Abstract
A rare case of fibrosing mediastinitis from histoplasmosis with extrinsic compression of the right pulmonary artery is reported. A 41-year-old patient presented with worsening symptoms of cough, fever, migratory arthralgia, chest pain, and progressive dyspnea. The pulmonary artery involvement was suspected by transthoracic echo and was confirmed by transesophageal echo, CT scan of chest, and right heart catheterization. Diagnosis of histoplasmosis was confirmed by biopsy and serological tests. Patient has been free from symptoms of pulmonary stenosis for 4 years after successful pulmonary artery stenting.
| Original language | English |
|---|---|
| Journal | International Journal of Cardiology |
| Volume | 118 |
| Issue number | 3 |
| DOIs | |
| State | Published - Jun 12 2007 |
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All Science Journal Classification (ASJC) codes
- Cardiology and Cardiovascular Medicine
Cite this
Fibrosing mediastinitis presenting as pulmonary stenosis : Stenting works. / Satpathy, Ruby; Aguila, Virginia; Mohiuddin, Syed M.; Khan, Ijaz A.
In: International Journal of Cardiology, Vol. 118, No. 3, 12.06.2007.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Fibrosing mediastinitis presenting as pulmonary stenosis
T2 - Stenting works
AU - Satpathy, Ruby
AU - Aguila, Virginia
AU - Mohiuddin, Syed M.
AU - Khan, Ijaz A.
PY - 2007/6/12
Y1 - 2007/6/12
N2 - A rare case of fibrosing mediastinitis from histoplasmosis with extrinsic compression of the right pulmonary artery is reported. A 41-year-old patient presented with worsening symptoms of cough, fever, migratory arthralgia, chest pain, and progressive dyspnea. The pulmonary artery involvement was suspected by transthoracic echo and was confirmed by transesophageal echo, CT scan of chest, and right heart catheterization. Diagnosis of histoplasmosis was confirmed by biopsy and serological tests. Patient has been free from symptoms of pulmonary stenosis for 4 years after successful pulmonary artery stenting.
AB - A rare case of fibrosing mediastinitis from histoplasmosis with extrinsic compression of the right pulmonary artery is reported. A 41-year-old patient presented with worsening symptoms of cough, fever, migratory arthralgia, chest pain, and progressive dyspnea. The pulmonary artery involvement was suspected by transthoracic echo and was confirmed by transesophageal echo, CT scan of chest, and right heart catheterization. Diagnosis of histoplasmosis was confirmed by biopsy and serological tests. Patient has been free from symptoms of pulmonary stenosis for 4 years after successful pulmonary artery stenting.
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UR - http://www.scopus.com/inward/citedby.url?scp=34247619841&partnerID=8YFLogxK
U2 - 10.1016/j.ijcard.2007.01.030
DO - 10.1016/j.ijcard.2007.01.030
M3 - Article
VL - 118
JO - International Journal of Cardiology
JF - International Journal of Cardiology
SN - 0167-5273
IS - 3
ER -