| Literature DB >> 27531150 |
Masahiko Sumi1, Kazumi Norose2, Kenji Hikosaka2, Hiroko Kaiume3, Wataru Takeda3, Takehiko Kirihara3, Taro Kurihara3, Keijiro Sato3, Toshimitsu Ueki3, Yuki Hiroshima3, Hiroshi Kuraishi4, Masahide Watanabe5, Hikaru Kobayashi3.
Abstract
The prognosis of pulmonary toxoplasmosis, including disseminated toxoplasmosis involving the lungs, following hematopoietic stem cell transplantation (HSCT) is extremely poor due to the difficulties associated with early diagnosis and the rapidly progressive deterioration of multiorgan function. In our institution, we identified nine cases of toxoplasmosis, representing incidences of 2.2 and 19.6 % among all HSCT recipients and seropositive HSCT recipients, respectively. Of the patients with toxoplasmosis, six had pulmonary toxoplasmosis. Chest computed tomography (CT) findings revealed centrilobular, patchy ground-glass opacities (n = 3), diffuse ground-glass opacities (n = 2), ground-glass opacities with septal thickening (n = 1), and marked pleural effusion (n = 1). All cases died, except for one with suspected pulmonary toxoplasmosis who was diagnosed by a polymerase chain reaction assay 2 days after the onset of symptoms. In pulmonary toxoplasmosis, CT findings are non-specific and may mimic pulmonary congestion, atypical pneumonia, viral pneumonitis, and bronchopneumonia. Early diagnosis and treatment is crucial for overcoming this serious infectious complication. Pulmonary toxoplasmosis should be considered during differential diagnosis in a recipient with otherwise unexplained signs of infection and CT findings with ground-glass opacities, regardless of the distribution.Entities:
Keywords: Disseminated toxoplasmosis; Pulmonary toxoplasmosis; Stem cell transplantation; Toxoplasma gondii
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Year: 2016 PMID: 27531150 DOI: 10.1007/s12185-016-2077-0
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490