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            <record>
              <language>eng</language>
              <publisher>Turkish Society of Thoracic Surgery</publisher>
              <journalTitle>Current Thoracic Surgery</journalTitle>
              <issn></issn>
              <eissn>2548-0316</eissn>
              <publicationDate>2019-12-31</publicationDate>
              <volume>4</volume>
              <issue>1</issue>
              <startPage>1</startPage>
              <endPage>7</endPage>
              <doi>10.26663/cts.2019.0001</doi>
              <publisherRecordId>67</publisherRecordId>
              <documentType>article</documentType>
              <title language="eng">Routine practical contribution of innovations with 2015 world health organization classification in the diagnosis of large cell lung carcinoma</title>
                <authors>
                              <author>
                                <name>Funda  Incekara</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Gokturk  Findik</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Ebru Guven Sayilir</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Koray  Aydogdu</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Mustafa Sevki Demiroz</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Funda  Demirag</name>
                                <affiliationId>2</affiliationId>
                              </author>
                              <author>
                                <name>Hakan  Nomenoglu</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Selim Sakir Erkmen Gülhan</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Abdullah İrfan Tastepe</name>
                                <affiliationId>3</affiliationId>
                              </author>
                              <author>
                                <name>Sadi  Kaya</name>
                                <affiliationId>1</affiliationId>
                              </author>
                      </authors>
              <affiliationsList><affiliationName affiliationId="1">Department of Thoracic Surgery, Atatürk Chest Diseases and Thoracic Surgery Training and Research Hospital, Ankara, Turkey</affiliationName><affiliationName affiliationId="2">Department of Pathology, Atatürk Chest Diseases and Thoracic Surgery Training and Research Hospital, Ankara, Turkey</affiliationName><affiliationName affiliationId="3">Department of Thoracic Surgery, Gazi University Faculty of Medicine, Ankara, Turkey</affiliationName></affiliationsList><abstract language="eng">&lt;b&gt;Background:&lt;/b&gt; Large-cell lung carcinoma (LCLC) is a relatively aggressive tumor and constitutes a small
proportion of non-small-cell lung carcinoma (NSCLC). The purpose of this study was to investigate the
clinicopathological characteristics of LCLC and reclassify patients according to the 2015 World Health
Organization (WHO) criteria to improve the diagnosis rate of LCLC.&lt;p&gt;
&lt;b&gt;Materials and Methods: &lt;/b&gt;The clinicopathological data of 32 patients who were diagnosed as LCLC
in our clinic between January 1999 and December 2016 and underwent surgery were retrospectively
investigated. The 32 patients with LCLC accounted for 1.6% of the total 1935 patients who were
diagnosed as having pulmonary cancer during the corresponding time period at our institution.&lt;p&gt;
&lt;b&gt;Results:&lt;/b&gt; There were 30 males and 2 females with a mean age of 56.4 (range, 39-76) years. The ratio of
smoking / non-smoking patients was 22/32 (68.7%). Based on the new definition of LCLC, a total of
32 patients with LCLC were detected. 16 patients with null immunohistochemical features, 12 with no
stains available, and 4 with unclear immunohistochemical features. Our 1, 3, and 5-year survival rates
were 65.6%, 53.1%, and 46.9%, respectively.&lt;p&gt;
&lt;b&gt;Conclusions: &lt;/b&gt;According to the new classification, formerly diagnosed LCLCs were mostly reclassified
as adenocarcinoma and non-keratinizing squamous cell carcinoma. LCLC, which became a more
homogeneous group with the 2015 WHO classification, may significantly benefit from multimodal
treatment with surgery.</abstract>
              <fullTextUrl format="pdf">https://cts.tgcd.org.tr/pdf.php?id=67</fullTextUrl>
              <keywords><keyword>large-cell carcinoma</keyword><keyword>surgery</keyword><keyword>chemotherapy</keyword><keyword>radiotherapy</keyword>
                  </keywords>
            </record>


            <record>
              <language>eng</language>
              <publisher>Turkish Society of Thoracic Surgery</publisher>
              <journalTitle>Current Thoracic Surgery</journalTitle>
              <issn></issn>
              <eissn>2548-0316</eissn>
              <publicationDate>2019-12-31</publicationDate>
              <volume>4</volume>
              <issue>1</issue>
              <startPage>8</startPage>
              <endPage>12</endPage>
              <doi>10.26663/cts.2019.0002</doi>
              <publisherRecordId>68</publisherRecordId>
              <documentType>article</documentType>
              <title language="eng">The effect of polyglycolic acid mesh application in tracheal anastomoses on pressure and tensile strength: an ex vivo experimental study</title>
                <authors>
                              <author>
                                <name>Ali  Kılıcgün</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Yusuf Özgür Biçer</name>
                                <affiliationId>2</affiliationId>
                              </author>
                              <author>
                                <name>Ali Cevat Kutluk</name>
                                <affiliationId>3</affiliationId>
                              </author>
                              <author>
                                <name>Sinan  Seyhan</name>
                                <affiliationId>2</affiliationId>
                              </author>
                              <author>
                                <name>Serap Köybaşı Sanal</name>
                                <affiliationId>2</affiliationId>
                              </author>
                      </authors>
              <affiliationsList><affiliationName affiliationId="1">Department of Thoracic Surgery, Abant İzzet Baysal University, Medical School, Bolu, Turkey</affiliationName><affiliationName affiliationId="2">Department of Head and Neck Surgery, Abant Izzet Baysal University, Medical School, Bolu, Turkey</affiliationName><affiliationName affiliationId="3">Department of Thoracic Surgery, Yedikule Chest Disease and Thoracic Surgery Training and Research Hospital, İstanbul, Turkey</affiliationName></affiliationsList><abstract language="eng">&lt;b&gt;Background:&lt;/b&gt; This study aims to investigate the effect of polyglycolic acid (PGA) mesh application in
tracheal anastomosis on the air-leakage and tension resistance.&lt;p&gt;
&lt;b&gt;Materials and Methods: &lt;/b&gt;Tracheae were collected from freshly slaughtered healthy sheep weighing
25-30 kg (2-3 years old) that were acquired from the local slaughterhouse. Twenty-eight tracheae were
transported to the laboratory within an hour of slaughter and then dissected to remove the esophagus
before obtaining 20-cm long tracheae. All tracheae were transected at the midpoint. In Groups 1 and 2,
the transected tracheae were anastomosed by using interrupted 3-0 Vicryl sutures. In Groups 3 and 4, after
anastomosing the transected tracheae with interrupted 3-0 Vicryl, the sites of anastomosis were reinforced
by using Polyglycolic acid mesh. Groups 1 and 3 were tested for tensile strength, while Groups 2 and 4
were tested for pressure resistance.&lt;p&gt;
&lt;b&gt;Results: &lt;/b&gt;The median pressure was 49.00 ± 7.47 mmHg in the group anastomosed with only Vicryl,
whereas it was measured as 70 ± 13.49 mmHg in the group on which the anastomoses were reinforced
with PGA mesh. The median force needed to break anastomoses were 166.40 ± 24.28 Newton in the
Vicryl-only group and 136.80 ± 34.93 newton in the PGA- reinforced group. The difference between the
pressure resistance values of the Vicryl-only group and the PGA reinforced group was significant (p =
0.006). However, the difference with regard to the tensile strength was insignificant (p = 0.201).&lt;p&gt;
&lt;b&gt;Conclusion: &lt;/b&gt;We found that the reinforcement of the anastomosis site with polyglycolic acid mesh
significantly increases the pressure resistance but does not significantly affect tensile strength.</abstract>
              <fullTextUrl format="pdf">https://cts.tgcd.org.tr/pdf.php?id=68</fullTextUrl>
              <keywords><keyword>trachea</keyword><keyword>anastomoses</keyword><keyword>polyglycolic acid</keyword>
                  </keywords>
            </record>


            <record>
              <language>eng</language>
              <publisher>Turkish Society of Thoracic Surgery</publisher>
              <journalTitle>Current Thoracic Surgery</journalTitle>
              <issn></issn>
              <eissn>2548-0316</eissn>
              <publicationDate>2019-12-31</publicationDate>
              <volume>4</volume>
              <issue>1</issue>
              <startPage>13</startPage>
              <endPage>20</endPage>
              <doi>10.26663/cts.2019.0003</doi>
              <publisherRecordId>69</publisherRecordId>
              <documentType>article</documentType>
              <title language="eng">The role of fluids in postpneumonectomic pulmonary edema: an experimental study</title>
                <authors>
                              <author>
                                <name>Murat  Akkuş</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Ali Cevat Kutluk</name>
                                <affiliationId>2</affiliationId>
                              </author>
                      </authors>
              <affiliationsList><affiliationName affiliationId="1">Department of Thoracic Surgery, Mehmet Akif Ersoy Thoracic and Cardiovascular Surgery Training and Research Hospital, Istanbul, Turkey</affiliationName><affiliationName affiliationId="2">Department of Thoracic Surgery, Yedikule Thoracic Surgery Training and Research Hospital, Istanbul, Turkey</affiliationName></affiliationsList><abstract language="eng">&lt;b&gt;Background: &lt;/b&gt;The role of fluids in the etiology of postpneumonectomy pulmonary edema (PPE) is
controversial. The aim of this experimental study was to assess the effect of crystalloid or colloid fluids
and normal or high volume on the etiology of PPE.&lt;p&gt;
&lt;b&gt;Materials and Methods: &lt;/b&gt;20 New Zealand rabbits were used and divided into 4 groups. Pneumonectomy
had performed firstly in each subject, then for 3 hours, normal and high volume of crystalloid and
colloid fluids were administered. The first group were administered 3 ml/kg/h crystalloid (0.9% NaCl),
the second group received 10 ml/kg/h of the same crystalloid, the third group were administered 3 ml/
kg/h colloid (6% HES/0.7) and the fourth group received 10 ml/kg/h of the same colloid infusion.
Pneumonectomy and remaining lung materials were weighed when wet and dry and pathologic
investigation was performed with a light microscopy.&lt;p&gt;
&lt;b&gt;Results: &lt;/b&gt;There was no significant difference between the preoperative and postoperative wet/dry ratio
(W/DR) of pneumonectomy and remaining lung material in all groups administered crystalloid and
colloid (1st Group Z = 0.707; p = 0.480, 2nd Group Z = 0.577; p = 0.564, 3rd Group Z = 0.577; p
= 0.564, 4th Group Z = 0.677; p = 0.498). There was no significant difference identified between
pneumonectomy material W/DR for all crystalloid and colloid groups (x2 = 2.787; p = 0.426) and again
between the remaining lung material W/DR (x2 = 2.858; p = 0.414). The histopathologic assessments
of all groups were similar.&lt;p&gt;
&lt;b&gt;Conclusion: &lt;/b&gt;Administration of crystalloid or colloid fluids at normal or high volume was assessed not
be responsible alone for the PPE etiology in subjects with normal cardiac function. Histopathologic
findings were similar in all groups.</abstract>
              <fullTextUrl format="pdf">https://cts.tgcd.org.tr/pdf.php?id=69</fullTextUrl>
              <keywords><keyword>pulmonary edema</keyword><keyword>pneumonectomy complications</keyword><keyword>pulmonary resection</keyword>
                  </keywords>
            </record>


            <record>
              <language>eng</language>
              <publisher>Turkish Society of Thoracic Surgery</publisher>
              <journalTitle>Current Thoracic Surgery</journalTitle>
              <issn></issn>
              <eissn>2548-0316</eissn>
              <publicationDate>2019-12-31</publicationDate>
              <volume>4</volume>
              <issue>1</issue>
              <startPage>21</startPage>
              <endPage>25</endPage>
              <doi>10.26663/cts.2019.0004</doi>
              <publisherRecordId>70</publisherRecordId>
              <documentType>article</documentType>
              <title language="eng">Is delayed puberty a new etiological factor for primary spontaneous pneumothorax?</title>
                <authors>
                              <author>
                                <name>Tevfik Ilker Akcam</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Sukran  Darcan</name>
                                <affiliationId>2</affiliationId>
                              </author>
                              <author>
                                <name>Ali  Ozdil</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Onder  Kavurmaci</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Ayse Gul Ergonul</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Kutsal  Turhan</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Alpaslan  Cakan</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Ufuk  Cagirici</name>
                                <affiliationId>1</affiliationId>
                              </author>
                      </authors>
              <affiliationsList><affiliationName affiliationId="1">Department of Thoracic Surgery, Ege University, School of Medicine, Izmir, Turkey</affiliationName><affiliationName affiliationId="2">Department of Pediatric Endocrinology, Ege University, School of Medicine, Izmir, Turkey</affiliationName></affiliationsList><abstract language="eng">&lt;b&gt;Background:&lt;/b&gt; Although the etiology of primer spontaneous pneumothorax (PSP) is not exactly
understood, it has been suggested to be associated with rupture of bulla/bleb formations at the lung
apices in thin, tall, young adults. In this study, we aim to evaluate whether delayed puberty is a new
etiological factor for PSP.&lt;p&gt;
&lt;b&gt;Materials and Methods: &lt;/b&gt;A total of 91 patients who were treated for PSP in our clinic between January
2013 and September 2016 and who were scheduled for a follow-up visit by phone call and underwent
pubertal-stage assessment were retrospectively analyzed.&lt;p&gt;
&lt;b&gt;Results:&lt;/b&gt; Of all patients, 10 (12.1%) were females and 81 (87.9%) were males. The mean age was 25.90
± 6.83 (range, 17 to 38) years and the mean height was 178.90 ± 7.6 (range, 161 to 197) cm. The mean
age at menarche of female patients was 14.20 ± 1.31 (range, 12 to 17) years. The women had a late
age at menarche compared to the overall Turkish female population (p &lt; 0.0001). The mean age for the
development of facial hairs in the men was 16.63 ± 1.69 (range, 13 to 22) years, showing a later age,
compared to the overall Turkish male population (p &lt; 0.0001).&lt;p&gt;
&lt;b&gt;Conclusion:&lt;/b&gt; Our study results showed that the patients with pneumothorax had an advanced age at
puberty, compared to the normal overall population, and that the pubertal growth spurt occurred within
a short period of time. This condition is also suggested to have an effect on the lung maturity and the
development of pneumothorax.</abstract>
              <fullTextUrl format="pdf">https://cts.tgcd.org.tr/pdf.php?id=70</fullTextUrl>
              <keywords><keyword>primer spontaneous pneumothorax</keyword><keyword>pubertal growth</keyword><keyword>lung maturity</keyword>
                  </keywords>
            </record>


            <record>
              <language>eng</language>
              <publisher>Turkish Society of Thoracic Surgery</publisher>
              <journalTitle>Current Thoracic Surgery</journalTitle>
              <issn></issn>
              <eissn>2548-0316</eissn>
              <publicationDate>2019-12-31</publicationDate>
              <volume>4</volume>
              <issue>1</issue>
              <startPage>26</startPage>
              <endPage>33</endPage>
              <doi>10.26663/cts.2019.0005</doi>
              <publisherRecordId>71</publisherRecordId>
              <documentType>article</documentType>
              <title language="eng">Is intercostal nerve protection necessary and safe technique for postthoracotomy pain?</title>
                <authors>
                              <author>
                                <name>Celal Bugra Sezen</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Cemal  Aker</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Anil  Gokce</name>
                                <affiliationId>2</affiliationId>
                              </author>
                              <author>
                                <name>Cem Emrah Kalafat</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Suleyman Anıl Akboga</name>
                                <affiliationId>2</affiliationId>
                              </author>
                              <author>
                                <name>Muhammet  Sayan</name>
                                <affiliationId>2</affiliationId>
                              </author>
                              <author>
                                <name>Ali  Celik</name>
                                <affiliationId>2</affiliationId>
                              </author>
                              <author>
                                <name>Abdullah Irfan Tastepe</name>
                                <affiliationId>2</affiliationId>
                              </author>
                      </authors>
              <affiliationsList><affiliationName affiliationId="1">Department of Thoracic Surgery,Yedikule Chest Diseases and Thoracic Surgery Education and Research Hospital, İstanbul, Turkey</affiliationName><affiliationName affiliationId="2">Department of Thoracic Surgery, Gazi University, School of Medicine, Ankara, Turkey</affiliationName></affiliationsList><abstract language="eng">&lt;b&gt;Background:&lt;/b&gt; Our objective in this study was to prospectively evaluate the effects of conventional closure
techniques, intracostal suture, and intercostal nerve preservation on postoperative morbidity and longterm
pain management.&lt;p&gt;
&lt;b&gt;Materials and Methods: &lt;/b&gt;This prospective study was conducted between 2012 and 2015. Three different
closure techniques were applied to patients who underwent posterolateral thoracotomy: conventional
suture technique, intracostal suture technique, and intracostal suture technique with intercostal nerve
preservation. Early postoperative pain level was assessed using a visual analog scale; pain at postoperative
six months was assessed with the LANNS pain scale.&lt;p&gt;
&lt;b&gt;Results: &lt;/b&gt;Seventy-three male patients (82%) and 16 (18%) female patients were included in the study.
Suturing time differed significantly between the groups. At postoperative day 0, 1, and 2, there were
significant differences between the groups in pain scores when at rest and while coughing (p &lt; 0.001).
Complications occurred in 22 patients (24.7%). There were no significant differences in complications
between the groups (p = 0.603). Chronic pain at postoperative six months was more prevalent in group A
compared to groups B and C (p &lt; 0.05).&lt;p&gt;
&lt;b&gt;Conclusion:&lt;/b&gt; Compared to the conventional technique, the intracostal suture technique with intercostal
muscle flap is yields better outcomes in terms of early and chronic postoperative pain.</abstract>
              <fullTextUrl format="pdf">https://cts.tgcd.org.tr/pdf.php?id=71</fullTextUrl>
              <keywords><keyword>pain</keyword><keyword>chronic pain</keyword><keyword>thoracotomy</keyword><keyword>intercostal nerve</keyword>
                  </keywords>
            </record>


            <record>
              <language>eng</language>
              <publisher>Turkish Society of Thoracic Surgery</publisher>
              <journalTitle>Current Thoracic Surgery</journalTitle>
              <issn></issn>
              <eissn>2548-0316</eissn>
              <publicationDate>2019-12-31</publicationDate>
              <volume>4</volume>
              <issue>1</issue>
              <startPage>34</startPage>
              <endPage>41</endPage>
              <doi>10.26663/cts.2019.0006</doi>
              <publisherRecordId>72</publisherRecordId>
              <documentType>article</documentType>
              <title language="eng">Primary sarcomas of the lung: report of five cases and review of the literature</title>
                <authors>
                              <author>
                                <name>Makbule  Ergin</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Hakan  Keskin</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Abdullah  Erdogan</name>
                                <affiliationId>1</affiliationId>
                              </author>
                      </authors>
              <affiliationsList><affiliationName affiliationId="1">Department of Thoracic Surgery, School of Medicine, Akdeniz University, Antalya, Turkey Case Report Corresponding</affiliationName></affiliationsList><abstract language="eng">Primary pulmonary sarcomas of the lung are rare tumors with a low incidence. We reviewed the
literature and analyzed 5 patients retrospectively. All clinical datas and therapeutic protocols were
recorded. The required surgical procedure was lobectomy in 4 patients and diagnostic broncoscopy
and mediastinoscopy in one patient. At histological examination; 2 carcinosarcoma, 1 undifferentiated
pleomorphic sarcoma, 1 leiomyosarcoma and 1 synovial sarcoma diagnosed. Primary sarcomas of the
lung cannot be differentieted from more common tumors of the lung tumors clinically. Early diagnosis
and complete surgical resection is critical for prognosis.</abstract>
              <fullTextUrl format="pdf">https://cts.tgcd.org.tr/pdf.php?id=72</fullTextUrl>
              <keywords><keyword>carcinosarcoma</keyword><keyword>leiomyosarcoma</keyword><keyword>sarcoma</keyword><keyword>synovial sarcoma</keyword>
                  </keywords>
            </record>


            <record>
              <language>eng</language>
              <publisher>Turkish Society of Thoracic Surgery</publisher>
              <journalTitle>Current Thoracic Surgery</journalTitle>
              <issn></issn>
              <eissn>2548-0316</eissn>
              <publicationDate>2019-12-31</publicationDate>
              <volume>4</volume>
              <issue>1</issue>
              <startPage>42</startPage>
              <endPage>45</endPage>
              <doi>10.26663/cts.2019.0007</doi>
              <publisherRecordId>73</publisherRecordId>
              <documentType>article</documentType>
              <title language="eng">A rare lung tumor: pulmonary carcinosarcoma</title>
                <authors>
                              <author>
                                <name>Murat  Kara</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Berker  Özkan</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Berk  Çimenoğlu</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Fahmin  Amirov</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Yasemin  Özlük</name>
                                <affiliationId>2</affiliationId>
                              </author>
                      </authors>
              <affiliationsList><affiliationName affiliationId="1">Department of Thoracic Surgery, Istanbul University, Istanbul Medical Faculty, Istanbul, Turkey</affiliationName><affiliationName affiliationId="2">Department of Pathology, Istanbul University, Istanbul Medical Faculty, Istanbul, Turkey</affiliationName></affiliationsList><abstract language="eng">Pulmonary sarcomatoid carcinoma is an extremely rare malignant lung tumor with an unfavorable
prognosis, which shows carcinomatous and sarcomatous components. We present a case of 78-year-old
patient with a middle lobe tumor who underwent a bronchial sleeve middle lobectomy. The tumor was a
carcinosarcoma with squamous cell carcinoma and rhabdomyosarcoma components histologically. We
tried to emphasize this extreme lung tumor and its clinicopathological features.</abstract>
              <fullTextUrl format="pdf">https://cts.tgcd.org.tr/pdf.php?id=73</fullTextUrl>
              <keywords><keyword>pulmonary carcinosarcoma</keyword><keyword>surgery</keyword><keyword>resection</keyword>
                  </keywords>
            </record>


            <record>
              <language>eng</language>
              <publisher>Turkish Society of Thoracic Surgery</publisher>
              <journalTitle>Current Thoracic Surgery</journalTitle>
              <issn></issn>
              <eissn>2548-0316</eissn>
              <publicationDate>2019-12-31</publicationDate>
              <volume>4</volume>
              <issue>1</issue>
              <startPage>46</startPage>
              <endPage>48</endPage>
              <doi>10.26663/cts.2019.0008</doi>
              <publisherRecordId>74</publisherRecordId>
              <documentType>article</documentType>
              <title language="eng">Poland’s anomaly with contralateral spontaneous pneumothorax: is this a coincidence?</title>
                <authors>
                              <author>
                                <name>Güntuğ  Batıhan</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Kenan Can Ceylan</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Şeyda Örs Kaya</name>
                                <affiliationId>1</affiliationId>
                              </author>
                      </authors>
              <affiliationsList><affiliationName affiliationId="1">Department of Thoracic Surgery, Dr Suat Seren Chest Diseases and Surgery, Medical Practice and Research Center, University of Health Sciences, Izmir, Turkey</affiliationName></affiliationsList><abstract language="eng">Poland’s syndrome is a rare developmental anomaly characterized by absence of pectoralis major
muscle and presence of ipsilateral hand abnormalities (mostly syndactyly). Numerous malformations
as a component of this syndrome was defined in literature such as congenital heart diseases, upper limb
anomalies and pulmonary or renal hypoplasia. The incidence of Poland’s syndrome ranges from 1 in
7,000 to 1 in 100,000 live births. Here we describe a rare case of patient with Poland’s syndrome with
contralateral spontaneous pneumothorax.</abstract>
              <fullTextUrl format="pdf">https://cts.tgcd.org.tr/pdf.php?id=74</fullTextUrl>
              <keywords><keyword>Poland’s anomaly</keyword><keyword>pneumothorax</keyword><keyword>congenital malformation</keyword>
                  </keywords>
            </record>


            <record>
              <language>eng</language>
              <publisher>Turkish Society of Thoracic Surgery</publisher>
              <journalTitle>Current Thoracic Surgery</journalTitle>
              <issn></issn>
              <eissn>2548-0316</eissn>
              <publicationDate>2019-12-31</publicationDate>
              <volume>4</volume>
              <issue>1</issue>
              <startPage>49</startPage>
              <endPage>51</endPage>
              <doi>10.26663/cts.2019.0009</doi>
              <publisherRecordId>75</publisherRecordId>
              <documentType>article</documentType>
              <title language="eng">A rare case: extramedullary plasmacytoma of the mediastinum</title>
                <authors>
                              <author>
                                <name>Yiğit  Yılmaz</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Mesut Melih Özercan</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Burcu  Ancın</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Ulaş  Kumbasar</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Erkan  Dikmen</name>
                                <affiliationId>1</affiliationId>
                              </author>
                      </authors>
              <affiliationsList><affiliationName affiliationId="1">Department of Thoracic Surgery, Hacettepe University, School of Medicine, Ankara, Turkey</affiliationName></affiliationsList><abstract language="eng">Plasmacytomas are localized proliferations of plasma cells in bone marrow. Extraosseous tissue
involvement is uncommon. Herein, we report a case of mediastinal extramedullary plasmacytoma
in a 54-year-old woman. A 85 mm lesion was reported in computed chest tomography of the patient
who referred to ourvhospital with dyspnea. Since interventional radiologists did not think the patient
was suitable for percutaneous biopsy, a surgical biopsy was performed and the pathology reported a
plasmacytoma. Various investigations were done to rule out multiple myeloma. Since no result in favor
of multiple myeloma was obtained, mass was diagnosed as extramedullary plasmacytoma. Radiotherapy
was scheduled for the patient.</abstract>
              <fullTextUrl format="pdf">https://cts.tgcd.org.tr/pdf.php?id=75</fullTextUrl>
              <keywords><keyword>extramedullary plasmacytoma</keyword><keyword>mediastinum</keyword><keyword>mediastinal mass</keyword>
                  </keywords>
            </record>


            <record>
              <language>eng</language>
              <publisher>Turkish Society of Thoracic Surgery</publisher>
              <journalTitle>Current Thoracic Surgery</journalTitle>
              <issn></issn>
              <eissn>2548-0316</eissn>
              <publicationDate>2019-12-31</publicationDate>
              <volume>4</volume>
              <issue>1</issue>
              <startPage>52</startPage>
              <endPage>55</endPage>
              <doi>10.26663/cts.2019.00010</doi>
              <publisherRecordId>76</publisherRecordId>
              <documentType>article</documentType>
              <title language="eng">A rare cause of mediastinal mass: tuberculosis</title>
                <authors>
                              <author>
                                <name>Kenan Can Ceylan</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Guntug  Batıhan</name>
                                <affiliationId>1</affiliationId>
                              </author>
                              <author>
                                <name>Seyda Ors Kaya</name>
                                <affiliationId>1</affiliationId>
                              </author>
                      </authors>
              <affiliationsList><affiliationName affiliationId="1">Department of Thoracic Surgery, Dr Suat Seren Chest Diseases and Surgery, Medical Practice and Research Center, University of Health Sciences, Izmir, Turkey</affiliationName></affiliationsList><abstract language="eng">Neoplastic and non-neoplastic pathologies can cause lesions in the mediastinum. Bronchogenic cysts,
germ cell tumors, lymphoma, lymph node hyperplasia, thymoma, thymic cysts, and thyroid masses
tend to develop in mediastinal compartments. Tuberculosis would cause lymph node enlargement in
many areas of the body but it is a very rare cause of mediastinal mass. We report a case of tuberculosis
presenting with isolated, large middle mediastinal mass with high FDG uptake in PET/CT. We also
present a short review of reported cases of mediastinal tuberculosis.</abstract>
              <fullTextUrl format="pdf">https://cts.tgcd.org.tr/pdf.php?id=76</fullTextUrl>
              <keywords><keyword>mediastinal mass</keyword><keyword>tuberculosis</keyword><keyword>video-assisted thoracoscopic surgery</keyword>
                  </keywords>
            </record></records>