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引用本文的文献

1
Multimodal imaging findings in an adult case of Swyer-James-MacLeod syndrome.
Respirol Case Rep. 2017 Apr 17;5(4):e00236. doi: 10.1002/rcr2.236. eCollection 2017 Jul.
2
An uncommon obliterative lung disease: Swyer-James-MacLeod syndrome.一种罕见的闭塞性肺部疾病:斯怀尔-詹姆斯-麦克劳德综合征。
Intern Emerg Med. 2015 Oct;10(7):881-2. doi: 10.1007/s11739-015-1239-z. Epub 2015 May 5.

本文引用的文献

1
A 63-year-old man with recurrent pulmonary infections: a case of Swyer-James Macleod syndrome.一名63岁反复发生肺部感染的男性:1例斯怀尔-詹姆斯-麦克劳德综合征病例。
J La State Med Soc. 2010 Nov-Dec;162(6):346-9.
2
Swyer-James-MacLeod syndrome; repeated chest drainages in a patient misdiagnosed with pneumothorax.斯威耶-詹姆斯-麦克劳德综合征;一名被误诊为气胸的患者反复进行胸腔引流
Interact Cardiovasc Thorac Surg. 2009 Apr;8(4):482-4. doi: 10.1510/icvts.2008.197566. Epub 2009 Jan 22.
3
[Diagnostic considerations in unilateral hyperlucency of the lung (Swyer-James-MacLeod Syndrome)].[肺单侧透亮的诊断考量(斯怀尔-詹姆斯-麦克劳德综合征)]
Allergol Immunopathol (Madr). 2004 Sep-Oct;32(5):265-70. doi: 10.1016/s0301-0546(04)79253-8.
4
Abnormal transradiancy of one lung.一侧肺透亮度异常。
Thorax. 1954 Jun;9(2):147-53. doi: 10.1136/thx.9.2.147.
5
A case of unilateral pulmonary emphysema.一例单侧肺气肿病例。
Thorax. 1953 Jun;8(2):133-6. doi: 10.1136/thx.8.2.133.
6
Clinical, physiologic, and roentgenographic changes after pneumonectomy in a boy with Macleod/Swyer-James syndrome and bronchiectasis.麦克劳德/斯怀尔-詹姆斯综合征合并支气管扩张症男孩肺切除术后的临床、生理及影像学变化
Pediatr Pulmonol. 2002 Nov;34(5):412-6. doi: 10.1002/ppul.10178.
7
[Swyer-James syndrome: diagnostic contributions of helical computerized tomography].
Arch Bronconeumol. 2000 Jul-Aug;36(7):421.
8
Ventilation-perfusion scintigraphic correlation with multimodality imaging in a proven case of Swyer-James (Macleod's) syndrome.在一例经证实的斯怀尔-詹姆斯(麦克劳德)综合征病例中,通气-灌注闪烁扫描与多模态成像的相关性
Clin Nucl Med. 1997 Feb;22(2):115-8. doi: 10.1097/00003072-199702000-00009.
9
Unilateral hyperlucent lung: a complication of viral pneumonia.单侧肺透亮度增加:病毒性肺炎的一种并发症。
J Can Assoc Radiol. 1969 Dec;20(4):225-31.

患有斯怀尔-詹姆斯综合征的幼儿的典型影像学三联征。

Classical imaging triad in a very young child with swyer-james syndrome.

作者信息

Damle Nishikant A, Mishra Rohini, Wadhwa Jasmeet Kaur

机构信息

Department of Nuclear Medicine, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, 110029 India.

Department of Nuclear Medicine, B.L Kapur Memorial Hospital, New Delhi, India.

出版信息

Nucl Med Mol Imaging. 2012 Jun;46(2):115-8. doi: 10.1007/s13139-012-0131-2. Epub 2012 Apr 14.

DOI:10.1007/s13139-012-0131-2
PMID:24900044
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4043000/
Abstract

Swyer-James syndrome (SJS) or Swyer-James-MacLeod syndrome is a rare disorder characterized by roentgenographical hyperlucency of one lung, lobe, or part of a lobe. As originally described, it shows a unilateral small lung with hyperlucency and air trapping on radiographs. It is postinfectious obliterative bronchiolitis due to childhood respiratory infection. In SJS, the involved lung or portion of the lung does not grow normally. The characteristic radiologic appearance is that of pulmonary hyperlucency on chest X-ray/CT caused by over-distention of the alveoli in conjunction with diminished arterial flow detected on Tc-99 m MAA pulmonary perfusion scan. Radionuclide pulmonary ventilation studies are considered difficult to perform in very young children as patient co-operation is crucial to achieve adequate tracer entry into the lungs. We present here the case of a female child aged 2 years, who presented with chronic productive cough and fever off and on for 1.5 years. She had classical features on imaging and markedly diminished ventilation on Tc-99 m DTPA aerosol study. Our case highlights the typical findings on ventilation-perfusion scan (V/Q scan) and suggests that it is possible to conduct a satisfactory ventilation study with Tc-99 m DTPA aerosol even in very young children.

摘要

斯怀尔-詹姆斯综合征(SJS)或斯怀尔-詹姆斯-麦克劳德综合征是一种罕见的疾病,其特征为一侧肺、肺叶或部分肺叶在X线片上呈现透亮度增加。最初描述时,它在X线片上表现为单侧小肺伴透亮度增加和空气潴留。它是儿童期呼吸道感染后导致的闭塞性细支气管炎。在SJS中,受累的肺或肺的部分不能正常生长。其典型的放射学表现是胸部X线/CT上肺透亮度增加,这是由于肺泡过度扩张以及在锝-99m聚合人血清白蛋白(Tc-99m MAA)肺灌注扫描中检测到动脉血流减少所致。放射性核素肺通气研究被认为在幼儿中很难进行,因为患者的配合对于使示踪剂充分进入肺部至关重要。我们在此报告一名2岁女童的病例,该女童断断续续慢性咳痰伴发热1.5年。她在影像学上有典型表现,并且在锝-99m二乙三胺五乙酸(Tc-99m DTPA)气溶胶研究中通气明显减少。我们的病例突出了通气-灌注扫描(V/Q扫描)的典型表现,并表明即使在幼儿中,使用Tc-99m DTPA气溶胶也有可能进行令人满意的通气研究。