2017
DOI: 10.4322/acr.2017.027
|View full text |Cite
|
Sign up to set email alerts
|

Pulmonary placental transmogrification associated with adenocarcinoma of the lung: A case report with a comprehensive review of the literature

Abstract: Pulmonary placental transmogrification (PT) is a rare entity with less than 40 cases reported in the literature. Most reported cases are associated with either bullous emphysema or with pulmonary fibrochondromatous hamartomas. We present only the second case of PT associated with adenocarcinoma of the lung. A 67-year-old female with multiple chronic medical ailments presented with shortness of breath and was found to have a 6-cm mass in the upper lobe of her right lung. A computed tomography (CT) guided core b… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4

Citation Types

0
13
0

Year Published

2018
2018
2024
2024

Publication Types

Select...
6

Relationship

1
5

Authors

Journals

citations
Cited by 8 publications
(13 citation statements)
references
References 15 publications
0
13
0
Order By: Relevance
“…It has never been mentioned in a pediatric patient and previously described age ranges were in the third to seventh decades of life. Radiographically, it can appear as bullous emphysema, thin‐walled cystic lesions, or nodular lesions . Definitive diagnosis is obtained through histopathology, showing papillary structures resembling placental chorionic villi.…”
Section: Discussionmentioning
confidence: 99%
See 3 more Smart Citations
“…It has never been mentioned in a pediatric patient and previously described age ranges were in the third to seventh decades of life. Radiographically, it can appear as bullous emphysema, thin‐walled cystic lesions, or nodular lesions . Definitive diagnosis is obtained through histopathology, showing papillary structures resembling placental chorionic villi.…”
Section: Discussionmentioning
confidence: 99%
“…Definitive diagnosis is obtained through histopathology, showing papillary structures resembling placental chorionic villi. Treatment is resection of the affected areas and is considered curative except in two cases that described malignant transformation . Resection usually results in improvement of respiratory symptoms and lung function testing.…”
Section: Discussionmentioning
confidence: 99%
See 2 more Smart Citations
“…Similarly, the clinical cases are also of great educational value. Only within the last volume of the journal, there were some clinical case reports of rare entities including, undifferentiated carcinoma of the pancreas with osteoclast-like giant cells, 18 concurrent BRAF V600E mutation driven hairy cell leukemia and melanoma, 19 spontaneous regression of a pulmonary adenocarcinoma, 20 phosphaturic mesenchymal tumor, 21 perianal Langerhans cell histiocytosis, 22 pulmonary placental transmogrification, 23 native-valve endocarditis caused by Achromobacter xylosoxidans , 24 centronuclear myopathy 25 and migrainous infarction. 26 Even if the cases are not rare entities, the intrigue discussions are always worth reading.…”
mentioning
confidence: 99%