Thoracoabdominal duplication cyst: US, CT and MR findings

Savcı, Gürsel; Balkan, Emin; Ozyaman, T.; Doğruyol, Hasan; Tuncel, Ercan

doi:10.1007/s003300050170

Cited by 6 publications

(3 citation statements)

References 13 publications

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“…4,5 In addition to chest radiography, computed tomography, and magnetic resonance images, fluoroscopy helps in diagnosis. 6 Treatment is total excision of the cyst. If the cyst is related to the gastrointestinal system, this relationship should be eliminated.…”

Section: Discussionmentioning

confidence: 99%

A rare cause of respiratory distress in pediatric palliative care: Thoracic Duplication Cyst

Harputluoğlu

Çelik

Temır

et al. 2021

Preprint

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Gastrointestinal duplication cysts are actually rare congenital anomalies that can accompany various anomalies and are most frequently seen in the small intestine. Gastrointestinal duplication may accompany anomalies such as vertebral anomalies, spinal cord malformations. Depending on the location, symptoms such as chest pain, shortness of breath, cough, asthma-like symptoms, hemoptysis, cyanosis, vomiting, difficulty swallowing, weight loss, hematemesis and melena can be observed. To our knowledge, we report a rare case that has not been reported in pediatric palliative care. We present a case operated for diaphragmatic hernia in the neonatal period. A 3-month-old patient with respiratory distress who was followed up in pediatric palliative care was reoperated and pathologically diagnosed as gastrointestinal duplication cyst. Thoracic cysts can have a wide variety of etiology. The correct diagnosis can be made by performing further examinations and appropriate surgery.

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Section: Discussionmentioning

confidence: 99%

A rare cause of respiratory distress in pediatric palliative care: Thoracic Duplication Cyst

Harputluoğlu

Çelik

Temır

et al. 2021

Preprint

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“…Two cases in the literature included combination of duplications of bowel and malrotation ( 6 ). Thoracoabdominal duplications constitute approximately 2–4% of all duplications ( 7 ). They tend to be long, often large tubular lesions located in the posterior mediastinum, usually to the right of midline.…”

Section: Discussionmentioning

confidence: 99%

Thoraco-abdominal enteric duplication cyst in association with neurenteric cyst, axial skeletal anomalies, and malrotation

Bui

Bankhart

Mandell

et al. 2013

Radiology Case Reports

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We report a case of a 2-year old boy with cervicothoracic deformity with vertebral rib anomalies, neurenteric cyst, separate thoracoabominal enteric duplication cyst, concurrent intestinal malrotation, and dextroposition of the heart. This combination of abnormalities is very rare. When these lesions are suspected, the patient must be investigated carefully. This case is presented to show the importance of cross-sectional imaging (MR and CT) for surgical planning.

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“…Embriyolojik dönemdeki ortak kökenden dolayı duplikasyonların vertebra anomalileri, diğer ön barsak anomalileri ve split kord malformasyonları ile birlikte görülme sıklığı fazladır. TADK'lerinin çoğunda vertebra anomalisine rastlandığı bildirilmiştir (13). Çalışmamızdaki olgulardan ilkinde multipl vertebra anomalisi saptanırken, ikinci olguda vertebra anomalisine rastlanmadı ve iki lezyonun da spinal kanalla ilişkisi yoktu.…”

Section: Olguunclassified

Thoracoabdominal Duplication Cyst: Two Different Clinical Application in a Rare Variant

B¹,

Divarcı²,

Dökümcü³

et al. 2016

jpr

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Gastrointestinal duplikasyon (GİD) kisti, gastrointestinal sistemin nadir görülen bir konjenital anomalisidir. Tüm gastrointestinal sistemde saptanabilen bu anomali en sık ince barsaklarda görülmektedir (%40) (1,2). Özofagus duplikasyon kistleri tüm olguların %20'sini oluşturmaktadır. Özofagus duplikasyon kisti diyafragmatik hiatustan geçip abdomen içine uzanırsa torakoabdominal duplikasyon kisti (TADK) olarak adlandırılmakta ve oldukça nadir görülmektedir (3). Bu çalışmada, TADK tanısı almış ve birbirinden farklı klinik özellikler ile başvuran iki olgunun sunulması amaçlanmıştır. Olgu Sunumları Olgu 1 Yirmi beş yaşındaki annenin üçüncü gebeliğinden ikinci yaşayan olarak 37 haftalık, 3280 gr doğan olgu, intrauterin 8. ayda konjenital diyafragma hernisi tanısı almıştır. Doğum sonrası yapılan radyolojik incelemelerde özofagus Öz ABS TRACT Gastrointestinal duplikasyonlar çocuklarda nadir gözlenen konjenital anomalilerdir. Ağızdan anüse kadar tüm gastrointestinal sistem boyunca görülebilirler. Torakoabdominal varyantları ile oldukça nadir karşılaşılmaktadır. Bu çalışmada birbirinden farklı klinik tablolar ile başvuran iki torako-abdominal duplikasyon kisti olgusunun sunulması amaçlanmıştır. Anahtar Kelimeler: Duplikasyon kisti, konjenital anomaliler, gastrointestinal duplikasyon Gastrointestinal duplications are rare congenital anomalies in children. They may be localized throughout the entire gastrointestinal tract from mouth to anus. Thoracoabdominal variants are not usual in this clinical entity. In this study, two cases with thoracoabdominal duplication cysts are presented with different clinical presentations.

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Thoracoabdominal duplication cyst: US, CT and MR findings

Cited by 6 publications

References 13 publications

A rare cause of respiratory distress in pediatric palliative care: Thoracic Duplication Cyst

A rare cause of respiratory distress in pediatric palliative care: Thoracic Duplication Cyst

Thoraco-abdominal enteric duplication cyst in association with neurenteric cyst, axial skeletal anomalies, and malrotation

Thoracoabdominal Duplication Cyst: Two Different Clinical Application in a Rare Variant

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