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Nadir Görülen Bir Sendrom: Swyer James Macleod Olgusu

Year 2020, Volume: 3 Issue: 2, 77 - 79, 27.06.2020

Abstract

Swyer James MacLeod Sendromu (SJMS) özellikle çocukluk çağında sık pulmoner enfeksiyon sonrası geliştiği düşünülen radyolojik olarak tek taraflı radyolüsen görünümü olan nadir bir sendromdur. Genellikle asemptomatik olup insidental olarak saptanır. Unilateral radyolüsensi yapacak nedenler ekarte edildikten sonra radyolojik olarak tek taraflı hava hapsi, hiperlüsensi bulguları, küçük ya da normal boyutlarda akciğer, pulmoner damarların sayısı ve boyutlarında azalma karakteristik özellikleridir. Swyer James MacLeod Sendromu tedavisi, çoğu vakada konservatif olup hastaların enfeksiyon-lara karşı korunması, grip ve pnömokok aşılarını yaptırmaları önerilmektedir. Burada 27 yaşında erkek olgumuzu nadir görülen bir sendrom olması nedeniyle sunmaktayız. 

References

  • Swyer PR, James GC. A case of unilateral pulmonary emphysema. Thorax. 1953;8:133-136. doi:10.1136/thx.8.2.133
  • Alaygut D, Babayiğit A, Ölmez D, ve ark. Swyer James MacLeod Sendromlu bir çocuk olgu. Dokuz Eylül Üniversitesi Tıp Fakültesi Dergisi. 2008;22(1):19-22.
  • Capela C, Gouveia P, Sousa M, Regades MJ. Adult diagnosis of Swyer‐James‐MacLeod syndrome: A case report. J Med Case Reports. 2011;5:2. doi:10.1186/1752-1947-5-2
  • Piquette CA, Rennard SI, Snider GL. Chronic bronchitis andepmphysema. İçinde: Murray JF, Nadel JA, eds. Textbook of Respiratory Medicine. 3. Baskı. Philadelphia, PA: WB Saunders Company;2000:1187-1245.
  • Marchiori E, Hochhegger B, Zanetti G. Unilateral hyperlucent lung. J Bras Pneumol. 2018;44(3):182. doi:10.1590/S1806-37562018000000092
  • Sulaiman A, Cavaille A, Vaunois B, Tiffet O. Swyer‐James‐MacLeod syndrome; repeated chest drainages in a patient misdiagnosed with pneumothorax. Interact Cardiovasc Thorac Surg. 2009;8(4):482-484. doi:10.1510/icvts.2008.197566
  • Chaucer B, Chevenon M, Toro C, Lemma T,Grageda, M. Swyer-James-Macleod syndrome: A rare finding and important differential in the ED setting. Am J Emerg Med. 2016;7:1329-1329. doi:10.1016/j.ajem.2015.12.045
  • Fregonese L, Girosi D, Battistini E, et al. Clinical, physiologic, and roentgenographic changes after pneumonectomy in a boy with Macleod/Swyer-James syndrome and bronchiectasis. Pediatr Pulmonol. 2002;5:412-416. doi:10.1002/ppul.10178
  • Gómez Belda AB, Martínez-Moragón E, Fabrellas FE. Swyer-James syndrome: Diagnostic contributions of helical computerized tomography. Arch Bronconeumol. 2000;7:421-422.
  • da Silva PS, Lopes R, Neto HM. Swyer-James-MacLeodsyndrome in a surgically treated child: a case report and briefliterature review. J Pediatr Surg. 2012;47(4):e17-22. doi:10.1016/j.jpedsurg.2011.12.011

A RARE SYNDROME: A CASE OF SWYER JAMES MACLEOD

Year 2020, Volume: 3 Issue: 2, 77 - 79, 27.06.2020

Abstract

Swyer James MacLeod Syndrome (SJMS) is a rare syndrome with a unilateral radiolucent appearance that is thought to develop after frequent pulmonary infection in childhood. It is usually asymptomatic and incidentally detected. Radiologically, unilateral air confinement, signs of hyperlucency, small or normal lungs, pulmonary vessels and decrease in size are seen. Swyer James MacLeod Syndrome treatment is conservative in most cases and it is recommended to protect patients against infections and to receive influenza and pneumococcal vaccines. Herein, we present a 27-year-old man with a rare syndrome.

References

  • Swyer PR, James GC. A case of unilateral pulmonary emphysema. Thorax. 1953;8:133-136. doi:10.1136/thx.8.2.133
  • Alaygut D, Babayiğit A, Ölmez D, ve ark. Swyer James MacLeod Sendromlu bir çocuk olgu. Dokuz Eylül Üniversitesi Tıp Fakültesi Dergisi. 2008;22(1):19-22.
  • Capela C, Gouveia P, Sousa M, Regades MJ. Adult diagnosis of Swyer‐James‐MacLeod syndrome: A case report. J Med Case Reports. 2011;5:2. doi:10.1186/1752-1947-5-2
  • Piquette CA, Rennard SI, Snider GL. Chronic bronchitis andepmphysema. İçinde: Murray JF, Nadel JA, eds. Textbook of Respiratory Medicine. 3. Baskı. Philadelphia, PA: WB Saunders Company;2000:1187-1245.
  • Marchiori E, Hochhegger B, Zanetti G. Unilateral hyperlucent lung. J Bras Pneumol. 2018;44(3):182. doi:10.1590/S1806-37562018000000092
  • Sulaiman A, Cavaille A, Vaunois B, Tiffet O. Swyer‐James‐MacLeod syndrome; repeated chest drainages in a patient misdiagnosed with pneumothorax. Interact Cardiovasc Thorac Surg. 2009;8(4):482-484. doi:10.1510/icvts.2008.197566
  • Chaucer B, Chevenon M, Toro C, Lemma T,Grageda, M. Swyer-James-Macleod syndrome: A rare finding and important differential in the ED setting. Am J Emerg Med. 2016;7:1329-1329. doi:10.1016/j.ajem.2015.12.045
  • Fregonese L, Girosi D, Battistini E, et al. Clinical, physiologic, and roentgenographic changes after pneumonectomy in a boy with Macleod/Swyer-James syndrome and bronchiectasis. Pediatr Pulmonol. 2002;5:412-416. doi:10.1002/ppul.10178
  • Gómez Belda AB, Martínez-Moragón E, Fabrellas FE. Swyer-James syndrome: Diagnostic contributions of helical computerized tomography. Arch Bronconeumol. 2000;7:421-422.
  • da Silva PS, Lopes R, Neto HM. Swyer-James-MacLeodsyndrome in a surgically treated child: a case report and briefliterature review. J Pediatr Surg. 2012;47(4):e17-22. doi:10.1016/j.jpedsurg.2011.12.011
There are 10 citations in total.

Details

Primary Language Turkish
Subjects ​Internal Diseases
Journal Section Olgu Sunumu
Authors

Mehmet Fatih Elverişli 0000-0002-5103-4089

Pinar Yıldız Gülhan

Ege Güleç Balbay

Şule Yıldız

Publication Date June 27, 2020
Submission Date December 19, 2019
Acceptance Date June 2, 2020
Published in Issue Year 2020 Volume: 3 Issue: 2

Cite

AMA Elverişli MF, Yıldız Gülhan P, Güleç Balbay E, Yıldız Ş. Nadir Görülen Bir Sendrom: Swyer James Macleod Olgusu. Acta Med Nicomedia. June 2020;3(2):77-79.

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