2014
DOI: 10.5152/ttd.2013.37
|View full text |Cite
|
Sign up to set email alerts
|

Pulmonary Alveolar Microlithiasis and Preterm Delivery: A Case Report

Abstract: Pulmonary alveolar microlithiasis (PAM) is a rare, chronic lung disease characterised by extensive intra-alveolar calcium and phosphorus deposition throughout the parenchyma of both lungs. The etiology and pathogenesis of the disease is unclear. In our case, PAM with pregnancy was presented; respiratory distress had been observed during the first and second trimesters. In the following weeks, premature activity developed and the foetus was not able to stay alive. This is the third case of PAM in pregnancy desc… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2015
2015
2021
2021

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(2 citation statements)
references
References 8 publications
0
2
0
Order By: Relevance
“…In such cases, the child is usually delivered prematurely by Caesarean section. [3] and in some cases full term delivery has been reported. It should be considered that this disease with no effective treatment may rarely progress into end-stage pulmonary disease due to conditions which alter pulmonary functions, such as pregnancy.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…In such cases, the child is usually delivered prematurely by Caesarean section. [3] and in some cases full term delivery has been reported. It should be considered that this disease with no effective treatment may rarely progress into end-stage pulmonary disease due to conditions which alter pulmonary functions, such as pregnancy.…”
Section: Discussionmentioning
confidence: 99%
“…[2] Familial cases predominantly affect females, whereas sporadic cases are usually seen in males. [3] The etiopathogenesis is unclear. The present implication for intraalveolar microlith deposition is: Na Pi co-transporter (Npt2b) deletion following defective mutation in the gene "SLC34A2" (In short arm of chromosome 4) in the apical portions of alveolar type II cells.…”
Section: Introductionmentioning
confidence: 99%