Laparoscopic Repair of Bilateral Congenital Diaphragmatic Hernia Without Pulmonary Hypoplasia
Copyright © 2020, Mahmood et al..
We report the case of a 14-month-old female who had a right-sided congenital diaphragmatic hernia (CDH) without pulmonary hypoplasia. The patient was preoperatively diagnosed with a Morgagni hernia due to the size and location of the hernia seen on imaging. However, the patient was found to have bilateral diaphragmatic defects intraoperatively, and her right diaphragm was almost completely absent. Our patient did not have pulmonary hypoplasia or any of the respiratory comorbidities that CDH patients typically present with, though she did have repeated respiratory infections and cough. This case demonstrates that CDH is not always diagnosed in an accurate or timely manner radiographically and that the surgeon should be prepared to potentially repair more of the diaphragm than expected. Additionally, there is a need to study the pathophysiology and genetics of CDHs further.
| Medienart: |
E-Artikel |
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| Erscheinungsjahr: |
2020 |
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| Erschienen: |
2020 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:12 |
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| Enthalten in: |
Cureus - 12(2020), 9 vom: 09. Sept., Seite e10335 |
| Sprache: |
Englisch |
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| Beteiligte Personen: |
Mahmood, Mehreen [VerfasserIn] |
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| Links: |
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| Themen: |
Bilateral diaphragmatic hernia |
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| Anmerkungen: |
Date Revised 20.10.2020 published: Electronic Citation Status PubMed-not-MEDLINE |
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| doi: |
10.7759/cureus.10335 |
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| funding: |
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| Förderinstitution / Projekttitel: |
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| PPN (Katalog-ID): |
NLM316219436 |
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| 500 | |a Citation Status PubMed-not-MEDLINE | ||
| 520 | |a Copyright © 2020, Mahmood et al. | ||
| 520 | |a We report the case of a 14-month-old female who had a right-sided congenital diaphragmatic hernia (CDH) without pulmonary hypoplasia. The patient was preoperatively diagnosed with a Morgagni hernia due to the size and location of the hernia seen on imaging. However, the patient was found to have bilateral diaphragmatic defects intraoperatively, and her right diaphragm was almost completely absent. Our patient did not have pulmonary hypoplasia or any of the respiratory comorbidities that CDH patients typically present with, though she did have repeated respiratory infections and cough. This case demonstrates that CDH is not always diagnosed in an accurate or timely manner radiographically and that the surgeon should be prepared to potentially repair more of the diaphragm than expected. Additionally, there is a need to study the pathophysiology and genetics of CDHs further | ||
| 650 | 4 | |a Case Reports | |
| 650 | 4 | |a bilateral diaphragmatic hernia | |
| 650 | 4 | |a congenital diaphragmatic hernia | |
| 650 | 4 | |a laparascopic repair | |
| 650 | 4 | |a laparoscopy | |
| 650 | 4 | |a pulmonary hypoplasia | |
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| 700 | 1 | |a Westmoreland, Tamarah |e verfasserin |4 aut | |
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