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Radiological Case of the Month
Nighat F. Mehdi, MD;
Miles Weinberger, MD;
Mutasim N. Abu-Hasan, MD
From the Pediatric Allergy and Pulmonary Division, University of Iowa
College of Medicine, Iowa City.
Arch Pediatr Adolesc Med. 2002;156:81-82.
A 20-MONTH-OLD infant had a 4-week history of bilaterally bulging neck
masses that were apparent while crying. The masses were initially noted after
an upper respiratory infection, and they became progressively more prominent.
The infant had several episodes of difficulty swallowing, mild hoarseness,
and occasional perioral cyanosis during a 5-day hospitalization to evaluate
the neck masses. The infant's medical history was notable for respiratory
syncytial virus bronchiolitis at age 6 months and several episodes of otitis
media. There was no history of trauma or surgery.
Physical examination showed a playful child in no respiratory distress
but with prominent bulging of the supraclavicular fossae bilaterally (Figure 1) on crying. The swelling disappeared
when the infant was consoled (Figure 2),
and the remainder of the physical examination was normal.
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Figure 1.
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Figure 2.
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A flexible fiberoptic bronchoscopy showed no laryngeal or tracheal abnormality
during quiet breathing, crying, or coughing. A barium esophagogram and chest
computed tomography scan were normal. Chest and neck radiographs were obtained
under fluoroscopy while the child was crying
(Figure 3) and quiet
(Figure 4).
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Figure 3.
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Figure 4.
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Denouement and Discussion: Bilateral Congenital Apical Lung Herniation
Figure 1. The infant while
crying showing a lower mass with obliteration of the supraclavicular fossa.
Figure 2. The infant while
quiet with disappearance of the neck mass.
Figure 3. Radiograph of the
neck and upper chest at fluoroscopy while the infant is crying. There is protrusion
of both lung apices (right more than left) into the neck (arrows). Slight
deviation of the trachea is also apparent.
Figure 4. Radiograph of the
neck and upper chest at fluoroscopy while the infant is quiet. The lung apices
returned to their normal location in the chest, and the tracheal deviation
disappeared.
Lung herniation is a protrusion of the lung parenchyma beyond the musculoskeletal
thorax. It was initially described by Roland in 1499 and later by Hildanus
and Loysean in 1606 and 1617, respectively.1-2
Fewer than 300 cases are reported in the literature.
Lung hernias are classified by location and etiology.1-2
Categories are intercostal, cervical, and diaphragmatic. Sixty-five percent
of lung hernias occur through the intercostal spaces, 33% are cervical through
the thoracic inlet, and 1% are diaphragmatic.1-2
Herniation of 1 lung across the mediastinum occurs because of overinflation
of the ipsilateral lungs and small or absent contralateral lung. Lung hernias
are mostly acquired from penetrating injuries or blunt trauma to the chest
wall, multiple rib fractures, and tear of intercostal muscles. Only 18% of
lung hernias are congenital. Congenital herniation of the lung occurs mainly
in the cervical region due to weakness of the paratracheal fascia. Congenital
intercostal herniation through defects of the anterior thoracic wall has been
associated with costal cartilage malformation.3
Pathological hernias can occur when breast or chest wall malignancy, tuberculous
osteitis, or empyema weaken the thoracic wall.4
Congenital cervical lung hernia usually manifests during the first year
of life but may not be apparent at birth. Familial cases are associated with
hernias in other locations.5 Cervical lung
herniation occurs through the apex of the hemithorax at the thoracic inlet.
The trachea, esophagus, and neurovascular structures are flanked dorsally
by the trapezius and the 3 scalenus muscles. However, a gap exists ventrally
between the scalenus anterior and the sternocleidomastoid muscle and serves
as the herniation site.
The ascent of the lung beyond the thoracic inlet is prevented by Sibson
fascia, an opposed 2-layered fascia in the neck, the parietal pleura, and
the neck muscles. Cervical lung hernia occurs with partial absence, laxity,
or attenuation of Sibson fascia or with an increase in space between the sternocleidomastoid
and scalenus anterior muscles.
Unilateral or bilateral lung herniation is usually noted during the
first year of life as a bulging mass with a Valsalva maneuver and increased
intrathoracic pressure that is apparent during crying. Lung apex herniation
is temporary, and the lung apices return to the thoracic cavity spontaneously.
Cervical hernia may produce hoarseness, chronic cough, or stridor from external
compression of the trachea6 or transient
impairment of jugular venous drainage.7
Pain or tenderness is rarely present at the hernia site. The lung apices feel
like an elastic, compressible mass with crepitus, and cough can be elicited
by palpation. Acute respiratory distress from incarceration with an ischemic
or perforated lung has been reported in isolated cases.1-2,8-9
Congenital cervical hernias are apparent on chest and neck radiographs.
With accompanying tracheal deviation,10
chest computed tomography scans determine the location and size of the cervical
defect and exclude other masses. The radiological differential diagnosis of
apical lung hernias includes pharyngocele, laryngocele, and esophageal diverticulum.
Contrast esophagogram helps to differentiate esophageal diverticula. Recognition
of lung hernia helps avoid accidental iatrogenic lung trauma when placing
a central venous catheter.11
Adults with cervical lung hernia may have chronic cough or emphysema12-13 or occupations with repetitive
respiratory maneuvers and increased intrathoracic pressure, such as playing
wind instruments, glass blowing, or lifting weights. The combination of increased
intrathoracic pressure and focal weakening of the thoracic wall leads to herniation.10
Apical hernias in infants and children usually resolve spontaneously.
Treatment is warranted if incarceration or significant compression of nearby
structures occurs. Surgical reduction and repair using tissues such as periosteum,
muscle, or synthetic materials can be performed. Video-assisted thoracoscopic
repair of lung hernias has also been reported.14
AUTHOR INFORMATION
Accepted for publication July 12, 2000.
Reprints: Nighat F. Mehdi, MD, Pediatric Allergy and Pulmonary Division,
University of Iowa College of Medicine, 200 Hawkins Dr, Iowa City, IA 52242-1083
(e-mail: MehdiN{at}mail.medicine.uiowa.edu).
REFERENCES
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1. Ross RT, Burnett CM. Atraumatic lung hernia. Ann Thorac Surg. 1999;67:1496-1497.
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2. Minai OA, Hammond G, Curtis A. Hernia of the lung: a case report and review of literature. Conn Med. 1997;61:77-81.
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3. Neilands PS, Kurczynski TW, ElShafie MAF, Uraizee F. Brief clinical report: congenital lung herniation. Am J Med Genet. 1991;40:97-99.
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4. Bhalla M, Leitman BS, Forcade C, Stern E, Naidich DP, McCauley DI. Lung hernia: radiograghic features. AJR Am J Roentgenol. 1990;154:51-53.
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5. Chen RD, Liu XD, Liu LX. Familial cervical lung hernia: a report of 4 cases in a family. Chung Hua Chish Ho Ho Hu Hsi Tsa Chih. 1994;17:230-231,255.
6. Gonzalez del Rey J, Cunha C. Cervical lung herniation associated with upper airway obstruction. Ann Emerg Med. 1990;19:935-937.
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7. Siegelman SS, Shanser J-D, Attai LA. Cervical herniation of the lung associated with transient venous occlusion:
report of a case. Dis Chest. 1968;53:785-787.
8. Grunebaum M, Griscom NT. Protrusion of lung apex through Sibson's fascia in infancy. Thorax. 1978;33:290-294.
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9. Bronsther B, Coryllos E, Epstein B. Lung hernias in children. J Pediatr Surg. 1968;3:544-550.
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10. McAdams HP, Gordon DS, White CS. Apical lung hernia: radiologic findings in 6 cases. AJR Am J Roentgenol. 1996;167:927-930.
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11. Moncada R, Vade A, Giminez C, et al. Congenital and acquired lung hernias. J Thorac Imaging. 1992;11:75-81.
12. Aoki T, Takagi H, Ando T, et al. Cervical lung hernia in a case of severe chronic asthma and bronchitis. Nihon Kyobu Shikkan Gakkai Zasshi. 1991;29:632-637.
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13. Scullion DA, Negus R, AL-Kutoubi A. Case report: extrathoracic herniation of the lung with a review of
the literature. Br J Radiol. 1994;67:94-96.
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14. Brown WT, Hauser M, Keller FA. Hernia of the lung repaired by VATS: a case report. J Laparoendosc Surg. 1996;6:427-430.
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SECTION EDITOR: BEVERLY P. WOOD, MD
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