Isolated unilateral absence of the pulmonary artery (IUAPA) presenting with progressive interstitial shadows: A case report

被引:0
|
作者
Takeshige, Tomohito [1 ,2 ,3 ]
Koyama, Ryo [1 ]
Kohmaru, Makiko [1 ]
Akimoto, Takashi [1 ]
Watanabe, Junko [1 ]
Yae, Toshifumi [1 ]
Kido, Kenji [1 ]
Takahashi, Kazuhisa [2 ,3 ]
机构
[1] Juntendo Univ, Nerima Hosp, Dept Resp Med, Tokyo, Japan
[2] Juntendo Univ, Fac Med, Dept Resp Med, 3-1-3Hongo,Bunkyo Ku, Tokyo 1138431, Japan
[3] Grad Sch Med, 3-1-3 Hongo,Bunkyo Ku, Tokyo 1138431, Japan
来源
RESPIROLOGY CASE REPORTS | 2024年 / 12卷 / 10期
关键词
interstitial change; interstitial lung disease (ILD); interstitial shadow; isolated unilateral absence of the pulmonary artery (IUAPA); unilateral absence of pulmonary artery (UAPA);
D O I
10.1002/rcr2.70048
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Unilateral absence of the pulmonary artery (UAPA) is a rare congenital condition. When UAPA occurs without associated congenital heart disease, it is referred to as isolated unilateral absence of the pulmonary artery (IUAPA). IUAPA is frequently not diagnosed until adulthood. A 61-year-old female patient presented with right chest pain and a worsening interstitial shadow over 9 years. Contrast-enhanced computed tomography revealed the absence of blood flow from the pulmonary artery in the right lung, leading to the diagnosis of IUAPA. In this case, the diagnosis of UAPA was established after approximately 40 years. This case underscores the importance of identifying vascular abnormalities to differentiate this condition in patients presenting with nonspecific symptoms and interstitial shadows.
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页数:4
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