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  1. Article ; Online: Concurrent Localized Pulmonary Edema in a Patient With Pulmonary Embolism: An Atypical Clinical Presentation.

    Vrouvaki, Iro / Mouratidou, Nefeli / Katsenos, Stamatis

    Archivos de bronconeumologia

    2023  Volume 60, Issue 2, Page(s) 114

    MeSH term(s) Humans ; Pulmonary Edema/diagnostic imaging ; Pulmonary Edema/etiology ; Pulmonary Embolism/complications ; Pulmonary Embolism/diagnostic imaging ; Lung
    Language Spanish
    Publishing date 2023-12-18
    Publishing country Spain
    Document type Journal Article
    ZDB-ID 733126-5
    ISSN 1579-2129 ; 0300-2896
    ISSN (online) 1579-2129
    ISSN 0300-2896
    DOI 10.1016/j.arbres.2023.11.017
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Pharyngeal Papilloma: a Rare Non-Pulmonary Cause of Hemoptysis.

    Katsenos, Stamatis / Nikolopoulou, Melita

    Acta medica (Hradec Kralove)

    2019  Volume 61, Issue 4, Page(s) 158–161

    Abstract: The most common benign neoplasm of the pharynx is papilloma. It is characterized by bulging brittle lesions, which are pedicled or sessile, whitish-grey or pinkish colour. Progressive hoarseness is the main clinical feature. When the papillomata spread ... ...

    Abstract The most common benign neoplasm of the pharynx is papilloma. It is characterized by bulging brittle lesions, which are pedicled or sessile, whitish-grey or pinkish colour. Progressive hoarseness is the main clinical feature. When the papillomata spread throughout the tracheobronchial tree symptoms such as chronic cough, stridor, dyspnea or acute respiratory distress are mostly present. Hemoptysis as a presenting symptom is exceptionally rare in patients with pharyngeal papillomatosis. Herein, we report a case of pharyngeal papillomatosis in which hemoptysis was the primary clinical manifestation. The clinical and therapeutic aspects of the disease are briefly discussed.
    MeSH term(s) Adult ; Biopsy ; Bronchoscopy ; Diagnosis, Differential ; Hemoptysis/etiology ; Hemoptysis/surgery ; Humans ; Male ; Papilloma/complications ; Papilloma/pathology ; Papilloma/surgery ; Pharyngeal Neoplasms/complications ; Pharyngeal Neoplasms/pathology ; Pharyngeal Neoplasms/surgery ; Polymerase Chain Reaction ; Tomography, X-Ray Computed
    Language English
    Publishing date 2019-01-21
    Publishing country Czech Republic
    Document type Case Reports ; Journal Article
    ZDB-ID 1360995-6
    ISSN 1211-4286
    ISSN 1211-4286
    DOI 10.14712/18059694.2018.136
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Klinefelter syndrome and bronchial asthma: Is there any relationship between the low testosterone levels and asthma exacerbations?

    Ladias, Spyros / Katsenos, Stamatis

    Lung India : official organ of Indian Chest Society

    2018  Volume 35, Issue 4, Page(s) 368–369

    Language English
    Publishing date 2018-07-03
    Publishing country India
    Document type Letter
    ZDB-ID 2410801-7
    ISSN 0974-598X ; 0970-2113
    ISSN (online) 0974-598X
    ISSN 0970-2113
    DOI 10.4103/lungindia.lungindia_40_18
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Pharyngeal Papilloma

    Stamatis Katsenos / Melita Nikolopoulou

    Acta Medica, Vol 61, Iss 4, Pp 158-

    a Rare Non-Pulmonary Cause of Hemoptysis

    2019  Volume 161

    Abstract: The most common benign neoplasm of the pharynx is papilloma. It is characterized by bulging brittle lesions, which are pedicled or sessile, whitish-grey or pinkish colour. Progressive hoarseness is the main clinical feature. When the papillomata spread ... ...

    Abstract The most common benign neoplasm of the pharynx is papilloma. It is characterized by bulging brittle lesions, which are pedicled or sessile, whitish-grey or pinkish colour. Progressive hoarseness is the main clinical feature. When the papillomata spread throughout the tracheobronchial tree symptoms such as chronic cough, stridor, dyspnea or acute respiratory distress are mostly present. Hemoptysis as a presenting symptom is exceptionally rare in patients with pharyngeal papillomatosis. Herein, we report a case of pharyngeal papillomatosis in which hemoptysis was the primary clinical manifestation. The clinical and therapeutic aspects of the disease are briefly discussed.
    Keywords hemoptysis ; pharynx ; papilloma ; Medicine ; R
    Language English
    Publishing date 2019-01-01T00:00:00Z
    Publisher Karolinum Press
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  5. Article: Primary pulmonary lymphangiectasia in Noonan syndrome: apropos of an extremely rare manifestation and a brief literature review.

    Dendrinou, Georgia-Emmanuela / Zagarelos, Panagiotis / Sofronas, Angelos / Katsenos, Stamatis

    Monaldi archives for chest disease = Archivio Monaldi per le malattie del torace

    2020  Volume 90, Issue 4

    Abstract: Noonan syndrome (NS) is a genetic multisystem disorder characterised by distinctive facial features, developmental delay, learning difficulties, short stature, congenital heart disease, renal anomalies, bleeding difficulties and lymphatic malformations. ... ...

    Abstract Noonan syndrome (NS) is a genetic multisystem disorder characterised by distinctive facial features, developmental delay, learning difficulties, short stature, congenital heart disease, renal anomalies, bleeding difficulties and lymphatic malformations. Although lymphatic dysplasias are present in 20% of patients with NS, however pulmonary lymphangiectasia has rarely been described. In this present paper, we report a 24-year-old male who was diagnosed with Noonan syndrome and primary pulmonary lymphangiectasia by using chest imaging modalities. A brief overview of the current literature is also provided laying emphasis on the clinical, pathogenetic and diagnostic aspects of this uncommon Noonan syndrome complication.
    MeSH term(s) Adult ; Heart Defects, Congenital ; Humans ; Lung Diseases ; Lymphangiectasis/diagnostic imaging ; Male ; Noonan Syndrome/complications ; Noonan Syndrome/genetics ; Young Adult
    Language English
    Publishing date 2020-12-10
    Publishing country Italy
    Document type Case Reports ; Journal Article
    ZDB-ID 1160940-0
    ISSN 1122-0643 ; 1120-0391
    ISSN 1122-0643 ; 1120-0391
    DOI 10.4081/monaldi.2020.1576
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: The value of radial probe endobronchial ultrasound-guided transbronchial needle aspiration in the diagnosis of mediastinal lymph node metastasis from primary papillary thyroid cancer.

    Katsenos, Stamatis / Archondakis, Stavros

    Diagnostic cytopathology

    2016  Volume 44, Issue 9, Page(s) 748–752

    MeSH term(s) Bronchoscopy/methods ; Carcinoma/diagnostic imaging ; Carcinoma/pathology ; Endoscopic Ultrasound-Guided Fine Needle Aspiration/methods ; Female ; Humans ; Lymphatic Metastasis ; Mediastinal Neoplasms/diagnostic imaging ; Mediastinal Neoplasms/pathology ; Mediastinal Neoplasms/secondary ; Middle Aged ; Thyroid Neoplasms/diagnostic imaging ; Thyroid Neoplasms/pathology
    Language English
    Publishing date 2016-09
    Publishing country United States
    Document type Case Reports ; Journal Article
    ZDB-ID 632710-2
    ISSN 1097-0339 ; 8755-1039
    ISSN (online) 1097-0339
    ISSN 8755-1039
    DOI 10.1002/dc.23534
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Primary pulmonary lymphangiectasia in Noonan syndrome

    Georgia-Emmanuela Dendrinou / Panagiotis Zagarelos / Angelos Sofronas / Stamatis Katsenos

    Monaldi Archives for Chest Disease, Vol 90, Iss

    apropos of an extremely rare manifestation and a brief literature review

    2020  Volume 4

    Abstract: Noonan syndrome (NS) is a genetic multisystem disorder characterised by distinctive facial features, developmental delay, learning difficulties, short stature, congenital heart disease, renal anomalies, bleeding difficulties and lymphatic malformations. ... ...

    Abstract Noonan syndrome (NS) is a genetic multisystem disorder characterised by distinctive facial features, developmental delay, learning difficulties, short stature, congenital heart disease, renal anomalies, bleeding difficulties and lymphatic malformations. Although lymphatic dysplasias are present in 20% of patients with NS, however pulmonary lymphangiectasia has rarely been described. In this present paper, we report a 24-year-old male who was diagnosed with Noonan syndrome and primary pulmonary lymphangiectasia by using chest imaging modalities. A brief overview of the current literature is also provided laying emphasis on the clinical, pathogenetic and diagnostic aspects of this uncommon Noonan syndrome complication.
    Keywords Noonan syndrome ; pulmonary lymphangiectasia ; Medicine ; R
    Language English
    Publishing date 2020-12-01T00:00:00Z
    Publisher PAGEPress Publications
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  8. Article ; Online: Sulfasalazine-induced Hypereosinophilic Obliterative Bronchiolitis.

    Katsenos, Stamatis / Antonogiannaki, Elvira-Markela / Psathakis, Konstantinos

    Archivos de bronconeumologia

    2016  Volume 52, Issue 2, Page(s) 108

    MeSH term(s) Anti-Inflammatory Agents, Non-Steroidal/adverse effects ; Bronchiolitis Obliterans/chemically induced ; Eosinophilia/chemically induced ; Humans ; Male ; Middle Aged ; Sulfasalazine/adverse effects
    Chemical Substances Anti-Inflammatory Agents, Non-Steroidal ; Sulfasalazine (3XC8GUZ6CB)
    Language Spanish
    Publishing date 2016-02
    Publishing country Spain
    Document type Case Reports ; Letter
    ZDB-ID 733126-5
    ISSN 1579-2129 ; 0300-2896
    ISSN (online) 1579-2129
    ISSN 0300-2896
    DOI 10.1016/j.arbres.2015.01.013
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article: Solitary gastric metastasis from primary lung adenocarcinoma: a rare site of extra-thoracic metastatic disease.

    Katsenos, Stamatis / Archondakis, Stavros

    Journal of gastrointestinal oncology

    2013  Volume 4, Issue 2, Page(s) E11–5

    Abstract: Lung cancer metastasizing to gastrointestinal (GI)-tract is a rare event. Gastric metastasis is usually asymptomatic but when mucosal in location it may cause symptoms as demonstrated in the current case. This report describes a 60-year old male who was ... ...

    Abstract Lung cancer metastasizing to gastrointestinal (GI)-tract is a rare event. Gastric metastasis is usually asymptomatic but when mucosal in location it may cause symptoms as demonstrated in the current case. This report describes a 60-year old male who was admitted for evaluation of a left upper lobe lung mass with associated bilateral nodular opacities and mediastinal lymphadenopathy. After thorough work-up the diagnosis of advanced lung adenocarcinoma was made. During hospitalization period and prior to starting chemotherapy, he exhibited upper gastrointentinal bleeding. Esophagogastroduodenoscopy revealed an ulcerative lesion in the gastric corpus representing metastasis of the primary lung carcinoma that ensued from immunohistochemical analysis. Clinical, pathological and therapeutic aspects of this uncommon site of extrathoracic metastatic disease are discussed, emphasizing the importance of the immunohistochemistry in the differential diagnosis of lung carcinomas whether primary or secondary to the lung.
    Language English
    Publishing date 2013-05-17
    Publishing country China
    Document type Case Reports
    ZDB-ID 2594644-4
    ISSN 2219-679X ; 2078-6891
    ISSN (online) 2219-679X
    ISSN 2078-6891
    DOI 10.3978/j.issn.2078-6891.2012.057
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Orange-Pigmented Sputum as a Manifestation of Smoke Grenade Inhalation Injury.

    Chatzivasiloglou, Fotini / Katsenos, Stamatis / Psara, Anthoula / Tsintiris, Konstantinos

    Journal of bronchology & interventional pulmonology

    2016  Volume 23, Issue 1, Page(s) 76–78

    Abstract: A 34-year-old man presented with scanty hemoptysis, orange-colored expectoration, and mild dyspnea. He was in an enclosed building taking part in a military training exercise inhaling an orange-colored smoke from a smoke grenade ignition. His symptoms ... ...

    Abstract A 34-year-old man presented with scanty hemoptysis, orange-colored expectoration, and mild dyspnea. He was in an enclosed building taking part in a military training exercise inhaling an orange-colored smoke from a smoke grenade ignition. His symptoms developed immediately after the initial exposure but he sought medical assistance 20 hours later because of their persistence. Fiberoptic bronchoscopy was performed revealing diffuse inflammatory tracheobronchial tree with streaky orange-pigmented secretions in the trachea and both main-stem bronchi. Acute tracheobronchitis was diagnosed and the patient was treated with nebulized bronchodilators and intravenous corticosteroids showing complete recovery. To our knowledge, this is the first well-documented report of inhalation injury induced by a smoke bomb explosion including potassium chlorate oxidizer and Sudan I and presenting with orange-pigmented sputum production. Smoke inhalation injury is associated with significant morbidity and mortality. The heterogeneity of the smoke and the large variety of the resulting symptoms may be the reason why a definition, specific diagnostic criteria, and therapeutic guidelines are still lacking.
    MeSH term(s) Adrenal Cortex Hormones/therapeutic use ; Adult ; Bombs ; Bronchitis/drug therapy ; Bronchitis/etiology ; Bronchodilator Agents/therapeutic use ; Bronchoscopy ; Chlorates/adverse effects ; Humans ; Male ; Naphthols/adverse effects ; Smoke Inhalation Injury/diagnosis ; Smoke Inhalation Injury/drug therapy ; Sputum ; Tracheitis/drug therapy ; Tracheitis/etiology
    Chemical Substances Adrenal Cortex Hormones ; Bronchodilator Agents ; Chlorates ; Naphthols ; 1-phenylazo-2-naphthol (48I7IBB68J) ; chloric acid (Z0V9L75H3K)
    Language English
    Publishing date 2016-01
    Publishing country United States
    Document type Case Reports ; Journal Article
    ZDB-ID 2478320-1
    ISSN 1948-8270 ; 1944-6586
    ISSN (online) 1948-8270
    ISSN 1944-6586
    DOI 10.1097/LBR.0000000000000191
    Database MEDical Literature Analysis and Retrieval System OnLINE

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