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{{Congenital diaphragmatic hernia}}
{{Congenital diaphragmatic hernia}}
{{CMG}}; {{AE}}[[User:AroojNaz|Arooj Naz, M.B.B.S]]


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==Overview==
Congenital diaphragmatic hernia is a condition that often presents in infants, but there are differential diagnosis' to be considered. Some of these include [[Congenital Cystic Adenomatoid Malformation|congenital cystic adenomatoid malformation]], [[Bronchopulmonary Sequestration|bronchopulmonary sequestration]], [[Bronchogenic cyst|bronchogenic cyst]], [[Cystic Teratoma|cystic teratoma]], [[Neurogenic Tumors|neurogenic tumors]], and [[pulmonary agenesis]]. [[Hiatal Hernia|Hiatal hernia]] is often seen in adults rather than [[neonates]], but should still be differentiated from congenital hernias. Various imaging modalities may be utilized to further differentiate the potential diagnosis'.
 
==Differential Diagnosis==
{| class="wikitable"
|+Differential Diagnosis for CDH<ref name="pmid32310536">{{cite journal| author=| title=StatPearls | journal= | year= 2022 | volume=  | issue=  | pages= | pmid=32310536 | doi= | pmc= | url= }}</ref><ref name="pmid20301533">{{cite journal| author=Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Gripp KW | display-authors=etal| title=GeneReviews® | journal= | year= 1993 | volume=  | issue=  | pages=  | pmid=20301533 | doi= | pmc= | url= }}</ref>
!Condition
!Cause
!Presenting Symptoms
!Workup to differentiate condition from CDH
|-
|[[Congenital Cystic Adenomatoid Malformation]]<ref name="pmid27867411">{{cite journal| author=Adin ME| title=Ultrasound as a screening tool in the follow-up of asymptomatic congenital cystic adenomatoid malformation. | journal=Ultrasound | year= 2016 | volume= 24 | issue= 3 | pages= 175-179 | pmid=27867411 | doi=10.1177/1742271X16657120 | pmc=5105364 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=27867411  }}</ref>
|Abnormal cell [[proliferation]] and [[apoptosis]]; a developmental abnormality
|Symptoms present upon compression of surrounding structures in the [[mediastinum]] upon growth of [[cyst]]
|[[Ultrasound]]
|-
|[[Bronchopulmonary Sequestration]]<ref name="pmid30335347">{{cite journal| author=| title=StatPearls | journal= | year= 2022 | volume=  | issue=  | pages= | pmid=30335347 | doi= | pmc= | url= }}</ref>
|Lung tissue unconnected to the [[tracheobronchial tree]]
|Often asymptomatic; larger defects may present with [[respiratory distress]], [[high output cardiac failure]] or [[pleural hemorrhage]]
|Imaging ([[digital angiography]], [[CT]], [[MRA]])
|-
|[[Bronchogenic cyst|Bronchogenic Cyst]]<ref name="pmid15125186">{{cite journal| author=Elahi S, Fecher A, Birdas T, Bridas T| title=Mediastinal bronchogenic cyst. | journal=J Ayub Med Coll Abbottabad | year= 2004 | volume= 16 | issue= 1 | pages= 64-5 | pmid=15125186 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15125186  }}</ref>
|Abnormal  budding of the [[Foregut|ventral foregut]]
|These often remain asymptomatic and undiagnosed, but may be detected in the setting of an underlying [[infection]]
|[[CT]]
|-
|[[Cystic Teratoma]]<ref name="pmid33231995">{{cite journal| author=| title=StatPearls | journal= | year= 2022 | volume=  | issue=  | pages= | pmid=33231995 | doi= | pmc= | url= }}</ref>
|Rare [[tumors]] composed of cells derived from the [[endoderm]], [[ectoderm]], and or [[mesoderm]]
|Often asymptomatic; an increase in size may result in increased [[abdominal girth]], and [[gastrointestinal]] and [[urinary]] symptoms due to compression
|[[Ultrasound]], [[Pathology]] specimen examination
|-
|[[Neurogenic Tumors]]
|A lesion of [[Neural crest|neural crest origin]] most commonly found in the [[posterior mediastinum]]
|Symptoms of compression of surrounding structures; [[cough]], [[shortness of breath]], [[hoarseness]]
|[[CT]], [[MRI]]<ref name="pmid12533638">{{cite journal| author=Rha SE, Byun JY, Jung SE, Chun HJ, Lee HG, Lee JM| title=Neurogenic tumors in the abdomen: tumor types and imaging characteristics. | journal=Radiographics | year= 2003 | volume= 23 | issue= 1 | pages= 29-43 | pmid=12533638 | doi=10.1148/rg.231025050 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12533638  }}</ref>
|-
|[[Hiatal Hernia]] (Paraesophageal)<ref name="pmid24503366">{{cite journal| author=Chang P, Friedenberg F| title=Obesity and GERD. | journal=Gastroenterol Clin North Am | year= 2014 | volume= 43 | issue= 1 | pages= 161-73 | pmid=24503366 | doi=10.1016/j.gtc.2013.11.009 | pmc=3920303 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24503366  }}</ref>
|[[Herniation]] of a portion of the [[stomach]] through the [[Phrenoesophageal ligament|phrenoesophageal]] membrane
|[[Heart burn]], [[Regurgitation]], [[Dysphagia]]; most commonly present in adults
|[[Manometry]], [[Endoscopy]]
|-
|[[Pulmonary agenesis]]<ref name="pmid27164736">{{cite journal| author=Chawla RK, Madan A, Chawla A, Arora HN, Chawla K| title=Pulmonary Agenesis. | journal=Indian J Chest Dis Allied Sci | year= 2015 | volume= 57 | issue= 4 | pages= 251-3 | pmid=27164736 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=27164736  }}</ref>
|Failure of [[Lung bud|lung bud development]] resulting in complete or partial absence of lung tissue; associated with [[congenital defects]]
|[[Respiratory distress]] in newborns
|[[Chest X-ray]]
|}


==References==
==References==
{{Reflist|2}}
{{Reflist|2}}


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Latest revision as of 01:30, 7 August 2022

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Arooj Naz, M.B.B.S

Overview

Congenital diaphragmatic hernia is a condition that often presents in infants, but there are differential diagnosis' to be considered. Some of these include congenital cystic adenomatoid malformation, bronchopulmonary sequestration, bronchogenic cyst, cystic teratoma, neurogenic tumors, and pulmonary agenesis. Hiatal hernia is often seen in adults rather than neonates, but should still be differentiated from congenital hernias. Various imaging modalities may be utilized to further differentiate the potential diagnosis'.

Differential Diagnosis

Differential Diagnosis for CDH[1][2]
Condition Cause Presenting Symptoms Workup to differentiate condition from CDH
Congenital Cystic Adenomatoid Malformation[3] Abnormal cell proliferation and apoptosis; a developmental abnormality Symptoms present upon compression of surrounding structures in the mediastinum upon growth of cyst Ultrasound
Bronchopulmonary Sequestration[4] Lung tissue unconnected to the tracheobronchial tree Often asymptomatic; larger defects may present with respiratory distress, high output cardiac failure or pleural hemorrhage Imaging (digital angiography, CT, MRA)
Bronchogenic Cyst[5] Abnormal budding of the ventral foregut These often remain asymptomatic and undiagnosed, but may be detected in the setting of an underlying infection CT
Cystic Teratoma[6] Rare tumors composed of cells derived from the endoderm, ectoderm, and or mesoderm Often asymptomatic; an increase in size may result in increased abdominal girth, and gastrointestinal and urinary symptoms due to compression Ultrasound, Pathology specimen examination
Neurogenic Tumors A lesion of neural crest origin most commonly found in the posterior mediastinum Symptoms of compression of surrounding structures; cough, shortness of breath, hoarseness CT, MRI[7]
Hiatal Hernia (Paraesophageal)[8] Herniation of a portion of the stomach through the phrenoesophageal membrane Heart burn, Regurgitation, Dysphagia; most commonly present in adults Manometry, Endoscopy
Pulmonary agenesis[9] Failure of lung bud development resulting in complete or partial absence of lung tissue; associated with congenital defects Respiratory distress in newborns Chest X-ray

References

  1. "StatPearls". 2022. PMID 32310536 Check |pmid= value (help).
  2. Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Gripp KW; et al. (1993). "GeneReviews®".   ( ):  . PMID 20301533.
  3. Adin ME (2016). "Ultrasound as a screening tool in the follow-up of asymptomatic congenital cystic adenomatoid malformation". Ultrasound. 24 (3): 175–179. doi:10.1177/1742271X16657120. PMC 5105364. PMID 27867411.
  4. "StatPearls". 2022. PMID 30335347.
  5. Elahi S, Fecher A, Birdas T, Bridas T (2004). "Mediastinal bronchogenic cyst". J Ayub Med Coll Abbottabad. 16 (1): 64–5. PMID 15125186.
  6. "StatPearls". 2022. PMID 33231995 Check |pmid= value (help).
  7. Rha SE, Byun JY, Jung SE, Chun HJ, Lee HG, Lee JM (2003). "Neurogenic tumors in the abdomen: tumor types and imaging characteristics". Radiographics. 23 (1): 29–43. doi:10.1148/rg.231025050. PMID 12533638.
  8. Chang P, Friedenberg F (2014). "Obesity and GERD". Gastroenterol Clin North Am. 43 (1): 161–73. doi:10.1016/j.gtc.2013.11.009. PMC 3920303. PMID 24503366.
  9. Chawla RK, Madan A, Chawla A, Arora HN, Chawla K (2015). "Pulmonary Agenesis". Indian J Chest Dis Allied Sci. 57 (4): 251–3. PMID 27164736.