09 August 2021>: Articles
Autopsy Case of Pfeiffer Syndrome Type 2, a Phenotype of Fibroblast Growth Factor Receptor-Associated Craniosynostosis Syndromes, with Tracheal Cartilage Sleeve and Abnormal Hyperplasia of Bronchial Cartilages
Rare disease
Shin-ya Katsuragi A , Etsuko Hirose A , Yoshifumi Arai A , Yoshiro Otsuki C* , Shigeru Ohki B , Hiroshi Kobayashi ADOI: 10.12659/AJCR.932450
Am J Case Rep 2021; 22:e932450
Figure 4. (A) Geographically fused infarct is found in the spleen. (B) The splenic infarction (hematoxylin and eosin staining [H&E], ×40, inset: organized thrombus). (C) Renal cortex (H&E, ×100, inset: immature glomeruli).