Eine seltene Mißbildung der oberen Luftwege

Fritz, Erich

doi:10.1007/bf01892234

Cited by 14 publications

(6 citation statements)

References 3 publications

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“…Tracheal agenesis appears to have been described first by Payne [ 19001; subsequently 41 other patients were reported [Walcher, 1928;Fritz, 1933;Benesova and Peter, 1934;Marek, 1940;Morison, 1949;Milles and Dorsey, 1950;Kessel and Smith, 1953;Sandison, 1955;Hempel, 1956;Devenis and Otis, 1957;Onarir and Sariyalcin, 1961;Floyd et al, 1962;Witzleben, 1963;Fonkalsrud et al, 1963;McCracken et al, 1964;Devi and More, 1966;Stowens, 1966;Colavecchio, 1968;Lyons and Bruce, 1968;Eimer, 1969;Joshi, 1969;McNie and Pryse-Davies, 1970;Altman et al, 1972;Hopkinson, 1972;Hong et al, 1973;Effman et al, 1975;Chaurasia, 1976;Warfel, 1976;Donovan and Friedman, 1979;Far0 et al, 1979;Buchino et al, 1982; DFC:23 24 Evans, Reggin, and Greenberg Haupt and Edwards, 19831. In these cases tracheal agenesis was partial or total and various classifications of this malformation have been described [Floyd et al, 1962;Faro et al, 1979;Kluth, 19761.…”

Section: Pathogenesismentioning

confidence: 96%

Tracheal agenesis and associated malformations: A comparison with tracheoesophageal fistula and the VACTERL association

Reggin

Greenberg

1985

Am. J. Med. Genet.

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Tracheal agenesis is a rare malformation of the lower respiratory tract. Investigation of a patient with multiple congenital anomalies and tracheal agenesis prompted a review of the literature which uncovered 42 previously published cases, most of whom had other defects. The presence in our patient of a tracheal abnormality in association with radial hypoplasia, single umbilical artery, tetralogy of Fallot, and left hydroureter initially suggested presence of the VACTERL association. However, numerical classification of malformation patterns in the reported patients with tracheal agenesis and in a series of patients with tracheoesophageal fistula and other components of the VACTERL association suggests that tracheal agenesis does not occur in the VACTERL association and may be part of another pattern of malformations which includes laryngeal atresia, complex congenital heart anomalies, radial ray defects, and duodenal atresia.

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Section: Pathogenesismentioning

confidence: 96%

Tracheal agenesis and associated malformations: A comparison with tracheoesophageal fistula and the VACTERL association

Reggin

Greenberg

1985

Am. J. Med. Genet.

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“…In cyanosed after the cord is clamped. Despite this one (Fritz, 1933) the obstruction was partially rapidly developing cyanosis the child does not cartilaginous and partially membranous. Only 3 of appear shocked or asphyxiated, is active, and makes these infants were stillborn, the remaining 7 having strong respiratory movements.…”

Section: Discussionmentioning

confidence: 96%

“…Group B consisted of four cases in which laryngeal atresia was associated with deformities of the oesophagus or trachea, such as partial atresia of the trachea and tracheo-oesophageal fistula (Fritz, 1933;Sandison, 1955), oesophageal atresia and tracheooesophageal fistula (Sayre and Hall, 1954) or tracheo-oesophageal fistula (Heineken, 1952) can result in membranous laryngeal atresia.…”

Section: Discussionmentioning

confidence: 99%

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Laryngeal Atresia

Fox¹,

Cocker²

1964

Archives of Disease in Childhood

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“…On the other hand, recorded examples of absence of the trachea are very rare. Fritz (1933) and Sandison (1955) have each reported a case where the bronchi opened normally into a short lower segment of trachea from the roof of which a fistula passed to a normal oesophagus. In the infants described by Kessel and Smith (1953) and Hempel (1956) the conjoined bronchi connected by a fistula to the oesophagus whilst in those recorded by Walcher (1928), Benesova and Peter (1934) and Marek (1940) the bronchi opened directly into the oesophagus.…”

Section: Discussionmentioning

confidence: 99%

Atresia of the Oesophagus with Common Tracho-Oesophageal Tube

Welch¹,

Husain²

1958

Archives of Disease in Childhood

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The clinical picture and anatomical variants of oesophageal atresia are well known now that this condition can be treated surgically with fair hope of success. In about 90 % of cases there is a fistula connecting the lower segment ofthe oesophagus to the trachea and in some 9 % the atresia is present alone without a fistula. Amongst the remainder there are instances where the fistula passes from the upper pouch to the trachea, where there is a fistula connecting each segment to the trachea and where a fistula occurs without any atresia (Waterston, 1954). In the case of the infant described here, however,though in life the findings did not appear out of the ordinary, autopsy revealed a most unusual malformation and it is perhaps fortunate that the child's general condition precluded any attempt at surgical correction.Case History A male child, birth weight 6 lb., was born rapidly at home five weeks before term. The pregnancy had been uneventful and he was the third child of healthy parents, the mother's age being 23. Respiration could not be established and atresia of the oesophagus became apparent when a catheter could not be passed into the stomach. Intermittent gasping respiration followed mouth-to-mouth insufflation and the child was transferred to hospital where, following intra-tracheal oxygen, a more regular, but stertorous and rattling, respiration was established about two and a half hours after birth.The child remained limp and unresponsive, with intermittent cyanotic attacks and a low temperature. Numerous rales were audible all over the chest and the intestines filled with air. After some hours the intra-tracheal tube was removed but, as the child's condition and colour promptly deteriorated, it was reinserted, this time rather further than before. It was then noted that the condition remained poor until the tube was withdrawn a short way, but the significance of this was not appreciated until autopsy. After 36 hours, during which time the child never developed muscle tone or became responsive, the stertorous respirations became periodic and death followed at 48 hours.

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Eine seltene Mißbildung der oberen Luftwege

Cited by 14 publications

References 3 publications

Tracheal agenesis and associated malformations: A comparison with tracheoesophageal fistula and the VACTERL association

Tracheal agenesis and associated malformations: A comparison with tracheoesophageal fistula and the VACTERL association

Laryngeal Atresia

Atresia of the Oesophagus with Common Tracho-Oesophageal Tube

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