Case Report Pulmonary Hyalinizing Granuloma Mimicking Metastatic Lung Cancer

Pulmonary hyalinizing granuloma is a very rare benign condition, which usually manifests as solitary and sometimes as multiple pulmonary nodules. Deposition of immune complexes in the lung parenchyma due to hypersensitivity reactions is implicated in the etiology of pulmonary hyalinizing granuloma. A 59-year-old female patient who presented to our clinic with complaints of chest pain and cough had bilateral, multiple, and rounded lesions with regular margins suggesting metastatic lung disease. A transthoracic needle biopsy of the nodule was performed in the left pulmonary anterior segment. Biopsy showed no malignancy. Since no diagnosis was made by the biopsy, the patient underwent a video-assisted thoracic surgery. The wedge biopsy reported pulmonary hyalinizing granuloma. We aimed to present the diagnosis and treatment stages of our patient who was diagnosed with pulmonary hyalinizing granuloma in the light of literature review

Konjenital Lobar Amfizemi Taklit Eden Konjenital Segmenter Amfizem Olgusu

Konjenital lobar amfizem, akciğerin etkilenen lobunun aşırı distansiyonu ve hava hapsi ile karakterize, infantil respiratuar distres sendromunun nadir görülen nedenlerinden biridir. Operasyon öncesi akciğer radyografisi ve akciğer bilgisayarlı tomografisi ile kon- jenital lobar amfizem tanısı konan ancak operasyon sırasında segmenter düzeyde tutulum tespit edildiği için segmenter rezeksiyon yapılan ve başarılı sonuç alınan bir olgumuzu sunuyoru

Case of congenital segmental emphysema mimicking congenital lobar emphysema

Konjenital lobar amfizem, akciğerin etkilenen lobunun aşırı distansiyonu ve hava hapsi ile karakterize, infantil respiratuar distres sendromunun nadir görülen nedenlerinden biridir. Operasyon öncesi akciğer radyografisi ve akciğer bilgisayarlı tomografisi ile kon- jenital lobar amfizem tanısı konan ancak operasyon sırasında segmenter düzeyde tutulum tespit edildiği için segmenter rezeksiyon yapılan ve başarılı sonuç alınan bir olgumuzu sunuyoruzCongenital lobar emphysema characterized by over distension and air trapping in the affected lobe is one of the rare causes of infantile respiratory distress syndrome. Surgical removal of the affected lobe is the most commonly accepted form of treatment. We reported an infant case that diagnosed congenital lobar emphysema on both chest radiography and computed tomography preoperatively. Resection of the only affected segment that realized intraoperatively was performed with good resul

The Cause of Decortication Material, 1.5 kg in Weight, In a Child Patient: Tuberculous Pleurisy

Tuberculosis still remains an important cause of morbidity and mortality in the world. Tuberculous pleurisy develops due to delayedtype hypersensitivity caused by tuberculosis bacteria and antigen-stimulated CD4+ T lymphocytes in patients with open and bacilli disseminating sub-pleural tuberculosis lesion. The increase in capillary permeability is the most important reason for effusion development after pleurisy. Effusions can be detected on plain chest X-ray or computed tomography. When pleural thickening reaches serious dimensions, lung expansion is prevented. In this case, the removal of thickened pleura by decortication is a necessity. Total decortication was performed on a 15-year-old male patient who applied to our clinic due to shortness of breath, chest pain, cough and fever upon detecting massive pleural effusion on the right and serious pleural thickening. In this study, the patient’s clinical presentation, diagnosis and treatment steps were presented in company with a review of the literature

A oase of H Type isolated Tracheo-Oesophageal fistula

H-tipi fistül, nadir görülen izole bir trakea- özofageal fistül (TÖF) şeklidir. Bu terim, trakea arka duvarı ve yemek borusu ön duvarı arasında 'H' şekli oluşturan oblik bir bağlantıdan gelir. Tipik olarak, tanı yaşamın üçüncü yılından önce konulur. Ancak bazı raporlarda kronik öksürük ve sık solunum yolu infeksiyonu tanıları ile takip edilen ve yetişkin yaş grubunda tanı alan olgular da bildirilmiştir. Bu yazımızda izole H tipi trakeo-özofageal fistüllü, beslenme ile morarma ve hırıltı şikayeti olan 13 aylık bir erkek hasta literatür eşliğinde sunuldu.H-type fistula is a rare, isolated form of tracheo-oesophageal fistula (TEF).This term refers to a connection at an oblique course between the posterior wall of the trachea and the anterior wall of the esophagus, presenting as an 'H' form. Typically, the diagnosis is made before the third year of life; however, some reports have been made of late presentation in adults who present chronic cough and frequent respiratory infections. We present thirteen month-old male patient, complaints of wheezing and bruising of the diet with a H type TEF

Pulmonary Hyalinizing Granuloma Mimicking Metastatic Lung Cancer

Pulmonary hyalinizing granuloma is a very rare benign condition, which usually manifests as solitary and sometimes as multiple pulmonary nodules. Deposition of immune complexes in the lung parenchyma due to hypersensitivity reactions is implicated in the etiology of pulmonary hyalinizing granuloma. A 59-year-old female patient who presented to our clinic with complaints of chest pain and cough had bilateral, multiple, and rounded lesions with regular margins suggesting metastatic lung disease. A transthoracic needle biopsy of the nodule was performed in the left pulmonary anterior segment. Biopsy showed no malignancy. Since no diagnosis was made by the biopsy, the patient underwent a video-assisted thoracic surgery. The wedge biopsy reported pulmonary hyalinizing granuloma. We aimed to present the diagnosis and treatment stages of our patient who was diagnosed with pulmonary hyalinizing granuloma in the light of literature review

A oase of H Type isolated Tracheo-Oesophageal fistula

H-tipi fistül, nadir görülen izole bir trakea- özofageal fistül (TÖF) şeklidir. Bu terim, trakea arka duvarı ve yemek borusu ön duvarı arasında 'H' şekli oluşturan oblik bir bağlantıdan gelir. Tipik olarak, tanı yaşamın üçüncü yılından önce konulur. Ancak bazı raporlarda kronik öksürük ve sık solunum yolu infeksiyonu tanıları ile takip edilen ve yetişkin yaş grubunda tanı alan olgular da bildirilmiştir. Bu yazımızda izole H tipi trakeo-özofageal fistüllü, beslenme ile morarma ve hırıltı şikayeti olan 13 aylık bir erkek hasta literatür eşliğinde sunuldu.H-type fistula is a rare, isolated form of tracheo-oesophageal fistula (TEF).This term refers to a connection at an oblique course between the posterior wall of the trachea and the anterior wall of the esophagus, presenting as an 'H' form. Typically, the diagnosis is made before the third year of life; however, some reports have been made of late presentation in adults who present chronic cough and frequent respiratory infections. We present thirteen month-old male patient, complaints of wheezing and bruising of the diet with a H type TEF