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Showing 1 to 12 of 319 entries
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Lymphoepithelioma-like carcinoma of the lung: an unusual case and literature review.

Case reports in pulmonology

Huang YC, Hsueh C, Ho SY, Liao CY.
PMID: 24288644
Case Rep Pulmonol. 2013;2013:143405. doi: 10.1155/2013/143405. Epub 2013 Oct 30.

We described a case of lymphoepithelioma-like carcinoma (LELC) of the lung of a 65-year-old man with initial symptoms of intermittent chest pain and mild shortness of breath for 2 weeks. A right-lung mass was noted on chest computed tomography...

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Huang YC, Hsueh C, Ho SY, et al. Lymphoepithelioma-like carcinoma of the lung: an unusual case and literature review. Case Rep Pulmonol. 2013;2013:143405doi: 10.1155/2013/143405.
Huang, Y. C., Hsueh, C., Ho, S. Y., & Liao, C. Y. (2013). Lymphoepithelioma-like carcinoma of the lung: an unusual case and literature review. Case reports in pulmonology, 2013143405. https://doi.org/10.1155/2013/143405
Huang, Yuan-Chun, et al. "Lymphoepithelioma-like carcinoma of the lung: an unusual case and literature review." Case reports in pulmonology vol. 2013 (2013): 143405. doi: https://doi.org/10.1155/2013/143405
Huang YC, Hsueh C, Ho SY, Liao CY. Lymphoepithelioma-like carcinoma of the lung: an unusual case and literature review. Case Rep Pulmonol. 2013;2013:143405. doi: 10.1155/2013/143405. Epub 2013 Oct 30. PMID: 24288644; PMCID: PMC3833058.
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Endobronchial Cartilage Rupture: A Rare Cause of Lobar Collapse.

Case reports in pulmonology

Dasa O, Siddiqui N, Ruzieh M, Javaid T.
PMID: 27525149
Case Rep Pulmonol. 2016;2016:8178129. doi: 10.1155/2016/8178129. Epub 2016 Jul 25.

Endobronchial cartilage rupture is a rare clinical condition, which can present in patients with severe emphysema with sudden onset shortness of breath. We present a case of a 62-year-old male who presented to our emergency department with sudden onset...

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Dasa O, Siddiqui N, Ruzieh M, et al. Endobronchial Cartilage Rupture: A Rare Cause of Lobar Collapse. Case Rep Pulmonol. 2016;2016:8178129doi: 10.1155/2016/8178129.
Dasa, O., Siddiqui, N., Ruzieh, M., & Javaid, T. (2016). Endobronchial Cartilage Rupture: A Rare Cause of Lobar Collapse. Case reports in pulmonology, 20168178129. https://doi.org/10.1155/2016/8178129
Dasa, Osama, et al. "Endobronchial Cartilage Rupture: A Rare Cause of Lobar Collapse." Case reports in pulmonology vol. 2016 (2016): 8178129. doi: https://doi.org/10.1155/2016/8178129
Dasa O, Siddiqui N, Ruzieh M, Javaid T. Endobronchial Cartilage Rupture: A Rare Cause of Lobar Collapse. Case Rep Pulmonol. 2016;2016:8178129. doi: 10.1155/2016/8178129. Epub 2016 Jul 25. PMID: 27525149; PMCID: PMC4976168.
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Biphasic Malignant Pleural Mesothelioma Masquerading as a Primary Skeletal Tumor.

Case reports in pulmonology

Gleason JB, Tashtoush B, Diacovo MJ.
PMID: 27660729
Case Rep Pulmonol. 2016;2016:7560929. doi: 10.1155/2016/7560929. Epub 2016 Aug 31.

Biphasic malignant pleural mesothelioma is a rare malignant tumor, usually presenting as a pleural-based mass in a patient with history of chronic asbestos exposure. We herein report a case of a 41-year-old man who presented with chest pain and...

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Gleason JB, Tashtoush B, Diacovo MJ. Biphasic Malignant Pleural Mesothelioma Masquerading as a Primary Skeletal Tumor. Case Rep Pulmonol. 2016;2016:7560929doi: 10.1155/2016/7560929.
Gleason, J. B., Tashtoush, B., & Diacovo, M. J. (2016). Biphasic Malignant Pleural Mesothelioma Masquerading as a Primary Skeletal Tumor. Case reports in pulmonology, 20167560929. https://doi.org/10.1155/2016/7560929
Gleason, James Benjamin, et al. "Biphasic Malignant Pleural Mesothelioma Masquerading as a Primary Skeletal Tumor." Case reports in pulmonology vol. 2016 (2016): 7560929. doi: https://doi.org/10.1155/2016/7560929
Gleason JB, Tashtoush B, Diacovo MJ. Biphasic Malignant Pleural Mesothelioma Masquerading as a Primary Skeletal Tumor. Case Rep Pulmonol. 2016;2016:7560929. doi: 10.1155/2016/7560929. Epub 2016 Aug 31. PMID: 27660729; PMCID: PMC5021854.
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Mediastinal Mature Teratoma Revealed by Empyema.

Case reports in pulmonology

Raoufi M, Herrak L, Benali A, Achaachi L, El Ftouh M, Bellarbi S, Tilfine C, Taouarsa F.
PMID: 27144046
Case Rep Pulmonol. 2016;2016:7869476. doi: 10.1155/2016/7869476. Epub 2016 Apr 07.

Teratomas are germ cell tumors, manifested with a great variety of clinical features; the most common extragonadal site is the anterior mediastinum. In this case, we report the patient with a large mature mediastinal teratoma with several components of...

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Raoufi M, Herrak L, Benali A, et al. Mediastinal Mature Teratoma Revealed by Empyema. Case Rep Pulmonol. 2016;2016:7869476doi: 10.1155/2016/7869476.
Raoufi, M., Herrak, L., Benali, A., Achaachi, L., El Ftouh, M., Bellarbi, S., Tilfine, C., & Taouarsa, F. (2016). Mediastinal Mature Teratoma Revealed by Empyema. Case reports in pulmonology, 20167869476. https://doi.org/10.1155/2016/7869476
Raoufi, Mohammed, et al. "Mediastinal Mature Teratoma Revealed by Empyema." Case reports in pulmonology vol. 2016 (2016): 7869476. doi: https://doi.org/10.1155/2016/7869476
Raoufi M, Herrak L, Benali A, Achaachi L, El Ftouh M, Bellarbi S, Tilfine C, Taouarsa F. Mediastinal Mature Teratoma Revealed by Empyema. Case Rep Pulmonol. 2016;2016:7869476. doi: 10.1155/2016/7869476. Epub 2016 Apr 07. PMID: 27144046; PMCID: PMC4838797.
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Severe Respiratory Distress in a Child with Pulmonary Idiopathic Hemosiderosis Initially Presenting with Iron-Deficiency Anemia.

Case reports in pulmonology

Potalivo A, Finessi L, Facondini F, Lupo A, Andreoni C, Giuliani G, Cavicchi C.
PMID: 26634166
Case Rep Pulmonol. 2015;2015:876904. doi: 10.1155/2015/876904. Epub 2015 Nov 08.

Idiopathic pulmonary hemosiderosis (IPH) is a rare cause of alveolar hemorrhage in children but should be considered in children with anemia of unknown origin who develop respiratory complications. It is commonly characterized by the triad of recurrent hemoptysis, diffuse...

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Potalivo A, Finessi L, Facondini F, et al. Severe Respiratory Distress in a Child with Pulmonary Idiopathic Hemosiderosis Initially Presenting with Iron-Deficiency Anemia. Case Rep Pulmonol. 2015;2015:876904doi: 10.1155/2015/876904.
Potalivo, A., Finessi, L., Facondini, F., Lupo, A., Andreoni, C., Giuliani, G., & Cavicchi, C. (2015). Severe Respiratory Distress in a Child with Pulmonary Idiopathic Hemosiderosis Initially Presenting with Iron-Deficiency Anemia. Case reports in pulmonology, 2015876904. https://doi.org/10.1155/2015/876904
Potalivo, A, et al. "Severe Respiratory Distress in a Child with Pulmonary Idiopathic Hemosiderosis Initially Presenting with Iron-Deficiency Anemia." Case reports in pulmonology vol. 2015 (2015): 876904. doi: https://doi.org/10.1155/2015/876904
Potalivo A, Finessi L, Facondini F, Lupo A, Andreoni C, Giuliani G, Cavicchi C. Severe Respiratory Distress in a Child with Pulmonary Idiopathic Hemosiderosis Initially Presenting with Iron-Deficiency Anemia. Case Rep Pulmonol. 2015;2015:876904. doi: 10.1155/2015/876904. Epub 2015 Nov 08. PMID: 26634166; PMCID: PMC4655028.
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Perioperative Identification of an Accessory Fissure of the Right Lung.

Case reports in pulmonology

Taverne Y, Kleinrensink GJ, de Rooij P.
PMID: 26185701
Case Rep Pulmonol. 2015;2015:954769. doi: 10.1155/2015/954769. Epub 2015 Jun 22.

Anatomical variations of lungs are common in clinical practice; however, they are sometimes overlooked in routine imaging. Surgical anatomy of the lung is complex and many variations are known to occur. A defective pulmonary development gives rise to variations...

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Taverne Y, Kleinrensink GJ, de Rooij P. Perioperative Identification of an Accessory Fissure of the Right Lung. Case Rep Pulmonol. 2015;2015:954769doi: 10.1155/2015/954769.
Taverne, Y., Kleinrensink, G. J., & de Rooij, P. (2015). Perioperative Identification of an Accessory Fissure of the Right Lung. Case reports in pulmonology, 2015954769. https://doi.org/10.1155/2015/954769
Taverne, Yannick, et al. "Perioperative Identification of an Accessory Fissure of the Right Lung." Case reports in pulmonology vol. 2015 (2015): 954769. doi: https://doi.org/10.1155/2015/954769
Taverne Y, Kleinrensink GJ, de Rooij P. Perioperative Identification of an Accessory Fissure of the Right Lung. Case Rep Pulmonol. 2015;2015:954769. doi: 10.1155/2015/954769. Epub 2015 Jun 22. PMID: 26185701; PMCID: PMC4491585.
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Pleural mycobacterium avium complex infection in an immunocompetent female with no risk factors.

Case reports in pulmonology

Manglani RP, Khaja M, Hennessey K, Kennedy O.
PMID: 25793135
Case Rep Pulmonol. 2015;2015:760614. doi: 10.1155/2015/760614. Epub 2015 Feb 22.

Mycobacterium avium complex (MAC) infections rarely affect the pleura, accounting for 5-15% of pulmonary MAC. We report a case of MAC pleural effusion in an otherwise immunocompetent young patient. A 37-year-old healthy female with no past medical history was...

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Manglani RP, Khaja M, Hennessey K, et al. Pleural mycobacterium avium complex infection in an immunocompetent female with no risk factors. Case Rep Pulmonol. 2015;2015:760614doi: 10.1155/2015/760614.
Manglani, R. P., Khaja, M., Hennessey, K., & Kennedy, O. (2015). Pleural mycobacterium avium complex infection in an immunocompetent female with no risk factors. Case reports in pulmonology, 2015760614. https://doi.org/10.1155/2015/760614
Manglani, Ravi P, et al. "Pleural mycobacterium avium complex infection in an immunocompetent female with no risk factors." Case reports in pulmonology vol. 2015 (2015): 760614. doi: https://doi.org/10.1155/2015/760614
Manglani RP, Khaja M, Hennessey K, Kennedy O. Pleural mycobacterium avium complex infection in an immunocompetent female with no risk factors. Case Rep Pulmonol. 2015;2015:760614. doi: 10.1155/2015/760614. Epub 2015 Feb 22. PMID: 25793135; PMCID: PMC4352468.
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An unusual case of pulmonary nocardiosis in immunocompetent patient.

Case reports in pulmonology

Yaşar Z, Acat M, Onaran H, Ozgül MA, Fener N, Talay F, Cetinkaya E.
PMID: 25506020
Case Rep Pulmonol. 2014;2014:963482. doi: 10.1155/2014/963482. Epub 2014 Nov 17.

Pulmonary nocardiosis is a subacute or chronic necrotizing pneumonia caused by aerobic actinomycetes of the genus Nocardia and rare in immune-competent patients. A 35-year-old male, who had treated with antituberculosis drugs, presented with cough, dyspnea, and expectoration with episodes...

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Yaşar Z, Acat M, Onaran H, et al. An unusual case of pulmonary nocardiosis in immunocompetent patient. Case Rep Pulmonol. 2014;2014:963482doi: 10.1155/2014/963482.
Yaşar, Z., Acat, M., Onaran, H., Ozgül, M. A., Fener, N., Talay, F., & Cetinkaya, E. (2014). An unusual case of pulmonary nocardiosis in immunocompetent patient. Case reports in pulmonology, 2014963482. https://doi.org/10.1155/2014/963482
Yaşar, Zehra, et al. "An unusual case of pulmonary nocardiosis in immunocompetent patient." Case reports in pulmonology vol. 2014 (2014): 963482. doi: https://doi.org/10.1155/2014/963482
Yaşar Z, Acat M, Onaran H, Ozgül MA, Fener N, Talay F, Cetinkaya E. An unusual case of pulmonary nocardiosis in immunocompetent patient. Case Rep Pulmonol. 2014;2014:963482. doi: 10.1155/2014/963482. Epub 2014 Nov 17. PMID: 25506020; PMCID: PMC4251818.
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Vocal cord dysfunction: a frequently forgotten entity.

Case reports in pulmonology

Campainha S, Ribeiro C, Guimarães M, Lima R.
PMID: 23024876
Case Rep Pulmonol. 2012;2012:525493. doi: 10.1155/2012/525493. Epub 2012 Sep 16.

Vocal cord dysfunction (VCD) is a disorder characterized by unintentional paradoxical adduction of the vocal cords, resulting in episodic shortness of breath, wheezing and stridor. Due to its clinical presentation, this entity is frequently mistaken for asthma. The diagnosis...

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Campainha S, Ribeiro C, Guimarães M, et al. Vocal cord dysfunction: a frequently forgotten entity. Case Rep Pulmonol. 2012;2012:525493doi: 10.1155/2012/525493.
Campainha, S., Ribeiro, C., Guimarães, M., & Lima, R. (2012). Vocal cord dysfunction: a frequently forgotten entity. Case reports in pulmonology, 2012525493. https://doi.org/10.1155/2012/525493
Campainha, S, et al. "Vocal cord dysfunction: a frequently forgotten entity." Case reports in pulmonology vol. 2012 (2012): 525493. doi: https://doi.org/10.1155/2012/525493
Campainha S, Ribeiro C, Guimarães M, Lima R. Vocal cord dysfunction: a frequently forgotten entity. Case Rep Pulmonol. 2012;2012:525493. doi: 10.1155/2012/525493. Epub 2012 Sep 16. PMID: 23024876; PMCID: PMC3457600.
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An unusual transudative pleural effusion succeeded by pulmonary and brain edema and death.

Case reports in pulmonology

Mortazavimoghaddam SG, Riasi HR.
PMID: 22934227
Case Rep Pulmonol. 2012;2012:896409. doi: 10.1155/2012/896409. Epub 2012 Mar 28.

Here we report a 22-year old woman with massive and bilateral transudative effusion succeeded by pulmonary edema and brain edema and death. Investigations for systemic disorders were negative. Exacerbation of dyspnea after intravenous fluid infusion was a main problem....

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Mortazavimoghaddam SG, Riasi HR. An unusual transudative pleural effusion succeeded by pulmonary and brain edema and death. Case Rep Pulmonol. 2012;2012:896409doi: 10.1155/2012/896409.
Mortazavimoghaddam, S. G., & Riasi, H. R. (2012). An unusual transudative pleural effusion succeeded by pulmonary and brain edema and death. Case reports in pulmonology, 2012896409. https://doi.org/10.1155/2012/896409
Mortazavimoghaddam, Sayyed Gholam Reza, and Riasi, H R. "An unusual transudative pleural effusion succeeded by pulmonary and brain edema and death." Case reports in pulmonology vol. 2012 (2012): 896409. doi: https://doi.org/10.1155/2012/896409
Mortazavimoghaddam SG, Riasi HR. An unusual transudative pleural effusion succeeded by pulmonary and brain edema and death. Case Rep Pulmonol. 2012;2012:896409. doi: 10.1155/2012/896409. Epub 2012 Mar 28. PMID: 22934227; PMCID: PMC3420735.
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Severe Emphysema Treated by Endoscopic Bronchial Volume Reduction with Lung Sealant (AeriSeal).

Case reports in pulmonology

Falkenstern-Ge RF, Ingerl H, Kohlhäufl M.
PMID: 23710404
Case Rep Pulmonol. 2013;2013:361391. doi: 10.1155/2013/361391. Epub 2013 Apr 23.

Endoscopic lung volume reduction using lung sealant is a very new and innovative treatment option for patients with severe progressive and irreversible lung emphysema. A 55-year-old ex-smoker (60 pack years) referred to our center because of severe lung emphysema...

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Falkenstern-Ge RF, Ingerl H, Kohlhäufl M. Severe Emphysema Treated by Endoscopic Bronchial Volume Reduction with Lung Sealant (AeriSeal). Case Rep Pulmonol. 2013;2013:361391doi: 10.1155/2013/361391.
Falkenstern-Ge, R. F., Ingerl, H., & Kohlhäufl, M. (2013). Severe Emphysema Treated by Endoscopic Bronchial Volume Reduction with Lung Sealant (AeriSeal). Case reports in pulmonology, 2013361391. https://doi.org/10.1155/2013/361391
Falkenstern-Ge, R F, et al. "Severe Emphysema Treated by Endoscopic Bronchial Volume Reduction with Lung Sealant (AeriSeal)." Case reports in pulmonology vol. 2013 (2013): 361391. doi: https://doi.org/10.1155/2013/361391
Falkenstern-Ge RF, Ingerl H, Kohlhäufl M. Severe Emphysema Treated by Endoscopic Bronchial Volume Reduction with Lung Sealant (AeriSeal). Case Rep Pulmonol. 2013;2013:361391. doi: 10.1155/2013/361391. Epub 2013 Apr 23. PMID: 23710404; PMCID: PMC3655495.
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Night Sweats as a Prominent Symptom of a Patient Presenting with Pulmonary Embolism.

Case reports in pulmonology

Feher A, Muhsin SA, Maw AM.
PMID: 26078907
Case Rep Pulmonol. 2015;2015:841272. doi: 10.1155/2015/841272. Epub 2015 May 11.

Pulmonary embolism is a common, potentially fatal disease. Making the correct diagnosis early can significantly reduce mortality and morbidity. We report the first case of drenching night sweats as one of the presenting symptoms of submassive pulmonary embolism. One...

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Feher A, Muhsin SA, Maw AM. Night Sweats as a Prominent Symptom of a Patient Presenting with Pulmonary Embolism. Case Rep Pulmonol. 2015;2015:841272doi: 10.1155/2015/841272.
Feher, A., Muhsin, S. A., & Maw, A. M. (2015). Night Sweats as a Prominent Symptom of a Patient Presenting with Pulmonary Embolism. Case reports in pulmonology, 2015841272. https://doi.org/10.1155/2015/841272
Feher, Attila, et al. "Night Sweats as a Prominent Symptom of a Patient Presenting with Pulmonary Embolism." Case reports in pulmonology vol. 2015 (2015): 841272. doi: https://doi.org/10.1155/2015/841272
Feher A, Muhsin SA, Maw AM. Night Sweats as a Prominent Symptom of a Patient Presenting with Pulmonary Embolism. Case Rep Pulmonol. 2015;2015:841272. doi: 10.1155/2015/841272. Epub 2015 May 11. PMID: 26078907; PMCID: PMC4442258.
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Showing 1 to 12 of 319 entries