Malformation lung cystic adenomatoidea

Introduction: Cystic adenomatoid malformation is an alteration of lung development caused by the replacement of the small airway and lung parenchyma by cysts. Objective: Describe a case with a diagnosis of cystic adenomatoid malformation. Case presentation: 16-year-old male adolescent, product of a pregnancy with low obstetric risk, normal delivery at 38.4 weeks, with a personal pathological history of bronchial asthma, surgery for glaucoma at age 13, surgery for umbilical hernia at 12 years old, no history of previous income. On this occasion he went to the emergency room due to having a dry, sporadic cough that had been going on for approximately 15 days. In addition to sometimes presenting pain in the tip of the side, an X-ray was performed, confirming a radiopaque image in the left lower lobe, deciding to admit him for better study and treatment. Conclusions: Cystic adenomatoid malformation is a rare anomaly, so it is important to keep in mind that any patient with symptoms and signs suggestive of this disease receives complete care to guarantee an early diagnosis. The role of radiological diagnosis is key to fully characterize MCPs. The characterization of the vascular contributions in the radiological report is of great importance for surgical planning.

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Publication Details

Journal
Multidisciplinar
Published
2025-04-20
DOI
https://doi.org/10.62486/agmu2025192
Primary Topic
Congenital Diaphragmatic Hernia Studies
Type
article
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article

Malformation lung cystic adenomatoidea

Adriel Herrero Díaz, Dionis Ruiz Reyes, Dania María García Rodríguez, Diana García Rodríguez et al.
Multidisciplinar
Congenital Diaphragmatic Hernia Studies
article

Malformation lung cystic adenomatoidea

Adriel Herrero Díaz, Dionis Ruiz Reyes, Dania María García Rodríguez, Diana García Rodríguez, Ileana Beatriz Quiroga-López
article en

Abstract

Introduction: Cystic adenomatoid malformation is an alteration of lung development caused by the replacement of the small airway and lung parenchyma by cysts. Objective: Describe a case with a diagnosis of cystic adenomatoid malformation. Case presentation: 16-year-old male adolescent, product of a pregnancy with low obstetric risk, normal delivery at 38.4 weeks, with a personal pathological history of bronchial asthma, surgery for glaucoma at age 13, surgery for umbilical hernia at 12 years old, no history of previous income. On this occasion he went to the emergency room due to having a dry, sporadic cough that had been going on for approximately 15 days. In addition to sometimes presenting pain in the tip of the side, an X-ray was performed, confirming a radiopaque image in the left lower lobe, deciding to admit him for better study and treatment. Conclusions: Cystic adenomatoid malformation is a rare anomaly, so it is important to keep in mind that any patient with symptoms and signs suggestive of this disease receives complete care to guarantee an early diagnosis. The role of radiological diagnosis is key to fully characterize MCPs. The characterization of the vascular contributions in the radiological report is of great importance for surgical planning.

MultidisciplinarVol. 3
Universidad de Ciencias Medicas (CR), Universidad Central "Marta Abreu" de las Villas (UCLV) (CU)
Openalex Percentile: Top 86%
Congenital Diaphragmatic Hernia Studies
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