Evidence map›Paper›PMID 42472247›Full record

ArticleCase reports in obstetrics and gynecology2026

Conservative Management on Antenatally Found Congenital Cystic Adenomatoid Malformation: A 1-Year Follow-Up Case Report.

Bambang Abimanyu, Muhammad Robyanoor Ahyadi Radaam, Ruth Widhiati Raharjo Putri, Yosef Dwi Cahyadi Salan, Hermin Sabarudin, Adek Yeary Wardhani, Yakob Togar

Abstract read
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Article in Case reports in obstetrics and gynecology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Bambang AbimanyuFaculty of Medicine and Health Sciences, Ulin Regional Hospital, Lambung Mangkurat University, Banjarmasin, Indonesia, unlam.ac.id.
Muhammad Robyanoor Ahyadi RadaamFaculty of Medicine and Health Sciences, Ulin Regional Hospital, Lambung Mangkurat University, Banjarmasin, Indonesia, unlam.ac.id.
Ruth Widhiati Raharjo PutriFaculty of Medicine and Health Sciences, Ulin Regional Hospital, Lambung Mangkurat University, Banjarmasin, Indonesia, unlam.ac.id.
Yosef Dwi Cahyadi SalanFaculty of Medicine and Health Sciences, Ulin Regional Hospital, Lambung Mangkurat University, Banjarmasin, Indonesia, unlam.ac.id.
Hermin SabarudinFaculty of Medicine and Health Sciences, Ulin Regional Hospital, Lambung Mangkurat University, Banjarmasin, Indonesia, unlam.ac.id.
Adek Yeary WardhaniFaculty of Medicine and Health Sciences, Ulin Regional Hospital, Lambung Mangkurat University, Banjarmasin, Indonesia, unlam.ac.id.
Yakob TogarFaculty of Medicine and Health Sciences, Ulin Regional Hospital, Lambung Mangkurat University, Banjarmasin, Indonesia, unlam.ac.id.ORCID https://orcid.org/0000-0001-6554-6379

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: We report a rare case of congenital cystic adenomatoid malformation (CCAM) diagnosed antenatally based on USG and postnatally based on babygram, CT scan, and chest x-ray. We follow up the baby up to 1 year of age. Method: This study is a retrospective case report describing the clinical presentation, diagnosis, and management of a single patient. Results: The patient is an outpatient clinic with a diagnosis of G2P1A0, gestational age 38-39 weeks with breech presentation, not in labor, and the fetus is suspected for CCAM. The patient was planned for termination with cesarean delivery. The patient was first diagnosed with CCAM based on antenatal USG examination: A cystic mass in the thorax region of the fetus measuring 1.5 cm was found. The baby was then born by CS in consideration of breech presentation. At birth, the baby had a good APGAR score of 7-8-9. The baby underwent a babygram at 2 days old, which showed a CPAM type III result; CT scan at 16 days old showed infected CPAM type I/CCAM. The baby has been observed for 1 year of life, and no signs of respiratory distress were found. The latest chest x-ray at 1 year of age showed left superior pulmonary cyst. Conclusion: CCAM can be diagnosed perinatally by ultrasound examination. Management of CCAM depends on the size of the lesion and whether significant respiratory distress is present in the newborn. In our case, the CCAM was established prenatally and postnatally; no signs of respiratory symptoms were found within 1 year of age.

Indexed as

case reportCCAMprenatal diagnosis

Identifiers

PMID42472247
PMCPMC13380031

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.