Congenital Cystic Adenomatoid Malformation: Case Report

Özdemir, Özmert Ma; Ergin, Hacer; Karaca, Abdullah; Koltuksuz, Uğur; Karabulut, Nevzat; Yalçin, Nagihan

doi:10.5336/medsci.2008-7564

Turkiye Klinikleri J Med Sci

2010

DOI: 10.5336/medsci.2008-7564

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Congenital Cystic Adenomatoid Malformation: Case Report

Özmert Ma Özdemir¹,

Hacer Ergin²,

Abdullah Karaca³

et al.

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Cited by 2 publications

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Doğum öncesi dönemde tanı alan doğuştan kistik adenomatoid malformasyon: olgu sunumu

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2012

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Sum maryCongenital cystic adenomatoid malformation is a hamartomatous malformation accepted as an embryonic differentiation anomaly characterized by replacement of normal lung parenchyma by cysts of various sizes and numbers. The primigravid presented on her 24 th week with the ultrasound findings of a fetus with unilateral cyts in left lung. Thoracoamniotic shunting was inserted at a mean gestational age of 24. Patient was born due to premature rupture of membranes and preterm delivery at a mean gestational age of 25. We present a case of congenital cystic adenomatoid malformation type I in a newborn who died in twelve hours after birth and discuss about pre-and postnatal diagnostic and therapeutic possibilities. (Turk Arch Ped 2012; 47: 290-293)

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Doğum öncesi dönemde tanı alan doğuştan kistik adenomatoid malformasyon: olgu sunumu

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2012

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Congenital pulmonary airway malformation type 2: a case report with review of the literature

Tastekin¹,

Usta²,

Kaynar³

et al. 2014

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A congenital pulmonary airway malformation is a rare disorder of the pulmonary airway and a hamartomatous mass of disorganized lung tissues with various degrees of cystic change. A 20-year-old pregnant woman who did not have previous clinical follow-up during her pregnancy visited the gynecology department for her first check on the 19th week of gestation. The sonogram, showed severe hydrops fetalis. Laboratory findings were consistent with non-immune hydrops fetalis. Medical abortion was performed and the fetus was sent to our department for a complete fetal autopsy. Macroscopically, whole parts of the fetus had striking oedema. Massive pleural and peritoneal effusions were seen on dissection. The left lung filled the whole thoracic cavity. The heart was displaced to the right and the right lung was compressed. Microscopically, the left lung mass showed dilated bronchiole-like structures (1-20 mm) that were lined with ciliated columnar cells without any intervening mucinous cells. The subepithelial stroma contained thin, interrupted smooth muscle fibers and elastic connective tissue without cartilage plates. Our case is a very good example of non-immune hydrops fetalis associated with congenital pulmonary airway malformation type 2. Prenatal clinical and ultrasonographic follow-ups during pregnancy are very important for early diagnosis of congenital malformations.

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Congenital Cystic Adenomatoid Malformation: Case Report

Cited by 2 publications

References 11 publications

Doğum öncesi dönemde tanı alan doğuştan kistik adenomatoid malformasyon: olgu sunumu

Doğum öncesi dönemde tanı alan doğuştan kistik adenomatoid malformasyon: olgu sunumu

Congenital pulmonary airway malformation type 2: a case report with review of the literature

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