplatin induced apoptosis more when they were added before somatostatin, whereas etoposide induced apoptosis more after somatostatin treatment. Navelbine alone or in combination with somatostatin showed no differences in apoptosis. Farmorubicin showed equal toxicity in all combinations. Fluorouracil and Carboplatin induced apoptosis more when added alone in HTB-175 cell line. However, increased apoptosis was also observed when Carboplatin was administered before somatostatin in higher concentrations. Conclusion: Our results indicated that depending on the drug, somatostatin treatment before or after chemotherapeutic drugs increased apoptosis in small cell lung cancer cells. We suggest that long acting somatostatin analogues could be used as additive and maintenance therapy in combination to antineoplastic agents in SCLC patients.


Annals of Translational Medicine | 2015

Surgical anatomy of the internal thoracic arteries and their branching pattern: a cadaveric study

Dimitrios Paliouras; Thomas Rallis; Apostolos Gogakos; Christos Asteriou; Fotios Chatzinikolaou; Tagarakis Georgios; Katerina Tsirgogianni; Kosmas Tsakiridis; Andreas Mpakas; Nikolaos Sachpekidis; Konstantinos Zarogoulidis; Antonis Papaiwannou; John Organtzis; Ilias Karapantzos; Chrysanthi Karapantzou; Paul Zarogoulidis; Nikolaos Barbetakis

BACKGROUND The purpose of this study is to review the anatomic characteristics of internal thoracic artery (ITA) and its branches, in order to pursue the extension of its utilization and avoid intraoperative and postoperative complications. METHODS The study was carried out on anterior chest walls obtained during routine autopsies of 50 specimens (30 male, 20 female). Macroscopic and microscopic dissection was performed and the following were studied: origin, length and termination of ITA, size and distance from the sternum, and types of branches. RESULTS From the origin to the termination point, the length of the left internal thoracic artery (LITA) varied from 159 to 220 mm; with a mean of 182.60 mm. The length of the right internal thoracic artery (RITA) varied from 150 to 231 mm; with a mean of 185 mm. Four types of branches were distinguished. The RITA mean diameter was 2.31 mm, measured at the 2(nd) intercostal space, while the distance from the sternum was 12.77 mm, measured at the 3(rd) intercostal space. The LITA mean diameter was 1.98 mm with the distance from the sternum measured at 12.01 mm. CONCLUSIONS ITA has become the primary conduit for cardiac bypass surgery; many studies have generated fundamental anatomical knowledge for its clinical utilization, which is always useful in order to avoid intraoperative and postoperative complications.


Annals of Translational Medicine | 2015

Chest drainage systems in use

Charalambos Zisis; Katerina Tsirgogianni; George Lazaridis; Sofia Lampaki; Sofia Baka; Ioannis Mpoukovinas; Vasilis Karavasilis; Ioannis Kioumis; Georgia Pitsiou; Nikolaos Katsikogiannis; Kosmas Tsakiridis; Aggeliki Rapti; Georgia Trakada; Ilias Karapantzos; Chrysanthi Karapantzou; Athanasios Zissimopoulos; Konstantinos Zarogoulidis; Paul Zarogoulidis

A chest tube is a flexible plastic tube that is inserted through the chest wall and into the pleural space or mediastinum. It is used to remove air in the case of pneumothorax or fluid such as in the case of pleural effusion, blood, chyle, or pus when empyema occurs from the intrathoracic space. It is also known as a Bülau drain or an intercostal catheter. Insertion of chest tubes is widely performed by radiologists, pulmonary physicians and thoracic surgeons. Large catheters or small catheters are used based on each situation that the medical doctor encounters. In the current review we will focus on the chest drain systems that are in use.


Annals of Translational Medicine | 2015

Heimlich valve and pneumothorax

Apostolos Gogakos; Nikolaos Barbetakis; George Lazaridis; Antonis Papaiwannou; Anastasia Karavergou; Sofia Lampaki; Sofia Baka; Ioannis Mpoukovinas; Vasilis Karavasilis; Ioannis Kioumis; Georgia Pitsiou; Nikolaos Katsikogiannis; Kosmas Tsakiridis; Aggeliki Rapti; Georgia Trakada; Athanasios Zissimopoulos; Katerina Tsirgogianni; Konstantinos Zarogoulidis; Paul Zarogoulidis

The Heimlich valve is a small one-way valve used for chest drainage that empties into a flexible collection device and prevents return of gases or fluids into the pleural space. The Heimlich valve is less than 13 cm (5 inches) long and facilitates patient ambulation. Currently there are several systems in the market. It can be used in many patients instead of a traditional water seal drainage system. The Heimlich chest drainage valve was developed so that the process of draining the pleural cavity could be accomplished in a safe, relatively simple, and efficient manner. This valve system has replaced the cumbersome underwater drainage bottle system. Moreover; the Heimlich valve system connects to chest tubing and allows fluid and air to pass in one direction only. This system functions in any position, and it does not ever need to be clamped, a regulated suction can be attached to it if necessary. The valve drains into a plastic bag that can be held at any level, allowing the patient undergoing chest drainage to be ambulatory simply by carrying the bag. In the current mini review we will present the Heimlich valve system and method of insertion.


Annals of Translational Medicine | 2015

Electric vs. harmonic scalpel in treatment of primary focal hyperhidrosis with thoracoscopic sympathectomy

Ivan Kuhajda; Dejan Durić; Milos Koledin; Miroslav Ilic; Drosos Tsavlis; Ioannis Kioumis; Katerina Tsirgogianni; Konstantinos Zarogoulidis; John Organtzis; Christoforos Kosmidis; Sofia Baka; Ilias Karapantzos; Chrysanthi Karapantzou; Kosmas Tsakiridis; Nikolaos Sachpekidis; Paul Zarogoulidis; Milorad Bijelovic

BACKGROUND Hyperhidrosis is defined as excessive sweating beyond the physiologic needs of a person. Palmar hyperhidrosis in the adolescent period may have an impact on school work and may cause psychological problems. Thoracoscopic sympathectomy is now used routinely to treat patients with disabling primary hyperhidrosis or facial blushing. PATIENTS AND METHODS From January 2008 to December of 2009 bilateral thoracoscopic sympathectomy Th2-Th4 was performed to 79 patients aged from 17 to 55, who suffered from palmar, axillar or craniofacial hyperhidrosis. For the first 39 patients (group A) thoracoscopic sympathectomy was performed using electric scalpel and for the next 40 patients (group B) thoracoscopic sympathectomy was performed using harmonic scalpel. RESULTS Based on our results we did not find any significant differences between electric or harmonic scalpel usages for thoracoscopic sympathectomy. Moreover, there was no significant difference between complications and the severity of pain, with slightly higher intensity of pain with harmonic scalpel usage. Both electric and harmonic scalpel provided adequate treatment for primary hyperhidrosis, with the fact that non-disposable electric scalpel costs were less than that of the disposable harmonic scalpel. CONCLUSIONS Sympathectomy should be preferred for palmar hyperhidrosis treatment, as it is much technically shorter, simpler to implement, and also easier to learn. Thoracoscopic sympathectomy is safe and effective for the treatment of primary palmar hyperhidrosis in the adolescent period without any major side effects.


Annals of Translational Medicine | 2015

Double primary non-small cell lung cancer with synchronous small cell lung cancer N2 nodes: a case report

Apostolos Gogakos; Dimitrios Paliouras; Thomas Rallis; Fotios Chatzinikolaou; Persefoni Xirou; Katerina Tsirgogianni; Drosos Tsavlis; Nikos Sachpekidis; Kosmas Tsakiridis; Andreas Mpakas; Konstantinos Zarogoulidis; Athanasios Zissimopoulos; Paul Zarogoulidis; Nikolaos Barbetakis

Synchronous multiple primary lung cancer (SMPLC) is rare and very hard to distinguish from metastatic disease. Recent studies indicate the presence of this entity in the lung, with no mention to the involvement of the mediastinum. An extremely rare case of a 68-year-old male with double primary non-small cell lung cancer (NSCLC) in the left upper lobe and N2 positive nodes for small cell lung cancer (SCLC) is presented. Modern diagnostic criteria as well as aggressive curative strategies are encouraged, in order to achieve better survival rates for such patients.


Annals of Translational Medicine | 2015

Pulmonary arteriovenous malformation-etiology, clinical four case presentations and review of the literature

Ivan Kuhajda; Misel Milosevic; Dejan Ilincic; Danijela Kuhajda; Sandra Pekovic; Katerina Tsirgogianni; Drosos Tsavlis; Kosmas Tsakiridis; Antonios Sakkas; Angeliki Kantzeli; Konstantinos Zarogoulidis; Paul Zarogoulidis; Athanasios Zissimopoulos; Dejan Durić

Pulmonary arteriovenous malformation (PAVM) is a rare clinical condition with abnormal direct communication between the branches of pulmonary artery and vein. It may occur as an isolated anomaly or in association with hereditary hemorrhagic telangiectasia (HHT). Although these vascular pulmonary pathologies are quite uncommon, they are the important part of the differential diagnosis of common pulmonary problems such as hypoxemia and pulmonary nodules. The diagnosis of PAVM in patients remains a diagnostic challenge to the emergency physician. The most common clinical signs of PAVM are recurrent episodes of epistaxis and hemoptysis, so surgical resection is deemed the best curative option to avoid further episodes and recurrence of hemoptysis. Quite often the diagnosis is established after pathohistological examinations. We report a case of a female patient with a massive recurrent hemoptysis and without pathologic radiological findings which would suggest to PAVM and who was successfully treated with lobectomy.

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Dive into the Katerina Tsirgogianni's collaboration.

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Paul Zarogoulidis

Aristotle University of Thessaloniki

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Konstantinos Zarogoulidis

Aristotle University of Thessaloniki

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Ioannis Kioumis

Aristotle University of Thessaloniki

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Athanasios Zissimopoulos

Democritus University of Thrace

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Kosmas Tsakiridis

Aristotle University of Thessaloniki

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Drosos Tsavlis

Aristotle University of Thessaloniki

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Sofia Lampaki

Aristotle University of Thessaloniki

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Antonis Papaiwannou

Aristotle University of Thessaloniki

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George Lazaridis

Aristotle University of Thessaloniki

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Georgia Pitsiou

Aristotle University of Thessaloniki

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