Anat Cell Biol 2022; 55(2): 264-268
Published online June 30, 2022
Copyright © Korean Association of ANATOMISTS.
1Department of Pathology, ESIC Medical College & Super Specialty Hospital, Sanathnagar, Hyderabad (Telangana), 2Department of Anatomy, All India Institute of Medical Sciences, Bibinagar, Hyderabad (Telangana), India
Correspondence to:Rohini Motwani
Department of Anatomy, All India Institute of Medical Sciences, Bibinagar, Hyderabad (Telangana) 508126, India
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Congenital cystic adenomatoid malformation (CCAM) is a rare developmental dysplastic lesion that affects the fetal bronchial tree. Etiopathogenesis is still poorly understood. Most accepted view is that of abnormal branching of bronchioles during the period of morphogenesis. We observed a rare congenital anomaly of the lungs during fetal autopsy. Routine antenatal ultrasonography revealed multiple echolucent cysts in the right lung of the fetus. Thorough external and internal examination was followed by sectioning of each organ for histopathological examination. Histopathology of the right lung showed distortion of the parenchyma with dilated bronchioles. Multiple cysts lined by columnar epithelium along with loose intervening connective tissue were observed along with many congested and dilated blood vessels. Knowledge of congenital anomalies of the respiratory system would help clinicians to plan the management at a very early stage. Accurate fetal autopsy along with clinical data is important in evaluating fetal deaths and can help in reducing unexplained stillbirths.
Keywords: Congenital, Cystic adenomatoid, Embryology, Lung malformation
Congenital cystic adenomatoid malformations (CCAM) are rare cystic lesions of the lung due to developmental anomaly of the lungs. It is characterized by the presence of cystic intrathoracic masses formed by proliferative terminal respiratory bronchioles as well as decrease in the number of normal alveoli . CCAM affects 1 in 11,000 to 1 in 35,000 live births , with male predominance . CCAM was first reported by Chin and Tang in 1949 , and later, Stocker et al.  in 1977 gave its classification. We report a rare case of unilateral cystic malformation of the right lung of a 24-week fetus during autopsy. We anticipate that with this case report, we will be able to gain a better understanding of this congenital defect and can increase awareness about its importance.
A 30-year-old multigravida, at 24 weeks of gestation with gravida 3, parity 1, abortion 1 and live birth 1 (G3P1A1L1) with a previous history of intra uterine death due to some congenital anomaly (not known to the parents), presented to the obstetrics outpatient department for a routine antenatal visit. Routine ultrasound examination revealed a large cystic lesion within the right chest along with ventriculomegaly and ascites. The left lung was found to be normal. The fetal diaphragm and stomach were found in normal positions. The most likely diagnosis made was CCAM of the right lung. Due to the high possibility of pulmonary hypoplasia and nonimmune hydrops fetalis, the parents intended a medical termination of the pregnancy.
Following termination of pregnancy, a male fetus of weight 750-gram was received, along with an attached placenta and umbilical cord for autopsy, that was conducted at the Department of Pathology, ESIC Super Specialty Hospital in collaboration with the Department of Anatomy, ESIC Medical College and Hospital at Hyderabad. The fetus was then kept in 10% formalin, with a small niche given on the scalp and abdomen for effective perfusion into all spaces. External inspection revealed no anomalies. An “I” shaped incision was given, followed by complete evisceration. All the organs were carefully observed for any gross anomalies and then processed for histopathological examination (Fig. 1A). While all the organs were grossly normal, the right lung was observed to be flattened with distorted architecture and presence of multiple small cysts measuring less than 1 cm on the posterior aspect (Fig. 1B, C).
Histopathology revealed distorted lung parenchyma with dilated bronchioles. Multiple small cystic spaces were lined by simple columnar epithelium along with loose intervening connective tissue and the presence of congested and dilated blood vessels (Fig. 2). Other viscera were found normal according to gestational age. With the above given findings, a diagnosis of CCAM Stocker Type III was suggested.
CCAM is predominantly unilateral, affecting only one lobe of the lung. Left-sided CCAMs account for the bulk of antenatally diagnosed CCAMs . Data is minimal on bilateral CCAMs as there are very less number of case series reported . Bilateral lesions may be associated with an inherited predisposition to an underlying cell signaling abnormality, which may increase the likelihood of eventual malignant transformation in the CCAM or elsewhere in the lung  Prenatally diagnosed CCAMs have been linked to a wide range of perinatal mortality rates, ranging from 9% to 49% . We tried to compare the findings which are listed in Table 1 [8-11].
CCAMs are hamartomatous lesions that can affect any part of the fetal respiratory system, starting from the trachea to the alveoli. As the etiopathogenesis of CCAM is still unclear, various theories have been suggested, which include abnormal tissue proliferation , hyperplasia, dysplasia or metaplasia. There are four distinct phases of vertebrate lung development and maturation based on the anatomical changes that occur in lung architecture: pseudo-glandular (5–16 weeks), canalicular (16–26 weeks), saccular (26–36 weeks), and alveolar (36 weeks to maturity) (Table 2) . Studies suggest that the majority of CCAMs occurs during the pseudo glandular stage. The bronchial type of epithelium is arrested at this phase of lung development, resulting in CCAM disease types I–III, whereas the alveolar acinar type of epithelium is arrested later in weeks 22–36, resulting in CCAM pathology type IV .
The presence of normal alveoli on the periphery of the lesion but abnormal growth in the middle, implies failure of terminal bronchiole to canalize during second trimester, resulting a discontinuity of the conducting and the respiratory elements . Bronchoscopic and microscopic studies revealed that bronchial atresia is the primary defect that contributed to the development of CCAM . Between 5 and 16 weeks of pregnancy, the pseudoglandular, or branching phase of lung development occurs. It involves a plethora of spatially and temporally controlled signaling molecules that allow broad communication between the pulmonary epithelium and the mesenchyme.
HOXB5, which affects lung growth during branching morphogenesis, is significant gene that may influence the development of CCAM. Its expression is kept at a level that is appropriate for early lung development. In comparison to normal fetal lung or term CCAM tissue, CCAM that expanded faster, progressed to hydrops fetalis, and required in utero resection exhibited increased platelet derived growth factor (
Stocker in 1977, was the first to classify CCAM, based on the number and size of the cyst and histopathological findings [2, 5]. CCAM classification schemes have changed over time, and there are now five primary categories based on the embryologic stage of genesis and histologic features that are presented in Table 3 and Fig. 3. According to this classification, we report a case of Type III CCAM.
CCAM has been linked to other congenital anomalies such as cardiovascular malformations, lung hypoplasia, congenital diaphragmatic hernia, extralobular sequestration, hydrocephalus, bilateral renal agenesia/dysgenesis, gastrointestinal atresia, polyhydramnios, mediastinal shift, and particularly nonimmune fetal hydrops . In the present case, no anomaly was observed, but antenatal ultrasonography revealed ascites, which could indicate the onset of hydrops.
Because lung disease is a prevalent cause of fetal death, clinicians should be aware of congenital defects of the respiratory system so that treatment can be planned at an early stage. CCAM is most commonly diagnosed in the antenatal or neonatal period. Serial ultrasonographic evaluation, fetal lung mass size, and fetal echocardiography are required for antenatal diagnosis of cases. To achieve the best results, very attentive monitoring during the perinatal period is required. Accurate fetal autopsy combined with clinical data is critical, and it can help reduce unexplained stillbirths.
We would like to express our gratitude to the parents of the fetus who chose to donate their fetus to the pathology department for research.
Conceptualization: RM. Data acquisition: RM, RG. Data analysis or interpretation: RM. Drafting of the manuscript: RM. Critical revision of the manuscript: RM, RG. Approval of the final version of the manuscript: all authors.
No potential conflict of interest relevant to this article was reported.